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Publikationen

Suchbegriffe: GENOME-WIDE ASSOCIATION STUDY - , . Treffer: 124

2021

Lagou, V; Mägi, R; Hottenga, JJ; Grallert, H; Perry, JRB; Bouatia-Naji, N; Marullo, L; Rybin, D; Jansen, R; Min, JL; Dimas, AS; Ulrich, A; Zudina, L; Gådin, JR; Jiang, L; Faggian, A; Bonnefond, A; Fadista, J; Stathopoulou, MG; Isaacs, A; Willems, SM; Navarro, P; Tanaka, T; Jackson, AU; Montasser, ME; O'Connell, JR; Bielak, LF; Webster, RJ; Saxena, R; Stafford, JM; Pourcain, BS; Timpson, NJ; Salo, P; Shin, SY; Amin, N; Smith, AV; Li, G; Verweij, N; Goel, A; Ford, I; Johnson, PCD; Johnson, T; Kapur, K; Thorleifsson, G; Strawbridge, RJ; Rasmussen-Torvik, LJ; Esko, T; Mihailov, E; Fall, T; Fraser, RM; Mahajan, A; Kanoni, S; Giedraitis, V; Kleber, ME; Silbernagel, G; Meyer, J; Müller-Nurasyid, M; Ganna, A; Sarin, AP; Yengo, L; Shungin, D; Luan, J; Horikoshi, M; An, P; Sanna, S; Boettcher, Y; Rayner, NW; Nolte, IM; Zemunik, T; Iperen, EV; Kovacs, P; Hastie, ND; Wild, SH; McLachlan, S; Campbell, S; Polasek, O; Carlson, O; Egan, J; Kiess, W; Willemsen, G; Kuusisto, J; Laakso, M; Dimitriou, M; Hicks, AA; Rauramaa, R; Bandinelli, S; Thorand, B; Liu, Y; Miljkovic, I; Lind, L; Doney, A; Perola, M; Hingorani, A; Kivimaki, M; Kumari, M; Bennett, AJ; Groves, CJ; Herder, C; Koistinen, HA; Kinnunen, L; Faire, U; Bakker, SJL; Uusitupa, M; Palmer, CNA; Jukema, JW; Sattar, N; Pouta, A; Snieder, H; Boerwinkle, E; Pankow, JS; Magnusson, PK; Krus, U; Scapoli, C; de Geus, EJCN; Blüher, M; Wolffenbuttel, BHR; Province, MA; Abecasis, GR; Meigs, JB; Hovingh, GK; Lindström, J; Wilson, JF; Wright, AF; Dedoussis, GV; Bornstein, SR; Schwarz, PEH; Tönjes, A; Winkelmann, BR; Boehm, BO; März, W; Metspalu, A; Price, JF; Deloukas, P; Körner, A; Lakka, TA; Keinanen-Kiukaanniemi, SM; Saaristo, TE; Bergman, RN; Tuomilehto, J; Wareham, NJ; Langenberg, C; Männistö, S; Franks, PW; Hayward, C; Vitart, V; Kaprio, J; Visvikis-Siest, S; Balkau, B; Altshuler, D; Rudan, I; Stumvoll, M; Campbell, H; van Duijn, CM; Gieger, C; Illig, T; Ferrucci, L; Pedersen, NL; Pramstaller, PP; Boehnke, M; Frayling, TM; Shuldiner, AR; Peyser, PA; Kardia, SLR; Palmer, LJ; Penninx, BW; Meneton, P; Harris, TB; Navis, G; Harst, PV; Smith, GD; Forouhi, NG; Loos, RJF; Salomaa, V; Soranzo, N; Boomsma, DI; Groop, L; Tuomi, T; Hofman, A; Munroe, PB; Gudnason, V; Siscovick, DS; Watkins, H; Lecoeur, C; Vollenweider, P; Franco-Cereceda, A; Eriksson, P; Jarvelin, MR; Stefansson, K; Hamsten, A; Nicholson, G; Karpe, F; Dermitzakis, ET; Lindgren, CM; McCarthy, MI; Froguel, P; Kaakinen, MA; Lyssenko, V; Watanabe, RM; Ingelsson, E; Florez, JC; Dupuis, J; Barroso, I; Morris, AP; Prokopenko, I; Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC) Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Nat Commun. 2021; 12(1): 24-24. Doi: 10.1038/s41467-020-19366-9 [OPEN ACCESS]
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2020

Falcone, GJ; Kirsch, E; Acosta, JN; Noche, RB; Leasure, A; Marini, S; Chung, J; Selim, M; Meschia, JF; Brown, DL; Worrall, BB; Tirschwell, DL; Jagiella, JM; Schmidt, H; Jimenez-Conde, J; Fernandez-Cadenas, I; Lindgren, A; Slowik, A; Gill, D; Holmes, M; Phuah, CL; Petersen, NH; Matouk Md, CN; Gunel, M; Sansing, L; Bennett, D; Chen, Z; Sun, LL; Clarke, R; Walters, RG; Gill, TM; Biffi, A; Kathiresan, S; Langefeld, CD; Woo, D; Rosand, J; Sheth, KN; Anderson, CD; International Stroke Genetics Consortium Genetically Elevated LDL Associates with Lower Risk of Intracerebral Hemorrhage.
