Search

Your search keyword '"Frants, Rune"' showing total 774 results
Start Over Author "Frants, Rune"
774 results on '"Frants, Rune"'

1. Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder

Author

Jacobsen, Kaya K, Nievergelt, Caroline M, Zayats, Tetyana, Greenwood, Tiffany A, Anttila, Verneri, Akiskal, Hagop S, Consortium, BiGS, Consortium, IHG, include:, BiGS Consortium Co-Authors, Kelsoe, John R, McKinney, Rebecca, Shilling, Paul D, Smith, Erin N, Schork, Nicholas J, Bloss, Cinnamon S, Nurnberger, John I, Edenberg, Howard J, Foroud, Tatiana, Koller, Daniel L, Gershon, Elliot S, Badner, Judith A, Liu, Chunyu, Scheftner, William A, Lawson, William B, Nwulia, Evaristus A, Hipolito, Maria, Potash, James, Coryell, William, Rice, John, Byerley, William, McMahon, Francis J, Berrettini, Wade H, Zandi, Peter P, Mahon, Pamela B, McInnis, Melvin G, Zöllner, Sebastian, Zhang, Peng, Craig, David W, Szelinger, Szabolics, Barrett, Thomas B, Schulze, Thomas G, include:, IHG Consortium Co-Authors, Wedenoja, Juho, Kaunisto, Mari A, Heikkilä, Kauko, Kaprio, Jaakko, Wessman, Maija, Kallela, Mikko, Färkkilä, Markus, Artto, Ville, Aromaa, Arpo, Eriksson, Johan G, Winsvold, Bendik S, Zwart, John-Anker, Gormley, Padhraig, Palotie, Aarno, Kurth, Tobias, Rose, Lynda M, Buring, Julie E, Ridker, Paul M, Chasman, Daniel I, Bettella, Francesco, Steinberg, Stacy, Stefansson, Hreinn, Stefansson, Kari, McMahon, George, Davey-Smith, George, Malik, Rainer, Freilinger, Tobias, Wichmann, Heinz Erich, Dichgans, Martin, Muller-Myhsok, Bertram, Meitinger, Thomas, de Vries, Boukje, Terwindt, Gisela, Stam, Anine H, Frants, Rune R, Pelzer, Nadine, Weller, Claudia M, Zielman, Ronald, Ferrari, Michel D, van den Maagdenberg, Arn MJM, Medland, Sarah E, Montgomery, Grant W, Martin, Nicholas G, Nyholt, Dale R, Todt, Unda, Borck, Guntram, Kubisch, Christian, Quaye, Lydia, Williams, Frances MK, Cherkas, Lynn, Koiranen, Markku, Hartikainen, Anna-Liisa, Pouta, Anneli, Jarvelin, Marjo-Riitta, Ikram, M Arfan, and van den Ende, Joyce

Subjects
Biomedical and Clinical Sciences, Headaches, Bipolar Disorder, Human Genome, Genetics, Mental Health, Pain Research, Migraines, Serious Mental Illness, Chronic Pain, Mental Illness, Neurosciences, Brain Disorders, 2.1 Biological and endogenous factors, Neurological, Adult, Carrier Proteins, Comorbidity, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Male, Migraine Disorders, Nerve Tissue Proteins, Polymorphism, Single Nucleotide, Bipolar disorder, Migraine, NBEA, Neurobeachin, BiGS Consortium, IHG Consortium, Medical and Health Sciences, Psychology and Cognitive Sciences, Psychiatry, Biomedical and clinical sciences, Health sciences, Psychology
Abstract

BackgroundMigraine is a common comorbidity among individuals with bipolar disorder, but the underlying mechanisms for this co-occurrence are poorly understood. The aim of this study was to investigate the genetic background of bipolar patients with and without migraine.MethodsWe performed a genome-wide association analysis contrasting 460 bipolar migraneurs with 914 bipolar patients without migraine from the Bipolar Genome Study (BiGS).ResultsWe identified one genome-wide significant association between migraine in bipolar disorder patients and rs1160720, an intronic single nucleotide polymorphism (SNP) in the NBEA gene (P=2.97 × 10(-8), OR: 1.82, 95% CI: 1.47-2.25), although this was not replicated in a smaller sample of 289 migraine cases.LimitationsOur study is based on self-reported migraine.ConclusionsNBEA encodes neurobeachin, a scaffolding protein primarily expressed in the brain and involved in trafficking of vesicles containing neurotransmitter receptors. This locus has not previously been implicated in migraine per se. We found no evidence of association in data from the GWAS migraine meta-analysis consortium (n=118,710 participants) suggesting that the association might be specific to migraine co-morbid with bipolar disorder.

Published
2015

2. Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.

