Remdesivir in adults with severe COVID-19: a randomised, double-blind, placebo-controlled, multicentre trial. by Wang, Y, Zhang, D, Du, G, Du, R, Zhao, J, Jin, Y, Fu, S, Gao, L, Cheng, Z, Lu, Q, Hu, Y, Luo, G, Wang, K, Lu, Y, Li, H, Wang, S, Ruan, S, Yang, C, Mei, C, Wang, Y, Ding, D, Wu, F, Tang, X, Ye, X, Ye, Y, Liu, B, Yang, J, Yin, W, Wang, A, Fan, G, Zhou, F, Liu, Z, Gu, X, Xu, J, Shang, L, Zhang, Y, Cao, L, Guo, T, Wan, Y, Qin, H, Jiang, Y, Jaki, T, Hayden, FG, Horby, PW, Cao, B, Wang, C

Body iron status and gastric cancer risk in the EURGAST study by Fonseca-Nunes, A., Agudo, A., Aranda, N., Arija, V., Cross, A.J., Molina, E., Jose Sanchez, M., Bueno-de-Mesquita, H.B, Siersema, P., Weiderpass, E., Krogh, V., Mattiello, A., Tumino, R., Saieva, C., Naccarati, A., Ohlsson, B., Sjoberg, K., Boutron-Ruault, M.C., Cadeau, C., Fagherazzi, G., Boeing, H., Steffen, A., Kuehn, T., Katzke, V., Tjonneland, A., Olsen, A., Khaw, K.T, Wareham, N., Key, T., Lu, Y., Riboli, E., Peeters, P.H., Gavrila, D., Dorronsoro, M., Ramon Quiros, J., Barricarte, A., Jenab, M., Zamora-Ros, R., Freisling, H., Trichopoulou, A., Lagiou, P., Bamia, C., Jakszyn, P.

Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose by Wu, P, Rybin, D, Bielak, LF, Feitosa, MF, Franceschini, N, Li, Y, Lu, Y, Marten, J, Musani, SK, Noordam, R, Raghavan, S, Rose, LM, Schwander, K, Smith, AV, Tajuddin, SM, Vojinovic, D, Amin, N, Arnett, DK, Bottinger, EP, Demirkan, A, Florez, JC, Ghanbari, M, Harris, TB, Launer, LJ, Liu, J, Liu, J, Mook-Kanamori, DO, Murray, AD, Nalls, MA, Peyser, PA, Uitterlinden, AG, Voortman, T, Bouchard, C, Chasman, D, Correa, A, de Mutsert, R, Evans, MK, Gudnason, V, Hayward, C, Kao, L, Kardia, SLR, Kooperberg, C, Loos, RJF, Province, MM, Rankinen, T, Redline, S, Ridker, PM, Rotter, JI, Siscovick, D, Smith, BH, van Duijn, C

Polygenic hazard score is associated with prostate cancer in multi-ethnic populations by Huynh-Le, M, Fan, CC, Karunamuni, R, Thompson, WK, Martinez, ME, Eeles, RA, Kote-Jarai, Z, Muir, K, Schleutker, J, Pashayan, N, Batra, J, Grönberg, H, Neal, DE, Donovan, JL, Hamdy, FC, Martin, RM, Nielsen, SF, Nordestgaard, BG, Wiklund, F, Tangen, CM, Giles, GG, Wolk, A, Albanes, D, Travis, RC, Blot, WJ, Zheng, W, Sanderson, M, Stanford, JL, Mucci, LA, West, CML, Kibel, AS, Cussenot, O, Berndt, SI, Koutros, S, Sørensen, KD, Cybulski, C, Grindedal, EM, Menegaux, F, Khaw, K, Park, JY, Ingles, SA, Maier, C, Hamilton, RJ, Thibodeau, SN, Rosenstein, BS, Lu, Y, Watya, S, Watya, S, Vega, A, Kogevinas, M, Penney, KL, Mills, IG

