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1. Whole brain MP2RAGE-based mapping of the longitudinal relaxation time at 9.4T

Author: Hagberg, G E, Bause, J, Ethofer, T, Ehses, P, Dresler, T, Herbert, C, Pohmann, R, Shajan, G, Fallgatter, A, Pavlova, M A, and Scheffler, K
Published: 2017
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2. Analysis of structural brain asymmetries in attention-deficit/hyperactivity disorder in 39 datasets

Author: Postema, M.C., Hoogman, M., Ambrosino, S., Asherson, P., Banaschewski, T., Bandeira, C.E., Baranov, A., Bau, C.H.D., Baumeister, S., Baur-Streubel, R., Bellgrove, Mark A., Biederman, J., Bralten, J.B., Brandeis, D., Brem, S., Buitelaar, J.K., Busatto, G.F., Castellanos, F.X., Cercignani, M., Chaim-Avancini, T.M., Chantiluke, K.C., Christakou, A., Coghill, D., Conzelmann, A., Cubillo, A.I., Cupertino, R.B., Zeeuw, P. de, Doyle, A.E., Durston, S., Earl, E.A., Epstein, J.N., Ethofer, T., Fair, D.A., Fallgatter, A.J., Faraone, S.V, Frodl, T., Gabel, M.C., Gogberashvili, T., Grevet, E.H., Haavik, J., Harrison, N.A., Hartman, Catharina A., Heslenfeld, D.J., Hoekstra, P.J., Hohmann, S., Høvik, M.F., Jernigan, T.L., Kardatzki, B., Karkashadze, G., Kelly, C., Kohls, G., Konrad, K., Kuntsi, J., Lazaro, L., Lera-Miguel, S., Lesch, K.P., Louza, M.R., Lundervold, A.J., Malpas, C.B., Mattos, P., McCarthy, H., Namazova-Baranova, L., Nicolau, R., Nigg, J.T., Novotny, S.E., Weiss, E. Oberwelland, Tuura, R.L. O'Gorman, Oosterlaan, J., Oranje, B., Paloyelis, Y., Pauli, P., Picon, F.A., Plessen, K.J., Ramos-Quiroga, J.A., Reif, A., Reneman, L., Rosa, P.G., Rubia, K., Schrantee, A., Schweren, L.J., Seitz, J., Shaw, P., Silk, T.J., Skokauskas, N., Vila, J.C. Soliva, Stevens, M.C., Sudre, G., Tamm, L., Tovar-Moll, F., Erp, T.G. van, Vance, A., Vilarroya, O., Vives-Gilabert, Y., Polier, G.G. von, Walitza, S., Yoncheva, Y.N., Zanetti, M.V., Ziegler, G.C., Glahn, D.C., Fisher, S.E., Franke, B., Francks, C., Postema, M.C., Hoogman, M., Ambrosino, S., Asherson, P., Banaschewski, T., Bandeira, C.E., Baranov, A., Bau, C.H.D., Baumeister, S., Baur-Streubel, R., Bellgrove, Mark A., Biederman, J., Bralten, J.B., Brandeis, D., Brem, S., Buitelaar, J.K., Busatto, G.F., Castellanos, F.X., Cercignani, M., Chaim-Avancini, T.M., Chantiluke, K.C., Christakou, A., Coghill, D., Conzelmann, A., Cubillo, A.I., Cupertino, R.B., Zeeuw, P. de, Doyle, A.E., Durston, S., Earl, E.A., Epstein, J.N., Ethofer, T., Fair, D.A., Fallgatter, A.J., Faraone, S.V, Frodl, T., Gabel, M.C., Gogberashvili, T., Grevet, E.H., Haavik, J., Harrison, N.A., Hartman, Catharina A., Heslenfeld, D.J., Hoekstra, P.J., Hohmann, S., Høvik, M.F., Jernigan, T.L., Kardatzki, B., Karkashadze, G., Kelly, C., Kohls, G., Konrad, K., Kuntsi, J., Lazaro, L., Lera-Miguel, S., Lesch, K.P., Louza, M.R., Lundervold, A.J., Malpas, C.B., Mattos, P., McCarthy, H., Namazova-Baranova, L., Nicolau, R., Nigg, J.T., Novotny, S.E., Weiss, E. Oberwelland, Tuura, R.L. O'Gorman, Oosterlaan, J., Oranje, B., Paloyelis, Y., Pauli, P., Picon, F.A., Plessen, K.J., Ramos-Quiroga, J.A., Reif, A., Reneman, L., Rosa, P.G., Rubia, K., Schrantee, A., Schweren, L.J., Seitz, J., Shaw, P., Silk, T.J., Skokauskas, N., Vila, J.C. Soliva, Stevens, M.C., Sudre, G., Tamm, L., Tovar-Moll, F., Erp, T.G. van, Vance, A., Vilarroya, O., Vives-Gilabert, Y., Polier, G.G. von, Walitza, S., Yoncheva, Y.N., Zanetti, M.V., Ziegler, G.C., Glahn, D.C., Fisher, S.E., Franke, B., and Francks, C.
Abstract: Item does not contain fulltext, OBJECTIVE: Some studies have suggested alterations of structural brain asymmetry in attention-deficit/hyperactivity disorder (ADHD), but findings have been contradictory and based on small samples. Here, we performed the largest ever analysis of brain left-right asymmetry in ADHD, using 39 datasets of the ENIGMA consortium. METHODS: We analyzed asymmetry of subcortical and cerebral cortical structures in up to 1,933 people with ADHD and 1,829 unaffected controls. Asymmetry Indexes (AIs) were calculated per participant for each bilaterally paired measure, and linear mixed effects modeling was applied separately in children, adolescents, adults, and the total sample, to test exhaustively for potential associations of ADHD with structural brain asymmetries. RESULTS: There was no evidence for altered caudate nucleus asymmetry in ADHD, in contrast to prior literature. In children, there was less rightward asymmetry of the total hemispheric surface area compared to controls (t = 2.1, p = .04). Lower rightward asymmetry of medial orbitofrontal cortex surface area in ADHD (t = 2.7, p = .01) was similar to a recent finding for autism spectrum disorder. There were also some differences in cortical thickness asymmetry across age groups. In adults with ADHD, globus pallidus asymmetry was altered compared to those without ADHD. However, all effects were small (Cohen's d from -0.18 to 0.18) and would not survive study-wide correction for multiple testing. CONCLUSION: Prior studies of altered structural brain asymmetry in ADHD were likely underpowered to detect the small effects reported here. Altered structural asymmetry is unlikely to provide a useful biomarker for ADHD, but may provide neurobiological insights into the trait.
Published: 2021

3. Virtual histology of cortical thickness and shared neurobiology in 6 psychiatric disorders

Author: Patel, Y, Parker, N, Shin, J, Howard, D, French, L, Thomopoulos, SI, Pozzi, E, Abe, Y, Abé, C, Anticevic, A, Alda, M, Aleman, A, Alloza, C, Alonso-Lana, S, Ameis, SH, Anagnostou, E, McIntosh, AA, Arango, C, Arnold, PD, Asherson, P, Assogna, F, Auzias, G, Ayesa-Arriola, R, Bakker, G, Banaj, N, Banaschewski, T, Bandeira, CE, Baranov, A, Bargalló, N, Bau, CHD, Baumeister, S, Baune, BT, Bellgrove, MA, Benedetti, F, Bertolino, A, Boedhoe, PSW, Boks, M, Bollettini, I, Del Mar Bonnin, C, Borgers, T, Borgwardt, S, Brandeis, D, Brennan, BP, Bruggemann, JM, Bülow, R, Busatto, GF, Calderoni, S, Calhoun, VD, Calvo, R, Canales-Rodríguez, EJ, Cannon, DM, Carr, VJ, Cascella, N, Cercignani, M, Chaim-Avancini, TM, Christakou, A, Coghill, D, Conzelmann, A, Crespo-Facorro, B, Cubillo, AI, Cullen, KR, Cupertino, RB, Daly, E, Dannlowski, U, Davey, CG, Denys, D, Deruelle, C, Di Giorgio, A, Dickie, EW, Dima, D, Dohm, K, Ehrlich, S, Ely, BA, Erwin-Grabner, T, Ethofer, T, Fair, DA, Fallgatter, AJ, Faraone, SV, Fatjó-Vilas, M, Fedor, JM, Fitzgerald, KD, Ford, JM, Frodl, T, Fu, CHY, Fullerton, JM, Gabel, MC, Glahn, DC, Roberts, G, Gogberashvili, T, Goikolea, JM, Gotlib, IH, Goya-Maldonado, R, Grabe, HJ, Green, MJ, Grevet, EH, Groenewold, NA, Grotegerd, D, Gruber, O, Gruner, P, Guerrero-Pedraza, A, Silk, Timothy, Patel, Y, Parker, N, Shin, J, Howard, D, French, L, Thomopoulos, SI, Pozzi, E, Abe, Y, Abé, C, Anticevic, A, Alda, M, Aleman, A, Alloza, C, Alonso-Lana, S, Ameis, SH, Anagnostou, E, McIntosh, AA, Arango, C, Arnold, PD, Asherson, P, Assogna, F, Auzias, G, Ayesa-Arriola, R, Bakker, G, Banaj, N, Banaschewski, T, Bandeira, CE, Baranov, A, Bargalló, N, Bau, CHD, Baumeister, S, Baune, BT, Bellgrove, MA, Benedetti, F, Bertolino, A, Boedhoe, PSW, Boks, M, Bollettini, I, Del Mar Bonnin, C, Borgers, T, Borgwardt, S, Brandeis, D, Brennan, BP, Bruggemann, JM, Bülow, R, Busatto, GF, Calderoni, S, Calhoun, VD, Calvo, R, Canales-Rodríguez, EJ, Cannon, DM, Carr, VJ, Cascella, N, Cercignani, M, Chaim-Avancini, TM, Christakou, A, Coghill, D, Conzelmann, A, Crespo-Facorro, B, Cubillo, AI, Cullen, KR, Cupertino, RB, Daly, E, Dannlowski, U, Davey, CG, Denys, D, Deruelle, C, Di Giorgio, A, Dickie, EW, Dima, D, Dohm, K, Ehrlich, S, Ely, BA, Erwin-Grabner, T, Ethofer, T, Fair, DA, Fallgatter, AJ, Faraone, SV, Fatjó-Vilas, M, Fedor, JM, Fitzgerald, KD, Ford, JM, Frodl, T, Fu, CHY, Fullerton, JM, Gabel, MC, Glahn, DC, Roberts, G, Gogberashvili, T, Goikolea, JM, Gotlib, IH, Goya-Maldonado, R, Grabe, HJ, Green, MJ, Grevet, EH, Groenewold, NA, Grotegerd, D, Gruber, O, Gruner, P, Guerrero-Pedraza, A, and Silk, Timothy
Published: 2021

4. Characterizing neuroanatomic heterogeneity in people with and without ADHD based on subcortical brain volumes

Author: Li, T, van Rooij, D, Roth Mota, N, Buitelaar, JK, Hoogman, M, Arias Vasquez, A, Franke, B, Ambrosino, S, Banaschewski, T, Bandeira, CE, Bau, CHD, Baumeister, S, Baur-Streubel, R, Bellgrove, MA, Biederman, J, Bralten, J, Bramati, IE, Brandeis, D, Berm, S, Busatto, GF, Calvo, A, Castellanos, FX, Cercignani, M, Chantiluke, KC, Christakou, A, Coghill, D, Conzelmann, A, Cubillo, AI, Cupertino, RB, de Zeeuw, P, Durston, S, Earl, EA, Epstein, JN, Ethofer, T, Fallgatter, AJ, Fair, DA, Faraone, SV, Frodl, T, Gabel, MC, Gogberashvili, T, Grevet, EH, Haavik, J, Harrison, NA, Hartman, CA, Heslenfeld, DJ, Hoekstra, PJ, Høvik, MF, Jahanshad, N, Kardatzki, B, Karkashadze, G, Kelly, C, Kohls, G, Konrad, K, Kuntsi, J, Lazaro, L, Lera-Miguel, S, Lesch, KP, Louza, MR, Lundervold, AJ, Malpas, CB, Mattos, P, McCarthy, H, Nicolau, R, Nigg, JT, O'Gorman Tuura, RL, Oosterlaan, J, Oranje, B, Paloyelis, Y, Pauli, P, Picon, FA, Plessen, KJ, Ramos-Quiroga, JA, Reif, A, Reneman, L, Rosa, PGP, Rubia, K, Schrantee, A, Schweren, LJS, Seitz, J, Shaw, P, Silk, Tim, Skokauskas, N, Carlos Soliva Vila, J, Soloveva, A, Stevens, MC, Sudre, G, Tamm, L, Thompson, PM, Tovar-Moll, F, van Erp, TGM, Vance, A, Vilarroya, O, Vives-Gilabert, Y, von Polier, GG, Walitza, S, Yoncheva, YN, Zanetti, MV, Ziegler, GC, Anikin, A, Asherson, P, Li, T, van Rooij, D, Roth Mota, N, Buitelaar, JK, Hoogman, M, Arias Vasquez, A, Franke, B, Ambrosino, S, Banaschewski, T, Bandeira, CE, Bau, CHD, Baumeister, S, Baur-Streubel, R, Bellgrove, MA, Biederman, J, Bralten, J, Bramati, IE, Brandeis, D, Berm, S, Busatto, GF, Calvo, A, Castellanos, FX, Cercignani, M, Chantiluke, KC, Christakou, A, Coghill, D, Conzelmann, A, Cubillo, AI, Cupertino, RB, de Zeeuw, P, Durston, S, Earl, EA, Epstein, JN, Ethofer, T, Fallgatter, AJ, Fair, DA, Faraone, SV, Frodl, T, Gabel, MC, Gogberashvili, T, Grevet, EH, Haavik, J, Harrison, NA, Hartman, CA, Heslenfeld, DJ, Hoekstra, PJ, Høvik, MF, Jahanshad, N, Kardatzki, B, Karkashadze, G, Kelly, C, Kohls, G, Konrad, K, Kuntsi, J, Lazaro, L, Lera-Miguel, S, Lesch, KP, Louza, MR, Lundervold, AJ, Malpas, CB, Mattos, P, McCarthy, H, Nicolau, R, Nigg, JT, O'Gorman Tuura, RL, Oosterlaan, J, Oranje, B, Paloyelis, Y, Pauli, P, Picon, FA, Plessen, KJ, Ramos-Quiroga, JA, Reif, A, Reneman, L, Rosa, PGP, Rubia, K, Schrantee, A, Schweren, LJS, Seitz, J, Shaw, P, Silk, Tim, Skokauskas, N, Carlos Soliva Vila, J, Soloveva, A, Stevens, MC, Sudre, G, Tamm, L, Thompson, PM, Tovar-Moll, F, van Erp, TGM, Vance, A, Vilarroya, O, Vives-Gilabert, Y, von Polier, GG, Walitza, S, Yoncheva, YN, Zanetti, MV, Ziegler, GC, Anikin, A, and Asherson, P
Published: 2021

5. Evidence for similar structural brain anomalies in youth and adult attention-deficit/hyperactivity disorder: a machine learning analysis

Author: Zhang-James, Y, Helminen, EC, Liu, J, Busatto, GF, Calvo, A, Cercignani, M, Chaim-Avancini, TM, Gabel, MC, Harrison, NA, Lazaro, L, Lera-Miguel, S, Louza, MR, Nicolau, R, Rosa, PGP, Schulte-Rutte, M, Zanetti, MV, Ambrosino, S, Asherson, P, Banaschewski, T, Baranov, A, Baumeister, S, Baur-Streubel, R, Bellgrove, MA, Biederman, J, Bralten, J, Bramati, IE, Brandeis, D, Brem, S, Buitelaar, JK, Castellanos, FX, Chantiluke, KC, Christakou, A, Coghill, D, Conzelmann, A, Cubillo, AI, Dale, AM, de Zeeuw, P, Doyle, AE, Durston, S, Earl, EA, Epstein, JN, Ethofer, T, Fair, DA, Fallgatter, AJ, Frodl, T, Gogberashvili, T, Haavik, J, Hartman, CA, Heslenfeld, DJ, Hoekstra, PJ, Hohmann, S, Høvik, MF, Jahanshad, N, Jernigan, TL, Kardatzki, B, Karkashadze, G, Kelly, C, Kohls, G, Konrad, K, Kuntsi, J, Lesch, KP, Lundervold, AJ, Malpas, CB, Mattos, P, McCarthy, H, Mehta, MA, Namazova-Baranova, L, Nigg, JT, Novotny, SE, O’Gorman Tuura, RL, Weiss, EO, Oosterlaan, J, Oranje, B, Paloyelis, Y, Pauli, P, Plessen, KJ, Ramos-Quiroga, JA, Reif, A, Reneman, L, Rubia, K, Schrantee, A, Schwarz, L, Schweren, LJS, Seitz, J, Shaw, P, Silk, Timothy, Skokauskas, N, Vila, JCS, Stevens, MC, Sudre, G, Tamm, L, Thompson, PM, Tovar-Moll, F, van Erp, TGM, Vance, A, Vilarroya, O, Vives-Gilabert, Y, von Polier, GG, Walitza, S, Yoncheva, YN, Zhang-James, Y, Helminen, EC, Liu, J, Busatto, GF, Calvo, A, Cercignani, M, Chaim-Avancini, TM, Gabel, MC, Harrison, NA, Lazaro, L, Lera-Miguel, S, Louza, MR, Nicolau, R, Rosa, PGP, Schulte-Rutte, M, Zanetti, MV, Ambrosino, S, Asherson, P, Banaschewski, T, Baranov, A, Baumeister, S, Baur-Streubel, R, Bellgrove, MA, Biederman, J, Bralten, J, Bramati, IE, Brandeis, D, Brem, S, Buitelaar, JK, Castellanos, FX, Chantiluke, KC, Christakou, A, Coghill, D, Conzelmann, A, Cubillo, AI, Dale, AM, de Zeeuw, P, Doyle, AE, Durston, S, Earl, EA, Epstein, JN, Ethofer, T, Fair, DA, Fallgatter, AJ, Frodl, T, Gogberashvili, T, Haavik, J, Hartman, CA, Heslenfeld, DJ, Hoekstra, PJ, Hohmann, S, Høvik, MF, Jahanshad, N, Jernigan, TL, Kardatzki, B, Karkashadze, G, Kelly, C, Kohls, G, Konrad, K, Kuntsi, J, Lesch, KP, Lundervold, AJ, Malpas, CB, Mattos, P, McCarthy, H, Mehta, MA, Namazova-Baranova, L, Nigg, JT, Novotny, SE, O’Gorman Tuura, RL, Weiss, EO, Oosterlaan, J, Oranje, B, Paloyelis, Y, Pauli, P, Plessen, KJ, Ramos-Quiroga, JA, Reif, A, Reneman, L, Rubia, K, Schrantee, A, Schwarz, L, Schweren, LJS, Seitz, J, Shaw, P, Silk, Timothy, Skokauskas, N, Vila, JCS, Stevens, MC, Sudre, G, Tamm, L, Thompson, PM, Tovar-Moll, F, van Erp, TGM, Vance, A, Vilarroya, O, Vives-Gilabert, Y, von Polier, GG, Walitza, S, and Yoncheva, YN
Published: 2021

