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28건, 그중 20건 표시.
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
Manousaki D,
Dudding T,
Haworth S,
Hsu YH,
Liu CT,
Medina-Gómez C,
Voortman T,
van der Velde N,
Melhus H,
Robinson-Cohen C,
Cousminer DL,
Nethander M
외 41명 — 모두 보기
Vandenput L,
Noordam R,
Forgetta V,
Greenwood CMT,
Biggs ML,
Psaty BM,
Rotter JI,
Zemel BS,
Mitchell JA,
Taylor B,
Lorentzon M,
Karlsson M,
Jaddoe VVW,
Tiemeier H,
Campos-Obando N,
Franco OH,
Utterlinden AG,
Broer L,
van Schoor NM,
Ham AC,
Ikram MA,
Karasik D,
de Mutsert R,
Rosendaal FR,
den Heijer M,
Wang TJ,
Lind L,
Orwoll ES,
Mook-Kanamori DO,
Michaëlsson K,
Kestenbaum B,
Ohlsson C,
Mellström D,
de Groot LCPGM,
Grant SFA,
Kiel DP,
Zillikens MC,
Rivadeneira F,
Sawcer S,
Timpson NJ,
Richards JB
American journal of human genetics · 2017 · PMID 28757204
페이지 12개+
Discovery of common and rare genetic risk variants for colorectal cancer
Huyghe JR,
Bien SA,
Harrison TA,
Kang HM,
Chen S,
Schmit SL,
Conti DV,
Qu C,
Jeon J,
Edlund CK,
Greenside P,
Wainberg M
외 188명 — 모두 보기
Schumacher FR,
Smith JD,
Levine DM,
Nelson SC,
Sinnott-Armstrong NA,
Albanes D,
Alonso MH,
Anderson K,
Arnau-Collell C,
Arndt V,
Bamia C,
Banbury BL,
Baron JA,
Berndt SI,
Bézieau S,
Bishop DT,
Boehm J,
Boeing H,
Brenner H,
Brezina S,
Buch S,
Buchanan DD,
Burnett-Hartman A,
Butterbach K,
Caan BJ,
Campbell PT,
Carlson CS,
Castellví-Bel S,
Chan AT,
Chang-Claude J,
Chanock SJ,
Chirlaque MD,
Cho SH,
Connolly CM,
Cross AJ,
Cuk K,
Curtis KR,
de la Chapelle A,
Doheny KF,
Duggan D,
Easton DF,
Elias SG,
Elliott F,
English DR,
Feskens EJM,
Figueiredo JC,
Fischer R,
FitzGerald LM,
Forman D,
Gala M,
Gallinger S,
Gauderman WJ,
Giles GG,
Gillanders E,
Gong J,
Goodman PJ,
Grady WM,
Grove JS,
Gsur A,
Gunter MJ,
Haile RW,
Hampe J,
Hampel H,
Harlid S,
Hayes RB,
Hofer P,
Hoffmeister M,
Hopper JL,
Hsu WL,
Huang WY,
Hudson TJ,
Hunter DJ,
Ibañez-Sanz G,
Idos GE,
Ingersoll R,
Jackson RD,
Jacobs EJ,
Jenkins MA,
Joshi AD,
Joshu CE,
Keku TO,
Key TJ,
Kim HR,
Kobayashi E,
Kolonel LN,
Kooperberg C,
Kühn T,
Küry S,
Kweon SS,
Larsson SC,
Laurie CA,
Le Marchand L,
Leal SM,
Lee SC,
Lejbkowicz F,
Lemire M,
Li CI,
Li L,
Lieb W,
Lin Y,
Lindblom A,
Lindor NM,
Ling H,
Louie TL,
Männistö S,
Markowitz SD,
Martín V,
Masala G,
McNeil CE,
Melas M,
Milne RL,
Moreno L,
Murphy N,
Myte R,
Naccarati A,
Newcomb PA,
Offit K,
Ogino S,
Onland-Moret NC,
Pardini B,
Parfrey PS,
Pearlman R,
Perduca V,
Pharoah PDP,
Pinchev M,
Platz EA,
Prentice RL,
Pugh E,
Raskin L,
Rennert G,
Rennert HS,
Riboli E,
Rodríguez-Barranco M,
Romm J,
Sakoda LC,
Schafmayer C,
Schoen RE,
Seminara D,
Shah M,
Shelford T,
Shin MH,
Shulman K,
Sieri S,
Slattery ML,
Southey MC,
Stadler ZK,
Stegmaier C,
Su YR,
Tangen CM,
Thibodeau SN,
Thomas DC,
Thomas SS,
Toland AE,
