Suchbegriffe: GENETIC LOCI - , . Treffer: 35
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
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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
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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
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Gorski, M; van der Most, PJ; Teumer, A; Chu, AY; Li, M; Mijatovic, V; Nolte, IM; Cocca, M; Taliun, D; Gomez, F; Li, Y; Tayo, B; Tin, A; Feitosa, MF; Aspelund, T; Attia, J; Biffar, R; Bochud, M; Boerwinkle, E; Borecki, I; Bottinger, EP; Chen, MH; Chouraki, V; Ciullo, M; Coresh, J; Cornelis, MC; Curhan, GC; d'Adamo, AP; Dehghan, A; Dengler, L; Ding, J; Eiriksdottir, G; Endlich, K; Enroth, S; Esko, T; Franco, OH; Gasparini, P; Gieger, C; Girotto, G; Gottesman, O; Gudnason, V; Gyllensten, U; Hancock, SJ; Harris, TB; Helmer, C; Höllerer, S; Hofer, E; Hofman, A; Holliday, EG; Homuth, G; Hu, FB; Huth, C; Hutri-Kähönen, N; Hwang, SJ; Imboden, M; Johansson, Å; Kähönen, M; König, W; Kramer, H; Krämer, BK; Kumar, A; Kutalik, Z; Lambert, JC; Launer, LJ; Lehtimäki, T; de Borst, M; Navis, G; Swertz, M; Liu, Y; Lohman, K; Loos, RJF; Lu, Y; Lyytikäinen, LP; McEvoy, MA; Meisinger, C; Meitinger, T; Metspalu, A; Metzger, M; Mihailov, E; Mitchell, P; Nauck, M; Oldehinkel, AJ; Olden, M; Wjh Penninx, B; Pistis, G; Pramstaller, PP; Probst-Hensch, N; Raitakari, OT; Rettig, R; Ridker, PM; Rivadeneira, F; Robino, A; Rosas, SE; Ruderfer, D; Ruggiero, D; Saba, Y; Sala, C; Schmidt, H; Schmidt, R; Scott, RJ; Sedaghat, S; Smith, AV; Sorice, R; Stengel, B; Stracke, S; Strauch, K; Toniolo, D; Uitterlinden, AG; Ulivi, S; Viikari, JS; Völker, U; Vollenweider, P; Völzke, H; Vuckovic, D; Waldenberger, M; Jin Wang, J; Yang, Q; Chasman, DI; Tromp, G; Snieder, H; Heid, IM; Fox, CS; Köttgen, A; Pattaro, C; Böger, CA; Fuchsberger, C
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
Sci Rep. 2017; 7(5):45040-45040
Doi: 10.1038/srep45040
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Hibar, DP; Adams, HHH; Jahanshad, N; Chauhan, G; Stein, JL; Hofer, E; Renteria, ME; Bis, JC; Arias-Vasquez, A; Ikram, MK; Desrivières, S; Vernooij, MW; Abramovic, L; Alhusaini, S; Amin, N; Andersson, M; Arfanakis, K; Aribisala, BS; Armstrong, NJ; Athanasiu, L; Axelsson, T; Beecham, AH; Beiser, A; Bernard, M; Blanton, SH; Bohlken, MM; Boks, MP; Bralten, J; Brickman, AM; Carmichael, O; Chakravarty, MM; Chen, Q; Ching, CRK; Chouraki, V; Cuellar-Partida, G; Crivello, F; Den Braber, A; Doan, NT; Ehrlich, S; Giddaluru, S; Goldman, AL; Gottesman, RF; Grimm, O; Griswold, ME; Guadalupe, T; Gutman, BA; Hass, J; Haukvik, UK; Hoehn, D; Holmes, AJ; Hoogman, M; Janowitz, D; Jia, T; Jørgensen, KN; Karbalai, N; Kasperaviciute, D; Kim, S; Klein, M; Kraemer, B; Lee, PH; Liewald, DCM; Lopez, LM; Luciano, M; Macare, C; Marquand, AF; Matarin, M; Mather, KA; Mattheisen, M; McKay, DR; Milaneschi, Y; Muñoz Maniega, S; Nho, K; Nugent, AC; Nyquist, P; Loohuis, LMO; Oosterlaan, J; Papmeyer, M; Pirpamer, L; Pütz, B; Ramasamy, A; Richards, JS; Risacher, SL; Roiz-Santiañez, R; Rommelse, N; Ropele, S; Rose, EJ; Royle, NA; Rundek, T; Sämann, PG; Saremi, A; Satizabal, CL; Schmaal, L; Schork, AJ; Shen, L; Shin, J; Shumskaya, E; Smith, AV; Sprooten, E; Strike, LT; Teumer, A; Tordesillas-Gutierrez, D; Toro, R; Trabzuni, D; Trompet, S; Vaidya, D; Van der Grond, J; Van der Lee, SJ; Van der Meer, D; Van Donkelaar, MMJ; Van Eijk, KR; Van Erp, TGM; Van Rooij, D; Walton, E; Westlye, LT; Whelan, CD; Windham, BG; Winkler, AM; Wittfeld, K; Woldehawariat, G; Wolf, C; Wolfers, T; Yanek, LR; Yang, J; Zijdenbos, A; Zwiers, MP; Agartz, I; Almasy, L; Ames, D; Amouyel, P; Andreassen, OA; Arepalli, S; Assareh, AA; Barral, S; Bastin, ME; Becker, DM; Becker, JT; Bennett, DA; Blangero, J; van