6. Analysis of structural brain asymmetries in attention-deficit/hyperactivity disorder in 39 datasets

Author: Postema, MC, Hoogman, M, Ambrosino, S, Asherson, P, Banaschewski, T, Bandeira, CE, Baranov, A, Bau, CHD, Baumeister, S, Baur-Streubel, R, Bellgrove, MA, Biederman, J, Bralten, J, Brandeis, D, Brem, S, Buitelaar, JK, Busatto, GF, Castellanos, FX, Cercignani, M, Chaim-Avancini, TM, Chantiluke, KC, Christakou, A, Coghill, D, Conzelmann, A, Cubillo, AI, Cupertino, RB, de Zeeuw, P, Doyle, AE, Durston, S, Earl, EA, Epstein, JN, Ethofer, T, Fair, DA, Fallgatter, AJ, Faraone, SV, Frodl, T, Gabel, MC, Gogberashvili, T, Grevet, EH, Haavik, J, Harrison, NA, Hartman, CA, Heslenfeld, DJ, Hoekstra, PJ, Hohmann, S, Høvik, MF, Jernigan, TL, Kardatzki, B, Karkashadze, G, Kelly, C, Kohls, G, Konrad, K, Kuntsi, J, Lazaro, L, Lera-Miguel, S, Lesch, KP, Louza, MR, Lundervold, AJ, Malpas, CB, Mattos, P, McCarthy, H, Namazova-Baranova, L, Nicolau, R, Nigg, JT, Novotny, SE, Oberwelland Weiss, E, O'Gorman Tuura, RL, Oosterlaan, J, Oranje, B, Paloyelis, Y, Pauli, P, Picon, FA, Plessen, KJ, Ramos-Quiroga, JA, Reif, A, Reneman, L, Rosa, PGP, Rubia, K, Schrantee, A, Schweren, LJS, Seitz, J, Shaw, P, Silk, Tim, Skokauskas, N, Soliva Vila, JC, Stevens, MC, Sudre, G, Tamm, L, Tovar-Moll, F, van Erp, TGM, Vance, A, Vilarroya, O, Vives-Gilabert, Y, von Polier, GG, Walitza, S, Yoncheva, YN, Zanetti, MV, Ziegler, GC, Glahn, DC, Jahanshad, N, Postema, MC, Hoogman, M, Ambrosino, S, Asherson, P, Banaschewski, T, Bandeira, CE, Baranov, A, Bau, CHD, Baumeister, S, Baur-Streubel, R, Bellgrove, MA, Biederman, J, Bralten, J, Brandeis, D, Brem, S, Buitelaar, JK, Busatto, GF, Castellanos, FX, Cercignani, M, Chaim-Avancini, TM, Chantiluke, KC, Christakou, A, Coghill, D, Conzelmann, A, Cubillo, AI, Cupertino, RB, de Zeeuw, P, Doyle, AE, Durston, S, Earl, EA, Epstein, JN, Ethofer, T, Fair, DA, Fallgatter, AJ, Faraone, SV, Frodl, T, Gabel, MC, Gogberashvili, T, Grevet, EH, Haavik, J, Harrison, NA, Hartman, CA, Heslenfeld, DJ, Hoekstra, PJ, Hohmann, S, Høvik, MF, Jernigan, TL, Kardatzki, B, Karkashadze, G, Kelly, C, Kohls, G, Konrad, K, Kuntsi, J, Lazaro, L, Lera-Miguel, S, Lesch, KP, Louza, MR, Lundervold, AJ, Malpas, CB, Mattos, P, McCarthy, H, Namazova-Baranova, L, Nicolau, R, Nigg, JT, Novotny, SE, Oberwelland Weiss, E, O'Gorman Tuura, RL, Oosterlaan, J, Oranje, B, Paloyelis, Y, Pauli, P, Picon, FA, Plessen, KJ, Ramos-Quiroga, JA, Reif, A, Reneman, L, Rosa, PGP, Rubia, K, Schrantee, A, Schweren, LJS, Seitz, J, Shaw, P, Silk, Tim, Skokauskas, N, Soliva Vila, JC, Stevens, MC, Sudre, G, Tamm, L, Tovar-Moll, F, van Erp, TGM, Vance, A, Vilarroya, O, Vives-Gilabert, Y, von Polier, GG, Walitza, S, Yoncheva, YN, Zanetti, MV, Ziegler, GC, Glahn, DC, and Jahanshad, N
Published: 2021

7. Individuals at increased risk for development of bipolar disorder display structural alterations similar to people with manifest disease.

Author: Mikolas, P, Bröckel, K, Vogelbacher, C, Müller, DK, Marxen, M, Berndt, C, Sauer, C, Jung, S, Fröhner, JH, Fallgatter, AJ, Ethofer, T, Rau, A, Kircher, T, Falkenberg, I, Lambert, M, Kraft, V, Leopold, K, Bechdolf, A, Reif, A, Matura, S, Stamm, T, Bermpohl, F, Fiebig, J, Juckel, G, Flasbeck, V, Correll, CU, Ritter, P, Bauer, M, Jansen, A, Pfennig, A, Mikolas, P, Bröckel, K, Vogelbacher, C, Müller, DK, Marxen, M, Berndt, C, Sauer, C, Jung, S, Fröhner, JH, Fallgatter, AJ, Ethofer, T, Rau, A, Kircher, T, Falkenberg, I, Lambert, M, Kraft, V, Leopold, K, Bechdolf, A, Reif, A, Matura, S, Stamm, T, Bermpohl, F, Fiebig, J, Juckel, G, Flasbeck, V, Correll, CU, Ritter, P, Bauer, M, Jansen, A, and Pfennig, A
Abstract: In psychiatry, there has been a growing focus on identifying at-risk populations. For schizophrenia, these efforts have led to the development of early recognition and intervention measures. Despite a similar disease burden, the populations at risk of bipolar disorder have not been sufficiently characterized. Within the BipoLife consortium, we used magnetic resonance imaging (MRI) data from a multicenter study to assess structural gray matter alterations in N = 263 help-seeking individuals from seven study sites. We defined the risk using the EPIbipolar assessment tool as no-risk, low-risk, and high-risk and used a region-of-interest approach (ROI) based on the results of two large-scale multicenter studies of bipolar disorder by the ENIGMA working group. We detected significant differences in the thickness of the left pars opercularis (Cohen's d = 0.47, p = 0.024) between groups. The cortex was significantly thinner in high-risk individuals compared to those in the no-risk group (p = 0.011). We detected no differences in the hippocampal volume. Exploratory analyses revealed no significant differences in other cortical or subcortical regions. The thinner cortex in help-seeking individuals at risk of bipolar disorder is in line with previous findings in patients with the established disorder and corresponds to the region of the highest effect size in the ENIGMA study of cortical alterations. Structural alterations in prefrontal cortex might be a trait marker of bipolar risk. This is the largest structural MRI study of help-seeking individuals at increased risk of bipolar disorder.
Published: 2021

8. Virtual Histology of Cortical Thickness and Shared Neurobiology in 6 Psychiatric Disorders

Author: Patel, Y., Parker, N., Shin, J., Howard, D., French, L., Thomopoulos, S.I., Pozzi, E., Abe, Y., Abé, C., Anticevic, A., Alda, M., Aleman, A., Alloza, C., Alonso-Lana, S., Ameis, S.H., Anagnostou, E., McIntosh, A.A., Arango, C., Arnold, P.D., Asherson, P., Assogna, F., Auzias, G., Ayesa-Arriola, R., Bakker, G., Banaj, N., Banaschewski, T., Bandeira, C.E., Baranov, A., Bargalló, N., Bau, C.H.D., Baumeister, S., Baune, B.T., Bellgrove, M.A., Benedetti, F., Bertolino, A., Boedhoe, P.S.W., Boks, M., Bollettini, I., Del Mar Bonnin, C., Borgers, T., Borgwardt, S., Brandeis, D., Brennan, B.P., Bruggemann, J.M., Bülow, R., Busatto, G.F., Calderoni, S., Calhoun, V.D., Calvo, R., Canales-Rodríguez, E.J., Cannon, D.M., Carr, V.J., Cascella, N., Cercignani, M., Chaim-Avancini, T.M., Christakou, A., Coghill, D., Conzelmann, A., Crespo-Facorro, B., Cubillo, A.I., Cullen, K.R., Cupertino, R.B., Daly, E., Dannlowski, U., Davey, C.G., Denys, D., Deruelle, C., Di Giorgio, A., Dickie, E.W., Dima, D., Dohm, K., Ehrlich, S., Ely, B.A., Erwin-Grabner, T., Ethofer, T., Fair, D.A., Fallgatter, A.J., Faraone, S.V., Fatjó-Vilas, M., Fedor, J.M., Fitzgerald, K.D., Ford, J.M., Frodl, T., Fu, C.H.Y., Fullerton, J.M., Gabel, M.C., Glahn, D.C., Roberts, G., Gogberashvili, T., Goikolea, J.M., Gotlib, I.H., Goya-Maldonado, R., Grabe, H.J., Green, M.J., Grevet, E.H., Groenewold, N.A., Grotegerd, D., Gruber, O., Gruner, P., Guerrero-Pedraza, A., Gur, R.E., Gur, R.C., Haar, S., Haarman, B.C.M., Haavik, J., Hahn, T., Hajek, T., Harrison, B.J., Harrison, N.A., Hartman, C.A., Whalley, H.C., Heslenfeld, D.J., Hibar, D.P., Hilland, E., Hirano, Y., Ho, T.C., Hoekstra, P.J., Hoekstra, L., Hohmann, S., Hong, L.E., Höschl, C., Høvik, M.F., Howells, F.M., Nenadic, I., Jalbrzikowski, M., James, A.C., Janssen, J., Jaspers-Fayer, F., Xu, J., Jonassen, R., Karkashadze, G., King, J.A., Kircher, T., Kirschner, M., Koch, K., Kochunov, P., Kohls, G., Konrad, K., Krämer, B., Krug, A., Kuntsi, J., Kwon, J.S., Landén, M., Landrø, N.I., Lazaro, L., Lebedeva, I.S., Leehr, E.J., Lera-Miguel, S., Lesch, K.-P., Lochner, C., Louza, M.R., Luna, B., Lundervold, A.J., Macmaster, F.P., Maglanoc, L.A., Malpas, C.B., Portella, M.J., Marsh, R., Martyn, F.M., Mataix-Cols, D., Mathalon, D.H., McCarthy, H., McDonald, C., McPhilemy, G., Meinert, S., Menchón, J.M., Minuzzi, L., Mitchell, P.B., Moreno, C., Morgado, P., Muratori, F., Murphy, C.M., Murphy, D., Mwangi, B., Nabulsi, L., Nakagawa, A., Nakamae, T., Namazova, L., Narayanaswamy, J., Jahanshad, N., Nguyen, D.D., Nicolau, R., O'Gorman Tuura, R.L., O'Hearn, K., Oosterlaan, J., Opel, N., Ophoff, R.A., Oranje, B., García De La Foz, V.O., Overs, B.J., Paloyelis, Y., Pantelis, C., Parellada, M., Pauli, P., Picó-Pérez, M., Picon, F.A., Piras, F., Plessen, K.J., Pomarol-Clotet, E., Preda, A., Puig, O., Quidé, Y., Radua, J., Ramos-Quiroga, J.A., Rasser, P.E., Rauer, L., Reddy, J., Redlich, R., Reif, A., Reneman, L., Repple, J., Retico, A., Richarte, V., Richter, A., Rosa, P.G.P., Rubia, K.K., Hashimoto, R., Sacchet, M.D., Salvador, R., Santonja, J., Sarink, K., Sarró, S., Satterthwaite, T.D., Sawa, A., Schall, U., Schofield, P.R., Schrantee, A., Seitz, J., Serpa, M.H., Setién-Suero, E., Shaw, P., Shook, D., Silk, T.J., Sim, K., Simon, S., Simpson, H.B., Singh, A., Skoch, A., Skokauskas, N., Soares, J.C., Soreni, N., Soriano-Mas, C., Spalletta, G., Spaniel, F., Lawrie, S.M., Stern, E.R., Stewart, S.E., Takayanagi, Y., Temmingh, H.S., Tolin, D.F., Tomecek, D., Tordesillas-Gutiérrez, D., Tosetti, M., Uhlmann, A., Van Amelsvoort, T., Van Der Wee, N.J.A., Van Der Werff, S.J.A., Van Haren, N.E.M., Van Wingen, G.A., Vance, A., Vázquez-Bourgon, J., Vecchio, D., Venkatasubramanian, G., Vieta, E., Vilarroya, O., Vives-Gilabert, Y., Voineskos, A.N., Völzke, H., Von Polier, G.G., Walton, E., Weickert, T.W., Weickert, C.S., Weideman, A.S., Wittfeld, K., Wolf, D.H., Wu, M.-J., Yang, T.T., Yang, K., Yoncheva, Y., Yun, J.-Y., Cheng, Y., Zanetti, M.V., Ziegler, G.C., Franke, B., Hoogman, M., Buitelaar, J.K., Van Rooij, D., Andreassen, O.A., Ching, C.R.K., Veltman, D.J., Schmaal, L., Stein, D.J., Van Den Heuvel, O.A., Turner, J.A., Van Erp, T.G.M., Pausova, Z., Thompson, P.M., Paus, T., Patel, Y., Parker, N., Shin, J., Howard, D., French, L., Thomopoulos, S.I., Pozzi, E., Abe, Y., Abé, C., Anticevic, A., Alda, M., Aleman, A., Alloza, C., Alonso-Lana, S., Ameis, S.H., Anagnostou, E., McIntosh, A.A., Arango, C., Arnold, P.D., Asherson, P., Assogna, F., Auzias, G., Ayesa-Arriola, R., Bakker, G., Banaj, N., Banaschewski, T., Bandeira, C.E., Baranov, A., Bargalló, N., Bau, C.H.D., Baumeister, S., Baune, B.T., Bellgrove, M.A., Benedetti, F., Bertolino, A., Boedhoe, P.S.W., Boks, M., Bollettini, I., Del Mar Bonnin, C., Borgers, T., Borgwardt, S., Brandeis, D., Brennan, B.P., Bruggemann, J.M., Bülow, R., Busatto, G.F., Calderoni, S., Calhoun, V.D., Calvo, R., Canales-Rodríguez, E.J., Cannon, D.M., Carr, V.J., Cascella, N., Cercignani, M., Chaim-Avancini, T.M., Christakou, A., Coghill, D., Conzelmann, A., Crespo-Facorro, B., Cubillo, A.I., Cullen, K.R., Cupertino, R.B., Daly, E., Dannlowski, U., Davey, C.G., Denys, D., Deruelle, C., Di Giorgio, A., Dickie, E.W., Dima, D., Dohm, K., Ehrlich, S., Ely, B.A., Erwin-Grabner, T., Ethofer, T., Fair, D.A., Fallgatter, A.J., Faraone, S.V., Fatjó-Vilas, M., Fedor, J.M., Fitzgerald, K.D., Ford, J.M., Frodl, T., Fu, C.H.Y., Fullerton, J.M., Gabel, M.C., Glahn, D.C., Roberts, G., Gogberashvili, T., Goikolea, J.M., Gotlib, I.H., Goya-Maldonado, R., Grabe, H.J., Green, M.J., Grevet, E.H., Groenewold, N.A., Grotegerd, D., Gruber, O., Gruner, P., Guerrero-Pedraza, A., Gur, R.E., Gur, R.C., Haar, S., Haarman, B.C.M., Haavik, J., Hahn, T., Hajek, T., Harrison, B.J., Harrison, N.A., Hartman, C.A., Whalley, H.C., Heslenfeld, D.J., Hibar, D.P., Hilland, E., Hirano, Y., Ho, T.C., Hoekstra, P.J., Hoekstra, L., Hohmann, S., Hong, L.E., Höschl, C., Høvik, M.F., Howells, F.M., Nenadic, I., Jalbrzikowski, M., James, A.C., Janssen, J., Jaspers-Fayer, F., Xu, J., Jonassen, R., Karkashadze, G., King, J.A., Kircher, T., Kirschner, M., Koch, K., Kochunov, P., Kohls, G., Konrad, K., Krämer, B., Krug, A., Kuntsi, J., Kwon, J.S., Landén, M., Landrø, N.I., Lazaro, L., Lebedeva, I.S., Leehr, E.J., Lera-Miguel, S., Lesch, K.-P., Lochner, C., Louza, M.R., Luna, B., Lundervold, A.J., Macmaster, F.P., Maglanoc, L.A., Malpas, C.B., Portella, M.J., Marsh, R., Martyn, F.M., Mataix-Cols, D., Mathalon, D.H., McCarthy, H., McDonald, C., McPhilemy, G., Meinert, S., Menchón, J.M., Minuzzi, L., Mitchell, P.B., Moreno, C., Morgado, P., Muratori, F., Murphy, C.M., Murphy, D., Mwangi, B., Nabulsi, L., Nakagawa, A., Nakamae, T., Namazova, L., Narayanaswamy, J., Jahanshad, N., Nguyen, D.D., Nicolau, R., O'Gorman Tuura, R.L., O'Hearn, K., Oosterlaan, J., Opel, N., Ophoff, R.A., Oranje, B., García De La Foz, V.O., Overs, B.J., Paloyelis, Y., Pantelis, C., Parellada, M., Pauli, P., Picó-Pérez, M., Picon, F.A., Piras, F., Plessen, K.J., Pomarol-Clotet, E., Preda, A., Puig, O., Quidé, Y., Radua, J., Ramos-Quiroga, J.A., Rasser, P.E., Rauer, L., Reddy, J., Redlich, R., Reif, A., Reneman, L., Repple, J., Retico, A., Richarte, V., Richter, A., Rosa, P.G.P., Rubia, K.K., Hashimoto, R., Sacchet, M.D., Salvador, R., Santonja, J., Sarink, K., Sarró, S., Satterthwaite, T.D., Sawa, A., Schall, U., Schofield, P.R., Schrantee, A., Seitz, J., Serpa, M.H., Setién-Suero, E., Shaw, P., Shook, D., Silk, T.J., Sim, K., Simon, S., Simpson, H.B., Singh, A., Skoch, A., Skokauskas, N., Soares, J.C., Soreni, N., Soriano-Mas, C., Spalletta, G., Spaniel, F., Lawrie, S.M., Stern, E.R., Stewart, S.E., Takayanagi, Y., Temmingh, H.S., Tolin, D.F., Tomecek, D., Tordesillas-Gutiérrez, D., Tosetti, M., Uhlmann, A., Van Amelsvoort, T., Van Der Wee, N.J.A., Van Der Werff, S.J.A., Van Haren, N.E.M., Van Wingen, G.A., Vance, A., Vázquez-Bourgon, J., Vecchio, D., Venkatasubramanian, G., Vieta, E., Vilarroya, O., Vives-Gilabert, Y., Voineskos, A.N., Völzke, H., Von Polier, G.G., Walton, E., Weickert, T.W., Weickert, C.S., Weideman, A.S., Wittfeld, K., Wolf, D.H., Wu, M.-J., Yang, T.T., Yang, K., Yoncheva, Y., Yun, J.-Y., Cheng, Y., Zanetti, M.V., Ziegler, G.C., Franke, B., Hoogman, M., Buitelaar, J.K., Van Rooij, D., Andreassen, O.A., Ching, C.R.K., Veltman, D.J., Schmaal, L., Stein, D.J., Van Den Heuvel, O.A., Turner, J.A., Van Erp, T.G.M., Pausova, Z., Thompson, P.M., and Paus, T.
Abstract: Importance Large-scale neuroimaging studies have revealed group differences in cortical thickness across many psychiatric disorders. The underlying neurobiology behind these differences is not well understood. Objective To determine neurobiologic correlates of group differences in cortical thickness between cases and controls in 6 disorders: attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder (ASD), bipolar disorder (BD), major depressive disorder (MDD), obsessive-compulsive disorder (OCD), and schizophrenia. Design, Setting, and Participants Profiles of group differences in cortical thickness between cases and controls were generated using T1-weighted magnetic resonance images. Similarity between interregional profiles of cell-specific gene expression and those in the group differences in cortical thickness were investigated in each disorder. Next, principal component analysis was used to reveal a shared profile of group difference in thickness across the disorders. Analysis for gene coexpression, clustering, and enrichment for genes associated with these disorders were conducted. Data analysis was conducted between June and December 2019. The analysis included 145 cohorts across 6 psychiatric disorders drawn from the ENIGMA consortium. The numbers of cases and controls in each of the 6 disorders were as follows: ADHD: 1814 and 1602; ASD: 1748 and 1770; BD: 1547 and 3405; MDD: 2658 and 3572; OCD: 2266 and 2007; and schizophrenia: 2688 and 3244. Main Outcomes and Measures Interregional profiles of group difference in cortical thickness between cases and controls. Results A total of 12 721 cases and 15 600 controls, ranging from ages 2 to 89 years, were included in this study. Interregional profiles of group differences in cortical thickness for each of the 6 psychiatric disorders were associated with profiles of gene expression specific to pyramidal (CA1) cells, astrocytes (except for BD), and microglia (exce
Published: 2021
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9. Subcortical brain volume, regional cortical thickness, and cortical surface area across disorders: Findings from the ENIGMA ADHD, ASD, and OCD Working Groups