Author

Dastani, Zari, Hivert, Marie-France, Timpson, Nicholas, Perry, John RB, Yuan, Xin, Scott, Robert A, Henneman, Peter, Heid, Iris M, Kizer, Jorge R, Lyytikäinen, Leo-Pekka, Fuchsberger, Christian, Tanaka, Toshiko, Morris, Andrew P, Small, Kerrin, Isaacs, Aaron, Beekman, Marian, Coassin, Stefan, Lohman, Kurt, Qi, Lu, Kanoni, Stavroula, Pankow, James S, Uh, Hae-Won, Wu, Ying, Bidulescu, Aurelian, Rasmussen-Torvik, Laura J, Greenwood, Celia MT, Ladouceur, Martin, Grimsby, Jonna, Manning, Alisa K, Liu, Ching-Ti, Kooner, Jaspal, Mooser, Vincent E, Vollenweider, Peter, Kapur, Karen A, Chambers, John, Wareham, Nicholas J, Langenberg, Claudia, Frants, Rune, Willems-Vandijk, Ko, Oostra, Ben A, Willems, Sara M, Lamina, Claudia, Winkler, Thomas W, Psaty, Bruce M, Tracy, Russell P, Brody, Jennifer, Chen, Ida, Viikari, Jorma, Kähönen, Mika, Pramstaller, Peter P, Evans, David M, St Pourcain, Beate, Sattar, Naveed, Wood, Andrew R, Bandinelli, Stefania, Carlson, Olga D, Egan, Josephine M, Böhringer, Stefan, van Heemst, Diana, Kedenko, Lyudmyla, Kristiansson, Kati, Nuotio, Marja-Liisa, Loo, Britt-Marie, Harris, Tamara, Garcia, Melissa, Kanaya, Alka, Haun, Margot, Klopp, Norman, Wichmann, H-Erich, Deloukas, Panos, Katsareli, Efi, Couper, David J, Duncan, Bruce B, Kloppenburg, Margreet, Adair, Linda S, Borja, Judith B, DIAGRAM+ Consortium, MAGIC Consortium, GLGC Investigators, MuTHER Consortium, Wilson, James G, Musani, Solomon, Guo, Xiuqing, Johnson, Toby, Semple, Robert, Teslovich, Tanya M, Allison, Matthew A, Redline, Susan, Buxbaum, Sarah G, Mohlke, Karen L, Meulenbelt, Ingrid, Ballantyne, Christie M, Dedoussis, George V, Hu, Frank B, Liu, Yongmei, Paulweber, Bernhard, Spector, Timothy D, Slagboom, P Eline, Ferrucci, Luigi, and Jula, Antti

Subjects
DIAGRAM+ Consortium, MAGIC Consortium, GLGC Investigators, MuTHER Consortium, DIAGRAM Consortium, GIANT Consortium, Global B Pgen Consortium, Procardis Consortium, MAGIC investigators, GLGC Consortium, Humans, Diabetes Mellitus, Type 2, Insulin Resistance, Genetic Predisposition to Disease, Glucose Tolerance Test, Waist-Hip Ratio, Gene Expression, Polymorphism, Single Nucleotide, African Americans, Asian Continental Ancestry Group, European Continental Ancestry Group, Female, Male, Adiponectin, Cholesterol, HDL, Metabolic Networks and Pathways, Genome-Wide Association Study, Diabetes Mellitus, Type 2, Polymorphism, Single Nucleotide, Cholesterol, HDL, Genetics, Developmental Biology
Abstract

Circulating levels of adiponectin, a hormone produced predominantly by adipocytes, are highly heritable and are inversely associated with type 2 diabetes mellitus (T2D) and other metabolic traits. We conducted a meta-analysis of genome-wide association studies in 39,883 individuals of European ancestry to identify genes associated with metabolic disease. We identified 8 novel loci associated with adiponectin levels and confirmed 2 previously reported loci (P = 4.5×10(-8)-1.2×10(-43)). Using a novel method to combine data across ethnicities (N = 4,232 African Americans, N = 1,776 Asians, and N = 29,347 Europeans), we identified two additional novel loci. Expression analyses of 436 human adipocyte samples revealed that mRNA levels of 18 genes at candidate regions were associated with adiponectin concentrations after accounting for multiple testing (p

Published
2012

3. Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD).

Author

Zeng, Weihua, de Greef, Jessica C, Chen, Yen-Yun, Chien, Richard, Kong, Xiangduo, Gregson, Heather C, Winokur, Sara T, Pyle, April, Robertson, Keith D, Schmiesing, John A, Kimonis, Virginia E, Balog, Judit, Frants, Rune R, Ball, Alexander R, Jr, Lock, Leslie F, Donovan, Peter J, van der Maarel, Silvère M, and Yokomori, Kyoko

