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3 results on '"Freudenberger, P. (Paul)"'

1. Genome-wide association study of kidney function decline in individuals of European descent

Author

Gorski, M. (Mathias), Tin, A. (Adrienne), Garnaas, M. (Maija), McMahon, G.M. (Gearoid M.), Chu, A.Y. (Audrey Y.), Tayo, B. (Bamidele), Pattaro, C. (Cristian), Teumer, A. (Alexander), Chasman, D.I. (Daniel), Chalmers, J. (John), Hamet, P. (Pavel), Tremblay, J. (Johanne), Woodward, M. (Mark), Aspelund, T. (Thor), Eiriksdottir, G. (Gudny), Gudnason, V. (Vilmundur), Harris, T.B. (Tamara), Launer, L.J. (Lenore), Smith, A.V. (Albert V.), Mitchell, B.D. (Braxton), O´Connell, J.R., Shuldiner, A.R. (Alan), Coresh, J. (Josef), Li, M. (Man), Freudenberger, P. (Paul), Hofer, E. (Edith), Schmidt, R. (Reinhold), Holliday, E.G. (Elizabeth), Mitchell, P. (Paul), Wang, J.J. (Jie Jin), Boer, I.H. (Ian) de, Li, G. (Guo), Siscovick, D.S. (David), Kutalik, Z., Corre, T. (Tanguy), Vollenweider, P. (Peter), Waeber, G. (Gérard), Gupta, J. (Jayanta), Kanetsky, P.P. (Peter P.), Hwang, S.J., Olden, M. (Matthias), Yang, Q. (Qiong Fang), Andrade, M. (Mariza) de, Atkinson, E.J. (Elizabeth J.), Kardia, S.L.R. (Sharon), Turner, S.T. (Stephen), Stafford, J.M. (Jeanette M.), Ding, J. (Jingzhong), Liu, Y., Barlassina, C. (Christina), Cusi, D. (Daniele), Salvi, E. (Erika), Staessen, J.A. (Jan), Ridker, P.M. (Paul), Grallert, H. (Harald), Meisinger, C. (Christa), Müller-Nurasyid, M. (Martina), Krämer, B.K. (Bernhard K.), Kramer, H. (Holly), Rosas, S.E. (Sylvia E.), Nolte, I.M. (Ilja M.), Penninx, B.W.J.H. (Brenda), Snieder, H. (Harold), Fabiola Del Greco, M., Franke, A. (Andre), Nöthlings, U. (Ute), Lieb, W. (Wolfgang), Bakker, S.J.L. (Stephan), Gansevoort, R.T. (Ron), Van Der Harst, P. (Pim), Dehghan, A. (Abbas), Franco, O.H. (Oscar), Hofman, A. (Albert), Rivadeneira Ramirez, F. (Fernando), Sedaghat, S. (Sanaz), Uitterlinden, A.G. (André), Coassin, S. (Stefan), Haun, M. (Margot), Kollerits, B. (Barbara), Kronenberg, F. (Florian), Paulweber, B. (Bernhard), Aumann, N. (Nicole), Endlich, K. (Karlhans), Pietzner, M. (Mike), Völker, U. (Uwe), Rettig, R. (Rainer), Chouraki, V. (Vincent), Helmer, C. (Catherine), Lambert, J.-C. (Jean-Charles), Metzger, M. (Marie), Stengel, B. (Benedicte), Lehtimäki, T. (Terho), Lyytikäinen, L.