Author: Boedhoe, P.S., Rooij, D. van, Hoogman, M., Twisk, J.W.R., Schmaal, L., Abe, Y., Alonso, P., Ameis, S.H., Anikin, A., Anticevic, A., Arango, C., Arnold, P.D., Asherson, P., Assogna, F., Auzias, G., Banaschewski, T., Baranov, A., Batistuzzo, M.C., Baumeister, S., Baur-Streubel, R., Behrmann, M., Bellgrove, M.A., Benedetti, F. De, Beucke, J.C., Biederman, J., Bollettini, I., Bose, A., Bralten, J., Bramati, I.E., Brandeis, D., Brem, S., Brennan, B.P., Busatto, G.F., Calderoni, S., Calvo, A., Calvo, R., Castellanos, F.X., Cercignani, M., Chaim-Avancini, T.M., Chantiluke, K.C., Cheng, Y., Cho, K.I.K., Christakou, A., Coghill, D., Conzelmann, A., Cubillo, A.I., Dale, A.M., Dallaspezia, S., Daly, E., Denys, D., Deruelle, C., Martino, A, Dinstein, I., Doyle, A.E., Durston, S., Earl, E.A., Ecker, C., Ehrlich, S., Ely, B.A., Epstein, J.N., Ethofer, T., Fair, D.A., Fallgatter, A.J., Faraone, S.V, Fedor, J., Feng, X., Feusner, J.D., Fitzgerald, J., Fitzgerald, K.D., Fouche, J.P., Freitag, C.M., Fridgeirsson, E.A., Frodl, T., Gabel, M.C., Gallagher, L., Gogberashvili, T., Gori, I., Gruner, P., Gürsel, D.A., Haar, S., Haavik, J., Hall, G.B., Harrison, N.A., Hartman, Catharina A., Heslenfeld, D.J., Hirano, Y., Hoekstra, P.J., Hoexter, M.Q., Hohmann, S., Høvik, M.F., Hu, H., Huyser, C., Jahanshad, N., Jalbrzikowski, M., James, A., Janssen, J, Jaspers-Fayer, F., Jernigan, T.L., Kapilushniy, D., Kardatzki, B., Buitelaar, J.K., Franke, B., Heuvel, O.A. van den, Boedhoe, P.S., Rooij, D. van, Hoogman, M., Twisk, J.W.R., Schmaal, L., Abe, Y., Alonso, P., Ameis, S.H., Anikin, A., Anticevic, A., Arango, C., Arnold, P.D., Asherson, P., Assogna, F., Auzias, G., Banaschewski, T., Baranov, A., Batistuzzo, M.C., Baumeister, S., Baur-Streubel, R., Behrmann, M., Bellgrove, M.A., Benedetti, F. De, Beucke, J.C., Biederman, J., Bollettini, I., Bose, A., Bralten, J., Bramati, I.E., Brandeis, D., Brem, S., Brennan, B.P., Busatto, G.F., Calderoni, S., Calvo, A., Calvo, R., Castellanos, F.X., Cercignani, M., Chaim-Avancini, T.M., Chantiluke, K.C., Cheng, Y., Cho, K.I.K., Christakou, A., Coghill, D., Conzelmann, A., Cubillo, A.I., Dale, A.M., Dallaspezia, S., Daly, E., Denys, D., Deruelle, C., Martino, A, Dinstein, I., Doyle, A.E., Durston, S., Earl, E.A., Ecker, C., Ehrlich, S., Ely, B.A., Epstein, J.N., Ethofer, T., Fair, D.A., Fallgatter, A.J., Faraone, S.V, Fedor, J., Feng, X., Feusner, J.D., Fitzgerald, J., Fitzgerald, K.D., Fouche, J.P., Freitag, C.M., Fridgeirsson, E.A., Frodl, T., Gabel, M.C., Gallagher, L., Gogberashvili, T., Gori, I., Gruner, P., Gürsel, D.A., Haar, S., Haavik, J., Hall, G.B., Harrison, N.A., Hartman, Catharina A., Heslenfeld, D.J., Hirano, Y., Hoekstra, P.J., Hoexter, M.Q., Hohmann, S., Høvik, M.F., Hu, H., Huyser, C., Jahanshad, N., Jalbrzikowski, M., James, A., Janssen, J, Jaspers-Fayer, F., Jernigan, T.L., Kapilushniy, D., Kardatzki, B., Buitelaar, J.K., Franke, B., and Heuvel, O.A. van den
Abstract: Contains fulltext : 225388.pdf (Publisher’s version ) (Closed access), OBJECTIVE: Attention deficit hyperactivity disorder (ADHD), autism spectrum disorder (ASD), and obsessive-compulsive disorder (OCD) are common neurodevelopmental disorders that frequently co-occur. The authors sought to directly compare these disorders using structural brain imaging data from ENIGMA consortium data. METHODS: Structural T(1)-weighted whole-brain MRI data from healthy control subjects (N=5,827) and from patients with ADHD (N=2,271), ASD (N=1,777), and OCD (N=2,323) from 151 cohorts worldwide were analyzed using standardized processing protocols. The authors examined subcortical volume, cortical thickness, and cortical surface area differences within a mega-analytical framework, pooling measures extracted from each cohort. Analyses were performed separately for children, adolescents, and adults, using linear mixed-effects models adjusting for age, sex, and site (and intracranial volume for subcortical and surface area measures). RESULTS: No shared differences were found among all three disorders, and shared differences between any two disorders did not survive correction for multiple comparisons. Children with ADHD compared with those with OCD had smaller hippocampal volumes, possibly influenced by IQ. Children and adolescents with ADHD also had smaller intracranial volume than control subjects and those with OCD or ASD. Adults with ASD showed thicker frontal cortices compared with adult control subjects and other clinical groups. No OCD-specific differences were observed across different age groups and surface area differences among all disorders in childhood and adulthood. CONCLUSIONS: The study findings suggest robust but subtle differences across different age groups among ADHD, ASD, and OCD. ADHD-specific intracranial volume and hippocampal differences in children and adolescents, and ASD-specific cortical thickness differences in the frontal cortex in adults, support previous work emphasizing structural brain differences in these disorders.
Published: 2020

10. Subcortical Brain Volume, Regional Cortical Thickness, and Cortical Surface Area Across Disorders: Findings From the ENIGMA ADHD, ASD, and OCD Working Groups

Author: Boedhoe, PSW, van Rooij, D, Hoogman, M, Twisk, JWR, Schmaal, L, Abe, Y, Alonso, P, Ameis, SH, Anikin, A, Anticevic, A, Arango, C, Arnold, PD, Asherson, P, Assogna, F, Auzias, G, Banaschewski, T, Baranov, A, Batistuzzo, MC, Baumeister, S, Baur-Streubel, R, Behrmann, M, Bellgrove, MA, Benedetti, F, Beucke, JC, Biederman, J, Bollettini, I, Bose, A, Bralten, J, Bramati, IE, Brandeis, D, Brem, S, Brennan, BP, Busatto, GF, Calderoni, S, Calvo, A, Calvo, R, Castellanos, FX, Cercignani, M, Chaim-Avancini, TM, Chantiluke, KC, Cheng, Y, Cho, KIK, Christakou, A, Coghill, D, Conzelmann, A, Cubillo, A, Dale, AM, Dallaspezia, S, Daly, E, Denys, D, Deruelle, C, Di Martino, A, Dinstein, I, Doyle, AE, Durston, S, Earl, EA, Ecker, C, Ehrlich, S, Ely, BA, Epstein, JN, Ethofer, T, Fair, DA, Fallgatter, AJ, Faraone, S, Fedor, J, Feng, X, Feusner, JD, Fitzgerald, J, Fitzgerald, KD, Fouche, J-P, Freitag, CM, Fridgeirsson, EA, Frodl, T, Gabel, MC, Gallagher, L, Gogberashvili, T, Gori, I, Gruner, P, Gursel, DA, Haar, S, Haavik, J, Hall, GB, Harrison, NA, Hartman, CA, Heslenfeld, DJ, Hirano, Y, Hoekstra, PJ, Hoexter, MQ, Hohmann, S, Hovik, MF, Hu, H, Huyser, C, Jahanshad, N, Jalbrzikowski, M, James, A, Janssen, J, Jaspers-Fayer, F, Jernigan, TL, Kapilushniy, D, Kardatzki, B, Karkashadze, G, Kathmann, N, Kaufmann, C, Kelly, C, Khadka, S, King, JA, Koch, K, Kohls, G, Konrad, K, Kuno, M, Kuntsi, J, Kvale, G, Kwon, JS, Lazaro, L, Lera-Miguel, S, Lesch, K-P, Hoekstra, L, Liu, Y, Lochner, C, Louza, MR, Luna, B, Lundervold, AJ, Malpas, CB, Marques, P, Marsh, R, Martinez-Zalacain, I, Mataix-Cols, D, Mattos, P, McCarthy, H, McGrath, J, Mehta, MA, Menchon, JM, Mennes, M, Martinho, MM, Moreira, PS, Morer, A, Morgado, P, Muratori, F, Murphy, CM, Murphy, DGM, Nakagawa, A, Nakamae, T, Nakao, T, Namazova-Baranova, L, Narayanaswamy, JC, Nicolau, R, Nigg, JT, Novotny, SE, Nurmi, EL, Weiss, EO, Tuura, RLO, O'Hearn, K, O'Neill, J, Oosterlaan, J, Oranje, B, Paloyelis, Y, Parellada, M, Pauli, P, Perriello, C, Piacentini, J, Piras, F, Plessen, KJ, Puig, O, Ramos-Quiroga, JA, Reddy, YCJ, Reif, A, Reneman, L, Retico, A, Rosa, PGP, Rubia, K, Rus, OG, Sakai, Y, Schrantee, A, Schwarz, L, Schweren, LJS, Seitz, J, Shaw, P, Shook, D, Silk, TJ, Simpson, HB, Skokauskas, N, Vila, JCS, Solovieva, A, Soreni, N, Soriano-Mas, C, Spalletta, G, Stern, ER, Stevens, MC, Stewart, SE, Sudre, G, Szeszko, PR, Tamm, L, Taylor, MJ, Tolin, DF, Tosetti, M, Tovar-Moll, F, Tsuchiyagaito, A, van Erp, TGM, van Wingen, GA, Vance, A, Venkatasubramanian, G, Vilarroya, O, Vives-Gilabert, Y, von Polier, GG, Walitza, S, Wallace, GL, Wang, Z, Wolfers, T, Yoncheva, YN, Yun, J-Y, Zanetti, M, Zhou, F, Ziegler, GC, Zierhut, KC, Zwiers, MP, Thompson, PM, Stein, DJ, Buitelaar, J, Franke, B, van den Heuvel, OA, Boedhoe, PSW, van Rooij, D, Hoogman, M, Twisk, JWR, Schmaal, L, Abe, Y, Alonso, P, Ameis, SH, Anikin, A, Anticevic, A, Arango, C, Arnold, PD, Asherson, P, Assogna, F, Auzias, G, Banaschewski, T, Baranov, A, Batistuzzo, MC, Baumeister, S, Baur-Streubel, R, Behrmann, M, Bellgrove, MA, Benedetti, F, Beucke, JC, Biederman, J, Bollettini, I, Bose, A, Bralten, J, Bramati, IE, Brandeis, D, Brem, S, Brennan, BP, Busatto, GF, Calderoni, S, Calvo, A, Calvo, R, Castellanos, FX, Cercignani, M, Chaim-Avancini, TM, Chantiluke, KC, Cheng, Y, Cho, KIK, Christakou, A, Coghill, D, Conzelmann, A, Cubillo, A, Dale, AM, Dallaspezia, S, Daly, E, Denys, D, Deruelle, C, Di Martino, A, Dinstein, I, Doyle, AE, Durston, S, Earl, EA, Ecker, C, Ehrlich, S, Ely, BA, Epstein, JN, Ethofer, T, Fair, DA, Fallgatter, AJ, Faraone, S, Fedor, J, Feng, X, Feusner, JD, Fitzgerald, J, Fitzgerald, KD, Fouche, J-P, Freitag, CM, Fridgeirsson, EA, Frodl, T, Gabel, MC, Gallagher, L, Gogberashvili, T, Gori, I, Gruner, P, Gursel, DA, Haar, S, Haavik, J, Hall, GB, Harrison, NA, Hartman, CA, Heslenfeld, DJ, Hirano, Y, Hoekstra, PJ, Hoexter, MQ, Hohmann, S, Hovik, MF, Hu, H, Huyser, C, Jahanshad, N, Jalbrzikowski, M, James, A, Janssen, J, Jaspers-Fayer, F, Jernigan, TL, Kapilushniy, D, Kardatzki, B, Karkashadze, G, Kathmann, N, Kaufmann, C, Kelly, C, Khadka, S, King, JA, Koch, K, Kohls, G, Konrad, K, Kuno, M, Kuntsi, J, Kvale, G, Kwon, JS, Lazaro, L, Lera-Miguel, S, Lesch, K-P, Hoekstra, L, Liu, Y, Lochner, C, Louza, MR, Luna, B, Lundervold, AJ, Malpas, CB, Marques, P, Marsh, R, Martinez-Zalacain, I, Mataix-Cols, D, Mattos, P, McCarthy, H, McGrath, J, Mehta, MA, Menchon, JM, Mennes, M, Martinho, MM, Moreira, PS, Morer, A, Morgado, P, Muratori, F, Murphy, CM, Murphy, DGM, Nakagawa, A, Nakamae, T, Nakao, T, Namazova-Baranova, L, Narayanaswamy, JC, Nicolau, R, Nigg, JT, Novotny, SE, Nurmi, EL, Weiss, EO, Tuura, RLO, O'Hearn, K, O'Neill, J, Oosterlaan, J, Oranje, B, Paloyelis, Y, Parellada, M, Pauli, P, Perriello, C, Piacentini, J, Piras, F, Plessen, KJ, Puig, O, Ramos-Quiroga, JA, Reddy, YCJ, Reif, A, Reneman, L, Retico, A, Rosa, PGP, Rubia, K, Rus, OG, Sakai, Y, Schrantee, A, Schwarz, L, Schweren, LJS, Seitz, J, Shaw, P, Shook, D, Silk, TJ, Simpson, HB, Skokauskas, N, Vila, JCS, Solovieva, A, Soreni, N, Soriano-Mas, C, Spalletta, G, Stern, ER, Stevens, MC, Stewart, SE, Sudre, G, Szeszko, PR, Tamm, L, Taylor, MJ, Tolin, DF, Tosetti, M, Tovar-Moll, F, Tsuchiyagaito, A, van Erp, TGM, van Wingen, GA, Vance, A, Venkatasubramanian, G, Vilarroya, O, Vives-Gilabert, Y, von Polier, GG, Walitza, S, Wallace, GL, Wang, Z, Wolfers, T, Yoncheva, YN, Yun, J-Y, Zanetti, M, Zhou, F, Ziegler, GC, Zierhut, KC, Zwiers, MP, Thompson, PM, Stein, DJ, Buitelaar, J, Franke, B, and van den Heuvel, OA
Abstract: Objective: Attention deficit hyperactivity disorder (ADHD), autism spectrum disorder (ASD), and obsessive-compulsive disorder (OCD) are common neurodevelopmental disorders that frequently co-occur. The authors sought to directly compare these disorders using structural brain imaging data from ENIGMA consortium data. Methods: Structural T1-weighted whole-brain MRI data from healthy control subjects (N=5,827) and from patients with ADHD (N=2,271), ASD (N=1,777), and OCD (N=2,323) from 151 cohorts worldwide were analyzed using standardized processing protocols. The authors examined subcortical volume, cortical thickness, and cortical surface area differences within a mega-analytical framework, pooling measures extracted from each cohort. Analyses were performed separately for children, adolescents, and adults, using linear mixed-effects models adjusting for age, sex, and site (and intracranial volume for subcortical and surface area measures). Results: No shared differences were found among all three disorders, and shared differences between any two disorders did not survive correction for multiple comparisons. Children with ADHD compared with those with OCD had smaller hippocampal volumes, possibly influenced by IQ. Children and adolescents with ADHD also had smaller intracranial volume than control subjects and those with OCD or ASD. Adults with ASD showed thicker frontal cortices compared with adult control subjects and other clinical groups. No OCD-specific differences were observed across different age groups and surface area differences among all disorders in childhood and adulthood. Conclusions: The study findings suggest robust but subtle differences across different age groups among ADHD, ASD, and OCD. ADHD-specific intracranial volume and hippocampal differences in children and adolescents, and ASD-specific cortical thickness differences in the frontal cortex in adults, support previous work emphasizing structural brain differences in these disorders.
Published: 2020