Appraising the relevance of DNA copy number loss and gain in prostate cancer using whole genome DNA sequence data by Camacho, N, Van Loo, P, Edwards, S, Kay, J, Matthews, L, Haase, K, Clark, J, Dennis, N, Thomas, S, Kremeyer, B, Zamora, J, Butler, A, Gundem, G, Merson, S, Luxton, H, Hawkins, S, Ghori, M, Marsden, L, Lambert, A, Karaszi, K, Pelvender, G, Massie, C, Kote-Jarai, Z, Raine, K, Jones, D, Howat, W, Hazell, S, Livni, N, Fisher, C, Ogden, C, Kumar, P, Thompson, A, Nicol, D, Mayer, E, Dudderidge, T, Yu, Y, Zhang, H, Shah, N, Gnanapragasam, V, Isaacs, W, Visakorpi, T, Hamdy, F, Berney, D, Verrill, C, Warren, A, Wedge, D, Lynch, A, Foster, C, Lu, Y, Bova, G, Whitaker, H, McDermott, U, Neal, D, Eeles, R, Cooper, C, Brewer, D

Genetic studies of leptin concentrations implicate leptin in the regulation of early adiposity by Yaghootkar, H, Zhang, Y, Spracklen, CN, Karaderi, T, Huang, LO, Bradfield, J, Schurmann, C, Fine, RS, Preuss, MH, Kutalik, Z, Wittemans, LB, Lu, Y, Metz, S, Willems, SM, Li-Gao, R, Grarup, N, Wang, S, Molnos, S, Sandoval-Zárate, AA, Nalls, MA, Lange, LA, Haesser, J, Guo, X, Lyytikäinen, L-P, Feitosa, MF, Sitlani, CM, Venturini, C, Mahajan, A, Kacprowski, T, Wang, CA, Chasman, DI, Amin, N, Broer, L, Robertson, N, Young, KL, Allison, M, Auer, PL, Blüher, M, Borja, JB, Bork-Jensen, J, Carrasquilla, GD, Christofidou, P, Demirkan, A, Doege, CA, Garcia, ME, Graff, M, Guo, K, Hakonarson, H, Hong, J, Ida Chen, Y-D, van Duijn, CM, Et al.

Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies by Morris, A, Le, T, Wu, H, Akbarov, A, Van Der Most, P, Hemani, G, Smith, G, Mahajan, A, Gaulton, K, Nadkarni, G, Valladares-Salgado, A, Wacher-Rodarte, N, Mychaleckyj, J, Dueker, N, Guo, X, Hai, Y, Haessler, J, Kamatani, Y, Stilp, A, Zhu, G, Cook, J, Ärnlöv, J, Blanton, S, De Borst, M, Bottinger, E, Buchanan, T, Cechova, S, Charchar, F, Chu, P, Damman, J, Eales, J, Gharavi, A, Giedraitis, V, Heath, A, Ipp, E, Kiryluk, K, Kramer, H, Kubo, M, Larsson, A, Lindgren, C, Lu, Y, Madden, P, Montgomery, G, Papanicolaou, G, Raffel, L, Sacco, R, Sanchez, E, Stark, H, Sundstrom, J, Taylor, K, Xiang, A, Zivkovic, A, Lind, L, Ingelsson, E, Martin, N, Whitfield, J, Cai, J, Laurie, C, Okada, Y, Matsuda, K, Kooperberg, C, Chen, Y, Rundek, T, Rich, S, Loos, R, Parra, E, Cruz, M, Rotter, J, Snieder, H, Tomaszewski, M, Humphreys, B, Franceschini, N

Association analyses based on false discovery rate implicate new loci for coronary artery disease by Nelson, CP, Goel, A, Butterworth, AS, Kanoni, S, Webb, TR, Marouli, E, Zeng, L, Ntalla, I, Lai, FY, Hopewell, JC, Giannakopoulou, O, Jiang, T, Hamby, SE, Di Angelantonio, E, Assimes, TL, Bottinger, EP, Chambers, JC, Clarke, R, Palmer, CNA, Cubbon, RM, Ellinor, P, Ermel, R, Evangelou, E, Franks, PW, Grace, C, Gu, D, Hingorani, AD, Howson, JMM, Ingelsson, E, Kastrati, A, Kessler, T, Kyriakou, T, Lehtimäki, T, Lu, X, Lu, Y, März, W, McPherson, R, Metspalu, A, Pujades-Rodriguez, M, Ruusalepp, A, Schadt, EE, Schmidt, AF, Sweeting, MJ, Zalloua, PA, AlGhalayini, K, Keavney, BD, Kooner, JS, Loos, RJF, Patel, RS, Rutter, MK, Tomaszewski, M, Tzoulaki, I, Zeggini, E, Erdmann, J, Dedoussis, G, Björkegren, JLM, EPIC-CVD Consortium, CARDIoGRAMplusC4D, UK Biobank CardioMetabolic Consortium CHD working group, Schunkert, H, Farrall, M, Danesh, J, Samani, NJ, Watkins, H, Deloukas, P