Bokhoven, H; Boomsma, DI; Brodaty, H; Brouwer, RM; Brunner, HG; Buckner, RL; Buitelaar, JK; Bulayeva, KB; Cahn, W; Calhoun, VD; Cannon, DM; Cavalleri, GL; Cheng, CY; Cichon, S; Cookson, MR; Corvin, A; Crespo-Facorro, B; Curran, JE; Czisch, M; Dale, AM; Davies, GE; De Craen, AJM; De Geus, EJC; De Jager, PL; De Zubicaray, GI; Deary, IJ; Debette, S; DeCarli, C; Delanty, N; Depondt, C; DeStefano, A; Dillman, A; Djurovic, S; Donohoe, G; Drevets, WC; Duggirala, R; Dyer, TD; Enzinger, C; Erk, S; Espeseth, T; Fedko, IO; Fernández, G; Ferrucci, L; Fisher, SE; Fleischman, DA; Ford, I; Fornage, M; Foroud, TM; Fox, PT; Francks, C; Fukunaga, M; Gibbs, JR; Glahn, DC; Gollub, RL; Göring, HHH; Green, RC; Gruber, O; Gudnason, V; Guelfi, S; Håberg, AK; Hansell, NK; Hardy, J; Hartman, CA; Hashimoto, R; Hegenscheid, K; Heinz, A; Le Hellard, S; Hernandez, DG; Heslenfeld, DJ; Ho, BC; Hoekstra, PJ; Hoffmann, W; Hofman, A; Holsboer, F; Homuth, G; Hosten, N; Hottenga, JJ; Huentelman, M; Hulshoff Pol, HE; Ikeda, M; Jack, CR; Jenkinson, M; Johnson, R; Jönsson, EG; Jukema, JW; Kahn, RS; Kanai, R; Kloszewska, I; Knopman, DS; Kochunov, P; Kwok, JB; Lawrie, SM; Lemaître, H; Liu, X; Longo, DL; Lopez, OL; Lovestone, S; Martinez, O; Martinot, JL; Mattay, VS; McDonald, C; McIntosh, AM; McMahon, FJ; McMahon, KL; Mecocci, P; Melle, I; Meyer-Lindenberg, A; Mohnke, S; Montgomery, GW; Morris, DW; Mosley, TH; Mühleisen, TW; Müller-Myhsok, B; Nalls, MA; Nauck, M; Nichols, TE; Niessen, WJ; Nöthen, MM; Nyberg, L; Ohi, K; Olvera, RL; Ophoff, RA; Pandolfo, M; Paus, T; Pausova, Z; Penninx, BWJH; Pike, GB; Potkin, SG; Psaty, BM; Reppermund, S; Rietschel, M; Roffman, JL; Romanczuk-Seiferth, N; Rotter, JI; Ryten, M; Sacco, RL; Sachdev, PS; Saykin, AJ; ...
Novel genetic loci associated with hippocampal volume.
Nat Commun. 2017; 8(6):13624-13624
Doi: 10.1038/ncomms13624
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Rigoutsos, I; Lee, SK; Nam, SY; Anfossi, S; Pasculli, B; Pichler, M; Jing, Y; Rodriguez-Aguayo, C; Telonis, AG; Rossi, S; Ivan, C; Catela Ivkovic, T; Fabris, L; Clark, PM; Ling, H; Shimizu, M; Redis, RS; Shah, MY; Zhang, X; Okugawa, Y; Jung, EJ; Tsirigos, A; Huang, L; Ferdin, J; Gafà, R; Spizzo, R; Nicoloso, MS; Paranjape, AN; Shariati, M; Tiron, A; Yeh, JJ; Teruel-Montoya, R; Xiao, L; Melo, SA; Menter, D; Jiang, ZQ; Flores, ER; Negrini, M; Goel, A; Bar-Eli, M; Mani, SA; Liu, CG; Lopez-Berestein, G; Berindan-Neagoe, I; Esteller, M; Kopetz, S; Lanza, G; Calin, GA
N-BLR, a primate-specific non-coding transcript leads to colorectal cancer invasion and migration.
Genome Biol. 2017; 18(1):98-98
Doi: 10.1186/s13059-017-1224-0
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Traylor, M; Malik, R; Nalls, MA; Cotlarciuc, I; Radmanesh, F; Thorleifsson, G; Hanscombe, KB; Langefeld, C; Saleheen, D; Rost, NS; Yet, I; Spector, TD; Bell, JT; Hannon, E; Mill, J; Chauhan, G; Debette, S; Bis, JC; Longstreth, WT; Ikram, MA; Launer, LJ; Seshadri, S; METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium; Hamilton-Bruce, MA; Jimenez-Conde, J; Cole, JW; Schmidt, R; Słowik, A; Lemmens, R; Lindgren, A; Melander, O; Grewal, RP; Sacco, RL; Rundek, T; Rexrode, K; Arnett, DK; Johnson, JA; Benavente, OR; Wasssertheil-Smoller, S; Lee, JM; Pulit, SL; Wong, Q; Rich, SS; de Bakker, PI; McArdle, PF; Woo, D; Anderson, CD; Xu, H; Heitsch, L; Fornage, M; Jern, C; Stefansson, K; Thorsteinsdottir, U; Gretarsdottir, S; Lewis, CM; Sharma, P; Sudlow, CL; Rothwell, PM; Boncoraglio, GB; Thijs, V; Levi, C; Meschia, JF; Rosand, J; Kittner, SJ; Mitchell, BD; Dichgans, M; Worrall, BB; Markus, HS; International Stroke Genetics Consortium
Genetic variation at 16q24.2 is associated with small vessel stroke.