11. Cerebral processing of linguistic and emotional prosody: fMRI studies

Author: Wildgruber, D., primary, Ackermann, H., additional, Kreifelts, B., additional, and Ethofer, T., additional
Published: 2006
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12. Decoding of emotional information in voice-sensitive cortices

Author: Ethofer, T, Van De Ville, D, Scherer, K, and Vuilleumier, P
Published: 2009
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13. Identification of emotional intonation evaluated by fMRI

Author: Wildgruber, D., Riecker, A., Hertrich, I., Erb, M., Grodd, W., Ethofer, T., and Ackermann, H.
Published: 2005
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14. Brain imaging of the cortex in ADHD: A coordinated analysis of large-scale clinical and population-based samples

Author: Hoogman, M., Muetzel, R., Guimaraes, J.P., Shumskaya, E., Mennes, M., Zwiers, M.P., Jahanshad, N., Sudre, G., Wolfers, T., Earl, E.A., oliva Vila, J.C. S, Vives-Gilabert, Y., Khadka, S., Novotny, S.E., Hartman, Catharina, Heslenfeld, D.J., Schweren, L.J., Ambrosino, S., Oranje, B., Zeeuw, P. de, Chaim-Avancini, T.M., Rosa, P.G., Zanetti, M.V., Malpas, C.B., Kohls, G., Polier, G.G. von, Seitz, J., Biederman, J., Doyle, A.E., Dale, A.M., Erp, T.G. van, Epstein, J.N., Jernigan, T.L., Baur-Streubel, R., Ziegler, G.C., Zierhut, K.C., Schrantee, A., Hovik, M.F., Lundervold, A.J., Kelly, C., McCarthy, H., Skokauskas, N., O'Gorman Tuura, R.L., Calvo, A., Lera-Miguel, S., Nicolau, R., Chantiluke, K.C., Christakou, A., Vance, A., Cercignani, M., Gabel, M.C., Asherson, P., Baumeister, S., Brandeis, D., Hohmann, S., Bramati, I.E., Tovar-Moll, F., Fallgatter, A.J., Kardatzki, B., Schwarz, L., Anikin, A., Baranov, A., Gogberashvili, T., Kapilushniy, D., Solovieva, A., Marroun, H. El, White, T., Karkashadze, G., Namazova-Baranova, L., Ethofer, T., Mattos, P., Banaschewski, T., Coghill, D., Plessen, K.J., Kuntsi, J., Mehta, M.A., Paloyelis, Y., Harrison, N.A., Bellgrove, M.A., Silk, T.J., Cubillo, A.I., Rubia, K., Lazaro, L., Brem, S., Walitza, S., Frodl, T., Zentis, M., Castellanos, F.X., Yoncheva, Y.N., Haavik, J., Reneman, L., Conzelmann, A., Lesch, K.P., Pauli, P., Reif, A., Tamm, L., Konrad, K., Oberwelland Weiss, E., Busatto, G.F., Louza, M.R., Durston, S., Hoekstra, P.J., Oosterlaan, J., Stevens, M.C., Ramos-Quiroga, J.A., Vilarroya, O., Fair, D.A., Nigg, J.T., Thompson, P.M., Buitelaar, J.K., Faraone, S.V, Shaw, P., Tiemeier, H., Bralten, J., Franke, B., Hoogman, M., Muetzel, R., Guimaraes, J.P., Shumskaya, E., Mennes, M., Zwiers, M.P., Jahanshad, N., Sudre, G., Wolfers, T., Earl, E.A., oliva Vila, J.C. S, Vives-Gilabert, Y., Khadka, S., Novotny, S.E., Hartman, Catharina, Heslenfeld, D.J., Schweren, L.J., Ambrosino, S., Oranje, B., Zeeuw, P. de, Chaim-Avancini, T.M., Rosa, P.G., Zanetti, M.V., Malpas, C.B., Kohls, G., Polier, G.G. von, Seitz, J., Biederman, J., Doyle, A.E., Dale, A.M., Erp, T.G. van, Epstein, J.N., Jernigan, T.L., Baur-Streubel, R., Ziegler, G.C., Zierhut, K.C., Schrantee, A., Hovik, M.F., Lundervold, A.J., Kelly, C., McCarthy, H., Skokauskas, N., O'Gorman Tuura, R.L., Calvo, A., Lera-Miguel, S., Nicolau, R., Chantiluke, K.C., Christakou, A., Vance, A., Cercignani, M., Gabel, M.C., Asherson, P., Baumeister, S., Brandeis, D., Hohmann, S., Bramati, I.E., Tovar-Moll, F., Fallgatter, A.J., Kardatzki, B., Schwarz, L., Anikin, A., Baranov, A., Gogberashvili, T., Kapilushniy, D., Solovieva, A., Marroun, H. El, White, T., Karkashadze, G., Namazova-Baranova, L., Ethofer, T., Mattos, P., Banaschewski, T., Coghill, D., Plessen, K.J., Kuntsi, J., Mehta, M.A., Paloyelis, Y., Harrison, N.A., Bellgrove, M.A., Silk, T.J., Cubillo, A.I., Rubia, K., Lazaro, L., Brem, S., Walitza, S., Frodl, T., Zentis, M., Castellanos, F.X., Yoncheva, Y.N., Haavik, J., Reneman, L., Conzelmann, A., Lesch, K.P., Pauli, P., Reif, A., Tamm, L., Konrad, K., Oberwelland Weiss, E., Busatto, G.F., Louza, M.R., Durston, S., Hoekstra, P.J., Oosterlaan, J., Stevens, M.C., Ramos-Quiroga, J.A., Vilarroya, O., Fair, D.A., Nigg, J.T., Thompson, P.M., Buitelaar, J.K., Faraone, S.V, Shaw, P., Tiemeier, H., Bralten, J., and Franke, B.
Abstract: Contains fulltext : 204879.pdf (publisher's version ) (Closed access) Contains fulltext : 204879pos.pdf (postprint version ) (Open Access), OBJECTIVE: Neuroimaging studies show structural alterations of various brain regions in children and adults with attention deficit hyperactivity disorder (ADHD), although nonreplications are frequent. The authors sought to identify cortical characteristics related to ADHD using large-scale studies. METHODS: Cortical thickness and surface area (based on the Desikan-Killiany atlas) were compared between case subjects with ADHD (N=2,246) and control subjects (N=1,934) for children, adolescents, and adults separately in ENIGMA-ADHD, a consortium of 36 centers. To assess familial effects on cortical measures, case subjects, unaffected siblings, and control subjects in the NeuroIMAGE study (N=506) were compared. Associations of the attention scale from the Child Behavior Checklist with cortical measures were determined in a pediatric population sample (Generation-R, N=2,707). RESULTS: In the ENIGMA-ADHD sample, lower surface area values were found in children with ADHD, mainly in frontal, cingulate, and temporal regions; the largest significant effect was for total surface area (Cohen's d=-0.21). Fusiform gyrus and temporal pole cortical thickness was also lower in children with ADHD. Neither surface area nor thickness differences were found in the adolescent or adult groups. Familial effects were seen for surface area in several regions. In an overlapping set of regions, surface area, but not thickness, was associated with attention problems in the Generation-R sample. CONCLUSIONS: Subtle differences in cortical surface area are widespread in children but not adolescents and adults with ADHD, confirming involvement of the frontal cortex and highlighting regions deserving further attention. Notably, the alterations behave like endophenotypes in families and are linked to ADHD symptoms in the population, extending evidence that ADHD behaves as a continuous trait in the population. Future longitudinal studies should clarify individual lifespan trajectories that lead to nons
Published: 2019

15. Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study

Author: Kalman, JL, Papiol, S, Forstner, AJ, Heilbronner, U, Degenhardt, F, Strohmaier, J, Adli, M, Adorjan, K, Akula, N, Alda, M, Anderson-Schmidt, H, Andlauer, TFM, Anghelescu, IG, Ardau, R, Arias, B, Arolt, V, Aubry, JM, Backlund, L, Bartholdi, K, Bauer, M, Baune, BT, Becker, T, Bellivier, F, Benabarre, A, Bengesser, S, Bhattacharjee, AK, Biernacka, JM, Birner, A, Brichant-Petitjean, C, Budde, M, Cervantes, P, Chillotti, C, Cichon, S, Clark, SR, Colom, F, Comes, AL, Cruceanu, C, Czerski, PM, Dannlowski, U, Dayer, A, Del Zompo, M, DePaulo, JR, Dietrich, DE, Étain, B, Ethofer, T, Falkai, P, Fallgatter, A, Figge, C, Flatau, L, Folkerts, H, Frisen, L, Frye, MA, Fullerton, JM, Gade, K, Gard, S, Garnham, JS, Goes, FS, Grigoroiu-Serbanescu, M, Gryaznova, A, Hake, M, Hauser, J, Herms, S, Hoffmann, P, Hou, L, Jäger, M, Jamain, S, Jiménez, E, Juckel, G, Kahn, JP, Kassem, L, Kelsoe, J, Kittel-Schneider, S, Kliwicki, S, Klohn-Sagatholislam, F, Koller, M, König, B, Konrad, C, Lackner, N, Laje, G, Landén, M, Lang, FU, Lavebratt, C, Leboyer, M, Leckband, SG, Maj, M, Manchia, M, Martinsson, L, McCarthy, MJ, McElroy, SL, McMahon, FJ, Mitchell, PB, Mitjans, M, Mondimore, FM, Monteleone, P, Nieratschker, V, Nievergelt, CM, Novák, T, Ösby, U, Pfennig, A, Potash, JB, Kalman, JL, Papiol, S, Forstner, AJ, Heilbronner, U, Degenhardt, F, Strohmaier, J, Adli, M, Adorjan, K, Akula, N, Alda, M, Anderson-Schmidt, H, Andlauer, TFM, Anghelescu, IG, Ardau, R, Arias, B, Arolt, V, Aubry, JM, Backlund, L, Bartholdi, K, Bauer, M, Baune, BT, Becker, T, Bellivier, F, Benabarre, A, Bengesser, S, Bhattacharjee, AK, Biernacka, JM, Birner, A, Brichant-Petitjean, C, Budde, M, Cervantes, P, Chillotti, C, Cichon, S, Clark, SR, Colom, F, Comes, AL, Cruceanu, C, Czerski, PM, Dannlowski, U, Dayer, A, Del Zompo, M, DePaulo, JR, Dietrich, DE, Étain, B, Ethofer, T, Falkai, P, Fallgatter, A, Figge, C, Flatau, L, Folkerts, H, Frisen, L, Frye, MA, Fullerton, JM, Gade, K, Gard, S, Garnham, JS, Goes, FS, Grigoroiu-Serbanescu, M, Gryaznova, A, Hake, M, Hauser, J, Herms, S, Hoffmann, P, Hou, L, Jäger, M, Jamain, S, Jiménez, E, Juckel, G, Kahn, JP, Kassem, L, Kelsoe, J, Kittel-Schneider, S, Kliwicki, S, Klohn-Sagatholislam, F, Koller, M, König, B, Konrad, C, Lackner, N, Laje, G, Landén, M, Lang, FU, Lavebratt, C, Leboyer, M, Leckband, SG, Maj, M, Manchia, M, Martinsson, L, McCarthy, MJ, McElroy, SL, McMahon, FJ, Mitchell, PB, Mitjans, M, Mondimore, FM, Monteleone, P, Nieratschker, V, Nievergelt, CM, Novák, T, Ösby, U, Pfennig, A, and Potash, JB
Abstract: Objectives: Bipolar disorder (BD) with early disease onset is associated with an unfavorable clinical outcome and constitutes a clinically and biologically homogenous subgroup within the heterogeneous BD spectrum. Previous studies have found an accumulation of early age at onset (AAO) in BD families and have therefore hypothesized that there is a larger genetic contribution to the early-onset cases than to late onset BD. To investigate the genetic background of this subphenotype, we evaluated whether an increased polygenic burden of BD- and schizophrenia (SCZ)-associated risk variants is associated with an earlier AAO in BD patients. Methods: A total of 1995 BD type 1 patients from the Consortium of Lithium Genetics (ConLiGen), PsyCourse and Bonn-Mannheim samples were genotyped and their BD and SCZ polygenic risk scores (PRSs) were calculated using the summary statistics of the Psychiatric Genomics Consortium as a training data set. AAO was either separated into onset groups of clinical interest (childhood and adolescence [≤18 years] vs adulthood [>18 years]) or considered as a continuous measure. The associations between BD- and SCZ-PRSs and AAO were evaluated with regression models. Results: BD- and SCZ-PRSs were not significantly associated with age at disease onset. Results remained the same when analyses were stratified by site of recruitment. Conclusions: The current study is the largest conducted so far to investigate the association between the cumulative BD and SCZ polygenic risk and AAO in BD patients. The reported negative results suggest that such a polygenic influence, if there is any, is not large, and highlight the importance of conducting further, larger scale studies to obtain more information on the genetic architecture of this clinically relevant phenotype.
Published: 2019

16. Properties of face localizer activations and their application in functional magnetic resonance imaging (fMRI) fingerprinting