An immunodominant NP105–113-B*07:02 cytotoxic T cell response controls viral replication and is associated with less severe COVID-19 disease by Peng, Y, Felce, SL, Dong, D, Penkava, F, Mentzer, AJ, Yao, X, Liu, G, Yin, Z, Chen, J-L, Lu, Y, Wellington, D, Wing, PAC, Dominey-Foy, DCC, Jin, C, Wang, W, Hamid, MA, Fernandes, RA, Wang, B, Fries, A, Zhuang, X, Ashley, N, Rostron, T, Waugh, C, Sopp, P, Hublitz, P, Beveridge, R, Tan, TK, Dold, C, Kwok, AJ, Rich-Griffin, C, Dejnirattisa, W, Liu, C, Kurupati, P, Nassiri, I, Watson, RA, Tong, O, Taylor, CA, Kumar Sharma, P, Sun, B, Curion, F, Revale, S, Garner, LC, Jansen, K, Ferreira, RC, Attar, M, Fry, JW, Russell, RA, Stauss, HJ, James, W, Townsend, A, Ho, L-P, Klenerman , P, Mongkolsapaya , P, Screaton, GR, Dendrou, C, Sansom , SN, Bashford-Rogers, R, Chain , B, Smith , GL, McKeating, JA, Fairfax, BP, Bowness , P, McMichael, AJ, Ogg, G, Knight, JC, Dong, T

No association of coronary artery disease with x-chromosomal variants in comprehensive international meta-analysis by Loley, C, Alver, M, Assimes, T, Bjonnes, A, Goel, A, Gustafsson, S, Hernesniemi, J, Hopewell, J, Kanoni, S, Kleber, M, Lau, K, Lu, Y, Lyytikäinen, L, Nelson, C, Nikpay, M, Qu, L, Salfati, E, Scholz, M, Tukiainen, T, Willenborg, C, Won, H, Zeng, L, Zhang, W, Anand, S, Beutner, F, Bottinger, E, Clarke, R, Dedoussis, G, Do, R, Esko, T, Eskola, M, Farrall, M, Gauguier, D, Giedraitis, V, Granger, C, Hall, A, Hamsten, A, Hazen, S, Huang, J, Kähönen, M, Kyriakou, T, Laaksonen, R, Lind, L, Lindgren, C, Magnusson, P, Marouli, E, Mihailov, E, Morris, A, Nikus, K, Pedersen, N, Rallidis, L, Salomaa, V, Shah, S, Stewart, A, Thompson, J, Zalloua, P, Chambers, J, Collins, R, Ingelsson, E, Iribarren, C, Karhunen, P, Kooner, J, Lehtimäki, T, Loos, R, März, W, McPherson, R, Metspalu, A, Reilly, M, Ripatti, S, Sanghera, D, Thiery, J, Watkins, H, Deloukas, P, Kathiresan, S, Samani, N, Schunkert, H, Erdmann, J, König, I

Germline variation at 8q24 and prostate cancer risk in men of European ancestry by Matejcic, M, Saunders, EJ, Dadaev, T, Brook, MN, Wang, K, Sheng, X, Olama, AAA, Schumacher, FR, Ingles, SA, Govindasami, K, Benlloch, S, Berndt, SI, Albanes, D, Koutros, S, Muir, K, Stevens, VL, Gapstur, SM, Tangen, CM, Batra, J, Clements, J, Gronberg, H, Pashayan, N, Schleutker, J, Wolk, A, West, C, Mucci, L, Kraft, P, Cancel-Tassin, G, Sorensen, KD, Maehle, L, Grindedal, EM, Strom, SS, Neal, DE, Hamdy, FC, Donovan, JL, Travis, RC, Hamilton, RJ, Rosenstein, B, Lu, Y-J, Giles, GG, Kibel, AS, Vega, A, Bensen, JT, Kogevinas, M, Penney, KL, Park, JY, Stanford, JL, Cybulski, C, Nordestgaard, BG, Brenner, H, Maier, C, Kim, J, Teixeira, MR, Neuhausen, SL, De Ruyck, K, Razack, A, Newcomb, LF, Lessel, D, Kaneva, R, Usmani, N, Claessens, F, Townsend, PA, Gago-Dominguez, M, Roobol, MJ, Menegaux, F, Khaw, K-T, Cannon-Albright, LA, Pandha, H, Thibodeau, SN, Schaid, DJ, Wiklund, F, Chanock, SJ, Easton, DF, Eeles, RA, Kote-Jarai, Z, Conti, DV, Haiman, CA