Ann Neurol. 2017; 81(3):383-394
Doi: 10.1002/ana.24840
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Wild, PS; Felix, JF; Schillert, A; Teumer, A; Chen, MH; Leening, MJG; Völker, U; Großmann, V; Brody, JA; Irvin, MR; Shah, SJ; Pramana, S; Lieb, W; Schmidt, R; Stanton, AV; Malzahn, D; Smith, AV; Sundström, J; Minelli, C; Ruggiero, D; Lyytikäinen, LP; Tiller, D; Smith, JG; Monnereau, C; Di Tullio, MR; Musani, SK; Morrison, AC; Pers, TH; Morley, M; Kleber, ME; Aragam, J; Benjamin, EJ; Bis, JC; Bisping, E; Broeckel, U; Cheng, S; Deckers, JW; Del Greco M, F; Edelmann, F; Fornage, M; Franke, L; Friedrich, N; Harris, TB; Hofer, E; Hofman, A; Huang, J; Hughes, AD; Kähönen, M; Investigators, K; Kruppa, J; Lackner, KJ; Lannfelt, L; Laskowski, R; Launer, LJ; Leosdottir, M; Lin, H; Lindgren, CM; Loley, C; MacRae, CA; Mascalzoni, D; Mayet, J; Medenwald, D; Morris, AP; Müller, C; Müller-Nurasyid, M; Nappo, S; Nilsson, PM; Nuding, S; Nutile, T; Peters, A; Pfeufer, A; Pietzner, D; Pramstaller, PP; Raitakari, OT; Rice, KM; Rivadeneira, F; Rotter, JI; Ruohonen, ST; Sacco, RL; Samdarshi, TE; Schmidt, H; Sharp, ASP; Shields, DC; Sorice, R; Sotoodehnia, N; Stricker, BH; Surendran, P; Thom, S; Töglhofer, AM; Uitterlinden, AG; Wachter, R; Völzke, H; Ziegler, A; Münzel, T; März, W; Cappola, TP; Hirschhorn, JN; Mitchell, GF; Smith, NL; Fox, ER; Dueker, ND; Jaddoe, VWV; Melander, O; Russ, M; Lehtimäki, T; Ciullo, M; Hicks, AA; Lind, L; Gudnason, V; Pieske, B; Barron, AJ; Zweiker, R; Schunkert, H; Ingelsson, E; Liu, K; Arnett, DK; Psaty, BM; Blankenberg, S; Larson, MG; Felix, SB; Franco, OH; Zeller, T; Vasan, RS; Dörr, M
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.
J Clin Invest. 2017; 127(5):1798-1812
Doi: 10.1172/JCI84840
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Iotchkova, V; Huang, J; Morris, JA; Jain, D; Barbieri, C; Walter, K; Min, JL; Chen, L; Astle, W; Cocca, M; Deelen, P; Elding, H; Farmaki, AE; Franklin, CS; Franberg, M; Gaunt, TR; Hofman, A; Jiang, T; Kleber, ME; Lachance, G; Luan, J; Malerba, G; Matchan, A; Mead, D; Memari, Y; Ntalla, I; Panoutsopoulou, K; Pazoki, R; Perry, JRB; Rivadeneira, F; Sabater-Lleal, M; Sennblad, B; Shin, SY; Southam, L; Traglia, M; van Dijk, F; van Leeuwen, EM; Zaza, G; Zhang, W; UK10K Consortium; Amin, N; Butterworth, A; Chambers, JC; Dedoussis, G; Dehghan, A; Franco, OH; Franke, L; Frontini, M; Gambaro, G; Gasparini, P; Hamsten, A; Issacs, A; Kooner, JS; Kooperberg, C; Langenberg, C; Marz, W; Scott, RA; Swertz, MA; Toniolo, D; Uitterlinden, AG; van Duijn, CM; Watkins, H; Zeggini, E; Maurano, MT; Timpson, NJ; Reiner, AP; Auer, PL; Soranzo, N
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.
Nat Genet. 2016; 48(11):1303-1312
Doi: 10.1038/ng.3668
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Khan, MA; Khan, S; Windpassinger, C; Badar, M; Nawaz, Z; Mohammad, RM
The Molecular Genetics of Autosomal Recessive Nonsyndromic Intellectual Disability: a Mutational Continuum and Future Recommendations.
Ann Hum Genet. 2016; 80(6):342-368
Doi: 10.1111/ahg.12176
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NINDS Stroke Genetics Network (SiGN); International Stroke Genetics Consortium (ISGC)
Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
Lancet Neurol. 2016; 15(2): 174-184.
Doi: 10.1016/S1474-4422(15)00338-5
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Verhaaren, BF; Debette, S; Bis, JC; Smith, JA; Ikram, MK; Adams, HH; Beecham, AH; Rajan, KB; Lopez, LM; Barral, S; van Buchem, MA; van der Grond, J; Smith, AV; Hegenscheid, K; Aggarwal, NT; de Andrade, M; Atkinson, EJ; Beekman, M; Beiser, AS; Blanton, SH; Boerwinkle, E; Brickman, AM; Bryan, RN; Chauhan, G; Chen, CP; Chouraki, V; de Craen, AJ; Crivello, F; Deary, IJ; Deelen, J; De Jager, PL; Dufouil, C; Elkind, MS; Evans, DA; Freudenberger, P; Gottesman, RF; Guðnason, V; Habes, M; Heckbert, SR; Heiss, G; Hilal, S; Hofer, E; Hofman, A; Ibrahim-Verbaas, CA; Knopman, DS; Lewis, CE; Liao, J; Liewald, DC; Luciano, M; van der Lugt, A; Martinez, OO; Mayeux, R; Mazoyer, B; Nalls, M; Nauck, M; Niessen, WJ; Oostra, BA; Psaty, BM; Rice, KM; Rotter, JI; von Sarnowski, B; Schmidt, H; Schreiner, PJ; Schuur, M; Sidney, SS; Sigurdsson, S; Slagboom, PE; Stott, DJ; van Swieten, JC; Teumer, A; Töglhofer, AM; Traylor, M; Trompet, S; Turner, ST; Tzourio, C; Uh, HW; Uitterlinden, AG; Vernooij, MW; Wang, JJ; Wong, TY; Wardlaw, JM; Windham, BG; Wittfeld, K; Wolf, C; Wright, CB; Yang, Q; Zhao, W; Zijdenbos, A; Jukema, JW; Sacco, RL; Kardia, SL; Amouyel, P; Mosley, TH; Longstreth, WT; DeCarli, CC; van Duijn, CM; Schmidt, R; Launer, LJ; Grabe, HJ; Seshadri, SS; Ikram, MA; Fornage, M
Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI.