Author: Schwarz, L., Kreifelts, B., Wildgruber, D., Erb, M., Scheffler, K., Ethofer, T., and https://orcid.org/0000-0002-4612-6018
Subjects: Adult, Male, Science, Face, Medicine, Humans, Female, Magnetic Resonance Imaging, Temporal Lobe, Research Article
Abstract: Functional localizers are particularly prevalent in functional magnetic resonance imaging (fMRI) studies concerning face processing. In this study, we extend the knowledge on face localizers regarding four important aspects: First, activation differences in occipital and fusiform face areas (OFA/FFA) and amygdala are characterized by increased activation while precuneus and medial prefrontal cortex show decreased deactivation to faces versus control stimuli. The face-selective posterior superior temporal sulcus is a hybrid area exhibiting increased activation within its inferior and decreased deactivation within its superior part. Second, the employed control stimuli can impact on whether a region is classified in group analyses as face-selective or not. We specifically investigated this for recently described cytoarchitectonic subregions of the fusiform cortex (FG-2/FG-4). Averaged activity across voxels in FG-4 was stronger for faces than objects, houses, or landscapes. In FG-2, averaged activity was only significantly stronger in comparison with landscapes, but small peaks within this area were detected for comparison versus objects and houses. Third, reproducibility of individual peak activations is excellent for right FFA and quite good for right OFA, whereas within all other areas it was too low to provide valid information on time-invariant individual peaks. Finally, the fine-grained spatial activation patterns in right OFA and FFA are both time-invariant within each individual and sufficiently different between individuals to enable identification of individual participants with near-perfect precision (fMRI fingerprinting).
Published: 2018

17. Evaluating the impact of fast-fMRI on dynamic functional connectivity in an event-based paradigm

Author: Sahib, A., Erb, M., Marquetand, J., Martin, P., Klamer, S., Vulliemoz, S., Scheffler, K., Ethofer, T., https://orcid.org/0000-0002-4612-6018, and Focke, N.
Abstract: The human brain is known to contain several functional networks that interact dynamically. Therefore, it is desirable to analyze the temporal features of these networks by dynamic functional connectivity (dFC). A sliding window approach was used in an event-related fMRI (visual stimulation using checkerboards) to assess the impact of repetition time (TR) and window size on the temporal features of BOLD dFC. In addition, we also examined the spatial distribution of dFC and tested the feasibility of this approach for the analysis of interictal epileptiforme discharges. 15 healthy controls (visual stimulation paradigm) and three patients with epilepsy (EEG-fMRI) were measured with EPI-fMRI. We calculated the functional connectivity degree (FCD) by determining the total number of connections of a given voxel above a predefined threshold based on Pearson correlation. FCD could capture hemodynamic changes relative to stimulus onset in controls. A significant effect of TR and window size was observed on FCD estimates. At a conventional TR of 2.6 s, FCD values were marginal compared to FCD values using sub-seconds TRs achievable with multiband (MB) fMRI. Concerning window sizes, a specific maximum of FCD values (inverted u-shape behavior) was found for each TR, indicating a limit to the possible gain in FCD for increasing window size. In patients, a dynamic FCD change was found relative to the onset of epileptiform EEG patterns, which was compatible with their clinical semiology. Our findings indicate that dynamic FCD transients are better detectable with sub-second TR than conventional TR. This approach was capable of capturing neuronal connectivity across various regions of the brain, indicating a potential to study the temporal characteristics of interictal epileptiform discharges and seizures in epilepsy patients or other brain diseases with brief events.
Published: 2018

18. Effect of temporal resolution and serial autocorrelations in event-related functional MRI

Author: Sahib, A., Mathiak, K., Erb, M., Elshahabi, K., Klamer, S., Scheffler, K., Focke, N., Ethofer, T., and https://orcid.org/0000-0002-4612-6018
Abstract: Purpose To assess the impact of colored noise on statistics in event-related functional MRI (fMRI) (visual stimulation using checkerboards) acquired by simultaneous multislice imaging enabling repetition times (TRs) between 2.64 to 0.26 s. Methods T-values within the visual cortex obtained with analysis tools that assume a first-order autoregressive plus white noise process (AR(1)+w) with a fixed AR coefficient versus higher-order AR models with spatially varying AR coefficients were compared. In addition, dependency of T-values on correction of physiological noise (respiration, heart rate) was evaluated. Results Optimal statistical power was obtained for a TR of 0.33 s, but T-values as obtained by AR(1)+w models were strongly dependent on the predefined AR coefficients in fMRI with short TRs which required higher-order AR models to achieve stable statistics. Direct estimation of AR coefficients revealed the highest values within the default mode network while physiological noise had little influence on statistics in cortical structures. Conclusion Colored noise in event-related fMRI obtained at short TRs originates mainly from neural sources and calls for more sophisticated correction of serial autocorrelations which cannot be achieved with standard methods relying on AR(1)+w models with globally fixed AR coefficients.
Published: 2016

19. V17. Functional and structural neuroimaging of the human midbrain at 9,4T

Author: Loureiro, J., Hagberg, G., Ethofer, T., Erb, M., Scheffler, K., and Himmelbach, M.
Published: 2015
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20. Funktionelle Konnektivität der Netzwerke für verbale und non-verbale emotionale Kommunikation: parallele oder hierarchische Informationsverarbeitung?

Author: Ethofer, T, Anders, S, Erb, M, Grodd, W, Wiethoff, S, Herbert, C, Kissler, J, and Wildgruber, D
Published: 2024
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21. Cerebrale Verarbeitung non-verbaler emotionaler Reize: fMRT-Studie zum Einfluss der emotionalen Ausdrucksstärke

Author: Wildgruber, D, Ethofer, T, Droll, C, Reiterer, S, Anders, S, and Grodd, W
Published: 2024
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22. Cerebrale Verarbeitung akustischer Signale: Diskrimination von Tondauer- und Tonhöhenunterschieden

Author: Reiterer, S, Erb, M, Droll, C, Anders, S, Ethofer, T, Grodd, W, and Wildgruber, D
Published: 2024
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23. Atypische hereditäre Creutzfeldt-Jakob-Krankheit (CJD) – diagnostische Relevanz von FDG-PET und MR-Spektroskopie

Author: Henkel, K, Grasbon-Frodl, EM, Mottaghy, FM, Ethofer, T, Uttner, I, Zerr, I, Reske, SN, Kretzschmar, HA, Ludolph, AC, and Bengel, D
Published: 2024
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24. Interaktionseffekte bei multimodaler Verarbeitung emotionaler Reize

Author: Ethofer, T, Saur, R, Anders, S, Erb, M, Royen, L, Droll, C, Grodd, W, and Wildgruber, D
Published: 2024
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25. Dissoziation kortikaler und subkortikaler Verarbeitung eines aversiven visuellen Stimulus bei partieller Rindenblindheit

Author: Anders, S, Reiterer, S, Ethofer, T, Lotze, M, Birbaumer, N, Grodd, W, and Wildgruber, D
Published: 2024
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26. P8. Social brain network and autism spectrum disorder: Reduced connectivity to the frontal cortex

Author: Hoffmann, E., primary, Brück, C., additional, Kreifelts, B., additional, Ethofer, T., additional, and Wildgruber, D., additional
Published: 2015
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27. Integrating face and voice in person perception

Author: Campanella, Salvatore, Belin, Pascal, Ethofer, T., Campanella, Salvatore, Belin, Pascal, and Ethofer, T.
Abstract: This book follows a successful symposium organized in June 2009 at the Human Brain Mapping conference. The topic is at the crossroads of two domains of increasing importance and appeal in the neuroimaging/neuroscience community: multi-modal integration, and social neuroscience. Most of our social interactions involve combining information from both the face and voice of other persons: speech information, but also crucial nonverbal information on the person's identity and affective state. The cerebral bases of the multimodal integration of speech have been intensively investigated; by contrast only few studies have focused on nonverbal aspects of face-voice integration. This work highlights recent advances in investigations of the behavioral and cerebral bases of face-voice multimodal integration in the context of person perception, focusing on the integration of affective and identity information. Several research domains are brought together. Behavioral and neuroimaging work in normal adult humans included are presented alongside evidence from other domains to provide complementary perspectives: studies in human children for a developmental perspective, studies in non-human primates for an evolutionary perspective, and studies in human clinical populations for a clinical perspective. Several research domains are brought together. Behavioral and neuroimaging work in normal adult humans included are presented alongside evidence from other domains to provide complementary perspectives: studies in human children for a developmental perspective, studies in non-human primates for an evolutionary perspective, and studies in human clinical populations for a clinical perspective. Several research domains are brought together. Behavioral and neuroimaging work in normal adult humans included are presented alongside evidence from other domains to provide complementary perspectives: studies in human children for a developmental perspective, studies in non-human primates for an, eBook: http://dx.doi.org/10.1007/978-1-4614-3585-3, SCOPUS: bk.b, info:eu-repo/semantics/published
Published: 2012

28. Funktionelle Konnektivität der Netzwerke für verbale und non-verbale emotionale Kommunikation: parallele oder hierarchische Informationsverarbeitung?

Author: Ethofer, T, primary, Anders, S, additional, Erb, M, additional, Grodd, W, additional, Wiethoff, S, additional, Herbert, C, additional, Kissler, J, additional, and Wildgruber, D, additional
Published: 2005
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29. Proton MR spectroscopy in succinic semialdehyde dehydrogenase deficiency

Author: Ethofer, T., primary, Seeger, U., additional, Klose, U., additional, Erb, M., additional, Kardatzki, B., additional, Kraft, E., additional, Landwehrmeyer, G. B., additional, Grodd, W., additional, and Storch, A., additional
Published: 2004
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30. Atypische hereditäre Creutzfeldt-Jakob-Krankheit (CJD) - diagnostische Relevanz von FDG-PET und MR-Spektroskopie

Author: Henkel, K, primary, Grasbon-Frodl, EM, additional, Mottaghy, FM, additional, Ethofer, T, additional, Uttner, I, additional, Zerr, I, additional, Reske, SN, additional, Kretzschmar, HA, additional, Ludolph, AC, additional, and Bengel, D, additional
Published: 2004
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31. Interaktionseffekte bei multimodaler Verarbeitung emotionaler Reize

Author: Ethofer, T, primary, Saur, R, additional, Anders, S, additional, Erb, M, additional, Royen, L, additional, Droll, C, additional, Grodd, W, additional, and Wildgruber, D, additional
Published: 2004
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32. Dissoziation kortikaler und subkortikaler Verarbeitung eines aversiven visuellen Stimulus bei partieller Rindenblindheit

Author: Anders, S, primary, Reiterer, S, additional, Ethofer, T, additional, Lotze, M, additional, Birbaumer, N, additional, Grodd, W, additional, and Wildgruber, D, additional
Published: 2004
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33. Cerebrale Verarbeitung akustischer Signale: Diskrimination von Tondauer- und Tonhöhenunterschieden

Author: Reiterer, S, primary, Erb, M, additional, Droll, C, additional, Anders, S, additional, Ethofer, T, additional, Grodd, W, additional, and Wildgruber, D, additional
Published: 2004
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34. Cerebrale Verarbeitung non-verbaler emotionaler Reize: fMRT-Studie zum Einfluss der emotionalen Ausdrucksstärke

Author: Wildgruber, D, primary, Ethofer, T, additional, Droll, C, additional, Reiterer, S, additional, Anders, S, additional, and Grodd, W, additional
Published: 2004
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35. Validation of an ESI-MS/MS screening method for acylcarnitine profiling in urine specimens of neonates, children, adolescents and adults

Author: Mueller, P, primary, Schulze, A, additional, Schindler, I, additional, Ethofer, T, additional, Buehrdel, P, additional, and Ceglarek, U, additional
Published: 2003
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36. Changes in cortical activation during retrieval of clock time representations in patients with mild cognitive impairment and early Alzheimer's disease.

Author: Leyhe T, Erb M, Milian M, Eschweiler GW, Ethofer T, Grodd W, and Saur R
Abstract: OBJECTIVE: We investigated healthy controls (HCs), and patients with mild cognitive impairment (MCI) and early Alzheimer's disease (AD) to identify neuronal correlates of clock time representation and changes resulting from neurodegenerative processes using functional magnetic resonance imaging. METHODS: Two clock-specific tasks demanding conceptual knowledge of clock hands, i.e. a minute hand and an hour hand task, were compared with a semantic control task. RESULTS: We observed that the minute hand task provoked a stronger activation of areas in the parietal lobes known to be involved in spatial mental imagery, while the semantic task primarily activated regions of the superior temporal lobes associated with verbal conceptual knowledge. The performance of the MCI group did not differ from that of the HC group, but additional activation was found in several brain regions. Decreased activation was detected during the minute hand task in the right middle temporal gyrus. Patients with early AD showed deteriorated performance in both clock tasks along with reduced activation in the occipital lobes and the left fusiform gyrus. Additional activation was detected in the precuneus. CONCLUSIONS: The fusiform gyrus might be crucial for the visual-semantic retrieval of clock time representation. In patients with early AD, access to this visual-semantic knowledge appears to be reduced. [ABSTRACT FROM AUTHOR]
Published: 2009
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37. Decoding Inter-individual Relations from Spatial Similarity of Brain Activity.

Author: Anders, S., Haynes, J.-D., and Ethofer, T.
Published: 2010
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38. Virtual Histology of Cortical Thickness and Shared Neurobiology in 6 Psychiatric Disorders

