Associations of autozygosity with a broad range of human phenotypes
DW Clark, Y Okada, KHS Moore, D Mason, N Pirastu, I Gandin, H Mattsson, CLK Barnes, K Lin, JH Zhao, P Deelen, R Rohde, C Schurmann, X Guo, F Giulianini, W Zhang, C Medina-Gomez, R Karlsson, Y Bao, TM Bartz, C Baumbach, G Biino, MJ Bixley, M Brumat, JF Chai, T Corre, DL Cousminer, AM Dekker, DA Eccles, KR van Eijk, C Fuchsberger, H Gao, M Germain, SD Gordon, HG de Haan, . Harris, E Hofer, A Huerta-Chagoya, C Igartua, IE Jansen, Y Jia, T Kacprowski, T Karlsson, ME Kleber, . Li, R Li-Gao, A Mahajan, K Matsuda, K Meidtner, W Meng, ME Montasser, PJ van der Most, M Munz, T Nutile, T Palviainen, G Prasad, RB Prasad, TDS Priyanka, F Rizzi, E Salvi, BR Sapkota, D Shriner, L Skotte, MC Smart, AV Smith, A van der Spek, CN Spracklen, RJ Strawbridge, SM Tajuddin, S Trompet, C Turman, N Verweij, C Viberti, L Wang, HR Warren, RE Wootton, LR Yanek, J Yao, NA Yousri, W Zhao, AA Adeyemo, S Afaq, CA Aguilar-Salinas, M Akiyama, ML Albert, MA Allison, M Alver, T Aung, F Azizi, AR Bentley, H Boeing, E Boerwinkle, JB Borja, GJ de Borst, EP Bottinger, L Broer, H Campbell, S Chanock, ML Chee, G Chen, Laura Scott, Jennifer Smith
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power (Nature, (2019), 572, 7769, (323-328), 10.1038/s41586-019-1457-z)
AE Locke, KM Steinberg, CWK Chiang, SK Service, AS Havulinna, L Stell, M Pirinen, HJ Abel, CC Chiang, RS Fulton, AU Jackson, CJ Kang, KL Kanchi, DC Koboldt, DE Larson, J Nelson, TJ Nicholas, A Pietilä, V Ramensky, D Ray, Laura Scott, HM Stringham, J Vangipurapu, R Welch, P Yajnik, X Yin, JG Eriksson, M Ala-Korpela, . Järvelin, M Männikkö, H Laivuori, SK Dutcher, NO Stitziel, RK Wilson, IM Hall, C Sabatti, A Palotie, V Salomaa, M Laakso, S Ripatti, Michael Boehnke, NB Freimer
New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders
E Evangelou, H Gao, C Chu, G Ntritsos, P Blakeley, AR Butts, R Pazoki, H Suzuki, F Koskeridis, AM Yiorkas, I Karaman, P Elliott, Q Luo, S Aeschbacher, TM Bartz, . Baumeister, PS Braund, . Brown, JA Brody, TK Clarke, N Dimou, JD Faul, G Homuth, AU Jackson, KA Kentistou, PK Joshi, RN Lemaitre, PA Lind, LP Lyytikäinen, M Mangino, Y Milaneschi, CP Nelson, IM Nolte, MM Perälä, O Polasek, D Porteous, SM Ratliff, Jennifer Smith, A Stančáková, A Teumer, S Tuominen, S Thériault, J Vangipurapu, JB Whitfield, A Wood, J Yao, B Yu, W Zhao, DE Arking, J Auvinen, C Liu, M Männikkö, L Risch, JI Rotter, H Snieder, J Veijola, AI Blakemore, Michael Boehnke, H Campbell, D Conen, JG Eriksson, HJ Grabe, X Guo, P van der Harst, CA Hartman, C Hayward, AC Heath, . Jarvelin, M Kähönen, SLR Kardia, M Kühne, J Kuusisto, M Laakso, J Lahti, T Lehtimäki, AM McIntosh, KL Mohlke, AC Morrison, NG Martin, AJ Oldehinkel, BWJH Penninx, BM Psaty, OT Raitakari, I Rudan, NJ Samani, Laura Scott, TD Spector, N Verweij, . Weir, JF Wilson, D Levy, I Tzoulaki, JD Bell, PM Matthews, A Rothenfluh, S Desrivières, G Schumann, Sharon Kardia
Exome sequencing of Finnish isolates enhances rare-variant association power
AE Locke, KM Steinberg, CWK Chiang, SK Service, AS Havulinna, L Stell, M Pirinen, HJ Abel, CC Chiang, RS Fulton, AU Jackson, CJ Kang, KL Kanchi, DC Koboldt, DE Larson, J Nelson, TJ Nicholas, A Pietilä, V Ramensky, D Ray, Laura Scott, HM Stringham, J Vangipurapu, R Welch, P Yajnik, X Yin, JG Eriksson, M Ala-Korpela, . Järvelin, M Männikkö, H Laivuori, SK Dutcher, NO Stitziel, RK Wilson, IM Hall, C Sabatti, A Palotie, V Salomaa, M Laakso, S Ripatti, Michael Boehnke, NB Freimer