Circ Cardiovasc Genet. 2015; 8(2):398-409
Doi: 10.1161/CIRCGENETICS.114.000858
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Huang, J; Huffman, JE; Yamkauchi, M; Trompet, S; Asselbergs, FW; Sabater-Lleal, M; Tregouet, DA; Chen, WM; Smith, NL; Kleber, ME; Shin, SY; Becker, DM; Tang, WH; Dehghan, A; Johnson, AD; Truong, V; Folkersen, L; Yang, Q; Oudot-Mellkah, T; Buckley, BM; Moore, JH; Williams, FMK; Campbell, H; Silbernagel, G; Vitart, V; Rudan, I; Tofler, GH; Navis, GJ; DeStefano, A; Wright, AF; Chen, MH; de Craen, AJM; Worrall, BB; Rudnicka, AR; Rumley, A; Bookman, EB; Psaty, BM; Chen, F; Keene, KL; Franco, OH; Bohm, BO; Uitterlinden, AG; Carter, AM; Jukema, JW; Sattar, N; Bis, JC; Ikram, MA; Sale, MM; McKnight, B; Fornage, M; Ford, I; Taylor, K; Slagboom, PE; McArdle, WL; Hsu, FC; Franco-Cereceda, A; Goodall, AH; Yanek, LR; Furie, KL; Cushman, M; Hofman, A; Witteman, JCM; Folsom, AR; Basu, S; Matijevic, N; van Gilst, WH; Wilson, JF; Westendorp, RGJ; Kathiresan, S; Reilly, MP; Tracy, RP; Polasek, O; Winkelmann, BR; Grant, PJ; Hillege, HL; Cambien, F; Stott, DJ; Lowe, GD; Spector, TD; Meigs, JB; Marz, W; Eriksson, P; Becker, LC; Morange, PE; Soranzo, N; Williams, SM; Hayward, C; van der Harst, P; Hamsten, A; Lowenstein, CJ; Strachan, DP; O'Donnell, CJ;
Genome-Wide Association Study for Circulating Tissue Plasminogen Activator Levels and Functional Follow-Up Implicates Endothelial STXBP5 and STX2.
ARTERIOSCLER THROMB VASC BIOL. 2014; 34(5): 1093-1101.
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Schiekofer, S; Bobak, I; Kleber, ME; Maerz, W; Rudofsky, G; Dugi, KA; Schneider, JG
Association between a gene variant near ataxia telangiectasia mutated and coronary artery disease in men.
Diab Vasc Dis Res. 2014; 11(1):60-63
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Tragante, V; Barnes, MR; Ganesh, SK; Lanktree, MB; Guo, W; Franceschini, N; Smith, EN; Johnson, T; Holmes, MV; Padmanabhan, S; Karczewski, KJ; Almoguera, B; Barnard, J; Baumert, J; Chang, YP; Elbers, CC; Farrall, M; Fischer, ME; Gaunt, TR; Gho, JM; Gieger, C; Goel, A; Gong, Y; Isaacs, A; Kleber, ME; Mateo Leach, I; McDonough, CW; Meijs, MF; Melander, O; Nelson, CP; Nolte, IM; Pankratz, N; Price, TS; Shaffer, J; Shah, S; Tomaszewski, M; van der Most, PJ; Van Iperen, EP; Vonk, JM; Witkowska, K; Wong, CO; Zhang, L; Beitelshees, AL; Berenson, GS; Bhatt, DL; Brown, M; Burt, A; Cooper-DeHoff, RM; Connell, JM; Cruickshanks, KJ; Curtis, SP; Davey-Smith, G; Delles, C; Gansevoort, RT; Guo, X; Haiqing, S; Hastie, CE; Hofker, MH; Hovingh, GK; Kim, DS; Kirkland, SA; Klein, BE; Klein, R; Li, YR; Maiwald, S; Newton-Cheh, C; O'Brien, ET; Onland-Moret, NC; Palmas, W; Parsa, A; Penninx, BW; Pettinger, M; Vasan, RS; Ranchalis, JE; M Ridker, P; Rose, LM; Sever, P; Shimbo, D; Steele, L; Stolk, RP; Thorand, B; Trip, MD; van Duijn, CM; Verschuren, WM; Wijmenga, C; Wyatt, S; Young, JH; Zwinderman, AH; Bezzina, CR; Boerwinkle, E; Casas, JP; Caulfield, MJ; Chakravarti, A; Chasman, DI; Davidson, KW; Doevendans, PA; Dominiczak, AF; FitzGerald, GA; Gums, JG; Fornage, M; Hakonarson, H; Halder, I; Hillege, HL; Illig, T; Jarvik, GP; Johnson, JA; Kastelein, JJ; Koenig, W; Kumari, M; März, W; Murray, SS; O'Connell, JR; Oldehinkel, AJ; Pankow, JS; Rader, DJ; Redline, S; Reilly, MP; Schadt, EE; Kottke-Marchant, K; Snieder, H; Snyder, M; Stanton, AV; Tobin, MD; Uitterlinden, AG; van der Harst, P; van der Schouw, YT; Samani, NJ; Watkins, H; Johnson, AD; Reiner, AP; Zhu, X; de Bakker, PI; Levy, D; Asselbergs, FW; Munroe, PB; Keating, BJ
Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci.
Am J Hum Genet. 2014; 94(3):349-360
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European Alzheimer's Disease Initiative (EADI); Genetic and Environmental Risk in Alzheimer's Disease; Alzheimer's Disease Genetic Consortium; Cohorts for Heart and Aging Research in Genomic Epidemiology
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease.
Nat Genet. 2013; 45(12):1452-1458
Doi: 10.1038/ng.2802
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Kodaganur, SG; Tontanahal, SJ; Sarda, A; Shah, MH; Bhat, V; Kumar, A
Clinical phenotype and the lack of mutations in the CHRNG, CHRND, and CHRNA1 genes in two Indian families with Escobar syndrome.
Clin Dysmorphol. 2013; 22(2): 54-58.
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Mayerle, J; den Hoed, CM; Schurmann, C; Stolk, L; Homuth, G; Peters, MJ; Capelle, LG; Zimmermann, K; Rivadeneira, F; Gruska, S; Völzke, H; de Vries, AC; Völker, U; Teumer, A; van Meurs, JB; Steinmetz, I; Nauck, M; Ernst, F; Weiss, FU; Hofman, A; Zenker, M; Kroemer, HK; Prokisch, H; Uitterlinden, AG; Lerch, MM; Kuipers, EJ; Kuipers, E
Identification of genetic loci associated with Helicobacter pylori serologic status.