Author: Committee, Writing, Disorder, Autism Spectrum, French, Leon, Grevet, Eugenio H, Groenewold, Nynke A, Grotegerd, Dominik, Gruber, Oliver, Gruner, Patricia, Guerrero-Pedraza, Amalia, Gur, Raquel E, Gur, Ruben C, Haar, Shlomi, Haarman, Bartholomeus C M, Thomopoulos, Sophia I, Haavik, Jan, Hahn, Tim, Hajek, Tomas, Harrison, Benjamin J, Harrison, Neil A, Hartman, Catharina A, Whalley, Heather C, Heslenfeld, Dirk J, Hibar, Derrek P, Hilland, Eva, Pozzi, Elena, Hirano, Yoshiyuki, Ho, Tiffany C, Hoekstra, Pieter J, Hoekstra, Liesbeth, Hohmann, Sarah, Hong, L. E., Höschl, Cyril, Høvik, Marie F, Howells, Fleur M, Nenadic, Igor, Abe, Yoshinari, Jalbrzikowski, Maria, James, Anthony C, Janssen, Joost, Jaspers-Fayer, Fern, Xu, Jian, Jonassen, Rune, Karkashadze, Georgii, King, Joseph A, Kircher, Tilo, Kirschner, Matthias, Abé, Christoph, Koch, Kathrin, Kochunov, Peter, Kohls, Gregor, Konrad, Kerstin, Krämer, Bernd, Krug, Axel, Kuntsi, Jonna, Kwon, Jun Soo, Landén, Mikael, Landrø, Nils I, Anticevic, Alan, Lazaro, Luisa, Lebedeva, Irina S, Leehr, Elisabeth J, Lera-Miguel, Sara, Lesch, Klaus-Peter, Lochner, Christine, Louza, Mario R, Luna, Beatriz, Lundervold, Astri J, MacMaster, Frank P, Alda, Martin, Maglanoc, Luigi A, Malpas, Charles B, Portella, Maria J, Marsh, Rachel, Martyn, Fiona M, Mataix-Cols, David, Mathalon, Daniel H, McCarthy, Hazel, McDonald, Colm, McPhilemy, Genevieve, Aleman, Andre, Meinert, Susanne, Menchón, José M, Minuzzi, Luciano, Mitchell, Philip B, Moreno, Carmen, Morgado, Pedro, Muratori, Filippo, Murphy, Clodagh M, Murphy, Declan, Mwangi, Benson, Alloza, Clara, Nabulsi, Leila, Nakagawa, Akiko, Nakamae, Takashi, Namazova, Leyla, Narayanaswamy, Janardhanan, Jahanshad, Neda, Nguyen, Danai D, Nicolau, Rosa, O'Gorman Tuura, Ruth L, O'Hearn, Kirsten, Alonso-Lana, Silvia, Oosterlaan, Jaap, Opel, Nils, Ophoff, Roel A, Oranje, Bob, García de la Foz, Victor Ortiz, Overs, Bronwyn J, Paloyelis, Yannis, Pantelis, Christos, Parellada, Mara, Pauli, Paul, Disorder, Bipolar, Ameis, Stephanie H, Picó-Pérez, Maria, Picon, Felipe A, Piras, Fabrizio, Piras, Federica, Plessen, Kerstin J, Pomarol-Clotet, Edith, Preda, Adrian, Puig, Olga, Quidé, Yann, Radua, Joaquim, Anagnostou, Evdokia, Ramos-Quiroga, J Antoni, Rasser, Paul E, Rauer, Lisa, Reddy, Janardhan, Redlich, Ronny, Reif, Andreas, Reneman, Liesbeth, Repple, Jonathan, Retico, Alessandra, Richarte, Vanesa, McIntosh, Andrew A, Richter, Anja, Rosa, Pedro G P, Rubia, Katya K, Hashimoto, Ryota, Sacchet, Matthew D, Salvador, Raymond, Santonja, Javier, Sarink, Kelvin, Sarró, Salvador, Satterthwaite, Theodore D, Arango, Celso, Sawa, Akira, Schall, Ulrich, Schofield, Peter R, Schrantee, Anouk, Seitz, Jochen, Serpa, Mauricio H, Setién-Suero, Esther, Shaw, Philip, Shook, Devon, Silk, Tim J, Arnold, Paul D, Sim, Kang, Simon, Schmitt, Simpson, Helen Blair, Singh, Aditya, Skoch, Antonin, Skokauskas, Norbert, Soares, Jair C, Soreni, Noam, Soriano-Mas, Carles, Spalletta, Gianfranco, Asherson, Philip, Spaniel, Filip, Lawrie, Stephen M, Stern, Emily R, Stewart, S Evelyn, Takayanagi, Yoichiro, Temmingh, Henk S, Tolin, David F, Tomecek, David, Tordesillas-Gutiérrez, Diana, Tosetti, Michela, Assogna, Francesca, Uhlmann, Anne, van Amelsvoort, Therese, van der Wee, Nic J A, van der Werff, Steven J A, van Haren, Neeltje E M, van Wingen, Guido A, Vance, Alasdair, Vázquez-Bourgon, Javier, Vecchio, Daniela, Venkatasubramanian, Ganesan, Auzias, Guillaume, Vieta, Eduard, Vilarroya, Oscar, Vives-Gilabert, Yolanda, Voineskos, Aristotle N, Völzke, Henry, von Polier, Georg G, Walton, Esther, Weickert, Thomas W, Weickert, Cynthia Shannon, Weideman, Andrea S, Ayesa-Arriola, Rosa, Wittfeld, Katharina, Wolf, Daniel H, Wu, Mon-Ju, Yang, T. T., Yang, Sikun, Yoncheva, Yuliya, Yun, Je-Yeon, Cheng, Yuqi, Zanetti, Marcus V, Ziegler, Georg C, Bakker, Geor, Franke, Barbara, Hoogman, Martine, Buitelaar, Jan K, van Rooij, Daan, Andreassen, Ole A, Ching, Christopher R K, Veltman, Dick J, Schmaal, Lianne, Stein, Dan J, van den Heuvel, Odile A, Disorder, Major Depressive, Banaj, Nerisa, Turner, Jessica A, van Erp, Theo G M, Pausova, Zdenka, Thompson, Paul M, Paus, Tomáš, Attention-Deficit/Hyperactivity Disorder, Banaschewski, Tobias, Bandeira, Cibele E, Baranov, Alexandr, Bargalló, Núria, Bau, Claiton H D, Baumeister, Sarah, Baune, Bernhard T, Bellgrove, Mark A, Benedetti, Francesco, Disorder, Obsessive-Compulsive, Bertolino, Alessandro, Boedhoe, Premika S W, Boks, Marco, Bollettini, Irene, Del Mar Bonnin, Caterina, Borgers, Tiana, Borgwardt, Stefan, Brandeis, Daniel, Brennan, Brian P, Bruggemann, Jason M, Groups, Schizophrenia ENIGMA Working, Bülow, Robin, Busatto, Geraldo F, Calderoni, Sara, Calhoun, Vince D, Calvo, Rosa, Canales-Rodríguez, Erick J, Cannon, Dara M, Carr, Vaughan J, Cascella, Nicola, Cercignani, Mara, Patel, Yash, Chaim-Avancini, Tiffany M, Christakou, Anastasia, Coghill, David, Conzelmann, Annette, Crespo-Facorro, Benedicto, Cubillo, Ana I, Cullen, Kathryn R, Cupertino, Renata B, Daly, Eileen, Dannlowski, Udo, Parker, Nadine, Davey, Christopher G, Denys, Damiaan, Deruelle, Christine, Di Giorgio, Annabella, Dickie, Erin W, Dima, Danai, Dohm, Katharina, Ehrlich, Stefan, Ely, Benjamin A, Erwin-Grabner, Tracy, Shin, Jean, Ethofer, Thomas, Fair, Damien A, Fallgatter, Andreas, Faraone, Stephen V, Fatjó-Vilas, Mar, Fedor, Jennifer M, Fitzgerald, Kate D, Ford, Judith M, Frodl, Thomas, Fu, Cynthia H Y, Howard, Derek, Fullerton, Janice M, Gabel, Matt C, Glahn, David C, Roberts, Gloria, Gogberashvili, Tinatin, Goikolea, Jose M, Gotlib, Ian H, Goya-Maldonado, Roberto, Grabe, Hans, Green, Melissa J, Patel, Y., Parker, N., Shin, J., Howard, D., French, L., Thomopoulos, S. I., Pozzi, E., Abe, Y., Abe, C., Anticevic, A., Alda, M., Aleman, A., Alloza, C., Alonso-Lana, S., Ameis, S. H., Anagnostou, E., Mcintosh, A. A., Arango, C., Arnold, P. D., Asherson, P., Assogna, F., Auzias, G., Ayesa-Arriola, R., Bakker, G., Banaj, N., Banaschewski, T., Bandeira, C. E., Baranov, A., Bargallo, N., Bau, C. H. D., Baumeister, S., Baune, B. T., Bellgrove, M. A., Benedetti, F., Bertolino, A., Boedhoe, P. S. W., Boks, M., Bollettini, I., Del Mar Bonnin, C., Borgers, T., Borgwardt, S., Brandeis, D., Brennan, B. P., Bruggemann, J. M., Bulow, R., Busatto, G. F., Calderoni, S., Calhoun, V. D., Calvo, R., Canales-Rodriguez, E. J., Cannon, D. M., Carr, V. J., Cascella, N., Cercignani, M., Chaim-Avancini, T. M., Christakou, A., Coghill, D., Conzelmann, A., Crespo-Facorro, B., Cubillo, A. I., Cullen, K. R., Cupertino, R. B., Daly, E., Dannlowski, U., Davey, C. G., Denys, D., Deruelle, C., Di Giorgio, A., Dickie, E. W., Dima, D., Dohm, K., Ehrlich, S., Ely, B. A., Erwin-Grabner, T., Ethofer, T., Fair, D. A., Fallgatter, A. J., Faraone, S. V., Fatjo-Vilas, M., Fedor, J. M., Fitzgerald, K. D., Ford, J. M., Frodl, T., Fu, C. H. Y., Fullerton, J. M., Gabel, M. C., Glahn, D. C., Roberts, G., Gogberashvili, T., Goikolea, J. M., Gotlib, I. H., Goya-Maldonado, R., Grabe, H. J., Green, M. J., Grevet, E. H., Groenewold, N. A., Grotegerd, D., Gruber, O., Gruner, P., Guerrero-Pedraza, A., Gur, R. E., Gur, R. C., Haar, S., Haarman, B. C. M., Haavik, J., Hahn, T., Hajek, T., Harrison, B. J., Harrison, N. A., Hartman, C. A., Whalley, H. C., Heslenfeld, D. J., Hibar, D. P., Hilland, E., Hirano, Y., Ho, T. C., Hoekstra, P. J., Hoekstra, L., Hohmann, S., Hong, L. E., Hoschl, C., Hovik, M. F., Howells, F. M., Nenadic, I., Jalbrzikowski, M., James, A. C., Janssen, J., Jaspers-Fayer, F., Xu, J., Jonassen, R., Karkashadze, G., King, J. A., Kircher, T., Kirschner, M., Koch, K., Kochunov, P., Kohls, G., Konrad, K., Kramer, B., Krug, A., Kuntsi, J., Kwon, J. S., Landen, M., Landro, N. I., Lazaro, L., Lebedeva, I. S., Leehr, E. J., Lera-Miguel, S., Lesch, K. -P., Lochner, C., Louza, M. R., Luna, B., Lundervold, A. J., Macmaster, F. P., Maglanoc, L. A., Malpas, C. B., Portella, M. J., Marsh, R., Martyn, F. M., Mataix-Cols, D., Mathalon, D. H., Mccarthy, H., Mcdonald, C., Mcphilemy, G., Meinert, S., Menchon, J. M., Minuzzi, L., Mitchell, P. B., Moreno, C., Morgado, P., Muratori, F., Murphy, C. M., Murphy, D., Mwangi, B., Nabulsi, L., Nakagawa, A., Nakamae, T., Namazova, L., Narayanaswamy, J., Jahanshad, N., Nguyen, D. D., Nicolau, R., O'Gorman Tuura, R. L., O'Hearn, K., Oosterlaan, J., Opel, N., Ophoff, R. A., Oranje, B., Garcia De La Foz, V. O., Overs, B. J., Paloyelis, Y., Pantelis, C., Parellada, M., Pauli, P., Pico-Perez, M., Picon, F. A., Piras, F., Plessen, K. J., Pomarol-Clotet, E., Preda, A., Puig, O., Quide, Y., Radua, J., Ramos-Quiroga, J. A., Rasser, P. E., Rauer, L., Reddy, J., Redlich, R., Reif, A., Reneman, L., Repple, J., Retico, A., Richarte, V., Richter, A., Rosa, P. G. P., Rubia, K. K., Hashimoto, R., Sacchet, M. D., Salvador, R., Santonja, J., Sarink, K., Sarro, S., Satterthwaite, T. D., Sawa, A., Schall, U., Schofield, P. R., Schrantee, A., Seitz, J., Serpa, M. H., Setien-Suero, E., Shaw, P., Shook, D., Silk, T. J., Sim, K., Simon, S., Simpson, H. B., Singh, A., Skoch, A., Skokauskas, N., Soares, J. C., Soreni, N., Soriano-Mas, C., Spalletta, G., Spaniel, F., Lawrie, S. M., Stern, E. R., Stewart, S. E., Takayanagi, Y., Temmingh, H. S., Tolin, D. F., Tomecek, D., Tordesillas-Gutierrez, D., Tosetti, M., Uhlmann, A., Van Amelsvoort, T., Van Der Wee, N. J. A., Van Der Werff, S. J. A., Van Haren, N. E. M., Van Wingen, G. A., Vance, A., Vazquez-Bourgon, J., Vecchio, D., Venkatasubramanian, G., Vieta, E., Vilarroya, O., Vives-Gilabert, Y., Voineskos, A. N., Volzke, H., Von Polier, G. G., Walton, E., Weickert, T. W., Weickert, C. S., Weideman, A. S., Wittfeld, K., Wolf, D. H., Wu, M. -J., Yang, T. T., Yang, K., Yoncheva, Y., Yun, J. -Y., Cheng, Y., Zanetti, M. V., Ziegler, G. C., Franke, B., Hoogman, M., Buitelaar, J. K., Van Rooij, D., Andreassen, O. A., Ching, C. R. K., Veltman, D. J., Schmaal, L., Stein, D. J., Van Den Heuvel, O. A., Turner, J. A., Van Erp, T. G. M., Pausova, Z., Thompson, P. M., Paus, T., Institut de Neurosciences de la Timone (INT), Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS), Pediatric surgery, Radiology and nuclear medicine, Anatomy and neurosciences, Psychiatry, Amsterdam Neuroscience - Brain Imaging, Amsterdam Neuroscience - Compulsivity, Impulsivity & Attention, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, Amsterdam Neuroscience - Neurodegeneration, Psychiatrie & Neuropsychologie, RS: MHeNs - R2 - Mental Health, MUMC+: MA Med Staf Spec Psychiatrie (9), Adult Psychiatry, ANS - Compulsivity, Impulsivity & Attention, General Paediatrics, ARD - Amsterdam Reproduction and Development, Radiology and Nuclear Medicine, APH - Personalized Medicine, ANS - Brain Imaging, ANS - Mood, Anxiety, Psychosis, Stress & Sleep, APH - Mental Health, University of Zurich, Clinical Cognitive Neuropsychiatry Research Program (CCNP), Clinical Neuropsychology, Interdisciplinary Centre Psychopathology and Emotion regulation (ICPE), Child and Adolescent Psychiatry / Psychology, IBBA, and Cognitive Psychology
Subjects: Male, Obsessive-Compulsive Disorder, Bipolar Disorder, Autism Spectrum Disorder, Autism, [SDV]Life Sciences [q-bio], Gene Expression, cytology [Cerebral Cortex], Cohort Studies, Fetal Development, physiology [Gene Expression], 2738 Psychiatry and Mental Health, 0302 clinical medicine, diagnostic imaging [Cerebral Cortex], SCHIZOPHRENIA, BRAIN, Child, Obsessive-compulsive disorder (OCD), Original Investigation, Aged, 80 and over, Cerebral Cortex, 0303 health sciences, pathology [Depressive Disorder, Major], Principal Component Analysis, Adolescent psychiatry, 10058 Department of Child and Adolescent Psychiatry, Middle Aged, diagnostic imaging [Obsessive-Compulsive Disorder], REGIONS, Magnetic Resonance Imaging, 3. Good health, FALSE DISCOVERY RATE, Psychiatry and Mental health, Autism spectrum disorder, Schizophrenia, growth & development [Cerebral Cortex], Child, Preschool, Major depressive disorder, diagnostic imaging [Schizophrenia], Esquizofrènia, Female, Psiquiatria infantil, Psiquiatria de l'adolescència, diagnostic imaging [Autism Spectrum Disorder], Adult, medicine.medical_specialty, Adolescent, Human Development, 610 Medicine & health, diagnostic imaging [Bipolar Disorder], pathology [Autism Spectrum Disorder], diagnostic imaging [Depressive Disorder, Major], 03 medical and health sciences, Young Adult, All institutes and research themes of the Radboud University Medical Center, Neuroimaging, SDG 3 - Good Health and Well-being, CEREBRAL-CORTEX, Child psychiatry, medicine, Attention deficit hyperactivity disorder, Humans, Bipolar disorder, ddc:610, Psychiatry, pathology [Schizophrenia], 030304 developmental biology, Aged, Depressive Disorder, Major, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], business.industry, DENDRITE, Computational Biology, Correction, pathology [Attention Deficit Disorder with Hyperactivity], physiology [Fetal Development], medicine.disease, PATHOLOGY, pathology [Bipolar Disorder], pathology [Obsessive-Compulsive Disorder], 10036 Medical Clinic, Attention Deficit Disorder with Hyperactivity, 10054 Clinic for Psychiatry, Psychotherapy, and Psychosomatics, Case-Control Studies, DENSITY, ORIGINS, HIPPOCAMPUS, diagnostic imaging [Attention Deficit Disorder with Hyperactivity], pathology [Cerebral Cortex], Autisme, business, Neuroscience, 030217 neurology & neurosurgery, physiology [Human Development]
Abstract: [Importance] Large-scale neuroimaging studies have revealed group differences in cortical thickness across many psychiatric disorders. The underlying neurobiology behind these differences is not well understood., [Objective] To determine neurobiologic correlates of group differences in cortical thickness between cases and controls in 6 disorders: attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder (ASD), bipolar disorder (BD), major depressive disorder (MDD), obsessive-compulsive disorder (OCD), and schizophrenia., [Design, Setting, and Participants] Profiles of group differences in cortical thickness between cases and controls were generated using T1-weighted magnetic resonance images. Similarity between interregional profiles of cell-specific gene expression and those in the group differences in cortical thickness were investigated in each disorder. Next, principal component analysis was used to reveal a shared profile of group difference in thickness across the disorders. Analysis for gene coexpression, clustering, and enrichment for genes associated with these disorders were conducted. Data analysis was conducted between June and December 2019. The analysis included 145 cohorts across 6 psychiatric disorders drawn from the ENIGMA consortium. The numbers of cases and controls in each of the 6 disorders were as follows: ADHD: 1814 and 1602; ASD: 1748 and 1770; BD: 1547 and 3405; MDD: 2658 and 3572; OCD: 2266 and 2007; and schizophrenia: 2688 and 3244., [Main Outcomes and Measures] Interregional profiles of group difference in cortical thickness between cases and controls., [Results] A total of 12 721 cases and 15 600 controls, ranging from ages 2 to 89 years, were included in this study. Interregional profiles of group differences in cortical thickness for each of the 6 psychiatric disorders were associated with profiles of gene expression specific to pyramidal (CA1) cells, astrocytes (except for BD), and microglia (except for OCD); collectively, gene-expression profiles of the 3 cell types explain between 25% and 54% of variance in interregional profiles of group differences in cortical thickness. Principal component analysis revealed a shared profile of difference in cortical thickness across the 6 disorders (48% variance explained); interregional profile of this principal component 1 was associated with that of the pyramidal-cell gene expression (explaining 56% of interregional variation). Coexpression analyses of these genes revealed 2 clusters: (1) a prenatal cluster enriched with genes involved in neurodevelopmental (axon guidance) processes and (2) a postnatal cluster enriched with genes involved in synaptic activity and plasticity-related processes. These clusters were enriched with genes associated with all 6 psychiatric disorders., [Conclusions and Relevance] In this study, shared neurobiologic processes were associated with differences in cortical thickness across multiple psychiatric disorders. These processes implicate a common role of prenatal development and postnatal functioning of the cerebral cortex in these disorders.
Published: 2021