Abstract

Facioscapulohumeral dystrophy (FSHD) is an autosomal dominant muscular dystrophy in which no mutation of pathogenic gene(s) has been identified. Instead, the disease is, in most cases, genetically linked to a contraction in the number of 3.3 kb D4Z4 repeats on chromosome 4q. How contraction of the 4qter D4Z4 repeats causes muscular dystrophy is not understood. In addition, a smaller group of FSHD cases are not associated with D4Z4 repeat contraction (termed "phenotypic" FSHD), and their etiology remains undefined. We carried out chromatin immunoprecipitation analysis using D4Z4-specific PCR primers to examine the D4Z4 chromatin structure in normal and patient cells as well as in small interfering RNA (siRNA)-treated cells. We found that SUV39H1-mediated H3K9 trimethylation at D4Z4 seen in normal cells is lost in FSHD. Furthermore, the loss of this histone modification occurs not only at the contracted 4q D4Z4 allele, but also at the genetically intact D4Z4 alleles on both chromosomes 4q and 10q, providing the first evidence that the genetic change (contraction) of one 4qD4Z4 allele spreads its effect to other genomic regions. Importantly, this epigenetic change was also observed in the phenotypic FSHD cases with no D4Z4 contraction, but not in other types of muscular dystrophies tested. We found that HP1gamma and cohesin are co-recruited to D4Z4 in an H3K9me3-dependent and cell type-specific manner, which is disrupted in FSHD. The results indicate that cohesin plays an active role in HP1 recruitment and is involved in cell type-specific D4Z4 chromatin regulation. Taken together, we identified the loss of both histone H3K9 trimethylation and HP1gamma/cohesin binding at D4Z4 to be a faithful marker for the FSHD phenotype. Based on these results, we propose a new model in which the epigenetic change initiated at 4q D4Z4 spreads its effect to other genomic regions, which compromises muscle-specific gene regulation leading to FSHD pathogenesis.

Published
2009

4. Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder

Author

Kelsoe, John R., Greenwood, Tiffany A., Nievergelt, Caroline M., McKinney, Rebecca, Shilling, Paul D., Smith, Erin N., Schork, Nicholas J., Bloss, Cinnamon S., Nurnberger, John I., Jr., Edenberg, Howard J., Foroud, Tatiana, Koller, Daniel L., Gershon, Elliot S., Badner, Judith A., Liu, Chunyu, Scheftner, William A., Lawson, William B., Nwulia, Evaristus A., Hipolito, Maria, Potash, James, Coryell, William, Rice, John, Byerley, William, McMahon, Francis J., Berrettini, Wade H., Zandi, Peter P., Mahon, Pamela B., McInnis, Melvin G., Zöllner, Sebastian, Zhang, Peng, Craig, David W., Szelinger, Szabolics, Barrett, Thomas B., Schulze, Thomas G., Wedenoja, Juho, Kaunisto, Mari A., Heikkilä, Kauko, Kaprio, Jaakko, Wessman, Maija, Kallela, Mikko, Färkkilä, Markus, Artto, Ville, Aromaa, Arpo, Eriksson, Johan G., Winsvold, Bendik S., Zwart, John-Anker, Gormley, Padhraig, Palotie, Aarno, Kurth, Tobias, Rose, Lynda M., Buring, Julie E., Ridker, Paul M., Chasman, Daniel I., Bettella, Francesco, Steinberg, Stacy, Stefansson, Hreinn, Stefansson, Kari, McMahon, George, Davey-Smith, George, Malik, Rainer, Freilinger, Tobias, Erich Wichmann, Heinz, Dichgans, Martin, Muller-Myhsok, Bertram, Meitinger, Thomas, de Vries, Boukje, Terwindt, Gisela, Stam, Anine H., Frants, Rune R., Pelzer, Nadine, Weller, Claudia M., Zielman, Ronald, Ferrari, Michel D., van den Maagdenberg, Arn M.J.M., Medland, Sarah E., Montgomery, Grant W., Martin, Nicholas G., Nyholt, Dale R., Todt, Unda, Borck, Guntram, Kubisch, Christian, Quaye, Lydia, Williams, Frances M.K., Cherkas, Lynn, Koiranen, Markku, Hartikainen, Anna-Liisa, Pouta, Anneli, Jarvelin, Marjo-Riitta, Arfan Ikram, M., van den Ende, Joyce, Uitterlinden, Andre G., Hofman, Albert, Amin, Najaf, van Duijn, Cornelia, Lehtimäki, Terho, Ligthart, Lannie, Hottenga, Jouke-Jan, Vink, Jacqueline M., Penninx, Brenda W., Boomsma, Dorret I., Schürks, Markus, Jakobsson, Finnbogi, Schoenen, Jean, Heath, Andrew C., Madden, Pamela A.F., Göbel, Hartmut, Heinze, Axel, Heinze-Kuhn, Katja, Schreiber, Stefan, Anttila, Verneri, Daly, Mark J., Alexander, Michael, Raitakari, Olli, Strachan, David P., Jacobsen, Kaya K., Zayats, Tetyana, Akiskal, Hagop S., Haavik, Jan, Bernt Fasmer, Ole, Johansson, Stefan, and Oedegaard, Ketil J.