JAMA. 2013; 309(18):1912-1920
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Rietveld, CA; Medland, SE; Derringer, J; Yang, J; Esko, T; Martin, NW; Westra, HJ; Shakhbazov, K; Abdellaoui, A; Agrawal, A; Albrecht, E; Alizadeh, BZ; Amin, N; Barnard, J; Baumeister, SE; Benke, KS; Bielak, LF; Boatman, JA; Boyle, PA; Davies, G; de Leeuw, C; Eklund, N; Evans, DS; Ferhmann, R; Fischer, K; Gieger, C; Gjessing, HK; Hägg, S; Harris, JR; Hayward, C; Holzapfel, C; Ibrahim-Verbaas, CA; Ingelsson, E; Jacobsson, B; Joshi, PK; Jugessur, A; Kaakinen, M; Kanoni, S; Karjalainen, J; Kolcic, I; Kristiansson, K; Kutalik, Z; Lahti, J; Lee, SH; Lin, P; Lind, PA; Liu, Y; Lohman, K; Loitfelder, M; McMahon, G; Vidal, PM; Meirelles, O; Milani, L; Myhre, R; Nuotio, ML; Oldmeadow, CJ; Petrovic, KE; Peyrot, WJ; Polasek, O; Quaye, L; Reinmaa, E; Rice, JP; Rizzi, TS; Schmidt, H; Schmidt, R; Smith, AV; Smith, JA; Tanaka, T; Terracciano, A; van der Loos, MJ; Vitart, V; Völzke, H; Wellmann, J; Yu, L; Zhao, W; Allik, J; Attia, JR; Bandinelli, S; Bastardot, F; Beauchamp, J; Bennett, DA; Berger, K; Bierut, LJ; Boomsma, DI; Bültmann, U; Campbell, H; Chabris, CF; Cherkas, L; Chung, MK; Cucca, F; de Andrade, M; De Jager, PL; De Neve, JE; Deary, IJ; Dedoussis, GV; Deloukas, P; Dimitriou, M; Eiríksdóttir, G; Elderson, MF; Eriksson, JG; Evans, DM; Faul, JD; Ferrucci, L; Garcia, ME; Grönberg, H; Guðnason, V; Hall, P; Harris, JM; Harris, TB; Hastie, ND; Heath, AC; Hernandez, DG; Hoffmann, W; Hofman, A; Holle, R; Holliday, EG; Hottenga, JJ; Iacono, WG; Illig, T; Järvelin, MR; Kähönen, M; Kaprio, J; Kirkpatrick, RM; Kowgier, M; Latvala, A; Launer, LJ; Lawlor, DA; Lehtimäki, T; Li, J; Lichtenstein, P; Lichtner, P; Liewald, DC; Madden, PA; Magnusson, PK; Mäkinen, TE; Masala, M; McGue, M; Metspalu, A; Mielck, A; Miller, MB; Montgomery, GW; Mukherjee, S; Nyholt, DR; Oostra, BA; Palmer, LJ; Palotie, A; Penninx, BW; Perola, M; Peyser, PA; Preisig, M; Räikkönen, K; Raitakari, OT; Realo, A; Ring, SM; Ripatti, S; Rivadeneira, F; Rudan, I; Rustichini, A; Salomaa, V; Sarin, AP; Schlessinger, D; Scott, RJ; Snieder, H; St Pourcain, B; Starr, JM; Sul, JH; Surakka, I; Svento, R; Teumer, A; LifeLines Cohort Study; Tiemeier, H; van Rooij, FJ; Van Wagoner, DR; Vartiainen, E; Viikari, J; Vollenweider, P; Vonk, JM; Waeber, G; Weir, DR; Wichmann, HE; Widen, E; Willemsen, G; Wilson, JF; Wright, AF; Conley, D; Davey-Smith, G; Franke, L; Groenen, PJ; Hofman, A; Johannesson, M; Kardia, SL; Krueger, RF; Laibson, D; Martin, NG; Meyer, MN; Posthuma, D; Thurik, AR; Timpson, NJ; Uitterlinden, AG; van Duijn, CM; Visscher, PM; Benjamin, DJ; Cesarini, D; Koellinger, PD
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.
Science. 2013; 340(6139):1467-1471
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Silbernagel, G; Genser, B; Nestel, P; März, W
Plant sterols and atherosclerosis.
Curr Opin Lipidol. 2013; 24(1):12-17
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Bis, JC; DeCarli, C; Smith, AV; van der Lijn, F; Crivello, F; Fornage, M; Debette, S; Shulman, JM; Schmidt, H; Srikanth, V; Schuur, M; Yu, L; Choi, SH; Sigurdsson, S; Verhaaren, BF; DeStefano, AL; Lambert, JC; Jack, CR; Struchalin, M; Stankovich, J; Ibrahim-Verbaas, CA; Fleischman, D; Zijdenbos, A; den Heijer, T; Mazoyer, B; Coker, LH; Enzinger, C; Danoy, P; Amin, N; Arfanakis, K; van Buchem, MA; de Bruijn, RF; Beiser, A; Dufouil, C; Huang, J; Cavalieri, M; Thomson, R; Niessen, WJ; Chibnik, LB; Gislason, GK; Hofman, A; Pikula, A; Amouyel, P; Freeman, KB; Phan, TG; Oostra, BA; Stein, JL; Medland, SE; Vasquez, AA; Hibar, DP; Wright, MJ; Franke, B; Martin, NG; Thompson, PM; Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium; Nalls, MA; Uitterlinden, AG; Au, R; Elbaz, A; Beare, RJ; van Swieten, JC; Lopez, OL; Harris, TB; Chouraki, V; Breteler, MM; De Jager, PL; Becker, JT; Vernooij, MW; Knopman, D; Fazekas, F; Wolf, PA; van der Lugt, A; Gudnason, V; Longstreth, WT; Brown, MA; Bennett, DA; van Duijn, CM; Mosley, TH; Schmidt, R; Tzourio, C; Launer, LJ; Ikram, MA; Seshadri, S; Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Common variants at 12q14 and 12q24 are associated with hippocampal volume.
