No association between polymorphisms in the INSIG1 gene and the risk of type 2 diabetes and related traits. by Szopa, M, Meirhaeghe, A, Luan, J, Moreno, L, Gonzalez-Gross, M, Vidal-Puig, A, Cooper, C, Hagen, R, Amouyel, P, Wareham, N, Loos, R

Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus. by Hamilton, G, Killick, R, Lambert, J, Amouyel, P, Carrasquillo, M, Pankratz, V, Graff-Radford, N, Dickson, D, Petersen, R, Younkin, S, Powell, J, Wade-Martins, R

Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus by Hamilton, G, Killick, R, Lambert, J, Amouyel, P, Carrasquillo, M, Pankratz, V, Graff-Radford, N, Dickson, D, Petersen, R, Younkin, S, Powell, J, Wade-Martins, R

Association between the T-381C polymorphism of the brain natriuretic peptide gene and risk of type 2 diabetes in human populations. by Meirhaeghe, A, Sandhu, MS, McCarthy, M, de Groote, P, Cottel, D, Arveiler, D, Ferrières, J, Groves, C, Hattersley, A, Hitman, G, Walker, M, Wareham, N, Amouyel, P

Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus. by Hamilton, G, Killick, R, Genetic, A, Translational, G, Lambert, J, Amouyel, P, European, A, Carrasquillo, M, Pankratz, V, Graff-Radford, N, Dickson, D, Petersen, R, Younkin, S, Powell, J, Wade-Martins, R

Mosaic loss of chromosome Y in blood is associated with Alzheimer disease by Dumanski, J, Lambert, J, Rasi, C, Giedraitis, V, Davies, H, Grenier-Boley, B, Lindgren, C, Campion, D, Dufouil, C, Pasquier, F, Amouyel, P, Lannfelt, L, Ingelsson, M, Kilander, L, Lind, L, Forsberg, L

The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism. by Klebe, S, Golmard, J, Nalls, M, Saad, M, Singleton, AB, Bras, J, Hardy, J, Simon-Sanchez, J, Heutink, P, Kuhlenbäumer, G, Charfi, R, Klein, C, Hagenah, J, Gasser, T, Wurster, I, Lesage, S, Lorenz, D, Deuschl, G, Durif, F, Pollak, P, Damier, P, Tison, F, Durr, A, Amouyel, P, Lambert, J

Ischemic stroke is associated with the ABO locus: the EuroCLOT study. by Williams, F, Carter, A, Hysi, P, Surdulescu, G, Hodgkiss, D, Soranzo, N, Traylor, M, Bevan, S, Dichgans, M, Rothwell, P, Sudlow, C, Farrall, M, Silander, K, Kaunisto, M, Wagner, P, Saarela, O, Kuulasmaa, K, Virtamo, J, Salomaa, V, Amouyel, P, Arveiler, D, Ferrieres, J, Wiklund, P, Ikram, M, Hofman, A

Ischemic stroke is associated with the ABO locus: The EuroCLOT study (vol 73, pg 16, 2013) by Williams, F, Carter, A, Hysi, P, Surdulescu, G, Hodgkiss, D, Soranzo, N, Traylor, M, Bevan, S, Dichgans, M, Rothwell, P, Sudlow, C, Farrall, M, Silander, K, Kaunisto, M, Wagner, P, Saarela, O, Kuulasmaa, K, Virtamo, J, Salomaa, V, Amouyel, P, Arveiler, D, Ferrieres, J, Wiklund, P, Ikram, M, Hofman, A

C-reactive protein, fibrinogen, and cardiovascular disease prediction. by Kaptoge, S, Di Angelantonio, E, Pennells, L, Wood, A, White, I, Gao, P, Walker, M, Thompson, A, Sarwar, N, Caslake, M, Butterworth, A, Amouyel, P, Assmann, G, Bakker, S, Barr, E, Barrett-Connor, E, Benjamin, E, Björkelund, C, Brenner, H, Brunner, E, Clarke, R, Cooper, J, Cremer, P, Cushman, M, Dagenais, G

Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer's disease by Gusareva, E, Twizere, J, Sleegers, K, Dourlen, P, Abisambra, J, Meier, S, Cloyd, R, Weiss, B, Dermaut, B, Bessonov, K, Van Der Lee, S, Carrasquillo, M, Katsumata, Y, Cherkaoui, M, Asselbergh, B, Ikram, M, Mayeux, R, Farrer, L, Haines, J, Pericak-Vance, M, Schellenberg, G, Genetic And Environmental Risk In Alzheimer'S Disease 1 Consortium (GERAD1), Alzheimer'S Disease Genetics Consortium (ADGC), European Alzheimer Disease Initiative Investigators (EADI1 Consortium), Sims, R, Williams, J, Amouyel, P, Van Duijn, C, Ertekin-Taner, N, Van Broeckhoven, C, Dequiedt, F, Fardo, D, Lambert, J, Van Steen, K