Published
2015
Full Text
View/download PDF

5. A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy

Author

Lemmers, Richard J. L. F., van der Vliet, Patrick J., Klooster, Rinse, Sacconi, Sabrina, Camaño, Pilar, Dauwerse, Johannes G., Snider, Lauren, Straasheijm, Kirsten R., van Ommen, Gert Jan, Padberg, George W., Miller, Daniel G., Tapscott, Stephen J., Tawil, Rabi, Frants, Rune R., and van der Maarel, Silvère M.

Published
2010

13. Worldwide population analysis of the 4q and 10q subtelomeres identifies only four discrete interchromosomal sequence transfers in human evolution

Author

Lemmers, Richard J.L.F., van der Vliet, Patrick J., van der Gaag, Kristiaan J., Zuniga, Sofia, Frants, Rune R., de Knijff, Peter, and van der Maarel, Silvere M.

Subjects
Telomeres -- Research, Human evolution -- Research, Nucleotide sequence -- Research, Haplotypes -- Research, Biological sciences
Abstract

A study of D4Z4 haplotypes in European and non-European world populations is conducted to gain better insights into the dynamic behavior of the subtelomeres of the chromosomes 4q and 10q. A constructed evolutionary network of the subtelomeres identifies only four discrete interchromosomal sequence transfers in human evolution, suggesting that subsequent intrachromosomal mutations must have resulted in the large number of standard and nonstandard haplotypes.

Published
2010

18. Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy

Author

Lemmers, Richard J.L.F., Wohlemuth, Marielle, van der Gaag, Kristiaan J., van der Vliet, Patrick J., van Teijlingen, Corrie M.M., de Knijff, Peter, Padberg, George W., Frants, Rune R., and Maarel, Silvere M. van der

Subjects
Haplotypes -- Research, Muscular dystrophy -- Genetic aspects, Muscular dystrophy -- Research, Single nucleotide polymorphisms -- Research, Biological sciences
Abstract

The studies about the allele-specific sequence differences among 4qA, 4qB, and 10q alleles which underlie the 4qA specificity of facioscapulohumeral muscular dystrophy (FSHD) are presented. Each of the haplotypes was found to have its unique sequence signature which is essential for the development of FSHD specific to single-nucleotide polymorphisms (SNPs) in the disease haplotype.