GWAS of suicide attempt in psychiatric disorders and association with major depression polygenic risk scores
N Mullins, TB Bigdeli, AD Børglum, JRI Coleman, D Demontis, D Mehta, RA Power, S Ripke, EA Stahl, A Starnawska, A Anjorin, A Corvin, AR Sanders, AJ Forstner, A Reif, AC Koller, BS Tkowska, BT Baune, B Müller-Myhsok, BWJH Penninx, C Pato, C Zai, D Rujescu, DM Hougaard, D Quested, DF Levinson, EB Binder, EM Byrne, E Agerbo, F Streit, F Mayoral, F Bellivier, F Degenhardt, G Breen, G Morken, G Turecki, GA Rouleau, HJ Grabe, H Völzke, I Jones, I Giegling, I Agartz, I Melle, J Lawrence, JTR Walters, J Strohmaier, J Shi, J Hauser, JM Biernacka, JB Vincent, J Kelsoe, JS Strauss, J Lissowska, J Pimm, JW Smoller, J Guzman-Parra, K Berger, Laura Scott, LA Jones, MH Azevedo, M Trzaskowski, M Kogevinas, M Rietschel, M Boks, M Ising, M Grigoroiu-Serbanescu, ML Hamshere, M Leboyer, M Frye, MM Nöthen, M Alda, M Preisig, M Nordentoft, Michael Boehnke, MC O’Donovan, MJ Owen, MT Pato, ME Renteria, M Budde, MM Weissman, NR Wray, N Bass, N Craddock, OB Smeland, OA Andreassen, O Mors, PV Gejman, P Sklar, P McGrath, P Hoffmann, P McGuffin, PH Lee, PB Mortensen, RS Kahn, RA Ophoff, R Adolfsson, S Van der Auwera, S Djurovic, S Kloiber, S Heilmann-Heimbach
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
A Giri, JN Hellwege, JM Keaton, J Park, C Qiu, HR Warren, ES Torstenson, CP Kovesdy, YV Sun, OD Wilson, C Robinson-Cohen, CL Roumie, CP Chung, KA Birdwell, SM Damrauer, SL DuVall, D Klarin, K Cho, Y Wang, E Evangelou, CP Cabrera, LV Wain, R Shrestha, BS Mautz, EA Akwo, M Sargurupremraj, S Debette, Michael Boehnke, Laura Scott, J Luan, JH Zhao, SM Willems, S Thériault, N Shah, C Oldmeadow, P Almgren, R Li-Gao, N Verweij, TS Boutin, M Mangino, I Ntalla, E Feofanova, P Surendran, JP Cook, S Karthikeyan, N Lahrouchi, C Liu, N Sepúlveda, TG Richardson, A Kraja, P Amouyel, M Farrall, NR Poulter, M Laakso, E Zeggini, P Sever, RA Scott, C Langenberg, NJ Wareham, D Conen, CNA Palmer, J Attia, DI Chasman, PM Ridker, O Melander, . Mook-Kanamori, P van der Harst, F Cucca, D Schlessinger, C Hayward, TD Spector, . Jarvelin, BJ Hennig, NJ Timpson, WQ Wei, JC Smith, Y Xu, ME Matheny, EE Siew, C Lindgren, KH Herzig, G Dedoussis, JC Denny, BM Psaty, JMM Howson, PB Munroe, C Newton-Cheh, MJ Caulfield, P Elliott, JM Gaziano, J Concato, PWF Wilson, PS Tsao, DR Velez Edwards, K Susztak, CJ O’Donnell, AM Hung, TL Edwards
Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans
J Carlson, AE Locke, M Flickinger, Matthew Zawistowski, S Levy, RM Myers, Michael Boehnke, HM Kang, Laura Scott, Jun Li, S Zöllner, D Absher, Huda Akil, G Breen, Margit Burmeister, S Cohen-Woods, WG Iacono, JA Knowles, L Legrand, Q Lu, M McGue, Melvin McInnis, MT Pato, M Rivera, JL Sobell, JB Vincent, SJ Watson, Stanley Watson Jr, Sebastian Zoellner
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, . 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, M Li, CH Newton-Cheh, S Padmanabhan, G Peloso, S Pulit, DJ Rader, D Reich, MP Reilly, MA Rivas, S Schwartz, Laura Scott, DS Siscovick, JA Spertus, NO Stitziel, N Stoletzki, . Sunyaev, BF Voight, Cristen 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, . Chen, P Concannon, J Crosby, LA Cupples, R D’Agostino, AL DeStefano, A Dreisbach, J Dupuis, JP Durda, J Ellis, AR Folsom, M Fornage, E Fox, V Funari, Santhi Ganesh, J Gardin, D Goff, O Gordon, W Grody, M Gross, X Guo, IM Hall, NL Heard-Costa, . Heckbert, N Heintz, DM Herrington, Jeffrey Kidd