Nat Genet. 2012; 44(5):545-551
Doi: 10.1038/ng.2237
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Demirkan, A; van Duijn, CM; Ugocsai, P; Isaacs, A; Pramstaller, PP; Liebisch, G; Wilson, JF; Johansson, Å; Rudan, I; Aulchenko, YS; Kirichenko, AV; Janssens, AC; Jansen, RC; Gnewuch, C; Domingues, FS; Pattaro, C; Wild, SH; Jonasson, I; Polasek, O; Zorkoltseva, IV; Hofman, A; Karssen, LC; Struchalin, M; Floyd, J; Igl, W; Biloglav, Z; Broer, L; Pfeufer, A; Pichler, I; Campbell, S; Zaboli, G; Kolcic, I; Rivadeneira, F; Huffman, J; Hastie, ND; Uitterlinden, A; Franke, L; Franklin, CS; Vitart, V; DIAGRAM Consortium; Nelson, CP; Preuss, M; CARDIoGRAM Consortium; Bis, JC; O'Donnell, CJ; Franceschini, N; CHARGE Consortium; Witteman, JC; Axenovich, T; Oostra, BA; Meitinger, T; Hicks, AA; Hayward, C; Wright, AF; Gyllensten, U; Campbell, H; Schmitz, G; EUROSPAN consortium
Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.
PLoS Genet. 2012; 8(2):e1002490-e1002490
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Ikram, MA; Fornage, M; Smith, AV; Seshadri, S; Schmidt, R; Debette, S; Vrooman, HA; Sigurdsson, S; Ropele, S; Taal, HR; Mook-Kanamori, DO; Coker, LH; Longstreth, WT; Niessen, WJ; DeStefano, AL; Beiser, A; Zijdenbos, AP; Struchalin, M; Jack, CR; Rivadeneira, F; Uitterlinden, AG; Knopman, DS; Hartikainen, AL; Pennell, CE; Thiering, E; Steegers, EA; Hakonarson, H; Heinrich, J; Palmer, LJ; Jarvelin, MR; McCarthy, MI; Grant, SF; St Pourcain, B; Timpson, NJ; Smith, GD; Sovio, U; Early Growth Genetics Consortium; Nalls, MA; Au, R; Hofman, A; Gudnason, H; van der Lugt, A; Harris, TB; Meeks, WM; Vernooij, MW; van Buchem, MA; Catellier, D; Jaddoe, VW; Gudnason, V; Windham, BG; Wolf, PA; van Duijn, CM; Mosley, TH; Schmidt, H; Launer, LJ; Breteler, MM; DeCarli, C; Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Common variants at 6q22 and 17q21 are associated with intracranial volume.
Nat Genet. 2012; 44(5):539-544
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Knight, J; Spain, SL; Capon, F; Hayday, A; Nestle, FO; Clop, A; Wellcome Trust Case Control Consortium; Genetic Analysis of Psoriasis Consortium; I-chip for Psoriasis Consortium; Barker, JN; Weale, ME; Trembath, RC
Conditional analysis identifies three novel major histocompatibility complex loci associated with psoriasis.
Hum Mol Genet. 2012; 21(23):5185-5192
Doi: 10.1093/hmg/dds344
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Saxena, R; Elbers, CC; Guo, Y; Peter, I; Gaunt, TR; Mega, JL; Lanktree, MB; Tare, A; Castillo, BA; Li, YR; Johnson, T; Bruinenberg, M; Gilbert-Diamond, D; Rajagopalan, R; Voight, BF; Balasubramanyam, A; Barnard, J; Bauer, F; Baumert, J; Bhangale, T; Böhm, BO; Braund, PS; Burton, PR; Chandrupatla, HR; Clarke, R; Cooper-DeHoff, RM; Crook, ED; Davey-Smith, G; Day, IN; de Boer, A; de Groot, MC; Drenos, F; Ferguson, J; Fox, CS; Furlong, CE; Gibson, Q; Gieger, C; Gilhuijs-Pederson, LA; Glessner, JT; Goel, A; Gong, Y; Grant, SF; Grobbee, DE; Hastie, C; Humphries, SE; Kim, CE; Kivimaki, M; Kleber, M; Meisinger, C; Kumari, M; Langaee, TY; Lawlor, DA; Li, M; Lobmeyer, MT; Maitland-van der Zee, AH; Meijs, MF; Molony, CM; Morrow, DA; Murugesan, G; Musani, SK; Nelson, CP; Newhouse, SJ; O'Connell, JR; Padmanabhan, S; Palmen, J; Patel, SR; Pepine, CJ; Pettinger, M; Price, TS; Rafelt, S; Ranchalis, J; Rasheed, A; Rosenthal, E; Ruczinski, I; Shah, S; Shen, H; Silbernagel, G; Smith, EN; Spijkerman, AW; Stanton, A; Steffes, MW; Thorand, B; Trip, M; van der Harst, P; van der A, DL; van Iperen, EP; van Setten, J; van Vliet-Ostaptchouk, JV; Verweij, N; Wolffenbuttel, BH; Young, T; Zafarmand, MH; Zmuda, JM; Look AHEAD Research Group; DIAGRAM consortium; Boehnke, M; Altshuler, D; McCarthy, M; Kao, WH; Pankow, JS; Cappola, TP; Sever, P; Poulter, N; Caulfield, M; Dominiczak, A; Shields, DC; Bhatt, DL; Bhatt, D; Zhang, L; Curtis, SP; Danesh, J; Casas, JP; van der Schouw, YT; Onland-Moret, NC; Doevendans, PA; Dorn, GW; Farrall, M; FitzGerald, GA; Hamsten, A; Hegele, R; Hingorani, AD; Hofker, MH; Huggins, GS; Illig, T; Jarvik, GP; Johnson, JA; Klungel, OH; Knowler, WC; Koenig, W; März, W; Meigs, JB; Melander, O; Munroe, PB; Mitchell, BD; Bielinski, SJ; Rader, DJ; Reilly, MP; Rich, SS; Rotter, JI; Saleheen, D; Samani, NJ; Schadt, EE; Shuldiner, AR; Silverstein, R; Kottke-Marchant, K; Talmud, PJ; Watkins, H; Asselbergs, FW; Asselbergs, F; de Bakker, PI; McCaffery, J; Wijmenga, C; Sabatine, MS; Wilson, JG; Reiner, A; Bowden, DW; Hakonarson, H; Siscovick, DS; Keating, BJ
Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci.