Ann Neurol. 2020; 88(1):56-66 Doi: 10.1002/ana.25740 [OPEN ACCESS]
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Hofer, E; Roshchupkin, GV; Adams, HHH; Knol, MJ; Lin, H; Li, S; Zare, H; Ahmad, S; Armstrong, NJ; Satizabal, CL; Bernard, M; Bis, JC; Gillespie, NA; Luciano, M; Mishra, A; Scholz, M; Teumer, A; Xia, R; Jian, X; Mosley, TH; Saba, Y; Pirpamer, L; Seiler, S; Becker, JT; Carmichael, O; Rotter, JI; Psaty, BM; Lopez, OL; Amin, N; van der Lee, SJ; Yang, Q; Himali, JJ; Maillard, P; Beiser, AS; DeCarli, C; Karama, S; Lewis, L; Harris, M; Bastin, ME; Deary, IJ; Veronica Witte, A; Beyer, F; Loeffler, M; Mather, KA; Schofield, PR; Thalamuthu, A; Kwok, JB; Wright, MJ; Ames, D; Trollor, J; Jiang, J; Brodaty, H; Wen, W; Vernooij, MW; Hofman, A; Uitterlinden, AG; Niessen, WJ; Wittfeld, K; Bülow, R; Völker, U; Pausova, Z; Bruce Pike, G; Maingault, S; Crivello, F; Tzourio, C; Amouyel, P; Mazoyer, B; Neale, MC; Franz, CE; Lyons, MJ; Panizzon, MS; Andreassen, OA; Dale, AM; Logue, M; Grasby, KL; Jahanshad, N; Painter, JN; Colodro-Conde, L; Bralten, J; Hibar, DP; Lind, PA; Pizzagalli, F; Stein, JL; Thompson, PM; Medland, SE; ENIGMA consortium; Sachdev, PS; Kremen, WS; Wardlaw, JM; Villringer, A; van Duijn, CM; Grabe, HJ; Longstreth, WT; Fornage, M; Paus, T; Debette, S; Arfan Ikram, M; Schmidt, H; Schmidt, R; Seshadri, S Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults.
Nat Commun. 2020; 11(1): 4796-4796. Doi: 10.1038/s41467-020-18367-y [OPEN ACCESS]
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Sargurupremraj, M; Suzuki, H; Jian, X; Sarnowski, C; Evans, TE; Bis, JC; Eiriksdottir, G; Sakaue, S; Terzikhan, N; Habes, M; Zhao, W; Armstrong, NJ; Hofer, E; Yanek, LR; Hagenaars, SP; Kumar, RB; van den Akker, EB; McWhirter, RE; Trompet, S; Mishra, A; Saba, Y; Satizabal, CL; Beaudet, G; Petit, L; Tsuchida, A; Zago, L; Schilling, S; Sigurdsson, S; Gottesman, RF; Lewis, CE; Aggarwal, NT; Lopez, OL; Smith, JA; Valdés Hernández, MC; van der Grond, J; Wright, MJ; Knol, MJ; Dörr, M; Thomson, RJ; Bordes, C; Le Grand, Q; Duperron, MG; Smith, AV; Knopman, DS; Schreiner, PJ; Evans, DA; Rotter, JI; Beiser, AS; Maniega, SM; Beekman, M; Trollor, J; Stott, DJ; Vernooij, MW; Wittfeld, K; Niessen, WJ; Soumaré, A; Boerwinkle, E; Sidney, S; Turner, ST; Davies, G; Thalamuthu, A; Völker, U; van Buchem, MA; Bryan, RN; Dupuis, J; Bastin, ME; Ames, D; Teumer, A; Amouyel, P; Kwok, JB; Bülow, R; Deary, IJ; Schofield, PR; Brodaty, H; Jiang, J; Tabara, Y; Setoh, K; Miyamoto, S; Yoshida, K; Nagata, M; Kamatani, Y; Matsuda, F; Psaty, BM; Bennett, DA; De Jager, PL; Mosley, TH; Sachdev, PS; Schmidt, R; Warren, HR; Evangelou, E; Trégouët, DA; International Network against Thrombosis (INVENT) Consortium; International Headache Genomics Consortium (IHGC); Ikram, MA; Wen, W; DeCarli, C; Srikanth, VK; Jukema, JW; Slagboom, EP; Kardia, SLR; Okada, Y; Mazoyer, B; Wardlaw, JM; Nyquist, PA; Mather, KA; Grabe, HJ; Schmidt, H; Van Duijn, CM; Gudnason, V; Longstreth, WT; Launer, LJ; Lathrop, M; Seshadri, S; Tzourio, C; Adams, HH; Matthews, PM; Fornage, M; Debette, S Cerebral small vessel disease genomics and its implications across the lifespan.