A genome-wide association study identifies genetic loci associated with specific lobar brain volumes by van der Lee, SJ, Knol, MJ, Chauhan, G, Satizabal, CL, Smith, AV, Hofer, E, Bis, JC, Hibar, DP, Hilal, S, van den Akker, EB, Arfanakis, K, Bernard, M, Yanek, LR, Amin, N, Crivello, F, Cheung, JW, Harris, TB, Saba, Y, Lopez, OL, Li, S, van der Grond, J, Yu, L, Paus, T, Roshchupkin, GV, Amouyel, P, Jahanshad, N, Taylor, KD, Yang, Q, Mathias, RA, Boehringer, S, Mazoyer, B, Rice, K, Cheng, CY, Maillard, P, van Heemst, D, Wong, TY, Niessen, WJ, Beiser, AS, Beekman, M, Zhao, W, Nyquist, PA, Chen, C, Launer, LJ, Psaty, BM, Ikram, MK, Vernooij, MW, Schmidt, H, Pausova, Z, Becker, DM, De Jager, PL

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease by Huang, K, Marcora, E, Pimenova, A, Di Narzo, A, Kapoor, M, Jin, S, Harari, O, Bertelsen, S, Fairfax, B, Czajkowski, J, Chouraki, V, Grenier-Boley, B, Bellenguez, C, Deming, Y, McKenzie, A, Raj, T, Renton, A, Budde, J, Smith, A, Fitzpatrick, A, Bis, J, Destefano, A, Adams, H, Ikram, M, Van Der Lee, S, Del-Aguila, J, Fernandez, M, Ibañez, L, Project, I, Alzheimer'S Disease Neuroimaging Initiative, Sims, R, Escott-Price, V, Mayeux, R, Haines, J, Farrer, L, Pericak-Vance, M, Lambert, J, Van Duijn, C, Launer, L, Seshadri, S, Williams, J, Amouyel, P, Schellenberg, G, Zhang, B, Borecki, I, Kauwe, J, Cruchaga, C, Hao, K, Goate, A

Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study by Jones, E, Hummerich, H, Viré, E, Uphill, J, Dimitriadis, A, Speedy, H, Campbell, T, Norsworthy, P, Quinn, L, Whitfield, J, Linehan, J, Jaunmuktane, Z, Brandner, S, Jat, P, Nihat, A, How Mok, T, Ahmed, P, Collins, S, Stehmann, C, Sarros, S, Kovacs, GG, Geschwind, MD, Golubjatnikov, A, Frontzek, K, Budka, H, Aguzzi, A, Karamujić-Čomić, H, van der Lee, SJ, Ibrahim-Verbaas, CA, van Duijn, CM, Sikorska, B, Golanska, E, Liberski, PP, Calero, M, Calero, O, Sanchez-Juan, P, Salas, A, Martinón-Torres, F, Bouaziz-Amar, E, Haïk, S, Laplanche, J-L, Brandel, J-P, Amouyel, P, Lambert, J-C, Parchi, P, Bartoletti-Stella, A, Capellari, S, Poleggi, A, Ladogana, A, Pocchiari, M

Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke by Cole, J, Xu, H, Ryan, K, Jaworek, T, Dueker, N, McArdle, P, Gaynor, B, Cheng, Y, O'Connell, J, Bevan, S, Malik, R, Ahmed, N, Amouyel, P, Anjum, S, Bis, J, Crosslin, D, Danesh, J, Engelter, S, Fornage, M, Frossard, P, Gieger, C, Giese, A, Grond-Ginsbach, C, Ho, W, Holliday, E, Hopewell, J, Hussain, M, Iqbal, W, Jabeen, S, Jannes, J, Kamal, A, Kamatani, Y, Kanse, S, Kloss, M, Lathrop, M, Leys, D, Lindgren, A, Longstreth, W, Mahmood, K, Meisinger, C, Metso, T, Mosley, T, Müller-Nurasyid, M, Norrving, B, Parati, E, Peters, A, Pezzini, A, Quereshi, I, Rasheed, A, Rauf, A, Salam, T, Shen, J, Słowik, A, Stanne, T, Strauch, K, Tatlisumak, T, Thijs, V, Tiedt, S, Traylor, M, Waldenberger, M, Walters, M, Zhao, W, Boncoraglio, G, Debette, S, Jern, C, Levi, C, Markus, H, Meschia, J, Rolfs, A, Rothwell, P, Saleheen, D, Seshadri, S, Sharma, P, Sudlow, C, Worrall, B, Metastroke Consortium Of The Isgc, Wtccc-2 Consortium, Stine, O, Kittner, S, Mitchell, B