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, . 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, EYH Chen, W Cheng, EFC Cheung, . Chong, CR Cloninger, 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, . 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, T Hansen, V Haroutunian, AM Hartmann, FA Henskens, S Herms, JN Hirschhorn, Michael Boehnke, Robert Thompson, Melvin McInnis, Stanley Watson Jr, Sebastian Zoellner, Margit Burmeister, Laura Scott, Fan Meng
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, Huda Akil, D Albani, M Albus, M Alda, M Alexander, N Alliey-Rodriguez, TD Als, F Amin, A Anjorin, MJ Arranz, S Awasthi, . 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, . Bergen, WH Berrettini, E Bevilacqua, JM Biernacka, TB Bigdeli, DW Black, H Blackburn, JM Blackwell, DHR Blackwood, CB Pedersen, Michael 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, Margit Burmeister, JD Buxbaum, J Bybjerg-Grauholm, W Byerley, W Cahn, G Cai, MJ Cairns, D Campion, RM Cantor, VJ Carr, N Carrera, M Casas, SV Catts, P Cervantes, KD Chambert, RCK Chan, RYL Chen, W Cheng, EFC Cheung, . Chong, TK Clarke, CR Cloninger, N Cohen, JRI Coleman, DA Collier, P Cormican, W Coryell, N Craddock, DW Craig, Laura Scott, Melvin McInnis, Stanley Watson Jr, Sebastian Zoellner, Robert Thompson, Fan Meng
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, P Chen, . Huyghe, M van de Bunt, RD Pearson, A Kumar, M Müller-Nurasyid, N Grarup, HM Stringham, ER Gamazon, HM Lee, J Scott, JE Below, 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, YJ Kim, . Kwon, KH Lin, TJ Maxwell, Y Nagai, X Wang, RP Welch, J Yoon, W Zhang, N Barzilai, BF Voight, . 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 Carey, P Kwan, G Grant, JD Smith, BM Neale, S Purcell, AS Butterworth, JMM Howson, Y Lu, SH Kwak, W Zhao, J Danesh, VKL Lam, KS Park, Goncalo Abecasis, Michael Boehnke, Laura Scott
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, . Huyghe, M Van De Bunt, RD Pearson, A Kumar, M Müller-Nurasyid, N Grarup, HM Stringham, ER Gamazon, S Lee, Y Chen, RA Scott, JE Below, P Chen, J Huang, MJ Go, ML Stitzel, D Pasko, Stephen Parker, TV Varga, T Green, NL Beer, AG Day-Williams, T Ferreira, T Fingerlin, M Horikoshi, C Hu, I Huh, MK Ikram, YJ Kim, Y Kim, . Kwon, J Lee, KH Lin, TJ Maxwell, Y Nagai, X Wang, RP Welch, J Yoon, W Zhang, N Barzilai, BF Voight, . 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, Laura Scott, Hyun Min Kang, Goncalo Abecasis, Michael Boehnke
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, Michael 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, . 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, J Grewal, . Han, RL Hanson, C Hayward, A Hofman, EP Hoffman, G Homuth, WC Hsueh, MJ Hubal, A Hubbard, KM Huffman, LB Husted, T Illig, E Ingelsson, T Ittermann, JO Jansson, JM Jordan, A Jula, M Karlsson, KT Khaw, TO Kilpelaïnen, N Klopp, JSL Kloth, HA Koistinen, WE Kraus, S Kritchevsky, T Kuulasmaa, J Kuusisto, M Laakso, J Lahti, T Lang, BL Langdahl, LJ Launer, JY Lee, MM Lerch, . Lewis, L Lind, C Lindgren, Y Liu, Stephen Parker, Laura Scott
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