Published
2007

19. Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease

Author

Bryois, Julien, Skene, Nathan G., Hansen, Thomas Folkmann, Kogelman, Lisette J.A., Watson, Hunna J., Liu, Zijing, Adan, Roger, Alfredsson, Lars, Ando, Tetsuya, Andreassen, Ole, Baker, Jessica, Bergen, Andrew, Berrettini, Wade, Birgegård, Andreas, Boden, Joseph, Boehm, Ilka, Boni, Claudette, Boraska Perica, Vesna, Brandt, Harry, Breen, Gerome, Buehren, Katharina, Bulik, Cynthia, Burghardt, Roland, Cassina, Matteo, Cichon, Sven, Clementi, Maurizio, Coleman, Jonathan, Cone, Roger, Courtet, Philippe, Crawford, Steven, Crow, Scott, Crowley, James, Danner, Unna, Davis, Oliver, de Zwaan, Martina, Dedoussis, George, Degortes, Daniela, DeSocio, Janiece, Dick, Danielle, Dikeos, Dimitris, Dina, Christian, Dmitrzak-Weglarz, Monika, Docampo Martinez, Elisa, Duncan, Laramie, Egberts, Karin, Ehrlich, Stefan, Escaramís, Geòrgia, Esko, Tõnu, Estivill, Xavier, Farmer, Anne, Favaro, Angela, Fernández-Aranda, Fernando, Fichter, Manfred, Fischer, Krista, Föcker, Manuel, Foretova, Lenka, Forstner, Andreas, Forzan, Monica, Franklin, Christopher, Gallinger, Steven, Gaspar, Héléna, Giegling, Ina, Giuranna, Johanna, Giusti-Rodríquez, Paola, Gonidakis, Fragiskos, Gordon, Scott, Gorwood, Philip, Gratacos Mayora, Monica, Grove, Jakob, Guillaume, Sébastien, Guo, Yiran, Hakonarson, Hakon, Halmi, Katherine, Hanscombe, Ken, Hatzikotoulas, Konstantinos, Hauser, Joanna, Hebebrand, Johannes, Helder, Sietske, Henders, Anjali, Herms, Stefan, Herpertz-Dahlmann, Beate, Herzog, Wolfgang, Hinney, Anke, Horwood, L. John, Hübel, Christopher, Huckins, Laura, Hudson, James, Imgart, Hartmut, Inoko, Hidetoshi, Janout, Vladimir, Jiménez-Murcia, Susana, Johnson, Craig, Jordan, Jennifer, Julià, Antonio, Juréus, Anders, Kalsi, Gursharan, Kaminská, Deborah, Kaplan, Allan, Kaprio, Jaakko, Karhunen, Leila, Karwautz, Andreas, Kas, Martien, Kaye, Walter, Kennedy, James, Kennedy, Martin, Keski-Rahkonen, Anna, Kiezebrink, Kirsty, Kim, Youl Ri, Kirk, Katherine, Klareskog, Lars, Klump, Kelly, Knudsen, Gun Peggy, La Via, Maria, Landén, Mikael, Larsen, Janne, Le Hellard, Stephanie, Leppä, Virpi, Levitan, Robert, Li, Dong, Lichtenstein, Paul, Lilenfeld, Lisa, Lin, Bochao Danae, Lissowska, Jolanta, Luykx, Jurjen, Magistretti, Pierre, Maj, Mario, Mannik, Katrin, Marsal, Sara, Marshall, Christian, Martin, Nicholas, Mattheisen, Manuel, Mattingsdal, Morten, McDevitt, Sara, McGuffin, Peter, Medland, Sarah, Metspalu, Andres, Meulenbelt, Ingrid, Micali, Nadia, Mitchell, James, Mitchell, Karen, Monteleone, Palmiero, Monteleone, Alessio Maria, Montgomery, Grant, Mortensen, Preben Bo, Munn-Chernoff, Melissa, Nacmias, Benedetta, Navratilova, Marie, Norring, Claes, Ntalla, Ioanna, Olsen, Catherine, Ophoff, Roel, O’Toole, Julie, Padyukov, Leonid, Palotie, Aarno, Pantel, Jacques, Papezova, Hana, Parker, Richard, Pearson, John, Pedersen, Nancy, Petersen, Liselotte, Pinto, Dalila, Purves, Kirstin, Rabionet, Raquel, Raevuori, Anu, Ramoz, Nicolas, Reichborn-Kjennerud, Ted, Ricca, Valdo, Ripatti, Samuli, Ripke, Stephan, Ritschel, Franziska, Roberts, Marion, Rotondo, Alessandro, Rujescu, Dan, Rybakowski, Filip, Santonastaso, Paolo, Scherag, André, Scherer, Stephen, Schmidt, Ulrike, Schork, Nicholas, Schosser, Alexandra, Seitz, Jochen, Slachtova, Lenka, Slagboom, P. Eline, Slof-Op ‘t Landt, Margarita, Slopien, Agnieszka, Sorbi, Sandro, Strober, Michael, Stuber, Garret, Sullivan, Patrick, Świątkowska, Beata, Szatkiewicz, Jin, Tachmazidou, Ioanna, Tenconi, Elena, Thornton, Laura, Tortorella, Alfonso, Tozzi, Federica, Treasure, Janet, Tsitsika, Artemis, Tyszkiewicz-Nwafor, Marta, Tziouvas, Konstantinos, van Elburg, Annemarie, van Furth, Eric, Wade, Tracey, Wagner, Gudrun, Walton, Esther, Watson, Hunna, Werge, Thomas, Whiteman, David, Widen, Elisabeth, Woodside, D. Blake, Yao, Shuyang, Yilmaz, Zeynep, Zeggini, Eleftheria, Zerwas, Stephanie, Zipfel, Stephan, Anttila, Verneri, Artto, Ville, Belin, Andrea Carmine, de Boer, Irene, Boomsma, Dorret I., Børte, Sigrid, Chasman, Daniel I., Cherkas, Lynn, Christensen, Anne Francke, Cormand, Bru, Cuenca-Leon, Ester, Davey-Smith, George, Dichgans, Martin, van Duijn, Cornelia, Esko, Tonu, Esserlind, Ann Louise, Ferrari, Michel, Frants, Rune R., Freilinger, Tobias, Furlotte, Nick, Gormley, Padhraig, Griffiths, Lyn, Hamalainen, Eija, Hiekkala, Marjo, Ikram, M. Arfan, Ingason, Andres, Järvelin, Marjo Riitta, Kajanne, Risto, Maagdenberg, Arn van den, Nyholt, Dale