-P. (Leo-Pekka), Raitakari, O. (Olli), Johnson, A.D. (Andrew), Parsa, A. (Afshin), Bochud, M. (Murielle), Heid, I.M. (Iris), Goessling, W. (Wolfram), Köttgen, A. (Anna), Kao, W.H.L. (Wen), Fox, C.S. (Caroline S.), Böger, C.A. (Carsten), Gorski, M. (Mathias), Tin, A. (Adrienne), Garnaas, M. (Maija), McMahon, G.M. (Gearoid M.), Chu, A.Y. (Audrey Y.), Tayo, B. (Bamidele), Pattaro, C. (Cristian), Teumer, A. (Alexander), Chasman, D.I. (Daniel), Chalmers, J. (John), Hamet, P. (Pavel), Tremblay, J. (Johanne), Woodward, M. (Mark), Aspelund, T. (Thor), Eiriksdottir, G. (Gudny), Gudnason, V. (Vilmundur), Harris, T.B. (Tamara), Launer, L.J. (Lenore), Smith, A.V. (Albert V.), Mitchell, B.D. (Braxton), O´Connell, J.R., Shuldiner, A.R. (Alan), Coresh, J. (Josef), Li, M. (Man), Freudenberger, P. (Paul), Hofer, E. (Edith), Schmidt, R. (Reinhold), Holliday, E.G. (Elizabeth), Mitchell, P. (Paul), Wang, J.J. (Jie Jin), Boer, I.H. (Ian) de, Li, G. (Guo), Siscovick, D.S. (David), Kutalik, Z., Corre, T. (Tanguy), Vollenweider, P. (Peter), Waeber, G. (Gérard), Gupta, J. (Jayanta), Kanetsky, P.P. (Peter P.), Hwang, S.J., Olden, M. (Matthias), Yang, Q. (Qiong Fang), Andrade, M. (Mariza) de, Atkinson, E.J. (Elizabeth J.), Kardia, S.L.R. (Sharon), Turner, S.T. (Stephen), Stafford, J.M. (Jeanette M.), Ding, J. (Jingzhong), Liu, Y., Barlassina, C. (Christina), Cusi, D. (Daniele), Salvi, E. (Erika), Staessen, J.A. (Jan), Ridker, P.M. (Paul), Grallert, H. (Harald), Meisinger, C. (Christa), Müller-Nurasyid, M. (Martina), Krämer, B.K. (Bernhard K.), Kramer, H. (Holly), Rosas, S.E. (Sylvia E.), Nolte, I.M. (Ilja M.), Penninx, B.W.J.H. (Brenda), Snieder, H. (Harold), Fabiola Del Greco, M., Franke, A. (Andre), Nöthlings, U. (Ute), Lieb, W. (Wolfgang), Bakker, S.J.L. (Stephan), Gansevoort, R.T. (Ron), Van Der Harst, P. (Pim), Dehghan, A. (Abbas), Franco, O.H. (Oscar), Hofman, A. (Albert), Rivadeneira Ramirez, F. (Fernando), Sedaghat, S. (Sanaz), Uitterlinden, A.G. (André), Coassin, S. (Stefan), Haun, M. (Margot), Kollerits, B. (Barbara), Kronenberg, F. (Florian), Paulweber, B. (Bernhard), Aumann, N. (Nicole), Endlich, K. (Karlhans), Pietzner, M. (Mike), Völker, U. (Uwe), Rettig, R. (Rainer), Chouraki, V. (Vincent), Helmer, C. (Catherine), Lambert, J.-C. (Jean-Charles), Metzger, M. (Marie), Stengel, B. (Benedicte), Lehtimäki, T. (Terho), Lyytikäinen, L.-P. (Leo-Pekka), Raitakari, O. (Olli), Johnson, A.D. (Andrew), Parsa, A. (Afshin), Bochud, M. (Murielle), Heid, I.M. (Iris), Goessling, W. (Wolfram), Köttgen, A. (Anna), Kao, W.H.L. (Wen), Fox, C.S. (Caroline S.), and Böger, C.A. (Carsten)