Trichopoulou A,
Ulrich CM,
Van Den Berg DJ,
van Duijnhoven FJB,
Van Guelpen B,
van Kranen H,
Vijai J,
Visvanathan K,
Vodicka P,
Vodickova L,
Vymetalkova V,
Weigl K,
Weinstein SJ,
White E,
Win AK,
Wolf CR,
Wolk A,
Woods MO,
Wu AH,
Zaidi SH,
Zanke BW,
Zhang Q,
Zheng W,
Zheng W,
Scacheri PC,
Potter JD,
Bassik MC,
Kundaje A,
Casey G,
Moreno V,
Abecasis GR,
Nickerson DA,
Gruber SB,
Hsu L,
Peters U
Nature genetics · 2019 · PMID 30510241 · open access
페이지 12개+
An atlas of genetic influences on osteoporosis in humans and mice
Morris JA,
Kemp JP,
Youlten SE,
Laurent L,
Logan JG,
Chai RC,
Vulpescu NA,
Forgetta V,
Kleinman A,
Mohanty ST,
Sergio CM,
Quinn J
외 47명 — 모두 보기
Nguyen-Yamamoto L,
Luco AL,
Vijay J,
Simon MM,
Pramatarova A,
Medina-Gomez C,
Trajanoska K,
Ghirardello EJ,
Butterfield NC,
Curry KF,
Leitch VD,
Sparkes PC,
Adoum AT,
Mannan NS,
Komla-Ebri DSK,
Pollard AS,
Dewhurst HF,
Hassall TAD,
Beltejar MG,
Adams DJ,
Vaillancourt SM,
Kaptoge S,
Baldock P,
Cooper C,
Reeve J,
Ntzani EE,
Evangelou E,
Ohlsson C,
Karasik D,
Rivadeneira F,
Kiel DP,
Tobias JH,
Gregson CL,
Harvey NC,
Grundberg E,
Goltzman D,
Adams DJ,
Lelliott CJ,
Hinds DA,
Ackert-Bicknell CL,
Hsu YH,
Maurano MT,
Croucher PI,
Williams GR,
Bassett JHD,
Evans DM,
Richards JB
23andMe Research Team
Nature genetics · 2019 · PMID 30598549 · open access
페이지 12개+
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
Graff M,
Justice AE,
Young KL,
Marouli E,
Zhang X,
Fine RS,
Lim E,
Buchanan V,
Rand K,
Feitosa MF,
Wojczynski MK,
Yanek LR
외 213명 — 모두 보기
Shao Y,
Rohde R,
Adeyemo AA,
Aldrich MC,
Allison MA,
Ambrosone CB,
Ambs S,
Amos C,
Arnett DK,
Atwood L,
Bandera EV,
Bartz T,
Becker DM,
Berndt SI,
Bernstein L,
Bielak LF,
Blot WJ,
Bottinger EP,
Bowden DW,
Bradfield JP,
Brody JA,
Broeckel U,
Burke G,
Cade BE,
Cai Q,
Caporaso N,
Carlson C,
Carpten J,
Casey G,
Chanock SJ,
Chen G,
Chen M,
Chen YI,
Chen WM,
Chesi A,
Chiang CWK,
Chu L,
Coetzee GA,
Conti DV,
Cooper RS,
Cushman M,
Demerath E,
Deming SL,
Dimitrov L,
Ding J,
Diver WR,
Duan Q,
Evans MK,
Falusi AG,
Faul JD,
Fornage M,
Fox C,
Freedman BI,
Garcia M,
Gillanders EM,
Goodman P,
Gottesman O,
Grant SFA,
Guo X,
Hakonarson H,
Haritunians T,
Harris TB,
Harris CC,
Henderson BE,
Hennis A,
Hernandez DG,
Hirschhorn JN,
McNeill LH,
Howard TD,
Howard B,
Hsing AW,
Hsu YH,
Hu JJ,
Huff CD,
Huo D,
Ingles SA,
Irvin MR,
John EM,
Johnson KC,
Jordan JM,
Kabagambe EK,
Kang SJ,
Kardia SL,
Keating BJ,
Kittles RA,
Klein EA,
Kolb S,
Kolonel LN,
Kooperberg C,
Kuller L,
Kutlar A,
Lange L,
Langefeld CD,
Le Marchand L,
Leonard H,
Lettre G,
Levin AM,
Li Y,
Li J,
Liu Y,
Liu Y,
Liu S,
Lohman K,
Lotay V,
Lu Y,
Maixner W,
Manson JE,
McKnight B,
Meng Y,
Monda KL,
Monroe K,
Moore JH,
Mosley TH,
Mudgal P,
Murphy AB,
Nadukuru R,
Nalls MA,
Nathanson KL,
Nayak U,
N'Diaye A,