R., Zhao, Huiying, Bell, Robert, Wilson, Catherine, other, and, Bryois, Julien, Skene, Nathan G., Hansen, Thomas Folkmann, Kogelman, Lisette J.A., Watson, Hunna J., Liu, Zijing, Adan, Roger, Alfredsson, Lars, Ando, Tetsuya, Andreassen, Ole, Baker, Jessica, Bergen, Andrew, Berrettini, Wade, Birgegård, Andreas, Boden, Joseph, Boehm, Ilka, Boni, Claudette, Boraska Perica, Vesna, Brandt, Harry, Breen, Gerome, Buehren, Katharina, Bulik, Cynthia, Burghardt, Roland, Cassina, Matteo, Cichon, Sven, Clementi, Maurizio, Coleman, Jonathan, Cone, Roger, Courtet, Philippe, Crawford, Steven, Crow, Scott, Crowley, James, Danner, Unna, Davis, Oliver, de Zwaan, Martina, Dedoussis, George, Degortes, Daniela, DeSocio, Janiece, Dick, Danielle, Dikeos, Dimitris, Dina, Christian, Dmitrzak-Weglarz, Monika, Docampo Martinez, Elisa, Duncan, Laramie, Egberts, Karin, Ehrlich, Stefan, Escaramís, Geòrgia, Esko, Tõnu, Estivill, Xavier, Farmer, Anne, Favaro, Angela, Fernández-Aranda, Fernando, Fichter, Manfred, Fischer, Krista, Föcker, Manuel, Foretova, Lenka, Forstner, Andreas, Forzan, Monica, Franklin, Christopher, Gallinger, Steven, Gaspar, Héléna, Giegling, Ina, Giuranna, Johanna, Giusti-Rodríquez, Paola, Gonidakis, Fragiskos, Gordon, Scott, Gorwood, Philip, Gratacos Mayora, Monica, Grove, Jakob, Guillaume, Sébastien, Guo, Yiran, Hakonarson, Hakon, Halmi, Katherine, Hanscombe, Ken, Hatzikotoulas, Konstantinos, Hauser, Joanna, Hebebrand, Johannes, Helder, Sietske, Henders, Anjali, Herms, Stefan, Herpertz-Dahlmann, Beate, Herzog, Wolfgang, Hinney, Anke, Horwood, L. John, Hübel, Christopher, Huckins, Laura, Hudson, James, Imgart, Hartmut, Inoko, Hidetoshi, Janout, Vladimir, Jiménez-Murcia, Susana, Johnson, Craig, Jordan, Jennifer, Julià, Antonio, Juréus, Anders, Kalsi, Gursharan, Kaminská, Deborah, Kaplan, Allan, Kaprio, Jaakko, Karhunen, Leila, Karwautz, Andreas, Kas, Martien, Kaye, Walter, Kennedy, James, Kennedy, Martin, Keski-Rahkonen, Anna, Kiezebrink, Kirsty, Kim, Youl Ri, Kirk, Katherine, Klareskog, Lars, Klump, Kelly, Knudsen, Gun Peggy, La Via, Maria, Landén, Mikael, Larsen, Janne, Le Hellard, Stephanie, Leppä, Virpi, Levitan, Robert, Li, Dong, Lichtenstein, Paul, Lilenfeld, Lisa, Lin, Bochao Danae, Lissowska, Jolanta, Luykx, Jurjen, Magistretti, Pierre, Maj, Mario, Mannik, Katrin, Marsal, Sara, Marshall, Christian, Martin, Nicholas, Mattheisen, Manuel, Mattingsdal, Morten, McDevitt, Sara, McGuffin, Peter, Medland, Sarah, Metspalu, Andres, Meulenbelt, Ingrid, Micali, Nadia, Mitchell, James, Mitchell, Karen, Monteleone, Palmiero, Monteleone, Alessio Maria, Montgomery, Grant, Mortensen, Preben Bo, Munn-Chernoff, Melissa, Nacmias, Benedetta, Navratilova, Marie, Norring, Claes, Ntalla, Ioanna, Olsen, Catherine, Ophoff, Roel, O’Toole, Julie, Padyukov, Leonid, Palotie, Aarno, Pantel, Jacques, Papezova, Hana, Parker, Richard, Pearson, John, Pedersen, Nancy, Petersen, Liselotte, Pinto, Dalila, Purves, Kirstin, Rabionet, Raquel, Raevuori, Anu, Ramoz, Nicolas, Reichborn-Kjennerud, Ted, Ricca, Valdo, Ripatti, Samuli, Ripke, Stephan, Ritschel, Franziska, Roberts, Marion, Rotondo, Alessandro, Rujescu, Dan, Rybakowski, Filip, Santonastaso, Paolo, Scherag, André, Scherer, Stephen, Schmidt, Ulrike, Schork, Nicholas, Schosser, Alexandra, Seitz, Jochen, Slachtova, Lenka, Slagboom, P. Eline, Slof-Op ‘t Landt, Margarita, Slopien, Agnieszka, Sorbi, Sandro, Strober, Michael, Stuber, Garret, Sullivan, Patrick, Świątkowska, Beata, Szatkiewicz, Jin, Tachmazidou, Ioanna, Tenconi, Elena, Thornton, Laura, Tortorella, Alfonso, Tozzi, Federica, Treasure, Janet, Tsitsika, Artemis, Tyszkiewicz-Nwafor, Marta, Tziouvas, Konstantinos, van Elburg, Annemarie, van Furth, Eric, Wade, Tracey, Wagner, Gudrun, Walton, Esther, Watson, Hunna, Werge, Thomas, Whiteman, David, Widen, Elisabeth, Woodside, D. Blake, Yao, Shuyang, Yilmaz, Zeynep, Zeggini, Eleftheria, Zerwas, Stephanie, Zipfel, Stephan, Anttila, Verneri, Artto, Ville, Belin, Andrea Carmine, de Boer, Irene, Boomsma, Dorret I., Børte, Sigrid, Chasman, Daniel I., Cherkas, Lynn, Christensen, Anne Francke, Cormand, Bru, Cuenca-Leon, Ester, Davey-Smith, George, Dichgans, Martin, van Duijn, Cornelia, Esko, Tonu, Esserlind, Ann Louise, Ferrari, Michel, Frants, Rune R., Freilinger, Tobias, Furlotte, Nick, Gormley, Padhraig, Griffiths, Lyn, Hamalainen, Eija, Hiekkala, Marjo, Ikram, M. Arfan, Ingason, Andres, Järvelin, Marjo Riitta, Kajanne, Risto, Maagdenberg, Arn van den, Nyholt, Dale R., Zhao, Huiying, Bell, Robert, Wilson, Catherine, and other, and