Nat Commun. 2020; 11(1):6285-6285 Doi: 10.1038/s41467-020-19111-2 [OPEN ACCESS]
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Shah, S; Henry, A; Roselli, C; Lin, H; Sveinbjörnsson, G; Fatemifar, G; Hedman, ÅK; Wilk, JB; Morley, MP; Chaffin, MD; Helgadottir, A; Verweij, N; Dehghan, A; Almgren, P; Andersson, C; Aragam, KG; Ärnlöv, J; Backman, JD; Biggs, ML; Bloom, HL; Brandimarto, J; Brown, MR; Buckbinder, L; Carey, DJ; Chasman, DI; Chen, X; Chen, X; Chung, J; Chutkow, W; Cook, JP; Delgado, GE; Denaxas, S; Doney, AS; Dörr, M; Dudley, SC; Dunn, ME; Engström, G; Esko, T; Felix, SB; Finan, C; Ford, I; Ghanbari, M; Ghasemi, S; Giedraitis, V; Giulianini, F; Gottdiener, JS; Gross, S; Guðbjartsson, DF; Gutmann, R; Haggerty, CM; van der Harst, P; Hyde, CL; Ingelsson, E; Jukema, JW; Kavousi, M; Khaw, KT; Kleber, ME; Køber, L; Koekemoer, A; Langenberg, C; Lind, L; Lindgren, CM; London, B; Lotta, LA; Lovering, RC; Luan, J; Magnusson, P; Mahajan, A; Margulies, KB; März, W; Melander, O; Mordi, IR; Morgan, T; Morris, AD; Morris, AP; Morrison, AC; Nagle, MW; Nelson, CP; Niessner, A; Niiranen, T; O'Donoghue, ML; Owens, AT; Palmer, CNA; Parry, HM; Perola, M; Portilla-Fernandez, E; Psaty, BM; Regeneron Genetics Center; Rice, KM; Ridker, PM; Romaine, SPR; Rotter, JI; Salo, P; Salomaa, V; van Setten, J; Shalaby, AA; Smelser, DT; Smith, NL; Stender, S; Stott, DJ; Svensson, P; Tammesoo, ML; Taylor, KD; Teder-Laving, M; Teumer, A; Thorgeirsson, G; Thorsteinsdottir, U; Torp-Pedersen, C; Trompet, S; Tyl, B; Uitterlinden, AG; Veluchamy, A; Völker, U; Voors, AA; Wang, X; Wareham, NJ; Waterworth, D; Weeke, PE; Weiss, R; Wiggins, KL; Xing, H; Yerges-Armstrong, LM; Yu, B; Zannad, F; Zhao, JH; Hemingway, H; Samani, NJ; McMurray, JJV; Yang, J; Visscher, PM; Newton-Cheh, C; Malarstig, A; Holm, H; Lubitz, SA; Sattar, N; Holmes, MV; Cappola, TP; Asselbergs, FW; Hingorani, AD; Kuchenbaecker, K; Ellinor, PT; Lang, CC; Stefansson, K; Smith, JG; Vasan, RS; Swerdlow, DI; Lumbers, RT Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.
Nat Commun. 2020; 11(1):163-163 Doi: 10.1038/s41467-019-13690-5 [OPEN ACCESS]
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Zhou, J; Passero, K; Palmiero, NE; Müller-Myhsok, B; Kleber, ME; Maerz, W; Hall, MA Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study.
PLoS One. 2020; 15(9):e0238304-e0238304 Doi: 10.1371/journal.pone.0238304 [OPEN ACCESS]
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2018

Day, F; Karaderi, T; Jones, MR; Meun, C; He, C; Drong, A; Kraft, P; Lin, N; Huang, H; Broer, L; Magi, R; Saxena, R; Laisk, T; Urbanek, M; Hayes, MG; Thorleifsson, G; Fernandez-Tajes, J; Mahajan, A; Mullin, BH; Stuckey, BGA; Spector, TD; Wilson, SG; Goodarzi, MO; Davis, L; Obermayer-Pietsch, B; Uitterlinden, AG; Anttila, V; Neale, BM; Jarvelin, MR; Fauser, B; Kowalska, I; Visser, JA; Andersen, M; Ong, K; Stener-Victorin, E; Ehrmann, D; Legro, RS; Salumets, A; McCarthy, MI; Morin-Papunen, L; Thorsteinsdottir, U; Stefansson, K; 23andMe Research Team; Styrkarsdottir, U; Perry, JRB; Dunaif, A; Laven, J; Franks, S; Lindgren, CM; Welt, CK Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria.
PLoS Genet. 2018; 14(12):e1007813-e1007813 Doi: 10.1371/journal.pgen.1007813 [OPEN ACCESS]
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Eriksson, AL; Perry, JRB; Coviello, AD; Delgado, GE; Ferrucci, L; Hoffman, AR; Huhtaniemi, IT; Ikram, MA; Karlsson, MK; Kleber, ME; Laughlin, GA; Liu, Y; Lorentzon, M; Lunetta, KL; Mellström, D; Murabito, JM; Murray, A; Nethander, M; Nielson, CM; Prokopenko, I; Pye, SR; Raffel, LJ; Rivadeneira, F; Srikanth, P; Stolk, L; Teumer, A; Travison, TG; Uitterlinden, AG; Vaidya, D; Vanderschueren, D; Zmuda, JM; März, W; Orwoll, ES; Ouyang, P; Vandenput, L; Wu, FCW; de Jong, FH; Bhasin, S; Kiel, DP; Ohlsson, C Genetic Determinants of Circulating Estrogen Levels and Evidence of a Causal Effect of Estradiol on Bone Density in Men.