Trans-ethnic association study of blood pressure determinants in over 750,000 individuals by Giri, A, Hellwege, JN, Keaton, JM, Park, J, Qiu, C, Warren, HR, Torstenson, ES, Kovesdy, CP, Sun, YV, Wilson, OD, Robinson-Cohen, C, Roumie, CL, Chung, CP, Birdwell, KA, Damrauer, SM, Duvall, SL, Klarin, D, Cho, K, Wang, Y, Evangelou, E, Cabrera, CP, Wain, LV, Shrestha, R, Mautz, BS, Akwo, EA, Sargurupremraj, M, Debette, S, Boehnke, M, Scott, LJ, Luan, J, Zhao, J-H, Willems, SM, Thériault, S, Shah, N, Oldmeadow, C, Almgren, P, Li-Gao, R, Verweij, N, Boutin, TS, Mangino, M, Ntalla, I, Feofanova, E, Surendran, P, Cook, JP, Karthikeyan, S, Lahrouchi, N, Liu, C, Sepúlveda, N, Richardson, TG, Kraja, A, Amouyel, P, Farrall, M, Poulter, NR, Understanding Society Scientific Group, International Consortium For Blood Pressure, Blood Pressure-International Consortium Of Exome Chip Studies, Laakso, M, Zeggini, E, Sever, P, Scott, RA, Langenberg, C, Wareham, NJ, Conen, D, Palmer, CNA, Attia, J, Chasman, DI, Ridker, PM, Melander, O, Mook-Kanamori, DO, Harst, PVD, Cucca, F, Schlessinger, D, Hayward, C, Spector, TD, Jarvelin, M-R, Hennig, BJ, Timpson, NJ, Wei, W-Q, Smith, JC, Xu, Y, Matheny, ME, Siew, EE, Lindgren, C, Herzig, K-H, Dedoussis, G, Denny, JC, Psaty, BM, Howson, JMM, Munroe, PB, Newton-Cheh, C, Caulfield, MJ, Elliott, P, Gaziano, JM, Concato, J, Wilson, PWF, Tsao, PS, Edwards, DR, Susztak, K, Million Veteran Program, O'Donnell, CJ, Hung, AM, Edwards, TL

The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis. by Fall, T, Hägg, S, Mägi, R, Ploner, A, Fischer, K, Horikoshi, M, Sarin, A, Thorleifsson, G, Ladenvall, C, Kals, M, Kuningas, M, Draisma, H, Ried, J, van Zuydam, N, Huikari, V, Mangino, M, Sonestedt, E, Benyamin, B, Nelson, C, Rivera, N, Kristiansson, K, Shen, H, Havulinna, A, Dehghan, A, Donnelly, L, Kaakinen, M, Nuotio, M, Robertson, N, de Bruijn, R, Ikram, M, Amin, N, Balmforth, A, Braund, P, Doney, A, Döring, A, Elliott, P, Esko, T, Franco, O, Gretarsdottir, S, Hartikainen, A, Heikkilä, K, Herzig, K, Holm, H, Hottenga, J, Hyppönen, E, Illig, T, Isaacs, A, Isomaa, B, Karssen, L, Kettunen, J, Koenig, W, Kuulasmaa, K, Laatikainen, T, Laitinen, J, Lindgren, C, Lyssenko, V, Läärä, E, Rayner, N, Männistö, S, Pouta, A, Rathmann, W, Rivadeneira, F, Ruokonen, A, Savolainen, M, Sijbrands, E, Small, K, Smit, J, Steinthorsdottir, V, Syvänen, A, Taanila, A, Tobin, MD, Uitterlinden, A, Willems, S, Willemsen, G, Witteman, J, Perola, M, Evans, A, Ferrières, J, Virtamo, J, Kee, F, Tregouet, D, Arveiler, D, Amouyel, P, Ferrario, M, Brambilla, P, Hall, A, Heath, A, Madden, P, Martin, N, Montgomery, G, Whitfield, J, Jula, A, Knekt, P, Oostra, B, van Duijn, C, Penninx, B, Davey Smith, G, Kaprio, J, Samani, N, Gieger, C, Peters, A, Wichmann, H, Boomsma, D, de Geus, E, Tuomi, T, Power, C, Hammond, C, Spector, T, Lind, L, Orho-Melander, M, Palmer, C, Morris, A, Groop, L, Järvelin, MR, Salomaa, V, Vartiainen, E, Hofman, A, Ripatti, S, Metspalu, A, Thorsteinsdottir, U, Stefansson, K, Pedersen, N, McCarthy, M, Ingelsson, E, Prokopenko, I

Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis by Rhodes, CJ, Batai, K, Bleda, M, Haimel, M, Southgate, L, Germain, M, Pauciulo, MW, Hadinnapola, C, Aman, J, Girerd, B, Arora, A, Knight, J, Hanscombe, KB, Karnes, JH, Kaakinen, M, Gall, H, Ulrich, A, Harbaum, L, Cebola, I, Ferrer, J, Lutz, K, Swietlik, EM, Ahmad, F, Amouyel, P, Archer, SL, Argula, R, Austin, ED, Badesch, D, Bakshi, S, Barnett, C, Benza, R, Bhatt, N, Bogaard, HJ, Burger, CD, Chakinala, M, Church, C, Coghlan, JG, Condliffe, R, Corris, PA, Danesino, C, Debette, S, Elliott, CG, Elwing, J, Eyries, M, Fortin, T, Franke, A, Frantz, RP, Frost, A, Garcia, JGN, Ghio, S, Ghofrani, H-A, Gibbs, JSR, Harley, J, He, H, Hill, NS, Hirsch, R, Houweling, AC, Howard, LS, Ivy, D, Kiely, DG, Klinger, J, Kovacs, G, Lahm, T, Laudes, M, Machado, RD, Ross, RV, Marsolo, K, Martin, LJ, Moledina, S, Montani, D, Nathan, SD, Newnham, M, Olschewski, A, Olschewski, H, Oudiz, RJ, Ouwehand, WH, Peacock, AJ, Pepke-Zaba, J, Rehman, Z, Robbins, I, Roden, DM, Rosenzweig, EB, Saydain, G, Scelsi, L, Schilz, R, Seeger, W, Shaffer, CM, Simms, RW, Simon, M, Sitbon, O, Suntharalingam, J, Tang, H, Tchourbanov, AY, Thenappan, T, Torres, F, Toshner, MR, Treacy, CM, Noordegraaf, A, Waisfisz, Q, Walsworth, AK, Walter, RE, Wharton, J, White, RJ, Wilt, J, Wort, SJ, Yung, D, Lawrie, A, Humbert, M, Soubrier, F, Trégouët, D-A, Prokopenko, I, Kittles, R, Gräf, S, Nichols, WC, Trembath, RC, Desai, AA, Morrell, NW, Wilkins, MR, UK NIHR Bioresource Rare Diseases Consortium, UK PAH Cohort Study Consortium, US PAH Biobank Consortium, McCarthy, M

A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease by Plagnol, V, Nalls, M, Bras, J, Hernandez, D, Sharma, M, Sheerin, U, Saad, M, Simon-Sanchez, J, Schulte, C, Lesage, S, Sveinbjornsdottir, S, Amouyel, P, Arepalli, S, Band, G, Barker, R, Bellinguez, C, Ben-Shlomo, Y, Berendse, H, Berg, D, Bhatia, K, de Bie, R, Biffi, A, Bloem, B, Bochdanovits, Z, Bonin, M, Brockmann, K, Brooks, J, Burn, D, Charlesworth, G, Chen, H, Chinnery, P, Chong, S, Clarke, C, Cookson, MR, Cooper, J, Corvol, J, Counsell, C, Damier, P, Dartigues, J, Deloukas, P, Deuschl, G, Dexter, D, van Dijk, K, Dillman, A, Durif, F, Duerr, A, Edkins, S, Evans, JR, Foltynie, T, Freeman, C, Gao, J, Gardner, M, Gibbs, JR, Goate, A, Gray, E, Guerreiro, R, Gustafsson, O, Harris, C, Hellenthal, G, van Hilten, J, Hofman, A, Hollenbeck, A, Holton, J, Hu, M, Huang, X, Huber, H, Hudson, G, Hunt, SE, Huttenlocher, J, Illig, T, Jonsson, P, Langford, C, Lees, A, Lichtner, P, Limousin, P, Lopez, G, Lorenz, D, McNeill, A, Moorby, C, Moore, M, Morris, H, Morrison, K, Mudanohwo, E, O'Sullivan, S, Pearson, J, Pearson, R, Perlmutter, J, Petursson, H, Pirinen, M, Pollak, P, Post, B, Potter, S, Ravina, B, Revesz, T, Riess, O, Rivadeneira, F, Rizzu, P, Ryten, M, Sawcer, S, Schapira, A, Scheffer, H, Shaw, K, Shoulson, I, Sidransky, E, de Silva, R, Smith, C, Spencer, C, Stefansson, H, Steinberg, S, Stockton, J, Strange, A, Su, Z, Talbot, K, Tanner, C, Tashakkori-Ghanbaria, A, Tison, F, Trabzuni, D, Traynor, B, Uitterlinden, A, Vandrovcova, J, Velseboer, D, Vidailhet, M, Vukcevic, D, Walker, R, van de Warrenburg, B, Weale, M, Wickremaratchi, M, Williams, N, Williams-Gray, C, Winder-Rhodes, S, Stefansson, K, Martinez, M, Donnelly, P, Singleton, AB, Hardy, J, Heutink, P, Brice, A, Gasser, T, Wood, N, WTCCC2

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