Abstract

Genome-wide association studies have discovered hundreds of loci associated with complex brain disorders, but it remains unclear in which cell types these loci are active. Here we integrate genome-wide association study results with single-cell transcriptomic data from the entire mouse nervous system to systematically identify cell types underlying brain complex traits. We show that psychiatric disorders are predominantly associated with projecting excitatory and inhibitory neurons. Neurological diseases were associated with different cell types, which is consistent with other lines of evidence. Notably, Parkinson’s disease was genetically associated not only with cholinergic and monoaminergic neurons (which include dopaminergic neurons) but also with enteric neurons and oligodendrocytes. Using post-mortem brain transcriptomic data, we confirmed alterations in these cells, even at the earliest stages of disease progression. Our study provides an important framework for understanding the cellular basis of complex brain maladies, and reveals an unexpected role of oligodendrocytes in Parkinson’s disease.

Published
2020

29. Genetics of headaches

Author

Van Den Maagdenberg, Arn M.J.M., primary, Terwindt, Gisela M., additional, Haan, Joost, additional, Frants, Rune R., additional, and Ferrari, Michel D., additional

Published
2010
Full Text
View/download PDF

35. Contributor's List

Author

Berkovic, Samuel F., primary, Bilguvar, Kaya, additional, Blackstone, Craig, additional, Bloch, Michael H., additional, Blumenfeld, Hal, additional, Bredesen, D.E., additional, Bressman, Susan B., additional, Brucal, Michelle, additional, Burton, Edward A., additional, Dalmau, Josep, additional, Dawson, Ted M., additional, Dawson, Valina L., additional, Depondt, Chantal, additional, DiLuna, Michael L., additional, DiMauro, Salvatore, additional, Ferrari, Michel D., additional, Fink, David J., additional, Flügel, Alexander, additional, Frants, Rune R., additional, Glorioso, Joseph C., additional, Goadsby, Peter J., additional, Goldin, Alan L., additional, Gunel, Murat, additional, Harel, Noam Y., additional, Helbig, Ingo, additional, Hemmen, Thomas M., additional, Hisama, Fuki M., additional, Hyman, Bradley T., additional, Ingelsson, Martin, additional, Johnson, Dennis R., additional, Kamholz, John, additional, Kaul, Marcus, additional, Kocsis, Jeffery D., additional, Lammers, Gert Jan, additional, Leckman, James F., additional, Li, Jun, additional, Lipton, Stuart A., additional, Maragakis, Nicholas J., additional, Mehlen, P., additional, Morimoto, Richard I., additional, Orton, Kai, additional, Overeem, Sebastiaan, additional, Ozelius, Laurie, additional, Pandolfo, Massimo, additional, Pascual, Juan M., additional, Paulson, Henry L., additional, Peroutka, Stephen J., additional, Petroff, Ognen A.C., additional, Ransom, Christopher B., additional, Rao, R.V., additional, Rismanchi, Neggy, additional, Rothstein, Jeffrey D., additional, Savitt, Joseph M., additional, Scheffer, Ingrid E., additional, Schon, Eric A., additional, Shy, Michael, additional, Strittmatter, Stephen M., additional, Tafti, Mehdi, additional, Tanriover, Gamze, additional, Todi, Sokol V., additional, van den Maagdenberg, Arn M.J.M., additional, Vance, Jeffery M., additional, Vincent, Angela, additional, Voisine, Cindy, additional, Waxman, Stephen G., additional, Wekerle, Hartmut, additional, Williams, Aislinn J., additional, Wood, John N., additional, Yang, Yvonne S., additional, and Zivin, Justin A., additional