39. Characterizing neuroanatomic heterogeneity in people with and without ADHD based on subcortical brain volumes

Author: Li, Ting, Rooij, Daan, Roth Mota, Nina, Buitelaar, Jan K., Hoogman, Martine, Arias Vasquez, Alejandro, Franke, Barbara, Ambrosino, Sara, Banaschewski, Tobias, Bandeira, Cibele E., Bau, Claiton H.D., Baumeister, Sarah, Baur‐Streubel, Ramona, Bellgrove, Mark A., Biederman, Joseph, Bralten, Janita, Bramati, Ivanei E., Brandeis, Daniel, Berm, Silvia, Busatto, Geraldo F., Calvo, Anna, Castellanos, Francisco X., Cercignani, Mara, Chantiluke, Kaylita C., Christakou, Anastasia, Coghill, David, Conzelmann, Annette, Cubillo, Ana I., Cupertino, Renata B., Zeeuw, Parick, Durston, Sarah, Earl, Eric A., Epstein, Jeffery N., Ethofer, Thomas, Fallgatter, Andreas J., Fair, Damien A., Faraone, Stephen V., Frodl, Thomas, Gabel, Matt C., Gogberashvili, Tinatin, Grevet, Eugenio H., Haavik, Jan, Harrison, Neil A., Hartman, Catharina A., Heslenfeld, Dirk J., Hoekstra, Pieter J., Høvik, Marie F., Jahanshad, Neda, Kardatzki, Bernd, Karkashadze, Georgii, Kelly, Clare, Kohls, Gregor, Konrad, Kerstin, Kuntsi, Jonna, Lazaro, Luisa, Lera‐Miguel, Sara, Lesch, Klaus‐Peter, Louza, Mario R., Lundervold, Astri J., Malpas, Charles B., Mattos, Paulo, McCarthy, Hazel, Nicolau, Rosa, Nigg, Joel T., O'Gorman Tuura, Ruth L., Oosterlaan, Jaap, Oranje, Bob, Paloyelis, Yannis, Pauli, Paul, Picon, Felipe A., Plessen, Kerstin J., Ramos‐Quiroga, J. Antoni, Reif, Andreas, Reneman, Liesbeth, Rosa, Pedro G.P., Rubia, Katya, Schrantee, Anouk, Schweren, Lizanne J.S., Seitz, Jochen, Shaw, Philip, Silk, Tim J., Skokauskas, Norbert, Carlos Soliva Vila, Juan, Soloveva, Anastasiia, Stevens, Michael C., Sudre, Gustavo, Tamm, Leanne, Thompson, Paul M., Tovar‐Moll, Fernanda, Erp, Theo GM, Vance, Alasdair, Vilarroya, Oscar, Vives‐Gilabert, Yolanda, Polier, Georg G., Walitza, Susanne, Yoncheva, Yuliya N., Zanetti, Marcus V., Ziegler, Georg C., Anikin, Anatoly, Asherson, Philip, Baranov, Alexandr, Chaim‐Avanicini, Tiffany, Dale, Anders M., Doyle, Alysa E., Jernigan, Terry, Hohmann, Sarah, Kapilushniy, Dmitry, Mehta, Mitul, Namazova‐Baranova, Leyla, Novotny, Stephanie E., Oberwelland Weiss, Eileen, Schwarz, Lena, General Paediatrics, ARD - Amsterdam Reproduction and Development, Radiology and Nuclear Medicine, APH - Mental Health, APH - Personalized Medicine, ANS - Brain Imaging, ANS - Compulsivity, Impulsivity & Attention, ENIGMA ADHD Working Group, Ambrosino, S., Banaschewski, T., Bandeira, C.E., Bau, CHD, Baumeister, S., Baur-Streubel, R., Bellgrove, M.A., Biederman, J., Bralten, J., Bramati, I.E., Brandeis, D., Berm, S., Busatto, G.F., Calvo, A., Castellanos, F.X., Cercignani, M., Chantiluke, K.C., Christakou, A., Coghill, D., Conzelmann, A., Cubillo, A.I., Cupertino, R.B., de Zeeuw, P., Durston, S., Earl, E.A., Epstein, J.N., Ethofer, T., Fallgatter, A.J., Fair, D.A., Faraone, S.V., Frodl, T., Gabel, M.C., Gogberashvili, T., Grevet, E.H., Haavik, J., Harrison, N.A., Hartman, C.A., Heslenfeld, D.J., Hoekstra, P.J., Høvik, M.F., Jahanshad, N., Kardatzki, B., Karkashadze, G., Kelly, C., Kohls, G., Konrad, K., Kuntsi, J., Lazaro, L., Lera-Miguel, S., Lesch, K.P., Louza, M.R., Lundervold, A.J., Malpas, C.B., Mattos, P., McCarthy, H., Nicolau, R., Nigg, J.T., O'Gorman Tuura, R.L., Oosterlaan, J., Oranje, B., Paloyelis, Y., Pauli, P., Picon, F.A., Plessen, K.J., Ramos-Quiroga, J.A., Reif, A., Reneman, L., Rosa, PGP, Rubia, K., Schrantee, A., Schweren, LJS, Seitz, J., Shaw, P., Silk, T.J., Skokauskas, N., Carlos Soliva Vila, J., Soloveva, A., Stevens, M.C., Sudre, G., Tamm, L., Thompson, P.M., Tovar-Moll, F., van Erp, T.G., Vance, A., Vilarroya, O., Vives-Gilabert, Y., von Polier, G.G., Walitza, S., Yoncheva, Y.N., Zanetti, M.V., Ziegler, G.C., Anikin, A., Asherson, P., Baranov, A., Chaim-Avanicini, T., Dale, A.M., Doyle, A.E., L Jernigan, T., Hohmann, S., Kapilushniy, D., Mehta, M., Namazova-Baranova, L., Novotny, S.E., Oberwelland Weiss, E., and Schwarz, L.
Subjects: Adult, Attention Deficit Disorder with Hyperactivity/diagnostic imaging, Attention Deficit Disorder with Hyperactivity/epidemiology, Brain/diagnostic imaging, Case-Control Studies, Female, Humans, Magnetic Resonance Imaging, Male, Thalamus/diagnostic imaging, ADHD, community detection, effect sizes, neuroanatomic heterogeneity, subcortical volume, INCREASED EFFECT, 0302 clinical medicine, Limbic system, Neurodevelopmental disorder, Thalamus, 130 000 Cognitive Neurology & Memory, Basal ganglia, Developmental and Educational Psychology, Psychology, Pediatric, 0303 health sciences, 05 social sciences, Brain, Exploratory factor analysis, Psychiatry and Mental health, Mental Health, medicine.anatomical_structure, Attention Deficit Disorder (ADD), Cognitive Sciences, Original Article, 050104 developmental & child psychology, Clinical psychology, Clinical Sciences, Patient subgroups, Developmental & Child Psychology, 03 medical and health sciences, ENIGMA ADHD Working Group, Clinical Research, mental disorders, medicine, In patient, 0501 psychology and cognitive sciences, ddc:610, 030304 developmental biology, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], business.industry, Neurosciences, Case-control study, Original Articles, medicine.disease, Attention Deficit Hyperactivity Disorder (ADHD), Brain Disorders, Attention Deficit Disorder with Hyperactivity, Sample size determination, Pediatrics, Perinatology and Child Health, Etiology, business, 030217 neurology & neurosurgery
Abstract: The journal of child psychology and psychiatry 62(9), 1140-1149 (2021). doi:10.1111/jcpp.13384, Published by Wiley-Blackwell, Oxford
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40. Validation of the Self-Report Version of the German Strengths and Weaknesses of ADHD Symptoms and Normal Behavior Scale (SWAN-DE-SB).

Author: Blume F, Buhr L, Kühnhausen J, Köpke R, Weber LA, Fallgatter AJ, Ethofer T, and Gawrilow C
Abstract: Adults with attention-deficit/hyperactivity disorder (ADHD) experience impairing levels of inattention and/or hyperactivity-impulsivity, while individuals without ADHD experience these symptoms to a lesser extent. Yet, ADHD self-report scales so far hardly captured continuous distributions across the general population. In addition, they focused on weaknesses and ignored strengths. To address these shortcomings, we present here the Strengths and Weaknesses of ADHD and Normal-Behavior Scale Self-Report (SWAN-DE-SB) . The normal distribution of the data collected and the scale's internal consistency, and factorial and convergent validity were assessed using data from a general population sample. Its clinical utility was evaluated by comparing scores from a clinical sample and a sample of individuals without ADHD and by calculating optimal cut-off values for specificity and sensitivity. The SWAN-DE-SB demonstrated normal distribution of the data collected, high internal consistency, and factorial and convergent validity. It reliably discriminated individuals with and without ADHD, with high specificity and sensitivity. It should therefore be considered a psychometrically convincing measure to assess strengths and weaknesses of ADHD symptoms and normal behavior in clinical and general population samples., Competing Interests: Declaration of Conflicting InterestsThe author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Published: 2024
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41. Investigating the effect of hippocampal sclerosis on parietal memory network.

Author: Ethofer S, Milian M, Erb M, Rona S, Honegger J, and Ethofer T
Subjects: Humans, Temporal Lobe surgery, Brain, Hippocampal Sclerosis, Epilepsy, Temporal Lobe surgery, Memory, Episodic
Abstract: Objective: We aimed to investigate differences in episodic memory networks between patients with temporal lobe epilepsy (TLE) due to hippocampal sclerosis and healthy controls, especially with regards to the parietal memory network (PMN), as well as their relation to neuropsychological memory performance after mesial temporal resection., Methods: 28 healthy subjects as well as 21 patients with TLE (12 left, 9 right) were investigated using a spatial memory fMRI paradigm, which has been shown to activate the PMN. Regions of interest (ROI) were defined based on the results of the second-level analyses and activations within the predefined ROIs were compared across groups and correlated with postoperative verbal and nonverbal memory scores., Results: Healthy subjects showed activations within regions belonging to the dorsal visual stream and the PMN as well as the bilateral parahippocampal place area, the bilateral frontal eye field, and the bilateral middle frontal gyrus. Comparison between groups revealed that TLE patients activated significantly less in the left middle occipital gyrus and the right precuneus. The activation pattern in left TLE patients showed further reductions, mainly in areas belonging to the dorsal visual stream and the PMN within the left hemisphere. Activations within the left superior parietal lobulus, bilateral inferior parietal lobulus, bilateral middle temporal gyrus, left precuneus, left frontal eye field, and left middle frontal gyrus correlated significantly with postoperative verbal memory scores, and activations within the left superior parietal lobulus, left inferior parietal lobulus, left middle temporal gyrus, and left precuneus correlated significantly with higher performance in postoperative nonverbal memory scores., Significance: The PMN is involved in episodic memory encoding. Higher activations in areas belonging to the PMN and the dorsal visual stream, especially within the left hemisphere, before amygdalohippocampectomy may result in higher postoperative memory scores., Plain Language Summary: This study aims to investigate the effects of epilepsy due to hippocampal sclerosis, i.e. scarring in the temporal lobe, on memory networks in the brain. We discovered that especially patients with left-sided hippocampal sclerosis show reduced brain activations in visual areas and memory networks within the left hemisphere of the brain during orientation in space. Importantly, higher activations within these areas may result in better memory after epilepsy surgery., (© 2023 The Authors. Epilepsia Open published by Wiley Periodicals LLC on behalf of International League Against Epilepsy.)
Published: 2024
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42. Treatment of adult attention-deficit hyperactivity disorder (ADHD) with transcranial direct current stimulation (tDCS): study protocol for a parallel, randomized, double-blinded, sham-controlled, multicenter trial (Stim-ADHD).

Author: Mauche N, Ulke C, Huang J, Franke A, Bogatsch H, Ethofer T, Grimm O, Frodl T, Hoffmann K, Juckel G, Kittel-Schneider S, Mehren A, Philipsen A, Plewnia C, Reif A, Ziegler GC, and Strauß M
Subjects: Adult, Humans, Cognition, Double-Blind Method, Multicenter Studies as Topic, Randomized Controlled Trials as Topic, Treatment Outcome, Attention Deficit Disorder with Hyperactivity diagnosis, Central Nervous System Stimulants therapeutic use, Transcranial Direct Current Stimulation methods
Abstract: Transcranial direct current stimulation (tDCS) is a non-invasive brain stimulation treatment used as an alternative or complementary treatment for various neuropsychiatric disorders, and could be an alternative or add-on therapy to psychostimulants in attention-deficit hyperactivity disorder (ADHD). Previous studies provided some evidence for improvements in cognition and clinical symptoms in pediatric and adult ADHD patients. However, data from multi-center randomized controlled trials (RCTs) for this condition are lacking. Thus, our aim is to evaluate short- and mid-term effects of tDCS in this multi-center, randomized, double blind, and sham-controlled, parallel group clinical trial with a 1:1 randomization ratio. Primary endpoint is the total score of DSM-IV scale of the internationally established Conners' Adult ADHD Rating Scales (German self-report screening version, CAARS-S-SR), at day 14 post-intervention (p.i.) to detect short-term lasting effects analyzed via analyses of covariance (ANCOVAs). In case of significant between-groups differences at day 14 p.i., hierarchically ordered hypotheses on mid-term lasting effects will be investigated by linear mixed models with visit (5 time points), treatment, treatment by visit interaction, and covariates as fixed categorical effects plus a patient-specific visit random effect, using an unstructured covariance structure to model the residual within-patient errors. Positive results of this clinical trial will expand the treatment options for adult ADHD patients with tDCS and provide an alternative or add-on therapy to psychostimulants with a low risk for side effects.Trial Registration The trial was registered on July 29, 2022 in the German Clinical Trials Register (DRKS00028148)., (© 2023. The Author(s).)
Published: 2024
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43. The impact of emotional dysregulation and comorbid depressive symptoms on clinical features, brain arousal, and treatment response in adults with ADHD.

Author: Huang J, Mauche N, Ahlers E, Bogatsch H, Böhme P, Ethofer T, Fallgatter AJ, Gallinat J, Hegerl U, Heuser I, Hoffmann K, Kittel-Schneider S, Reif A, Schöttle D, Unterecker S, and Strauß M
Abstract: Introduction: The role of emotional dysregulation (ED) in attention-deficit/hyperactivity disorder (ADHD) has become an important issue. This study, in which we analyzed data from a predictive pharmaco-EEG-trial, aimed to examine whether symptoms of ED in adult ADHD affect ADHD symptom severity, brain arousal regulation as measured by resting EEG, and the response to stimulant medication., Methods: ED is defined as having a sex- and age-corrected T -score of >70 on the emotional lability subscale of the German version of Conners' Adult ADHD Rating Scale. A total of 115 participants were included in the study, 56 of whom had ED. Participants with ED were more impaired in terms of the severity of core ADHD symptoms, especially inattentive symptoms, comorbid depressive symptoms, interpersonal relationships, and quality of life. In addition, participants with ED were more likely to report a total score above 13 on the Beck Depression Inventory-II, which was considered to be the cutoff for mild depression., Results: No differences were found between the ED and non-ED groups in response to stimulant medication or in brain arousal regulation. In addition, there was no significant effect of ED with comorbid depressive symptoms on treatment response. There was a trend for subgroups that showed a change in brain arousal regulation associated with symptom improvement., Discussion: Our findings may support the assumption that ED may be an important feature of ADHD. The use of EEG-based brain arousal regulation as a diagnostic and predictive tool in ADHD in the presence of ED and comorbid depressive symptoms should be further investigated., Competing Interests: MS has received speaker’s fees from MEDICE Arzneimittel Pütter GmbH & Co. KG and Takeda and was an advisory board member for Takeda in the past 3 years. AR has received honoraria for advisory boards or talks from MEDICE Arzneimittel Pütter GmbH & Co. KG, Takeda, Janssen, Boehringer Ingelheim, SAGE/Biogen, cyclerion, COMPASS and LivaNova. JG has received research funding from the German Federal Ministry of Education and Research, German Science Foundation, and speaker fees from Lundbeck, Janssen-Cilag, Lilly, and Boehringer. SK-S. has received author’s and speaker’s honoraria from Takeda and Medice Arzneimittel Pütter GmbH &Co. KG in the past 3 years. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2024 Huang, Mauche, Ahlers, Bogatsch, Böhme, Ethofer, Fallgatter, Gallinat, Hegerl, Heuser, Hoffmann, Kittel-Schneider, Reif, Schöttle, Unterecker and Strauß.)
Published: 2024
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44. Prediction of estimated risk for bipolar disorder using machine learning and structural MRI features.

Author: Mikolas P, Marxen M, Riedel P, Bröckel K, Martini J, Huth F, Berndt C, Vogelbacher C, Jansen A, Kircher T, Falkenberg I, Lambert M, Kraft V, Leicht G, Mulert C, Fallgatter AJ, Ethofer T, Rau A, Leopold K, Bechdolf A, Reif A, Matura S, Bermpohl F, Fiebig J, Stamm T, Correll CU, Juckel G, Flasbeck V, Ritter P, Bauer M, and Pfennig A
Subjects: Humans, Brain diagnostic imaging, Brain pathology, Magnetic Resonance Imaging methods, Machine Learning, Recognition, Psychology, Support Vector Machine, Bipolar Disorder diagnostic imaging, Bipolar Disorder pathology
Abstract: Background: Individuals with bipolar disorder are commonly correctly diagnosed a decade after symptom onset. Machine learning techniques may aid in early recognition and reduce the disease burden. As both individuals at risk and those with a manifest disease display structural brain markers, structural magnetic resonance imaging may provide relevant classification features., Methods: Following a pre-registered protocol, we trained linear support vector machine (SVM) to classify individuals according to their estimated risk for bipolar disorder using regional cortical thickness of help-seeking individuals from seven study sites ( N = 276). We estimated the risk using three state-of-the-art assessment instruments (BPSS-P, BARS, EPI bipolar )., Results: For BPSS-P, SVM achieved a fair performance of Cohen's κ of 0.235 (95% CI 0.11-0.361) and a balanced accuracy of 63.1% (95% CI 55.9-70.3) in the 10-fold cross-validation. In the leave-one-site-out cross-validation, the model performed with a Cohen's κ of 0.128 (95% CI -0.069 to 0.325) and a balanced accuracy of 56.2% (95% CI 44.6-67.8). BARS and EPI bipolar could not be predicted. In post hoc analyses, regional surface area, subcortical volumes as well as hyperparameter optimization did not improve the performance., Conclusions: Individuals at risk for bipolar disorder, as assessed by BPSS-P, display brain structural alterations that can be detected using machine learning. The achieved performance is comparable to previous studies which attempted to classify patients with manifest disease and healthy controls. Unlike previous studies of bipolar risk, our multicenter design permitted a leave-one-site-out cross-validation. Whole-brain cortical thickness seems to be superior to other structural brain features.
Published: 2024
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45. Association of polygenic score and the involvement of cholinergic and glutamatergic pathways with lithium treatment response in patients with bipolar disorder.