Sequencing of prostate cancers identifies new cancer genes, routes of progression and drug targets by Wedge, D, Gundem, G, Mitchell, T, Woodcock, D, Martincorena, I, Ghori, M, Zamora, J, Butler, A, Whitaker, H, Kote-Jarai, Z, Alexandrov, L, Van Loo, P, Massie, C, Dentro, S, Warren, A, Verrill, C, Berney, D, Dennis, N, Merson, S, Hawkins, S, Howat, W, Lu, Y, Lambert, A, Kay, J, Kremeyer, B, Karaszi, K, Luxton, H, Camacho, N, Marsden, L, Edwards, S, Matthews, L, Bo, V, Leongamornlert, D, McLaren, S, Ng, A, Yu, Y, Zhang, H, Dadaev, T, Thomas, S, Easton, D, Ahmed, M, Bancroft, E, Fisher, C, Livni, N, Nicol, D, Tavaré, S, Gill, P, Greenman, C, Khoo, V, Van As, N, Kumar, P, Ogden, C, Cahill, D, Thompson, A, Mayer, E, Rowe, E, Dudderidge, T, Gnanapragasam, V, Shah, N, Raine, K, Jones, D, Menzies, A, Stebbings, L, Teague, J, Hazell, S, Corbishley, C, de Bono, J, Attard, G, Isaacs, W, Visakorpi, T, Fraser, M, Boutros, P, Bristow, R, Workman, P, Sander, C, Hamdy, F, Futreal, A, McDermott, U, Al-Lazikani, B, Lynch, A, Bova, G, Foster, C, Brewer, D, Neal, D, Cooper, C, Eeles, R

Genomewide meta‐analysis identifies loci associated with IGF‐I and IGFBP‐3 levels with impact on age‐related traits by Teumer, A, Qi, Q, Nethander, M, Aschard, H, Bandinelli, S, Beekman, M, Berndt, SI, Bidlingmaier, M, Broer, L, Charge Longevity Working Group, Cappola, A, Ceda, GP, Chanock, S, Chen, M-H, Chen, TC, Chen, Y-DI, Chung, J, Del Greco Miglianico, F, Eriksson, J, Ferrucci, L, Friedrich, N, Gnewuch, C, Goodarzi, MO, Grarup, N, Guo, T, Hammer, E, Hayes, RB, Hicks, AA, Hofman, A, Houwing-Duistermaat, JJ, Hu, F, Hunter, DJ, Husemoen, LL, Isaacs, A, Jacobs, KB, Janssen, JAMJL, Jansson, J-O, Jehmlich, N, Johnson, S, Juul, A, Karlsson, M, Kilpelainen, TO, Kovacs, P, Kraft, P, Li, C, Linneberg, A, Liu, Y, Loos, RJF, Body Composition Genetics Consortium, Lorentzon, M, Lu, Y, Maggio, M, Magi, R, Meigs, J, Mellström, D, Nauck, M, Newman, AB, Pollak, MN, Pramstaller, PP, Prokopenko, I, Psaty, BM, Reincke, M, Rimm, EB, Rotter, JI, Pierre, A, Schurmann, C, Seshadri, S, Sjögren, K, Slagboom, PE, Strickler, HD, Stumvoll, M, Suh, Y, Sun, Q, Zhang, C, Svensson, J, Tanaka, T, Tare, A, Tönjes, A, Uh, H-W, Van Duijn, CM, Van Heemst, D, Vandenput, L, Vasan, RS, Völker, U, Willems, SM, Ohlsson, C, Wallaschofski, H, Kaplan, RC

Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. by Lange, L, Hu, Y, Zhang, H, Xue, C, Schmidt, E, Tang, Z, Bizon, C, Lange, E, Smith, J, Turner, E, Jun, G, Kang, H, Peloso, G, Auer, P, Li, K, Flannick, J, Zhang, J, Fuchsberger, C, Gaulton, K, Lindgren, C, Locke, A, Manning, A, Sim, X, Rivas, M, Holmen, O, Gottesman, O, Lu, Y, Ruderfer, D, Stahl, E, Duan, Q, Li, Y, Durda, P, Jiao, S, Isaacs, A, Hofman, A, Bis, J, Correa, A, Griswold, M, Jakobsdottir, J, Smith, A, Schreiner, P, Feitosa, M, Zhang, Q, Huffman, J, Crosby, J, Wassel, C, Do, R, Franceschini, N, Martin, L, Robinson, J, Assimes, T, Crosslin, DR, Rosenthal, E, Tsai, M, Rieder, M, Farlow, D, Folsom, A, Lumley, T, Fox, E, Carlson, C, Peters, U, Jackson, R, van Duijn, C, Uitterlinden, A, Levy, D, Rotter, J, Taylor, H, Gudnason, V, Siscovick, D, Fornage, M, Borecki, I, Hayward, C, Rudan, I, Chen, Y, Bottinger, E, Loos, R, Sætrom, P, Hveem, K, Boehnke, M, Groop, L, McCarthy, M, Meitinger, T, Ballantyne, C, Gabriel, S, O'Donnell, C, Post, W, North, K, Reiner, A, Boerwinkle, E, Psaty, B, Altshuler, D, Kathiresan, S, Lin, D, Jarvik, G, Cupples, L, Kooperberg, C, Wilson, J, Nickerson, D, Abecasis, G, Rich, S, Tracy, R, Willer, C

Exome-derived adiponectin-associated variants implicate obesity and lipid biology by Spracklen, CN, Karaderi, T, Yaghootkar, H, Schurmann, C, Fine, RS, Kutalik, Z, Preuss, MH, Lu, Y, Wittemans, LBL, Adair, LS, Allison, M, Amin, N, Auer, PL, Bartz, TM, Blüher, M, Boehnke, M, Borja, JB, Bork-Jensen, J, Broer, L, Chasman, DI, Chen, Y-DI, Chirstofidou, P, Demirkan, A, Van Duijn, CM, Feitosa, MF, Garcia, ME, Graff, M, Grallert, H, Grarup, N, Guo, X, Haesser, J, Hansen, T, Harris, TB, Highland, HM, Hong, J, Ikram, MA, Ingelsson, E, Jackson, R, Jousilahti, P, Kähönen, M, Kizer, JR, Kovacs, P, Kriebel, J, Laakso, M, Lange, LA, Lehtimäki, T, Li, J, Li-Gao, R, Lind, L, Luan, J, Lyytikäinen, L-P, Macgregor, S, Mackey, DA, Mahajan, A, Mangino, M, Männistö, S, McCarthy, MI, McKnight, B, Medina-Gomez, C, Meigs, JB, Molnos, S, Mook-Kanamori, D, Morris, AP, De Mutsert, R, Nalls, MA, Nedeljkovic, I, North, KE, Pennell, CE, Pradhan, AD, Province, MA, Raitakari, OT, Raulerson, CK, Reiner, AP, Ridker, PM, Ripatti, S, Roberston, N, Rotter, JI, Salomaa, V, Sandoval-Zárate, AA, Sitlani, CM, Spector, TD, Strauch, K, Stumvoll, M, Taylor, KD, Thuesen, B, Tönjes, A, Uitterlinden, AG, Venturini, C, Walker, M, Wang, CA, Wang, S, Wareham, NJ, Willems, SM, Van Dijk, K, Wilson, JG, Wu, Y, Yao, J, Young, KL, Langenberg, C, Frayling, TM, Kilpeläinen, TO, Lindgren, CM, Loos, RJF, Mohlke, KL