Am J Hum Genet. 2012; 90(3):410-425
Doi: 10.1016/j.ajhg.2011.12.022
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Taal, HR; St Pourcain, B; Thiering, E; Das, S; Mook-Kanamori, DO; Warrington, NM; Kaakinen, M; Kreiner-Møller, E; Bradfield, JP; Freathy, RM; Geller, F; Guxens, M; Cousminer, DL; Kerkhof, M; Timpson, NJ; Ikram, MA; Beilin, LJ; Bønnelykke, K; Buxton, JL; Charoen, P; Chawes, BL; Eriksson, J; Evans, DM; Hofman, A; Kemp, JP; Kim, CE; Klopp, N; Lahti, J; Lye, SJ; McMahon, G; Mentch, FD; Müller-Nurasyid, M; O'Reilly, PF; Prokopenko, I; Rivadeneira, F; Steegers, EA; Sunyer, J; Tiesler, C; Yaghootkar, H; Cohorts for Heart and Aging Research in Genetic Epidemiology Consortium; Breteler, MM; Decarli, C; Breteler, MM; Debette, S; Fornage, M; Gudnason, V; Launer, LJ; van der Lugt, A; Mosley, TH; Seshadri, S; Smith, AV; Vernooij, MW; Early Genetics & Lifecourse Epidemiology Consortium; Blakemore, AI; Chiavacci, RM; Feenstra, B; Fernandez-Banet, J; Grant, SF; Hartikainen, AL; van der Heijden, AJ; Iñiguez, C; Lathrop, M; McArdle, WL; Mølgaard, A; Newnham, JP; Palmer, LJ; Palotie, A; Pouta, A; Ring, SM; Sovio, U; Standl, M; Uitterlinden, AG; Wichmann, HE; Vissing, NH; DeCarli, C; van Duijn, CM; McCarthy, MI; Koppelman, GH; Estivill, X; Hattersley, AT; Melbye, M; Bisgaard, H; Pennell, CE; Widen, E; Hakonarson, H; Smith, GD; Heinrich, J; Jarvelin, MR; Jaddoe, VW; Early Growth Genetics Consortium
Common variants at 12q15 and 12q24 are associated with infant head circumference.
Nat Genet. 2012; 44(5):532-538
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Tsoi, LC; Spain, SL; Knight, J; Ellinghaus, E; Stuart, PE; Capon, F; Ding, J; Li, Y; Tejasvi, T; Gudjonsson, JE; Kang, HM; Allen, MH; McManus, R; Novelli, G; Samuelsson, L; Schalkwijk, J; Ståhle, M; Burden, AD; Smith, CH; Cork, MJ; Estivill, X; Bowcock, AM; Krueger, GG; Weger, W; Worthington, J; Tazi-Ahnini, R; Nestle, FO; Hayday, A; Hoffmann, P; Winkelmann, J; Wijmenga, C; Langford, C; Edkins, S; Andrews, R; Blackburn, H; Strange, A; Band, G; Pearson, RD; Vukcevic, D; Spencer, CC; Deloukas, P; Mrowietz, U; Schreiber, S; Weidinger, S; Koks, S; Kingo, K; Esko, T; Metspalu, A; Lim, HW; Voorhees, JJ; Weichenthal, M; Wichmann, HE; Chandran, V; Rosen, CF; Rahman, P; Gladman, DD; Griffiths, CE; Reis, A; Kere, J; Collaborative Association Study of Psoriasis (CASP); Genetic Analysis of Psoriasis Consortium; Psoriasis Association Genetics Extension; Wellcome Trust Case Control Consortium 2; Nair, RP; Franke, A; Barker, JN; Abecasis, GR; Elder, JT; Trembath, RC
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.
Nat Genet. 2012; 44(12):1341-1348
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Seventy-five genetic loci influencing the human red blood cell.
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Bis, JC; Kavousi, M; Franceschini, N; Isaacs, A; Abecasis, GR; Schminke, U; Post, WS; Smith, AV; Cupples, LA; Markus, HS; Schmidt, R; Huffman, JE; Lehtimäki, T; Baumert, J; Münzel, T; Heckbert, SR; Dehghan, A; North, K; Oostra, B; Bevan, S; Stoegerer, EM; Hayward, C; Raitakari, O; Meisinger, C; Schillert, A; Sanna, S; Völzke, H; Cheng, YC; Thorsson, B; Fox, CS; Rice, K; Rivadeneira, F; Nambi, V; Halperin, E; Petrovic, KE; Peltonen, L; Wichmann, HE; Schnabel, RB; Dörr, M; Parsa, A; Aspelund, T; Demissie, S; Kathiresan, S; Reilly, MP; Taylor, K; Uitterlinden, A; Couper, DJ; Sitzer, M; Kähönen, M; Illig, T; Wild, PS; Orru, M; Lüdemann, J; Shuldiner, AR; Eiriksdottir, G; White, CC; Rotter, JI; Hofman, A; Seissler, J; Zeller, T; Usala, G; Ernst, F; Launer, LJ; D'Agostino, RB; O'Leary, DH; Ballantyne, C; Thiery, J; Ziegler, A; Lakatta, EG; Chilukoti, RK; Harris, TB; Wolf, PA; Psaty, BM; Polak, JF; Li, X; Rathmann, W; Uda, M; Boerwinkle, E; Klopp, N; Schmidt, H; Wilson, JF; Viikari, J; Koenig, W; Blankenberg, S; Newman, AB; Witteman, J; Heiss, G; Duijn, Cv; Scuteri, A; Homuth, G; Mitchell, BD; Gudnason, V; O'Donnell, CJ; CARDIoGRAM Consortium
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.