Author: Amare AT, Thalamuthu A, Schubert KO, Fullerton JM, Ahmed M, Hartmann S, Papiol S, Heilbronner U, Degenhardt F, Tekola-Ayele F, Hou L, Hsu YH, Shekhtman T, Adli M, Akula N, Akiyama K, Ardau R, Arias B, Aubry JM, Hasler R, Richard-Lepouriel H, Perroud N, Backlund L, Bhattacharjee AK, Bellivier F, Benabarre A, Bengesser S, Biernacka JM, Birner A, Marie-Claire C, Cervantes P, Chen HC, Chillotti C, Cichon S, Cruceanu C, Czerski PM, Dalkner N, Del Zompo M, DePaulo JR, Étain B, Jamain S, Falkai P, Forstner AJ, Frisen L, Frye MA, Gard S, Garnham JS, Goes FS, Grigoroiu-Serbanescu M, Fallgatter AJ, Stegmaier S, Ethofer T, Biere S, Petrova K, Schuster C, Adorjan K, Budde M, Heilbronner M, Kalman JL, Kohshour MO, Reich-Erkelenz D, Schaupp SK, Schulte EC, Senner F, Vogl T, Anghelescu IG, Arolt V, Dannlowski U, Dietrich D, Figge C, Jäger M, Lang FU, Juckel G, Konrad C, Reimer J, Schmauß M, Schmitt A, Spitzer C, von Hagen M, Wiltfang J, Zimmermann J, Andlauer TFM, Fischer A, Bermpohl F, Ritter P, Matura S, Gryaznova A, Falkenberg I, Yildiz C, Kircher T, Schmidt J, Koch M, Gade K, Trost S, Haussleiter IS, Lambert M, Rohenkohl AC, Kraft V, Grof P, Hashimoto R, Hauser J, Herms S, Hoffmann P, Jiménez E, Kahn JP, Kassem L, Kuo PH, Kato T, Kelsoe J, Kittel-Schneider S, Ferensztajn-Rochowiak E, König B, Kusumi I, Laje G, Landén M, Lavebratt C, Leboyer M, Leckband SG, Tortorella A, Manchia M, Martinsson L, McCarthy MJ, McElroy S, Colom F, Millischer V, Mitjans M, Mondimore FM, Monteleone P, Nievergelt CM, Nöthen MM, Novák T, O'Donovan C, Ozaki N, Pfennig A, Pisanu C, Potash JB, Reif A, Reininghaus E, Rouleau GA, Rybakowski JK, Schalling M, Schofield PR, Schweizer BW, Severino G, Shilling PD, Shimoda K, Simhandl C, Slaney CM, Squassina A, Stamm T, Stopkova P, Maj M, Turecki G, Vieta E, Veeh J, Witt SH, Wright A, Zandi PP, Mitchell PB, Bauer M, Alda M, Rietschel M, McMahon FJ, Schulze TG, Clark SR, and Baune BT
Subjects: Humans, Female, Male, Adult, Middle Aged, Treatment Outcome, Bayes Theorem, Genome-Wide Association Study methods, Glutamic Acid metabolism, Cohort Studies, Lithium Compounds therapeutic use, Lithium Compounds pharmacology, Acetylcholine metabolism, Polymorphism, Single Nucleotide genetics, Antimanic Agents therapeutic use, Antimanic Agents pharmacology, Bipolar Disorder drug therapy, Bipolar Disorder genetics, Multifactorial Inheritance genetics, Lithium therapeutic use, Lithium pharmacology
Abstract: Lithium is regarded as the first-line treatment for bipolar disorder (BD), a severe and disabling mental health disorder that affects about 1% of the population worldwide. Nevertheless, lithium is not consistently effective, with only 30% of patients showing a favorable response to treatment. To provide personalized treatment options for bipolar patients, it is essential to identify prediction biomarkers such as polygenic scores. In this study, we developed a polygenic score for lithium treatment response (Li + PGS ) in patients with BD. To gain further insights into lithium's possible molecular mechanism of action, we performed a genome-wide gene-based analysis. Using polygenic score modeling, via methods incorporating Bayesian regression and continuous shrinkage priors, Li + PGS was developed in the International Consortium of Lithium Genetics cohort (ConLi + Gen: N = 2367) and replicated in the combined PsyCourse (N = 89) and BipoLife (N = 102) studies. The associations of Li + PGS and lithium treatment response - defined in a continuous ALDA scale and a categorical outcome (good response vs. poor response) were tested using regression models, each adjusted for the covariates: age, sex, and the first four genetic principal components. Statistical significance was determined at P < 0.05. Li + PGS was positively associated with lithium treatment response in the ConLi + Gen cohort, in both the categorical (P = 9.8 × 10 - 12 , R 2 = 1.9%) and continuous (P = 6.4 × 10 - 9 , R 2 = 2.6%) outcomes. Compared to bipolar patients in the 1 st decile of the risk distribution, individuals in the 10 th decile had 3.47-fold (95%CI: 2.22-5.47) higher odds of responding favorably to lithium. The results were replicated in the independent cohorts for the categorical treatment outcome (P = 3.9 × 10 - 4 , R 2 = 0.9%), but not for the continuous outcome (P = 0.13). Gene-based analyses revealed 36 candidate genes that are enriched in biological pathways controlled by glutamate and acetylcholine. Li + PGS may be useful in the development of pharmacogenomic testing strategies by enabling a classification of bipolar patients according to their response to treatment., (© 2023. The Author(s).)
Published: 2023
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46. Daring to Feel: Emotion-Focused Psychotherapy Increases Amygdala Activation and Connectivity in Euthymic Bipolar Disorder-A Randomized Controlled Trial.

Author: Meyer K, Hindi Attar C, Fiebig J, Stamm T, Bassett TR, Bauer M, Dannlowski U, Ethofer T, Falkenberg I, Jansen A, Juckel G, Kircher T, Mulert C, Leicht G, Rau A, Rauh J, Ritter D, Ritter P, Trost S, Vogelbacher C, Walter H, Wolter S, Hautzinger M, and Bermpohl F
Subjects: Humans, Brain Mapping, Neural Pathways, Amygdala, Emotions physiology, Psychotherapy, Bipolar Disorder
Abstract: Background: In bipolar disorder (BD), the alternation of extreme mood states indicates deficits in emotion processing, accompanied by aberrant neural function of the emotion network. The present study investigated the effects of an emotion-centered psychotherapeutic intervention on amygdala responsivity and connectivity during emotional face processing in BD., Methods: In a randomized controlled trial within the multicentric BipoLife project, euthymic patients with BD received one of two interventions over 6 months: an unstructured, emotion-focused intervention (FEST), where patients were guided to adequately perceive and label their emotions (n = 28), or a specific, structured, cognitive behavioral intervention (SEKT) (n = 31). Before and after interventions, functional magnetic resonance imaging was conducted while patients completed an emotional face-matching paradigm (final functional magnetic resonance imaging sample of patients completing both measurements: SEKT, n = 17; FEST, n = 17). Healthy control subjects (n = 32) were scanned twice after the same interval without receiving any intervention. Given the focus of FEST on emotion processing, we expected FEST to strengthen amygdala activation and connectivity., Results: Clinically, both interventions stabilized patients' euthymic states in terms of affective symptoms. At the neural level, FEST versus SEKT increased amygdala activation and amygdala-insula connectivity at postintervention relative to preintervention time point. In FEST, the increase in amygdala activation was associated with fewer depressive symptoms (r = 0.72) 6 months after intervention., Conclusions: Enhanced activation and functional connectivity of the amygdala after FEST versus SEKT may represent a neural marker of improved emotion processing, supporting the FEST intervention as an effective tool in relapse prevention in patients with BD., (Copyright © 2023. Published by Elsevier Inc.)
Published: 2023
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47. Machine Learning Prediction of Estimated Risk for Bipolar Disorders Using Hippocampal Subfield and Amygdala Nuclei Volumes.

Author: Huth F, Tozzi L, Marxen M, Riedel P, Bröckel K, Martini J, Berndt C, Sauer C, Vogelbacher C, Jansen A, Kircher T, Falkenberg I, Thomas-Odenthal F, Lambert M, Kraft V, Leicht G, Mulert C, Fallgatter AJ, Ethofer T, Rau A, Leopold K, Bechdolf A, Reif A, Matura S, Biere S, Bermpohl F, Fiebig J, Stamm T, Correll CU, Juckel G, Flasbeck V, Ritter P, Bauer M, Pfennig A, and Mikolas P
Abstract: The pathophysiology of bipolar disorder (BD) remains mostly unclear. Yet, a valid biomarker is necessary to improve upon the early detection of this serious disorder. Patients with manifest BD display reduced volumes of the hippocampal subfields and amygdala nuclei. In this pre-registered analysis, we used structural MRI ( n = 271, 7 sites) to compare volumes of hippocampus, amygdala and their subfields/nuclei between help-seeking subjects divided into risk groups for BD as estimated by BPSS-P, BARS and EPI bipolar . We performed between-group comparisons using linear mixed effects models for all three risk assessment tools. Additionally, we aimed to differentiate the risk groups using a linear support vector machine. We found no significant volume differences between the risk groups for all limbic structures during the main analysis. However, the SVM could still classify subjects at risk according to BPSS-P criteria with a balanced accuracy of 66.90% (95% CI 59.2-74.6) for 10-fold cross-validation and 61.9% (95% CI 52.0-71.9) for leave-one-site-out. Structural alterations of the hippocampus and amygdala may not be as pronounced in young people at risk; nonetheless, machine learning can predict the estimated risk for BD above chance. This suggests that neural changes may not merely be a consequence of BD and may have prognostic clinical value.
Published: 2023
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48. Boosting the Theory of Mind Network: Specific Psychotherapy Increases Neural Correlates of Affective Theory of Mind in Euthymic Bipolar Disorder.

Author: Meyer K, Hindi Attar C, Fiebig J, Stamm T, Bassett TR, Bauer M, Dannlowski U, Ethofer T, Falkenberg I, Jansen A, Juckel G, Kircher T, Mulert C, Leicht G, Rau A, Ritter D, Ritter P, Trost S, Vogelbacher C, Walter H, Wolter S, Hautzinger M, and Bermpohl F
Subjects: Humans, Brain, Cyclothymic Disorder, Psychotherapy, Bipolar Disorder, Theory of Mind physiology
Abstract: Background: In bipolar disorder, impaired affective theory of mind (aToM) performance and aberrant neural activation in the ToM brain network partly explain social functioning impairments. However, it is not yet known whether psychotherapy of bipolar disorder influences neuroimaging markers of aToM., Methods: In this study, conducted within the multicentric randomized controlled trial of the BipoLife consortium, patients with euthymic bipolar disorder underwent 2 group interventions over 6 months (mean = 28.45 weeks): 1) a specific, cognitive behavioral intervention (specific psychotherapeutic intervention [SEKT]) (n = 31) targeting impulse regulation, ToM, and social skills and 2) an emotion-focused intervention (FEST) (n = 28). To compare the effect of SEKT and FEST on neural correlates of aToM, patients performed an aToM task during functional magnetic resonance imaging before and after interventions (final functional magnetic resonance imaging sample of pre- and postcompleters, SEKT: n = 16; FEST: n = 17). Healthy control subjects (n = 32) were scanned twice with the same time interval. Because ToM was trained in SEKT, we expected an increased ToM network activation in SEKT relative to FEST postintervention., Results: Both treatments effectively stabilized patients' euthymic state in terms of affective symptoms, life satisfaction, and global functioning. Confirming our expectations, SEKT patients showed increased neural activation within regions of the ToM network, bilateral temporoparietal junction, posterior cingulate cortex, and precuneus, whereas FEST patients did not., Conclusions: The stabilizing effect of SEKT on clinical outcomes went along with increased neural activation of the ToM network, while FEST possibly exerted its positive effect by other, yet unexplored routes., (Copyright © 2022 Society of Biological Psychiatry. Published by Elsevier Inc. All rights reserved.)
Published: 2023
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49. Neurobiological correlates and attenuated positive social intention attribution during laughter perception associated with degree of autistic traits.

Author: Martinelli A, Hoffmann E, Brück C, Kreifelts B, Ethofer T, and Wildgruber D
Subjects: Adult, Humans, Female, Brain Mapping methods, Intention, Magnetic Resonance Imaging methods, Social Perception, Autistic Disorder, Laughter, Autism Spectrum Disorder
Abstract: Laughter plays an important role in group formation, signaling social belongingness by indicating a positive or negative social intention towards the receiver. In adults without autism, the intention of laughter can be correctly differentiated without further contextual information. In autism spectrum disorder (ASD), however, differences in the perception and interpretation of social cues represent a key characteristic of the disorder. Studies suggest that these differences are associated with hypoactivation and altered connectivity among key nodes of the social perception network. How laughter, as a multimodal nonverbal social cue, is perceived and processed neurobiologically in association with autistic traits has not been assessed previously. We investigated differences in social intention attribution, neurobiological activation, and connectivity during audiovisual laughter perception in association with the degree of autistic traits in adults [N = 31, M age (SD) = 30.7 (10.0) years, n female = 14]. An attenuated tendency to attribute positive social intention to laughter was found with increasing autistic traits. Neurobiologically, autistic trait scores were associated with decreased activation in the right inferior frontal cortex during laughter perception and with attenuated connectivity between the bilateral fusiform face area with bilateral inferior and lateral frontal, superior temporal, mid-cingulate and inferior parietal cortices. Results support hypoactivity and hypoconnectivity during social cue processing with increasing ASD symptoms between socioemotional face processing nodes and higher-order multimodal processing regions related to emotion identification and attribution of social intention. Furthermore, results reflect the importance of specifically including signals of positive social intention in future studies in ASD., (© 2023. The Author(s).)
Published: 2023
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50. Association of Polygenic Score and the involvement of Cholinergic and Glutamatergic Pathways with Lithium Treatment Response in Patients with Bipolar Disorder.

Author: Amare A, Thalamuthu A, Schubert KO, Fullerton J, Ahmed M, Hartmann S, Papiol S, Heilbronner U, Degenhardt F, Tekola-Ayele F, Hou L, Hsu YH, Shekhtman T, Adli M, Akula N, Akiyama K, Ardau R, Arias B, Aubry JM, Backlund L, Bhattacharjee AK, Bellivier F, Benabarre A, Bengesser S, Biernacka J, Birner A, Marie-Claire C, Cervantes P, Chen HC, Chillotti C, Cichon S, Cruceanu C, Czerski P, Dalkner N, Del Zompo M, DePaulo JR, Etain B, Jamain S, Falkai P, Forstner AJ, Frisén L, Frye M, Gard S, Garnham J, Goes F, Grigoroiu-Serbanescu M, Fallgatter A, Stegmaier S, Ethofer T, Biere S, Petrova K, Schuster C, Adorjan K, Budde M, Heilbronner M, Kalman J, Oraki Kohshour M, Reich-Erkelenz D, Schaupp S, Schulte E, Senner F, Vogl T, Anghelescu IG, Arolt V, Dannlowski U, Dietrich DE, Figge C, Jäger M, Lang F, Juckel G, Spitzer C, Reimer J, Schmauß M, Schmitt A, Konrad C, von Hagen M, Wiltfang J, Zimmermann J, Andlauer T, Fischer A, Bermpohl F, Kraft V, Matura S, Gryaznova A, Falkenberg I, Yildiz C, Kircher T, Schmidt J, Koch M, Gade K, Trost S, Haußleiter I, Lambert M, Rohenkohl AC, Kraft V, Grof P, Hashimoto R, Hauser J, Herms S, Hoffmann P, Jiménez E, Kahn JP, Kassem L, Kuo PH, Kato T, Kelsoe J, Kittel-Schneider S, Ferensztajn-Rochowiak E, König B, Kusumi I, Laje G, Landén M, Lavebratt C, Leboyer M, Leckband SG, Tortorella A, Manchia M, Martinsson L, McCarthy M, McElroy SL, Colom F, Mitjans M, Mondimore F, Monteleone P, Nievergelt C, Nöthen M, Novak T, O'Donovan C, Ozaki N, Pfennig A, Pisanu C, Potash J, Reif A, Reininghaus E, Rouleau G, Rybakowski JK, Schalling M, Schofield P, Schweizer BW, Severino G, Shilling PD, Shimoda K, Simhandl C, Slaney C, Squassina A, Stamm T, Stopkova P, Maj M, Turecki G, Vieta E, Veeh J, Witt S, Wright A, Zandi P, Mitchell P, Bauer M, Alda M, Rietschel M, McMahon F, Schulze TG, Millischer V, Clark S, and Baune B
Abstract: Lithium is regarded as the first-line treatment for bipolar disorder (BD), a severe and disabling mental disorder that affects about 1% of the population worldwide. Nevertheless, lithium is not consistently effective, with only 30% of patients showing a favorable response to treatment. To provide personalized treatment options for bipolar patients, it is essential to identify prediction biomarkers such as polygenic scores. In this study, we developed a polygenic score for lithium treatment response (Li+PGS) in patients with BD. To gain further insights into lithium's possible molecular mechanism of action, we performed a genome-wide gene-based analysis. Using polygenic score modeling, via methods incorporating Bayesian regression and continuous shrinkage priors, Li+PGS was developed in the International Consortium of Lithium Genetics cohort (ConLi+Gen: N=2,367) and replicated in the combined PsyCourse (N=89) and BipoLife (N=102) studies. The associations of Li+PGS and lithium treatment response - defined in a continuous ALDA scale and a categorical outcome (good response vs. poor response) were tested using regression models, each adjusted for the covariates: age, sex, and the first four genetic principal components. Statistical significance was determined at P<��.
Published: 2023
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