Trans-ethnic meta-analysis and functional annotation illuminates the genetic architecture of fasting glucose and insulin by Liu, C, Raghavan, S, Maruthur, N, Kabagambe, E, Hong, J, Ng, M, Hivert, M, Lu, Y, An, P, Bentley, A, Drolet, A, Gaulton, K, Guo, X, Armstrong, L, Irvin, M, Li, M, Lipovich, L, Rybin, D, Taylor, K, Agyemang, C, Palmer, N, Cade, B, Chen, W, Dauriz, M, Delaney, J, Edwards, T, Evans, D, Evans, M, Lange, L, Leong, A, Liu, J, Liu, Y, Nayak, U, Patel, S, Porneala, B, Rasmussen-Torvik, L, Snijder, M, Stallings, S, Tanaka, T, Yanek, L, Zhao, W, Becker, D, Bielak, L, Biggs, M, Bottinger, E, Bowden, D, Chen, G, Correa, A, Couper, D, Crawford, D, Cushman, M, Eicher, J, Fornage, M, Franceschini, N, Fu, Y, Goodarzi, M, Gottesman, O, Hara, K, Harris, T, Jensen, R, Johnson, A, Jhun, M, Karter, A, Keller, M, Kho, A, Kizer, J, Krauss, R, Langefeld, C, Li, X, Liang, J, Liu, S, Lowe, W, Mosley, T, North, K, Pacheco, J, Peyser, P, Patrick, A, Rice, K, Selvin, E, Sims, M, Smith, J, Tajuddin, S, Vaidya, D, Wren, M, Yao, J, Zhu, X, Ziegler, J, Zmuda, J, Zonderman, A, Zwinderman, A, Adeyemo, A, Boerwinkle, E, Ferrucci, L, Hayes, M, Kardia, S, Miljkovic, I, Pankow, J, Rotimi, C, Sale, M, Wagenknecht, L, Arnett, D, Chen, Y, Nalls, M, Province, M, Kao, W, Siscovick, D, Psaty, B, Wilson, J, Loos, R, Dupuis, J, Rich, S, Florez, J, Rotter, J, Morris, A, Meigs, J

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer by Bojesen, S.E., Pooley, K.A., Johnatty, S.E., Beesley, J., Michailidou, K., Tyrer, J.P., Edwards, S.L., Pickett, H.A., Shen, H.C., Smart, C.E., Hillman, K.M., Mai, P.L., Lawrenson, K., Stutz, M.D., Lu, Y., Karevan, R., Woods, N., Johnstonw, R.L., French, J.D., Chen, X.Q., Weischer, M., Nielsen, S.F., Maranian, M.J., Ghoussaini, M., Ahmed, S., Baynes, C., Bolla, M.K., Wang, Q., Dennis, J., McGuffog, L., Barrowdale, D., Lee, A., Healey, S., Lush, M., Tessier, D.C., Vincent, D., Bacot, F., Vergote, I., Lambrechts, S., Despierre, E., Risch, H.A., Gonzaalez-Neira, A., Rossing, M.A., Pita, G., Doherty, J.A., Alvarez, N., Larson, M.C., Fridley, B.L., Schoof, N., Chang-Claude, J., Cicek, M.S., Peto, J., Kalli, K.R., Broeks, A., Armasu, S.M., Schmidt, M.K., Braaf, L.M., Winterhoff, B., Nevanlinna, H., Konecny, G.E., Lambrechts, D., Rogmann, L., Guenel, P., Teoman, A., Milne, R.L., Garcia, J.J., Cox, A., Shridhar, V., Burwinkel, B., Marme, F., Hein, R., Sawyer, E.J., Haiman, C.A., Wang-Gohrke, S., Andrulis, I.L., Moysich, K.B., Hopper, J.L., Odunsi, K., Lindblom, A., Giles, G.G., Brenner, H., Simard, J., Lurie, G., Fasching, P.A., Carney, M.E., Radice, P., Wilkens, L.R., Swerdlow, A., Goodman, M.T., Brauch, H., Garcia-Closas, M., Hillemanns, P., Winqvist, R., Durst, M., Devilee, P., Runnebaum, I., Jakubowska, A., Lubinski, J., Mannermaa, A., Butzow, R., Omar, S.Z.

Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease by Stitziel, N, Stirrups, K, Masca, N, Erdmann, J, Ferrario, P, Koenig, I, Weeke, P, Webb, T, Auer, P, Schick, U, Lu, Y, Zhang, H, Dube, M, Goel, A, Farrall, M, Peloso, G, Won, H, Do, R, van Iperen, E, Kanoni, S, Kruppa, J, Mahajan, A, Scott, R, Willenborg, C, Braund, P, van Capelleveen, J, Doney, A, Donnelly, L, Asselta, R, Merlini, P, Duga, S, Marziliano, N, Denny, J, Shaffer, C, El-Mokhtari, N, Franke, A, Gottesman, O, Heilmann, S, Hengstenberg, C, Hoffmann, P, Holmen, O, Hveem, K, Jansson, J, Joeckel, K, Kessler, T, Kriebel, J, Laugwitz, K, Marouli, E, Martinelli, N, McCarthy, M, Van Zuydam, N, Meisinger, C, Esko, T, Mihailov, E, Escher, SA, Alver, M, Moebus, S, Morris, A, Mueller-Nurasyid, M, Nikpay, M, Olivieri, O, Perreault, L, AlQarawi, A, Robertson, N, Akinsanya, K, Reilly, D, Vogt, T, Yin, W, Asselbergs, F, Kooperberg, C, Jackson, R, Stahl, E, Strauch, K, Varga, T, Waldenberger, M, Zeng, L, Kraja, A, Liu, C, Ehret, G, Newton-Cheh, C, Chasman, D, Chowdhury, R, Ferrario, M, Ford, I, Jukema, J, Kee, F, Kuulasmaa, K, Nordestgaard, BG, Perola, M, Saleheen, D, Sattar, N, Surendran, P, Tregouet, D, Young, R, Howson, J, Butterworth, A, Danesh, J, Ardissino, D, Bottinger, E, Erbel, R, Franks, P, Girelli, D, Hall, A, Hovingh, G, Kastrati, A, Lieb, W, Meitinger, T, Kraus, W, Shah, S, McPherson, R, Orho-Melander, M, Melander, O, Metspalu, A, Palmer, C, Peters, A, Rader, D, Reilly, M, Loos, R, Reiner, A, Roden, D, Tardif, J, Thompson, JR, Wareham, N, Watkins, H, Willer, C, Kathiresan, S, Deloukas, P, Samani, N, Schunkert, H

Systematic evaluation of pleiotropy identifies 6 further loci associated with coronary artery disease by Webb, T, Erdmann, J, Stirrups, K, Stitziel, N, Masca, N, Jansen, H, Kanoni, S, Nelson, C, Ferrario, P, König, I, Eicher, J, Johnson, A, Hamby, S, Betsholtz, C, Ruusalepp, A, Franzén, O, Schadt, E, Björkegren, J, Weeke, P, Auer, P, Schick, U, Lu, Y, Zhang, H, Dube, M, Goel, A, Farrall, M, Peloso, G, Won, H, Do, R, van Iperen, E, Kruppa, J, Mahajan, A, Scott, R, Willenborg, C, Braund, P, van Capelleveen, J, Doney, A, Donnelly, L, Asselta, R, Merlini, P, Duga, S, Marziliano, N, Denny, J, Shaffer, C, El-Mokhtari, N, Franke, A, Heilmann, S, Hengstenberg, C, Hoffmann, P, Holmen, O, Hveem, K, Jansson, J, Jöckel, K, Kessler, T, Kriebel, J, Laugwitz, K, Marouli, E, Martinelli, N, McCarthy, M, Van Zuydam, N, Meisinger, C, Esko, T, Mihailov, E, Escher, S, Alver, M, Moebus, S, Morris, A, Virtamo, J, Nikpay, M, Olivieri, O, Provost, S, AlQarawi, A, Robertson, N, Akinsansya, K, Reilly, D, Vogt, T, Yin, W, Asselbergs, F, Kooperberg, C, Jackson, R, Stahl, E, Müller-Nurasyid, M, Strauch, K, Varga, T, Waldenberger, M, Wellcome Trust Case Control Consortium, Zeng, L, Chowdhury, R, Salomaa, V, Ford, I, Jukema, J, Amouyel, P, Kontto, J, MORGAM Investigators, Nordestgaard, B, Ferrières, J, Saleheen, D, Sattar, N, Surendran, P, Wagner, A, Young, R, Howson, J, Butterworth, A, Danesh, J, Ardissino, D, Bottinger, E, Erbel, R, Franks, P, Girelli, D, Hall, A, Hovingh, G, Kastrati, A, Lieb, W, Meitinger, T, Kraus, W, Shah, S, McPherson, R, Orho-Melander, M, Melander, O, Metspalu, A, Palmer, C, Peters, A, Rader, D, Reilly, M, Loos, R, Reiner, A, Roden, D, Tardif, J, Thompson, J, Wareham, N, Watkins, H, Willer, C, Samani, N, Schunkert, H, Deloukas, P, Kathiresan, S, Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation by 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