J CLIN ENDOCR METAB. 2018; 103(3): 991-1004. Doi: 10.1210/jc.2017-02060 [OPEN ACCESS]
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2017

Aung, T; Ozaki, M; Lee, MC; Schlötzer-Schrehardt, U; Thorleifsson, G; Mizoguchi, T; Igo, RP; Haripriya, A; Williams, SE; Astakhov, YS; Orr, AC; Burdon, KP; Nakano, S; Mori, K; Abu-Amero, K; Hauser, M; Li, Z; Prakadeeswari, G; Bailey, JNC; Cherecheanu, AP; Kang, JH; Nelson, S; Hayashi, K; Manabe, SI; Kazama, S; Zarnowski, T; Inoue, K; Irkec, M; Coca-Prados, M; Sugiyama, K; Järvelä, I; Schlottmann, P; Lerner, SF; Lamari, H; Nilgün, Y; Bikbov, M; Park, KH; Cha, SC; Yamashiro, K; Zenteno, JC; Jonas, JB; Kumar, RS; Perera, SA; Chan, ASY; Kobakhidze, N; George, R; Vijaya, L; Do, T; Edward, DP; de Juan Marcos, L; Pakravan, M; Moghimi, S; Ideta, R; Bach-Holm, D; Kappelgaard, P; Wirostko, B; Thomas, S; Gaston, D; Bedard, K; Greer, WL; Yang, Z; Chen, X; Huang, L; Sang, J; Jia, H; Jia, L; Qiao, C; Zhang, H; Liu, X; Zhao, B; Wang, YX; Xu, L; Leruez, S; Reynier, P; Chichua, G; Tabagari, S; Uebe, S; Zenkel, M; Berner, D; Mossböck, G; Weisschuh, N; Hoja, U; Welge-Luessen, UC; Mardin, C; Founti, P; Chatzikyriakidou, A; Pappas, T; Anastasopoulos, E; Lambropoulos, A; Ghosh, A; Shetty, R; Porporato, N; Saravanan, V; Venkatesh, R; Shivkumar, C; Kalpana, N; Sarangapani, S; Kanavi, MR; Beni, AN; Yazdani, S; Lashay, A; Naderifar, H; Khatibi, N; Fea, A; Lavia, C; Dallorto, L; Rolle, T; Frezzotti, P; Paoli, D; Salvi, E; Manunta, P; Mori, Y; Miyata, K; Higashide, T; Chihara, E; Ishiko, S; Yoshida, A; Yanagi, M; Kiuchi, Y; Ohashi, T; Sakurai, T; Sugimoto, T; Chuman, H; Aihara, M; Inatani, M; Miyake, M; Gotoh, N; Matsuda, F; Yoshimura, N; Ikeda, Y; Ueno, M; Sotozono, C; Jeoung, JW; Sagong, M; Park, KH; Ahn, J; Cruz-Aguilar, M; Ezzouhairi, SM; Rafei, A; Chong, YF; Ng, XY; Goh, SR; Chen, Y; Yong, VHK; Khan, MI; Olawoye, OO; Ashaye, AO; Ugbede, I; Onakoya, A; Kizor-Akaraiwe, N; Teekhasaenee, C; Suwan, Y; Supakontanasan, W; Okeke, S; Uche, NJ; Asimadu, I; Ayub, H; Akhtar, F; Kosior-Jarecka, E; Lukasik, U; Lischinsky, I; Castro, V; Grossmann, RP; Sunaric Megevand, G; Roy, S; Dervan, E; Silke, E; Rao, A; Sahay, P; Fornero, P; Cuello, O; Sivori, D; Zompa, T; Mills, RA; Souzeau, E; Mitchell, P; Wang, JJ; Hewitt, AW; Coote, M; Crowston, JG; Astakhov, SY; Akopov, EL; Emelyanov, A; Vysochinskaya, V; Kazakbaeva, G; Fayzrakhmanov, R; Al-Obeidan, SA; Owaidhah, O; Aljasim, LA; Chowbay, B; Foo, JN; Soh, RQ; Sim, KS; Xie, Z; Cheong, AWO; Mok, SQ; Soo, HM; Chen, XY; Peh, SQ; Heng, KK; Husain, R; Ho, SL; Hillmer, AM; Cheng, CY; Escudero-Domínguez, FA; González-Sarmiento, R; Martinon-Torres, F; Salas, A; Pathanapitoon, K; Hansapinyo, L; Wanichwecharugruang, B; Kitnarong, N; Sakuntabhai, A; Nguyn, HX; Nguyn, GTT; Nguyn, TV; Zenz, W; Binder, A; Klobassa, DS; Hibberd, ML; Davila, S; Herms, S; Nöthen, MM; Moebus, S; Rautenbach, RM; Ziskind, A; Carmichael, TR; Ramsay, M; Álvarez, L; García, M; González-Iglesias, H; Rodríguez-Calvo, PP; Fernández-Vega Cueto, L; Oguz, Ç; Tamcelik, N; Atalay, E; Batu, B; Aktas, D; Kasım, B; Wilson, MR; Coleman, AL; Liu, Y; Challa, P; Herndon, L; Kuchtey, RW; Kuchtey, J; Curtin, K; Chaya, CJ; Crandall, A; Zangwill, LM; Wong, TY; Nakano, M; Kinoshita, S; den Hollander, AI; Vesti, E; Fingert, JH; Lee, RK; Sit, AJ; Shingleton, BJ; Wang, N; Cusi, D; Qamar, R; Kraft, P; Pericak-Vance, MA; Raychaudhuri, S; Heegaard, S; Kivelä, T; Reis, A; Kruse, FE; Weinreb, RN; Pasquale, LR; Haines, JL; Thorsteinsdottir, U; Jonasson, F; Allingham, RR; Milea, D; Ritch, R; Kubota, T; Tashiro, K; Vithana, EN; Micheal, S; Topouzis, F; Craig, JE; Dubina, M; Sundaresan, P; Stefansson, K Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.