Abstract

Genome-wide association studies (GWASs) have identified multiple loci associated with cross-sectional eGFR, but a systematic genetic analysis of kidney function decline over time is missing. Here we conducted a GWAS meta-analysis among 63,558 participants of European descent, initially from 16 cohorts with serial kidney function measurements within the CKDGen Consortium, followed by independent replication among additional participants from 13 cohorts. In stage 1 GWAS meta-analysis, single-nucleotide polymorphisms (SNPs) at MEOX2, GALNT11, IL1RAP, NPPA, HPCAL1, and CDH23 showed the strongest associations for at least one trait, in addition to the known UMOD locus, which showed genome-wide significance with an annual change in eGFR. In stage 2 meta-analysis, the significant association at UMOD was replicated. Associations at GALNT11 with Rapid Decline (annual eGFR decline of 3 ml/min per 1.73 m 2 or more), and CDH23 with eGFR change among those with CKD showed significant suggestive evidence of replication. Combined stage 1 and 2 meta-analyses showed significance for UMOD, GALNT11, and CDH23. Morpholino knockdowns of galnt11 and cdh23 in zebrafish embryos each had signs of severe edema 72 h after gentamicin treatment compared with controls, but no gross morphological renal abnormalities before gentamicin administration. Thus, our results suggest a role in the deterioration of kidney function for the loci GALNT11 and CDH23, and show that the UMOD locus is significantly associated with kidney function decline.

Published
2015
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2. White Matter Lesion Progression: Genome-Wide Search for Genetic Influences

Author

Hofer, E. (Edith), Cavalieri, M. (Margherita), Bis, J.C. (Joshua), DeCarli, C. (Charles), Fornage, M. (Myriam), Sigurdsson, S. (Sigurdur), Srikanth, V. (Velandai), Trompet, S. (Stella), Verhaaren, B.F.J. (Benjamin), Wolf, C. (Christiane), Yang, Q. (Qiong Fang), Adams, H.H.H. (Hieab), Amouyel, P. (Philippe), Beiser, A. (Alexa), Buckley, B.M. (Brendan M.), Callisaya, M. (Michele), Chauhan, G. (Ganesh), De Craen, A.J.M. (Anton J. M.), Dufouil, C. (Carole), Duijn, C.M. (Cornelia) van, Ford, I., Freudenberger, P. (Paul), Gottesman, R.F. (Rebecca), Gudnason, V. (Vilmundur), Heiss, G. (Gerardo), Hofman, A. (Albert), Lumley, T. (Thomas), Martinez, O. (Oliver), Mazoyer, B. (Bernard), Moran, C. (Chris), Niessen, W.J. (Wiro), Phan, T.G. (Thanh), Psaty, B.M. (Bruce), Satizabal, C.L. (Claudia), Sattar, N. (Naveed), Schilling, S. (Sabrina), Shibata, D.K. (Dean), Slagboom, P.E. (Eline), Smith, A.V. (Davey), Stott, D.J. (David. J.), Taylor, K.D. (Kent), Thomson, R. (Russell), Töglhofer, A.M. (Anna Maria), Tzourio, C. (Christophe), Buchem, M.A. (Mark) van, Wang, J. (Jing), Westendorp, R.G.J. (Rudi), Windham, B.G. (Gwen), Vernooij, M.W. (Meike), Zijdenbos, A.P., Beare, R.J. (Richard), Debette, S. (Stéphanie), Ikram, M.A. (Arfan), Jukema, J.W. (Jan Wouter), Launer, L.J. (Lenore), Longstreth Jr, W.T., Mosley, T.H. (Thomas H.), Seshadri, S. (Sudha), Schmidt, R. (Reinhold), Hofer, E. (Edith), Cavalieri, M. (Margherita), Bis, J.C. (Joshua), DeCarli, C. (Charles), Fornage, M. (Myriam), Sigurdsson, S. (Sigurdur), Srikanth, V. (Velandai), Trompet, S. (Stella), Verhaaren, B.F.J. (Benjamin), Wolf, C. (Christiane), Yang, Q. (Qiong Fang), Adams, H.H.H. (Hieab), Amouyel, P. (Philippe), Beiser, A. (Alexa), Buckley, B.M. (Brendan M.), Callisaya, M. (Michele), Chauhan, G. (Ganesh), De Craen, A.J.M. (Anton J. M.), Dufouil, C. (Carole), Duijn, C.M. (Cornelia) van, Ford, I., Freudenberger, P. (Paul), Gottesman, R.F. (Rebecca), Gudnason, V. (Vilmundur), Heiss, G. (Gerardo), Hofman, A. (Albert), Lumley, T. (Thomas), Martinez, O. (Oliver), Mazoyer, B. (Bernard), Moran, C. (Chris), Niessen, W.J. (Wiro), Phan, T.G. (Thanh), Psaty, B.M. (Bruce), Satizabal, C.L. (Claudia), Sattar, N. (Naveed), Schilling, S. (Sabrina), Shibata, D.K. (Dean), Slagboom, P.E. (Eline), Smith, A.V. (Davey), Stott, D.J. (David. J.), Taylor, K.D. (Kent), Thomson, R. (Russell), Töglhofer, A.M. (Anna Maria), Tzourio, C. (Christophe), Buchem, M.A. (Mark) van, Wang, J. (Jing), Westendorp, R.G.J. (Rudi), Windham, B.G. (Gwen), Vernooij, M.W. (Meike), Zijdenbos, A.P., Beare, R.J. (Richard), Debette, S. (Stéphanie), Ikram, M.A. (Arfan), Jukema, J.W. (Jan Wouter), Launer, L.J. (Lenore), Longstreth Jr, W.T., Mosley, T.H. (Thomas H.), Seshadri, S. (Sudha), and Schmidt, R. (Reinhold)

