Rare loss of function variants in candidate genes and risk of colorectal cancer
EA Rosenthal, BH Shirts, LM Amendola, M Horike-Pyne, PD Robertson, FM Hisama, RL Bennett, MO Dorschner, DA Nickerson, IB Stanaway, R Nassir, KT Vickers, C Li, WM Grady, U Peters, GP Jarvik, SB Gabriel, DM Altshuler, GR Abecasis, H Allayee, S Cresci, MJ Daly, PIW de Bakker, MA DePristo, R Do, P Donnelly, DN Farlow, T Fennell, K Garimella, SL Hazen, Y Hu, DM Jordan, G Jun, S Kathiresan, HM Kang, A Kiezun, G Lettre, B Li, M Li, CH Newton-Cheh, S Padmanabhan, G Peloso, S Pulit, DJ Rader, D Reich, MP Reilly, MA Rivas, S Schwartz, L Scott, DS Siscovick, JA Spertus, NO Stitziel, N Stoletzki, SR Sunyaev, BF Voight, CJ Willer, SS Rich, E Akylbekova, LD Atwood, CM Ballantyne, M Barbalic, RG Barr, EJ Benjamin, J Bis, E Boerwinkle, DW Bowden, J Brody, M Budoff, G Burke, S Buxbaum, J Carr, DT Chen, IY Chen, WM Chen, P Concannon, J Crosby, LA Cupples, R D’Agostino, AL DeStefano, A Dreisbach, J Dupuis, JP Durda, J Ellis, AR Folsom, M Fornage, CS Fox, E Fox, V Funari, SK Ganesh, J Gardin, D Goff, O Gordon, W Grody
A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework
M LeBlanc, V Zuber, WK Thompson, OA Andreassen, A Frigessi, BK Andreassen, S Ripke, BM Neale, A Corvin, JTR Walters, KH Farh, P Lee, B Bulik-Sullivan, DA Collier, H Huang, TH Pers, I Agartz, E Agerbo, M Albus, M Alexander, F Amin, SA Bacanu, M Begemann, RA Belliveau, J Bene, E Bevilacqua, TB Bigdeli, DW Black, R Bruggeman, NG Buccola, RL Buckner, W Cahn, G Cai, MJ Cairns, D Campion, RM Cantor, VJ Carr, N Carrera, SV Catts, KD Chambert, RCK Chan, RYL Chen, EYH Chen, W Cheng, EFC Cheung, SA Chong, CR Cloninger, D Cohen, N Cohen, P Cormican, N Craddock, B Crespo-Facorro, JJ Crowley, D Curtis, M Davidson, KL Davis, F Degenhardt, JD Favero, LE DeLisi, D Demontis, D Dikeos, T Dinan, G Donohoe, E Drapeau, J Duan, F Dudbridge, N Durmishi, P Eichhammer, J Eriksson, V Escott-Price, L Essioux, AH Fanous, MS Farrell, J Frank, L Franke, R Freedman, NB Freimer, M Friedl, JI Friedman, M Fromer, G Genovese, L Georgieva, ES Gershon, I Giegling, P Giusti-Rodriguez, S Godard, JI Goldstein, V Golimbet, S Gopal, J Gratten, L de Haan, C Hammer, ML Hamshere, M Hansen, T Hansen, V Haroutunian, AM Hartmann, FA Henskens, S Herms
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes
DM Ruderfer, S Ripke, A McQuillin, J Boocock, EA Stahl, JMW Pavlides, N Mullins, AW Charney, APS Ori, LMO Loohuis, E Domenici, A Di Florio, S Papiol, JL Kalman, V Trubetskoy, R Adolfsson, I Agartz, E Agerbo, H Akil, D Albani, M Albus, M Alda, M Alexander, N Alliey-Rodriguez, TD Als, F Amin, A Anjorin, MJ Arranz, S Awasthi, SA Bacanu, JA Badner, M Baekvad-Hansen, S Bakker, G Band, JD Barchas, I Barroso, N Bass, M Bauer, BT Baune, M Begemann, C Bellenguez, RA Belliveau, F Bellivier, S Bender, J Bene, SE Bergen, WH Berrettini, E Bevilacqua, JM Biernacka, TB Bigdeli, DW Black, H Blackburn, JM