Nat Genet. 2017; 49(7):993-1004 Doi: 10.1038/ng.3875 [OPEN ACCESS]
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Christophersen, IE; Rienstra, M; Roselli, C; Yin, X; Geelhoed, B; Barnard, J; Lin, H; Arking, DE; Smith, AV; Albert, CM; Chaffin, M; Tucker, NR; Li, M; Klarin, D; Bihlmeyer, NA; Low, SK; Weeke, PE; Müller-Nurasyid, M; Smith, JG; Brody, JA; Niemeijer, MN; Dörr, M; Trompet, S; Huffman, J; Gustafsson, S; Schurmann, C; Kleber, ME; Lyytikäinen, LP; Seppälä, I; Malik, R; Horimoto, ARVR; Perez, M; Sinisalo, J; Aeschbacher, S; Thériault, S; Yao, J; Radmanesh, F; Weiss, S; Teumer, A; Choi, SH; Weng, LC; Clauss, S; Deo, R; Rader, DJ; Shah, SH; Sun, A; Hopewell, JC; Debette, S; Chauhan, G; Yang, Q; Worrall, BB; Paré, G; Kamatani, Y; Hagemeijer, YP; Verweij, N; Siland, JE; Kubo, M; Smith, JD; Van Wagoner, DR; Bis, JC; Perz, S; Psaty, BM; Ridker, PM; Magnani, JW; Harris, TB; Launer, LJ; Shoemaker, MB; Padmanabhan, S; Haessler, J; Bartz, TM; Waldenberger, M; Lichtner, P; Arendt, M; Krieger, JE; Kähönen, M; Risch, L; Mansur, AJ; Peters, A; Smith, BH; Lind, L; Scott, SA; Lu, Y; Bottinger, EB; Hernesniemi, J; Lindgren, CM; Wong, JA; Huang, J; Eskola, M; Morris, AP; Ford, I; Reiner, AP; Delgado, G; Chen, LY; Chen, YI; Sandhu, RK; Li, M; Boerwinkle, E; Eisele, L; Lannfelt, L; Rost, N; Anderson, CD; Taylor, KD; Campbell, A; Magnusson, PK; Porteous, D; Hocking, LJ; Vlachopoulou, E; Pedersen, NL; Nikus, K; Orho-Melander, M; Hamsten, A; Heeringa, J; Denny, JC; Kriebel, J; Darbar, D; Newton-Cheh, C; Shaffer, C; Macfarlane, PW; Heilmann-Heimbach, S; Almgren, P; Huang, PL; Sotoodehnia, N; Soliman, EZ; Uitterlinden, AG; Hofman, A; Franco, OH; Völker, U; Jöckel, KH; Sinner, MF; Lin, HJ; Guo, X; METASTROKE Consortium of the ISGC; Neurology Working Group of the CHARGE Consortium; Dichgans, M; Ingelsson, E; Kooperberg, C; Melander, O; Loos, RJF; Laurikka, J; Conen, D; Rosand, J; van der Harst, P; Lokki, ML; Kathiresan, S; Pereira, A; Jukema, JW; Hayward, C; Rotter, JI; März, W; Lehtimäki, T; Stricker, BH; Chung, MK; Felix, SB; Gudnason, V; Alonso, A; Roden, DM; Kääb, S; Chasman, DI; Heckbert, SR; Benjamin, EJ; Tanaka, T; Lunetta, KL; Lubitz, SA; Ellinor, PT; AFGen Consortium Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.
Nat Genet. 2017; 49(6):946-952 Doi: 10.1038/ng.3843 [OPEN ACCESS]
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de Vries, PS; Sabater-Lleal, M; Chasman, DI; Trompet, S; Ahluwalia, TS; Teumer, A; Kleber, ME; Chen, MH; Wang, JJ; Attia, JR; Marioni, RE; Steri, M; Weng, LC; Pool, R; Grossmann, V; Brody, JA; Venturini, C; Tanaka, T; Rose, LM; Oldmeadow, C; Mazur, J; Basu, S; Frånberg, M; Yang, Q; Ligthart, S; Hottenga, JJ; Rumley, A; Mulas, A; de Craen, AJ; Grotevendt, A; Taylor, KD; Delgado, GE; Kifley, A; Lopez, LM; Berentzen, TL; Mangino, M; Bandinelli, S; Morrison, AC; Hamsten, A; Tofler, G; de Maat, MP; Draisma, HH; Lowe, GD; Zoledziewska, M; Sattar, N; Lackner, KJ; Völker, U; McKnight, B; Huang, J; Holliday, EG; McEvoy, MA; Starr, JM; Hysi, PG; Hernandez, DG; Guan, W; Rivadeneira, F; McArdle, WL; Slagboom, PE; Zeller, T; Psaty, BM; Uitterlinden, AG; de Geus, EJ; Stott, DJ; Binder, H; Hofman, A; Franco, OH; Rotter, JI; Ferrucci, L; Spector, TD; Deary, IJ; März, W; Greinacher, A; Wild, PS; Cucca, F; Boomsma, DI; Watkins, H; Tang, W; Ridker, PM; Jukema, JW; Scott, RJ; Mitchell, P; Hansen, T; O'Donnell, CJ; Smith, NL; Strachan, DP; Dehghan, A Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study.