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Lanktree, MB; Guo, Y; Murtaza, M; Glessner, JT; Bailey, SD; Onland-Moret, NC; Lettre, G; Ongen, H; Rajagopalan, R; Johnson, T; Shen, H; Nelson, CP; Klopp, N; Baumert, J; Padmanabhan, S; Pankratz, N; Pankow, JS; Shah, S; Taylor, K; Barnard, J; Peters, BJ; Maloney, CM; Lobmeyer, MT; Stanton, A; Zafarmand, MH; Romaine, SP; Mehta, A; van Iperen, EP; Gong, Y; Price, TS; Smith, EN; Kim, CE; Li, YR; Asselbergs, FW; Atwood, LD; Bailey, KM; Bhatt, D; Bauer, F; Behr, ER; Bhangale, T; Boer, JM; Boehm, BO; Bradfield, JP; Brown, M; Braund, PS; Burton, PR; Carty, C; Chandrupatla, HR; Chen, W; Connell, J; Dalgeorgou, C; Boer, Ad; Drenos, F; Elbers, CC; Fang, JC; Fox, CS; Frackelton, EC; Fuchs, B; Furlong, CE; Gibson, Q; Gieger, C; Goel, A; Grobbee, DE; Hastie, C; Howard, PJ; Huang, GH; Johnson, WC; Li, Q; Kleber, ME; Klein, BE; Klein, R; Kooperberg, C; Ky, B; Lacroix, A; Lanken, P; Lathrop, M; Li, M; Marshall, V; Melander, O; Mentch, FD; Meyer, NJ; Monda, KL; Montpetit, A; Murugesan, G; Nakayama, K; Nondahl, D; Onipinla, A; Rafelt, S; Newhouse, SJ; Otieno, FG; Patel, SR; Putt, ME; Rodriguez, S; Safa, RN; Sawyer, DB; Schreiner, PJ; Simpson, C; Sivapalaratnam, S; Srinivasan, SR; Suver, C; Swergold, G; Sweitzer, NK; Thomas, KA; Thorand, B; Timpson, NJ; Tischfield, S; Tobin, M; Tomaszewski, M; Tomaszweski, M; Verschuren, WM; Wallace, C; Winkelmann, B; Zhang, H; Zheng, D; Zhang, L; Zmuda, JM; Clarke, R; Balmforth, AJ; Danesh, J; Day, IN; Schork, NJ; de Bakker, PI; Delles, C; Duggan, D; Hingorani, AD; Hirschhorn, JN; Hofker, MH; Humphries, SE; Kivimaki, M; Lawlor, DA; Kottke-Marchant, K; Mega, JL; Mitchell, BD; Morrow, DA; Palmen, J; Redline, S; Shields, DC; Shuldiner, AR; Sleiman, PM; Smith, GD; Farrall, M; Jamshidi, Y; Christiani, DC; Casas, JP; Hall, AS; Doevendans, PA; Christie, JD; Berenson, GS; Murray, SS; Illig, T; Dorn, GW; Cappola, TP; Boerwinkle, E; Sever, P; Rader, DJ; Reilly, MP; Caulfield, M; Talmud, PJ; Topol, E; Engert, JC; Wang, K; Dominiczak, A; Hamsten, A; Curtis, SP; Silverstein, RL; Lange, LA; Sabatine, MS; Trip, M; Saleheen, D; Peden, JF; Cruickshanks, KJ; März, W; O'Connell, JR; Klungel, OH; Wijmenga, C; Maitland-van der Zee, AH; Schadt, EE; Johnson, JA; Jarvik, GP; Papanicolaou, GJ; Hugh Watkins on behalf of PROCARDIS; Grant, SF; Munroe, PB; North, KE; Samani, NJ; Koenig, W; Gaunt, TR; Anand, SS; van der Schouw, YT; Meena Kumari on behalf of the Whitehall II Study and the WHII 50K Group; Soranzo, N; Fitzgerald, GA; Reiner, A; Hegele, RA; Hakonarson, H; Keating, BJ
Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height.
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Lerchbaum, E; Trummer, O; Giuliani, A; Gruber, HJ; Pieber, TR; Obermayer-Pietsch, B
Susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21, and 9q33.3 in a cohort of Caucasian women.
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Poetsch, M; Kamphausen, T; Bajanowski, T; Schwark, T; von Wurmb-Schwark, N
Powerplex® ES versus Powerplex® S5--casework testing of the new screening kit.
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Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
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Saleheen, D; Soranzo, N; Rasheed, A; Scharnagl, H; Gwilliam, R; Alexander, M; Inouye, M; Zaidi, M; Potter, S; Haycock, P; Bumpstead, S; Kaptoge, S; Di Angelantonio, E; Sarwar, N; Hunt, SE; Sheikh, N; Shah, N; Samuel, M; Haider, SR; Murtaza, M; Thompson, A; Gobin, R; Butterworth, A; Ahmad, U; Hakeem, A; Zaman, KS; Kundi, A; Yaqoob, Z; Cheema, LA; Qamar, N; Faruqui, A; Mallick, NH; Azhar, M; Samad, A; Ishaq, M; Rasheed, SZ; Jooma, R; Niazi, JH; Gardezi, AR; Memon, NA; Ghaffar, A; Rehman, FU; Hoffmann, MM; Renner, W; Kleber, ME; Grammer, TB; Stephens, J; Attwood, A; Koch, K; Hussain, M; Kumar, K; Saleem, A; Kumar, K; Daood, MS; Gul, AA; Abbas, S; Zafar, J; Shahid, F; Bhatti, SM; Ali, SS; Fahim, M; Sagoo, G; Bray, S; McGinnis, R; Dudbridge, F; Winkelmann, BR; Boehm, B; Thompson, S; Ouwehand, W; Marz, W; Frossard, P; Danesh, J; Deloukas, P
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Genome-wide analysis of genetic loci associated with Alzheimer disease.
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