Blackwell, DHR Blackwood, CB Pedersen, M Boehnke, M Boks, AD Borglum, E Bramon, G Breen, MA Brown, R Bruggeman, NG Buccola, RL Buckner, M Budde, B Bulik-Sullivan, SJ Bumpstead, W Bunney, M Burmeister, JD Buxbaum, J Bybjerg-Grauholm, W Byerley, W Cahn, G Cai, MJ Cairns, D Campion, RM Cantor, VJ Carr, N Carrera, JP Casas, M Casas, SV Catts, P Cervantes, KD Chambert, RCK Chan, EYH Chen, RYL Chen, W Cheng, EFC Cheung, SA Chong, TK Clarke, CR Cloninger, D Cohen, N Cohen, JRI Coleman, DA Collier, P Cormican, W Coryell, N Craddock, DW Craig
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
J Flannick, C Fuchsberger, A Mahajan, TM Teslovich, V Agarwala, KJ Gaulton, L Caulkins, R Koesterer, C Ma, L Moutsianas, DJ McCarthy, MA Rivas, JRB Perry, X Sim, TW Blackwell, NR Robertson, NW Rayner, P Cingolani, AE Locke, JF Tajes, HM Highland, J Dupuis, PS Chines, CM Lindgren, C Hartl, AU Jackson, H Chen, JR Huyghe, M van de Bunt, RD Pearson, A Kumar, M Müller-Nurasyid, N Grarup, HM Stringham, ER Gamazon, J Lee, Y Chen, RA Scott, JE Below, P Chen, J Huang, MJ Go, ML Stitzel, D Pasko, SCJ Parker, TV Varga, T Green, NL Beer, AG Day-Williams, T Ferreira, T Fingerlin, M Horikoshi, C Hu, I Huh, MK Ikram, BJ Kim, Y Kim, YJ Kim, MS Kwon, J Lee, S Lee, KH Lin, TJ Maxwell, Y Nagai, X Wang, RP Welch, J Yoon, W Zhang, N Barzilai, BF Voight, BG Han, CP Jenkinson, T Kuulasmaa, J Kuusisto, A Manning, MCY Ng, ND Palmer, B Balkau, A Stančáková, HE Abboud, H Boeing, V Giedraitis, D Prabhakaran, O Gottesman, J Scott, J Carey, P Kwan, G Grant, JD Smith, BM Neale, S Purcell, AS Butterworth, JMM Howson, HM Lee, Y Lu, SH Kwak, W Zhao, J Danesh, VKL Lam, KS Park
Data Descriptor: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
J Flannick, C Fuchsberger, A Mahajan, TM Teslovich, V Agarwala, KJ Gaulton, L Caulkins, R Koesterer, C Ma, L Moutsianas, DJ McCarthy, MA Rivas, JRB Perry, X Sim, TW Blackwell, NR Robertson, NW Rayner, P Cingolani, AE Locke, JF Tajes, HM Highland, J Dupuis, PS Chines, CM Lindgren, C Hartl, AU Jackson, H Chen, JR Huyghe, M Van De Bunt, RD Pearson, A Kumar, M Müller-Nurasyid, N Grarup, HM Stringham, ER Gamazon, J Lee, Y Chen, RA Scott, JE Below, P Chen, J Huang, MJ Go, ML Stitzel, D Pasko, SCJ Parker, TV Varga, T Green, NL Beer, AG Day-Williams, T Ferreira, T Fingerlin, M Horikoshi, C Hu, I Huh, MK Ikram, BJ Kim, Y Kim, YJ Kim, MS Kwon, J Lee, S Lee, KH Lin, TJ Maxwell, Y Nagai, X Wang, RP Welch, J Yoon, W Zhang, N Barzilai, BF Voight, BG Han, CP Jenkinson, T Kuulasmaa, J Kuusisto
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass
MC Zillikens, S Demissie, YH Hsu, LM Yerges-Armstrong, WC Chou, L Stolk, G Livshits, L Broer, T Johnson, DL Koller, Z Kutalik, J Luan, I Malkin, JS Ried, AV Smith, G Thorleifsson, L Vandenput, J Hua Zhao, W Zhang, A Aghdassi, K Åkesson, N Amin, LJ Baier, I Barroso, DA Bennett, L Bertram, R Biffar, M Bochud, M Boehnke, IB Borecki, AS Buchman, L Byberg, H Campbell, N Campos Obanda, JA Cauley, PM Cawthon, H Cederberg, Z Chen, NH Cho, H Jin Choi, M Claussnitzer, F Collins, SR Cummings, PL De Jager, I Demuth, RAM Dhonukshe-Rutten, L DIatchenko, G Eiriksdottir, AW Enneman, M Erdos, JG Eriksson, J Eriksson, K Estrada, DS Evans, MF Feitosa, M Fu, M Garcia, C Gieger, T Girke, NL Glazer, H Grallert
Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis
KJE van Hulzen, CJ Scholz, B Franke, S Ripke, M Klein, A McQuillin, EJ Sonuga-Barke, JR Kelsoe, M Landén, OA Andreassen, KP Lesch, H Weber, SV Faraone, A Arias-Vasquez, A Reif, RJL Anney, AA Vasquez, MJ Arranz, P Asherson, TJ Banaschewski, M Bayés, J Biederman, JK Buitelaar, M Casas, A Charach, B Cormand, J Crosbie, S Dalsgaard, MJ Daly, AE Doyle, RP Ebstein, J Elia, SV Faraone, B Franke, C Freitag, M Gill, H Hakonarson, A Hervas, P Holmans, L Kent, J Kuntsi, N Lambregts-Rommelse, K Langley, KP Lesch, SK Loo, J Martin, JJ McGough, SE Medland, J Meyer, E Mick, A Miranda, F Mulas, BM Neale, SF Nelson, MC O’Donovan, RD Oades, MJ Owen, H Palmason, JA Ramos-Quiroga, M Ribasés, S Ripke, H Roeyers, J Romanos, M Romanos, A Rothenberger, C Sánchez-Mora, R Schachar, J Sergeant, SL Smalley, EJS Sonuga-Barke, HC Steinhausen, A Thapar, A Todorov, S Walitza, Y Wang, A Warnke, N Williams, Y Zhang-James, D Absher, H Akil, OA Andreassen, A Anjorin, L Backlund, JA Badner, JD Barchas, TB Barrett, N Bass, M Bauer, F Bellivier
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
RA Scott, LJ Scott, R Mägi, L Marullo, KJ Gaulton, M Kaakinen, N Pervjakova, TH Pers, AD Johnson, JD Eicher, AU Jackson, T Ferreira, Y Lee, C Ma, V Steinthorsdottir, G Thorleifsson, L Qi, NR Van Zuydam, A Mahajan, H Chen, P Almgren, BF Voight, H Grallert, M Müller-Nurasyid, JS Ried, NW Rayner, N Robertson, LC Karssen, EM van Leeuwen, SM Willems, C Fuchsberger, P Kwan, TM Teslovich, P Chanda, M Li, Y Lu, C Dina, D Thuillier, L Yengo, L Jiang, T Sparso, HA Kestler, H Chheda, L Eisele, S Gustafsson, M Frånberg, RJ Strawbridge, R Benediktsson, AB Hreidarsson, A Kong, G Sigurðsson, ND Kerrison, J Luan, L Liang, T Meitinger, M Roden, B Thorand, T Esko, E Mihailov, C Fox, CT Liu, D Rybin, B Isomaa
Significant locus and metabolic genetic correlations revealed in genome-wide association study of anorexia nervosa
L Duncan, Z Yilmaz, H Gaspar, R Walters, J Goldstein, V Anttila, B Bulik-Sullivan, S Ripke, L Thornton, A Hinney, M Daly, PF Sullivan, E Zeggini, G Breen, CM Bulik, L Duncan, Z Yilmaz, H Gaspar, R Walters, J Goldstein, V Anttila, B Bulik-Sullivan, S Ripke, R Adan, L Alfredsson, T Ando, O Andreassen, H Aschauer, J Baker, J Barrett, V Bencko, A Bergen, W Berrettini, A Birgegård, C Boni, VB Perica, H Brandt, R Burghardt, L Carlberg, M Cassina
Causal effect of plasminogen activator inhibitor type 1 on coronary heart disease