PLoS One. 2017; 12(1):e0167742-e0167742 Doi: 10.1371/journal.pone.0167742 [OPEN ACCESS]
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J Clin Invest. 2017; 127(5):1798-1812 Doi: 10.1172/JCI84840 [OPEN ACCESS]
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Zadora, J; Singh, M; Herse, F; Przybyl, L; Haase, N; Golic, M; Yung, HW; Huppertz, B; Cartwright, JE; Whitley, G; Johnsen, GM; Levi, G; Isbruch, A; Schulz, H; Luft, FC; Müller, DN; Staff, AC; Hurst, LD; Dechend, R; Izsvák, Z Disturbed Placental Imprinting in Preeclampsia Leads to Altered Expression of DLX5, a Human-Specific Early Trophoblast Marker.
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Belic, J; Koch, M; Ulz, P; Auer, M; Gerhalter, T; Mohan, S; Fischereder, K; Petru, E; Bauernhofer, T; Geigl, JB; Speicher, MR; Heitzer, E mFast-SeqS as a Monitoring and Pre-screening Tool for Tumor-Specific Aneuploidy in Plasma DNA.
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Nat Genet. 2016; 48(11):1303-1312 Doi: 10.1038/ng.3668 [OPEN ACCESS]
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Jun, G; Ibrahim-Verbaas, CA; Vronskaya, M; Lambert, JC; Chung, J; Naj, AC; Kunkle, BW; Wang, LS; Bis, JC; Bellenguez, C; Harold, D; Lunetta, KL; Destefano, AL; Grenier-Boley, B; Sims, R; Beecham, GW; Smith, AV; Chouraki, V; Hamilton-Nelson, KL; Ikram, MA; Fievet, N; Denning, N; Martin, ER; Schmidt, H; Kamatani, Y; Dunstan, ML; Valladares, O; Laza, AR; Zelenika, D; Ramirez, A; Foroud, TM; Choi, SH; Boland, A; Becker, T; Kukull, WA; van der Lee, SJ; Pasquier, F; Cruchaga, C; Beekly, D; Fitzpatrick, AL; Hanon, O; Gill, M; Barber, R; Gudnason, V; Campion, D; Love, S; Bennett, DA; Amin, N; Berr, C; Tsolaki, M; Buxbaum, JD; Lopez, OL; Deramecourt, V; Fox, NC; Cantwell, LB; Tárraga, L; Dufouil, C; Hardy, J; Crane, PK; Eiriksdottir, G; Hannequin, D; Clarke, R; Evans, D; Mosley, TH; Letenneur, L; Brayne, C; Maier, W; De Jager, P; Emilsson, V; Dartigues, JF; Hampel, H; Kamboh, MI; de Bruijn, RF; Tzourio, C; Pastor, P; Larson, EB; Rotter, JI; O'Donovan, MC; Montine, TJ; Nalls, MA; Mead, S; Reiman, EM; Jonsson, PV; Holmes, C; St George-Hyslop, PH; Boada, M; Passmore, P; Wendland, JR; Schmidt, R; Morgan, K; Winslow, AR; Powell, JF; Carasquillo, M; Younkin, SG; Jakobsdóttir, J; Kauwe, JS; Wilhelmsen, KC; Rujescu, D; Nöthen, MM; Hofman, A; Jones, L; IGAP Consortium; Haines, JL; Psaty, BM; Van Broeckhoven, C; Holmans, P; Launer, LJ; Mayeux, R; Lathrop, M; Goate, AM; Escott-Price, V; Seshadri, S; Pericak-Vance, MA; Amouyel, P; Williams, J; van Duijn, CM; Schellenberg, GD; Farrer, LA A novel Alzheimer disease locus located near the gene encoding tau protein.
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Neurology Working Group of the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, the Stroke Genetics Network (SiGN), and the International Stroke Genetics Consortium (ISGC) Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies.
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Nature. 2016; 533(7604): 539-542. Doi: 10.1038/nature17671 [OPEN ACCESS]
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Proc Natl Acad Sci U S A. 2016; 113(50):14372-14377 Doi: 10.1073/pnas.1611243113 [OPEN ACCESS]
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Schweiger, R; Kaufman, S; Laaksonen, R; Kleber, ME; März, W; Eskin, E; Rosset, S; Halperin, E Fast and Accurate Construction of Confidence Intervals for Heritability.