Published
2007
Full Text
View/download PDF

38. Contributors

Author

Abu-Baker, Aida, primary, Ashizawa, Tetsuo, additional, Bachinski, Linda L., additional, Bacolla, Albino, additional, Bates, Gillian P., additional, Belt, John S., additional, Bezprozvanny, Dya, additional, Bidichandani, Sanjay, additional, Bissler, John J., additional, Brice, Alexis, additional, Carlson, Kerri M., additional, Chen, CheunJu, additional, Cooper, Thomas A., additional, Cortez-Apreza, Natividad, additional, Day, John W., additional, De Biase, Irene, additional, Dere, Ruhee, additional, Devys, Didier, additional, Dick, Katherine A., additional, Dion, Vincent, additional, Ellerby, Lisa M., additional, Epstein, Henry F., additional, Fischbeck, Kenneth H., additional, Foiry, Laurent, additional, Frants, Rune R., additional, Garden, Gwenn A., additional, Gomes-Pereira, M´rio, additional, Gourdon, Geneviéve, additional, Hagerman, Paul J., additional, Hagerman, Randi J, additional, Harper, Peter S., additional, Hashem, Vera I., additional, Hayden, Michael R., additional, Hebert, Micheal L., additional, Helmlinger, Dominique, additional, Hockly, Emma, additional, Holmes, Susan E., additional, Hwang, H.S., additional, Ikeda, Yoshio, additional, Ishikawa, Kinya, additional, Jackson, George R., additional, Kekis, Mariana, additional, Kosmider, Beata, additional, Kovtun, Irina V., additional, Krahe, Ralf, additional, Krzyzosiak, Wlodzimierz J., additional, La Spada, Albert R., additional, Larson, Jacquelynn E., additional, Lau, Rachel, additional, Leffak, Michael, additional, Leonard, Michelle R., additional, Lin, Yunfu, additional, Liu, Yuan, additional, Marcadier, Julien L., additional, Margolis, Jamie M., additional, Margolis, Russell L., additional, McMurray, Cynthia T., additional, Mirkin, Sergei M., additional, Mizusawa, Hidehiro, additional, Monckton, Darren G., additional, Montgomery, S. Erin, additional, Napierala, Marek, additional, Nelson, David L., additional, O'Hearn, Elizabeth, additional, Oostra, Ben A., additional, Orr, Harry T., additional, Padberg, George W., additional, Pandolfo, Massimo, additional, Panigrahi, Gagan B., additional, Paul, Sharan, additional, Paulson, Henry, additional, Pearson, Christopher E., additional, Pletnikova, Olga, additional, Potaman, Vladimir N., additional, Pouladi, Mahmoud A., additional, Prasad, Rajendra, additional, Puccio, Héléne, additional, Pulst, Stefan M., additional, Pytlos, Malgorzata J., additional, Ranum, Laura P.W., additional, Raymond, Lynn A., additional, Reddy, Sita, additional, Richards, Robert I., additional, Ross, Christopher A., additional, Rouleau, Guy, additional, Rudnicki, Dobrila D., additional, Sang, Tzu-Kang, additional, Shelbourne, Peggy E., additional, Siciliano, Michael J., additional, Sinden, Richard R., additional, Singh, Ram, additional, Sobczak, Krzysztof, additional, Son, LesHe S., additional, Stevanin, Giovanni, additional, Strack, S., additional, Swanson, Maurice S., additional, Taylor, J. Paul, additional, Thornton, Charles A., additional, Todd, Andrea, additional, Troncoso, Juan, additional, Truant, Ray, additional, Udd, Bjarne, additional, Usdin, Karen, additional, van der Maarel, Silvere M., additional, van Herpen, Rene E.M.A., additional, Vosch, Caroline, additional, Wansink, Derick G., additional, Wells, Robert D., additional, Wetzel, Ronald, additional, Wieringa, Bé, additional, Wilson, Robert B., additional, Wilson, Samuel H., additional, Wilson, John H., additional, and Wojciechowska, Marzena, additional

Published
2006
Full Text
View/download PDF

45. A high-density association screen of 155 ion transport genes for involvement with common migraine

Author

Nyholt, Dale R., LaForge, K. Steven, Kallela, Mikko, Alakurtti, Kirsi, Anttila, Verneri, Färkkilä, Markus, Hämaläinen, Eija, Kaprio, Jaakko, Kaunisto, Mari A., Heath, Andrew C., Montgomery, Grant W., Göbel, Hartmut, Todt, Unda, Ferrari, Michel D., Launer, Lenore J., Frants, Rune R., Terwindt, Gisela M., de Vries, Boukje, Verschuren, W.M. Monique, Brand, Jan, Freilinger, Tobias, Pfaffenrath, Volker, Straube, Andreas, Ballinger, Dennis G., Zhan, Yiping, Daly, Mark J., Cox, David R., Dichgans, Martin, van den Maagdenberg, Arn M.J.M., Kubisch, Christian, Martin, Nicholas G., Wessman, Maija, Peltonen, Leena, and Palotie, Aarno

Published
2008

50. Genetic Models of Migraine

Author

van de Ven, Rob C. G., Kaja, Simon, Plomp, Jaap J., Frants, Rune R., van den Maagdenberg, Arn M. J. M., and Ferrari, Michel D.

Published
2007

Catalog

Books, media, physical & digital resources
See catalog results