Abstract

Background and Purpose-White matter lesion (WML) progression on magnetic resonance imaging is related to cognitive decline and stroke, but its determinants besides baseline WML burden are largely unknown. Here, we estimated heritability of WML progression, and sought common genetic variants associated with WML progression in elderly participants from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium. Methods-Heritability of WML progression was calculated in the Framingham Heart Study. The genome-wide association study included 7773 elderly participants from 10 cohorts. To assess the relative contribution of genetic factors to progression of WML, we compared in 7 cohorts risk models including demographics, vascular risk factors plus single-nucleotide polymorphisms that have been shown to be associated cross-sectionally with WML in the current and previous association studies. Results-A total of 1085 subjects showed WML progression. The heritability estimate for WML progression was low at 6.5%, and no single-nucleotide polymorphisms achieved genome-wide significance (P<5×10-8). Four loci were suggestive (P<1×10-5) of an association with WML progression: 10q24.32 (rs10883817, P=1.46×10-6); 12q13.13 (rs4

Published
2015
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3. Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease

Author

Schmidt, R. (Reinhold), Zeginigg, M. (Marion), Wiltgen, M. (Marco), Freudenberger, P. (Paul), Petrovic, K. (Katja), Cavalieri, M. (Margherita), Gider, P. (Pierre), Enzinger, C. (Christian), Fornage, M. (Myriam), Debette, S. (Stéphanie), Rotter, J.I. (Jerome), Ikram, M.A. (Arfan), Launer, L.J. (Lenore), Schmidt, R. (Reinhold), Zeginigg, M. (Marion), Wiltgen, M. (Marco), Freudenberger, P. (Paul), Petrovic, K. (Katja), Cavalieri, M. (Margherita), Gider, P. (Pierre), Enzinger, C. (Christian), Fornage, M. (Myriam), Debette, S. (Stéphanie), Rotter, J.I. (Jerome), Ikram, M.A. (Arfan), and Launer, L.J. (Lenore)

Abstract

Cerebral small vessel disease-related brain lesions such as white matter lesions and lacunes are common findings of magnetic resonance imaging in the elderly. These lesions are thought to be major contributors to disability in old age, and risk factors that include age and hypertension have been established. The radiological, histopathologic and clinical phenotypes of age-related cerebral small vessel disease remarkably resemble autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy, which is caused by mutations in NOTCH3. We hypothesized that genetic variations in NOTCH3 also play a role in age-related cerebral small vessel disease. We directly sequenced all 33 exons, the promoter and 3′-untranslated region of NOTCH3 in 195 participants with either coalescent white matter lesions or lacunes and compared the results to 82 randomly selected participants with no focal changes on magnetic resonance images in the Austrian Stroke Prevention Study. We detected nine common and 33 rare single nucleotide polymorphisms, of which 20 were novel. All common single nucleotide polymorphisms were genotyped in the entire cohort (n=888), and four of them, rs1043994, rs10404382, rs10423702 and rs1043997, were associated significantly wit

Published
2011
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