Am J Hum Genet. 2016; 98(6):1181-1192 Doi: 10.1016/j.ajhg.2016.04.016 [OPEN ACCESS]
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Traylor, M; Zhang, CR; Adib-Samii, P; Devan, WJ; Parsons, OE; Lanfranconi, S; Gregory, S; Cloonan, L; Falcone, GJ; Radmanesh, F; Fitzpatrick, K; Kanakis, A; Barrick, TR; Moynihan, B; Lewis, CM; Boncoraglio, GB; Lemmens, R; Thijs, V; Sudlow, C; Wardlaw, J; Rothwell, PM; Meschia, JF; Worrall, BB; Levi, C; Bevan, S; Furie, KL; Dichgans, M; Rosand, J; Markus, HS; Rost, N; International Stroke Genetics Consortium Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke.
Neurology. 2016; 86(2):146-153 Doi: 10.1212/WNL.0000000000002263 [OPEN ACCESS]
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Weiss, A; Baselmans, BM; Hofer, E; Yang, J; Okbay, A; Lind, PA; Miller, MB; Nolte, IM; Zhao, W; Hagenaars, SP; Hottenga, JJ; Matteson, LK; Snieder, H; Faul, JD; Hartman, CA; Boyle, PA; Tiemeier, H; Mosing, MA; Pattie, A; Davies, G; Liewald, DC; Schmidt, R; De Jager, PL; Heath, AC; Jokela, M; Starr, JM; Oldehinkel, AJ; Johannesson, M; Cesarini, D; Hofman, A; Harris, SE; Smith, JA; Keltikangas-Järvinen, L; Pulkki-Råback, L; Schmidt, H; Smith, J; Iacono, WG; McGue, M; Bennett, DA; Pedersen, NL; Magnusson, PK; Deary, IJ; Martin, NG; Boomsma, DI; Bartels, M; Luciano, M Personality Polygenes, Positive Affect, and Life Satisfaction.
Twin Res Hum Genet. 2016; 19(5):407-417 Doi: 10.1017/thg.2016.65 [OPEN ACCESS]
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Biebl, A; Muendlein, A; Kinz, E; Drexel, H; Kabesch, M; Zenz, W; Elling, R; Müller, C; Keil, T; Lau, S; Simma, B Confirmation of Host Genetic Determinants in the CFH Region and Susceptibility to Meningococcal Disease in a Central European Study Sample.
Pediatr Infect Dis J. 2015; 34(10):1115-1117 Doi: 10.1097/INF.0000000000000823
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Chauhan, G; Adams, HHH; Bis, JC; Weinstein, G; Yu, L; Töglhofer, AM; Smith, AV; van der Lee, SJ; Gottesman, RF; Thomson, R; Wang, J; Yang, Q; Niessen, WJ; Lopez, OL; Becker, JT; Phan, TG; Beare, RJ; Arfanakis, K; Fleischman, D; Vernooij, MW; Mazoyer, B; Schmidt, H; Srikanth, V; Knopman, DS; Jack, CR; Amouyel, P; Hofman, A; DeCarli, C; Tzourio, C; van Duijn, CM; Bennett, DA; Schmidt, R; Longstreth, WT; Mosley, TH; Fornage, M; Launer, LJ; Seshadri, S; Ikram, MA; Debette, S Association of Alzheimer's disease GWAS loci with MRI markers of brain aging.
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Davies, G; Armstrong, N; Bis, JC; Bressler, J; Chouraki, V; Giddaluru, S; Hofer, E; Ibrahim-Verbaas, CA; Kirin, M; Lahti, J; van der Lee, SJ; Le Hellard, S; Liu, T; Marioni, RE; Oldmeadow, C; Postmus, I; Smith, AV; Smith, JA; Thalamuthu, A; Thomson, R; Vitart, V; Wang, J; Yu, L; Zgaga, L; Zhao, W; Boxall, R; Harris, SE; Hill, WD; Liewald, DC; Luciano, M; Adams, H; Ames, D; Amin, N; Amouyel, P; Assareh, AA; Au, R; Becker, JT; Beiser, A; Berr, C; Bertram, L; Boerwinkle, E; Buckley, BM; Campbell, H; Corley, J; De Jager, PL; Dufouil, C; Eriksson, JG; Espeseth, T; Faul, JD; Ford, I; Generation Scotland; Gottesman, RF; Griswold, ME; Gudnason, V; Harris, TB; Heiss, G; Hofman, A; Holliday, EG; Huffman, J; Kardia, SL; Kochan, N; Knopman, DS; Kwok, JB; Lambert, JC; Lee, T; Li, G; Li, SC; Loitfelder, M; Lopez, OL; Lundervold, AJ; Lundqvist, A; Mather, KA; Mirza, SS; Nyberg, L; Oostra, BA; Palotie, A; Papenberg, G; Pattie, A; Petrovic, K; Polasek, O; Psaty, BM; Redmond, P; Reppermund, S; Rotter, JI; Schmidt, H; Schuur, M; Schofield, PW; Scott, RJ; Steen, VM; Stott, DJ; van Swieten, JC; Taylor, KD; Trollor, J; Trompet, S; Uitterlinden, AG; Weinstein, G; Widen, E; Windham, BG; Jukema, JW; Wright, AF; Wright, MJ; Yang, Q; Amieva, H; Attia, JR; Bennett, DA; Brodaty, H; de Craen, AJ; Hayward, C; Ikram, MA; Lindenberger, U; Nilsson, LG; Porteous, DJ; Räikkönen, K; Reinvang, I; Rudan, I; Sachdev, PS; Schmidt, R; Schofield, PR; Srikanth, V; Starr, JM; Turner, ST; Weir, DR; Wilson, JF; van Duijn, C; Launer, L; Fitzpatrick, AL; Seshadri, S; Mosley, TH; Deary, IJ Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).