C Song, S Burgess, JD Eicher, CJ O'Donnell, AD Johnson, J Huang, M Sabater-Lleal, FW Asselbergs, D Tregouet, SY Shin, J Ding, J Baumert, T Oudot-Mellakh, L Folkersen, NL Smith, SM Williams, MA Ikram, ME Kleber, DM Becker, V Truong, JC Mychaleckyj, W Tang, Q Yang, B Sennblad, JH Moore, FMK Williams, A Dehghan, G Silbernagel, EMC Schrijvers, S Smith, M Karakas, GH Tofler, A Silveira, GJ Navis, K Lohman, MH Chen, A Peters, A Goel, JC Hopewell, JC Chambers, D Saleheen, P Lundmark, BM Psaty, RJ Strawbridge, BO Boehm, AM Carter, C Meisinger, JF Peden, JC Bis, B McKnight, J Öhrvik, K Taylor, MG Franzosi, U Seedorf, R Collins, A Franco-Cereceda, AC Syvänen, AH Goodall, LR Yanek, M Cushman, M Müller-Nurasyid, AR Folsom, S Basu, N Matijevic, WH van Gilst, JS Kooner, J Danesh, R Clarke, JB Meigs, S Kathiresan, MP Reilly, N Klopp, TB Harris, BR Winkelmann, PJ Grant, HL Hillege, H Watkins, TD Spector, LC Becker, RP Tracy, W März, AG Uitterlinden, P Eriksson, F Cambien, PE Morange, W Koenig, N Soranzo, P van der Harst, Y Liu, A Hamsten, GB Ehret, PB Munroe, KM Rice, M Bochud, DI Chasman, AV Smith
Genetic Regulation of Adipose Gene Expression and Cardio-Metabolic Traits
M Civelek, Y Wu, C Pan, CK Raulerson, A Ko, A He, C Tilford, NK Saleem, A Stančáková, LJ Scott, C Fuchsberger, HM Stringham, AU Jackson, N Narisu, PS Chines, KS Small, J Kuusisto, BW Parks, P Pajukanta, T Kirchgessner, FS Collins, PS Gargalovic, M Boehnke, M Laakso, KL Mohlke, AJ Lusis
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees
G Jun, A Manning, M Almeida, M Zawistowski, AR Wood, TM Teslovich, C Fuchsberger, S Feng, P Cingolani, KJ Gaulton, T Dyer, TW Blackwell, H Chen, PS Chines, S Choi, C Churchhouse, P Fontanillas, R King, SY Lee, SE Lincoln, V Trubetskoy, M DePristo, T Fingerlin, R Grossman, J Grundstad, A Heath, J Kim, YJ Kim, J Laramie, J Lee, H Li, X Liu, O Livne, AE Locke, J Maller, A Mazur, AP Morris, TI Pollin, D Ragona, D Reich, MA Rivas, LJ Scott, X Sim, RG Tearle, YY Teo, AL Williams, S Zöllner, JE Curran, J Peralta, B Akolkar, GI Bell, NP Burtt, NJ Cox, JC Florez, CL Hanis, C McKeon, KL Mohlke, M Seielstad, JG Wilson, G Atzmon, JE Below, J Dupuis, DL Nicolae, D Lehman, T Park, S Won, R Sladek
A reference panel of 64,976 haplotypes for genotype imputation
S McCarthy, S Das, W Kretzschmar, O Delaneau, AR Wood, A Teumer, HM Kang, C Fuchsberger, P Danecek, K Sharp, Y Luo, C Sidore, A Kwong, N Timpson, S Koskinen, S Vrieze, LJ Scott, H Zhang, A Mahajan, J Veldink, U Peters, C Pato, CM Van Duijn, CE Gillies, I Gandin, M Mezzavilla, A Gilly, M Cocca, M Traglia, A Angius, JC Barrett, D Boomsma, K Branham, G Breen, CM Brummett, F Busonero, H Campbell, A Chan, S Chen, E Chew, FS Collins, LJ Corbin, GD Smith, G Dedoussis, M Dorr, AE Farmaki, L Ferrucci, L Forer, RM Fraser, S Gabriel, S Levy, L Groop, T Harrison, A Hattersley, OL Holmen, K Hveem, M Kretzler, JC Lee, M McGue, T Meitinger, D Melzer, JL Min, KL Mohlke, JB Vincent, M Nauck, D Nickerson, A Palotie, M Pato, N Pirastu, M McInnis
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