Mol Psychiatry. 2015; 20(2):183-192 Doi: 10.1038/mp.2014.188 [OPEN ACCESS]
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Debette, S; Ibrahim Verbaas, CA; Bressler, J; Schuur, M; Smith, A; Bis, JC; Davies, G; Wolf, C; Gudnason, V; Chibnik, LB; Yang, Q; deStefano, AL; de Quervain, DJ; Srikanth, V; Lahti, J; Grabe, HJ; Smith, JA; Priebe, L; Yu, L; Karbalai, N; Hayward, C; Wilson, JF; Campbell, H; Petrovic, K; Fornage, M; Chauhan, G; Yeo, R; Boxall, R; Becker, J; Stegle, O; Mather, KA; Chouraki, V; Sun, Q; Rose, LM; Resnick, S; Oldmeadow, C; Kirin, M; Wright, AF; Jonsdottir, MK; Au, R; Becker, A; Amin, N; Nalls, MA; Turner, ST; Kardia, SL; Oostra, B; Windham, G; Coker, LH; Zhao, W; Knopman, DS; Heiss, G; Griswold, ME; Gottesman, RF; Vitart, V; Hastie, ND; Zgaga, L; Rudan, I; Polasek, O; Holliday, EG; Schofield, P; Choi, SH; Tanaka, T; An, Y; Perry, RT; Kennedy, RE; Sale, MM; Wang, J; Wadley, VG; Liewald, DC; Ridker, PM; Gow, AJ; Pattie, A; Starr, JM; Porteous, D; Liu, X; Thomson, R; Armstrong, NJ; Eiriksdottir, G; Assareh, AA; Kochan, NA; Widen, E; Palotie, A; Hsieh, YC; Eriksson, JG; Vogler, C; van Swieten, JC; Shulman, JM; Beiser, A; Rotter, J; Schmidt, CO; Hoffmann, W; Nöthen, MM; Ferrucci, L; Attia, J; Uitterlinden, AG; Amouyel, P; Dartigues, JF; Amieva, H; Räikkönen, K; Garcia, M; Wolf, PA; Hofman, A; Longstreth, WT; Psaty, BM; Boerwinkle, E; DeJager, PL; Sachdev, PS; Schmidt, R; Breteler, MM; Teumer, A; Lopez, OL; Cichon, S; Chasman, DI; Grodstein, F; Müller-Myhsok, B; Tzourio, C; Papassotiropoulos, A; Bennett, DA; Ikram, MA; Deary, IJ; van Duijn, CM; Launer, L; Fitzpatrick, AL; Seshadri, S; Mosley, TH; Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium.
Biol Psychiatry. 2015; 77(8):749-763 Doi: 10.1016/j.biopsych.2014.08.027 [OPEN ACCESS]
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Gorski, M; Tin, A; Garnaas, M; McMahon, GM; Chu, AY; Tayo, BO; Pattaro, C; Teumer, A; Chasman, DI; Chalmers, J; Hamet, P; Tremblay, J; Woodward, M; Aspelund, T; Eiriksdottir, G; Gudnason, V; Harris, TB; Launer, LJ; Smith, AV; Mitchell, BD; O'Connell, JR; Shuldiner, AR; Coresh, J; Li, M; Freudenberger, P; Hofer, E; Schmidt, H; Schmidt, R; Holliday, EG; Mitchell, P; Wang, JJ; de Boer, IH; Li, G; Siscovick, DS; Kutalik, Z; Corre, T; Vollenweider, P; Waeber, G; Gupta, J; Kanetsky, PA; Hwang, SJ; Olden, M; Yang, Q; de Andrade, M; Atkinson, EJ; Kardia, SL; Turner, ST; Stafford, JM; Ding, J; Liu, Y; Barlassina, C; Cusi, D; Salvi, E; Staessen, JA; Ridker, PM; Grallert, H; Meisinger, C; Müller-Nurasyid, M; Krämer, BK; Kramer, H; Rosas, SE; Nolte, IM; Penninx, BW; Snieder, H; Fabiola Del Greco, M; Franke, A; Nöthlings, U; Lieb, W; Bakker, SJ; Gansevoort, RT; van der Harst, P; Dehghan, A; Franco, OH; Hofman, A; Rivadeneira, F; Sedaghat, S; Uitterlinden, AG; Coassin, S; Haun, M; Kollerits, B; Kronenberg, F; Paulweber, B; Aumann, N; Endlich, K; Pietzner, M; Völker, U; Rettig, R; Chouraki, V; Helmer, C; Lambert, JC; Metzger, M; Stengel, B; Lehtimäki, T; Lyytikäinen, LP; Raitakari, O; Johnson, A; Parsa, A; Bochud, M; Heid, IM; Goessling, W; Köttgen, A; Kao, WH; Fox, CS; Böger, CA Genome-wide association study of kidney function decline in individuals of European descent.
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