Nemesure B,
Neslund-Dudas C,
Neuhouser ML,
Nyante S,
Ochs-Balcom H,
Ogundiran TO,
Ogunniyi A,
Ojengbede O,
Okut H,
Olopade OI,
Olshan A,
Padhukasahasram B,
Palmer J,
Palmer CD,
Palmer ND,
Papanicolaou G,
Patel SR,
Pettaway CA,
Peyser PA,
Press MF,
Rao DC,
Rasmussen-Torvik LJ,
Redline S,
Reiner AP,
Rhie SK,
Rodriguez-Gil JL,
Rotimi CN,
Rotter JI,
Ruiz-Narvaez EA,
Rybicki BA,
Salako B,
Sale MM,
Sanderson M,
Schadt E,
Schreiner PJ,
Schurmann C,
Schwartz AG,
Shriner DA,
Signorello LB,
Singleton AB,
Siscovick DS,
Smith JA,
Smith S,
Speliotes E,
Spitz M,
Stanford JL,
Stevens VL,
Stram A,
Strom SS,
Sucheston L,
Sun YV,
Tajuddin SM,
Taylor H,
Taylor K,
Tayo BO,
Thun MJ,
Tucker MA,
Vaidya D,
Van Den Berg DJ,
Vedantam S,
Vitolins M,
Wang Z,
Ware EB,
Wassertheil-Smoller S,
Weir DR,
Wiencke JK,
Williams SM,
Williams LK,
Wilson JG,
Witte JS,
Wrensch M,
Wu X,
Yao J,
Zakai N,
Zanetti K,
Zemel BS,
Zhao W,
Zhao JH,
Zheng W,
Zhi D,
Zhou J,
Zhu X,
Ziegler RG,
Zmuda J,
Zonderman AB,
Psaty BM,
Borecki IB,
Cupples LA,
Liu CT,
Haiman CA,
Loos R,
Ng MCY,
North KE
American journal of human genetics · 2021 · PMID 33713608
페이지 12개+
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries
Fernandez-Rozadilla C,
Timofeeva M,
Chen Z,
Law P,
Thomas M,
Schmit S,
Díez-Obrero V,
Hsu L,
Fernandez-Tajes J,
Palles C,
Sherwood K,
Briggs S
외 198명 — 모두 보기
Svinti V,
Donnelly K,
Farrington S,
Blackmur J,
Vaughan-Shaw P,
Shu XO,
Long J,
Cai Q,
Guo X,
Lu Y,
Broderick P,
Studd J,
Huyghe J,
Harrison T,
Conti D,
Dampier C,
Devall M,
Schumacher F,
Melas M,
Rennert G,
Obón-Santacana M,
Martín-Sánchez V,
Moratalla-Navarro F,
Oh JH,
Kim J,
Jee SH,
Jung KJ,
Kweon SS,
Shin MH,
Shin A,
Ahn YO,
Kim DH,
Oze I,
Wen W,
Matsuo K,
Matsuda K,
Tanikawa C,
Ren Z,
Gao YT,
Jia WH,
Hopper J,
Jenkins M,
Win AK,
Pai R,
Figueiredo J,
Haile R,
Gallinger S,
Woods M,
Newcomb P,
Duggan D,
Cheadle J,
Kaplan R,
Maughan T,
Kerr R,
Kerr D,
Kirac I,
Böhm J,
Mecklin LP,
Jousilahti P,
Knekt P,
Aaltonen L,
Rissanen H,
Pukkala E,
Eriksson J,
Cajuso T,
Hänninen U,
Kondelin J,
Palin K,
Tanskanen T,
Renkonen-Sinisalo L,
Zanke B,
Männistö S,
Albanes D,
Weinstein S,
Ruiz-Narvaez E,
Palmer J,
Buchanan D,
Platz E,
Visvanathan K,
Ulrich C,
Siegel E,
Brezina S,
Gsur A,
Campbell P,
Chang-Claude J,
Hoffmeister M,
Brenner H,
Slattery M,
Potter J,
Tsilidis K,
Schulze M,
Gunter M,
Murphy N,
Castells A,
Castellví-Bel S,
Moreira L,
Arndt V,
Shcherbina A,
Stern M,
Pardamean B,
Bishop T,
Giles G,
Southey M,
Idos G,
McDonnell K,
Abu-Ful Z,
Greenson J,
Shulman K,
Lejbkowicz F,
Offit K,
Su YR,
Steinfelder R,
Keku T,
van Guelpen B,
Hudson T,
Hampel H,
Pearlman R,
Berndt S,
Hayes R,
Martinez ME,
Thomas S,
Corley D,
Pharoah P,
Larsson S,
Yen Y,
Lenz HJ,
White E,
Li L,
Doheny K,
Pugh E,
Shelford T,
Chan A,
Cruz-Correa M,
Lindblom A,
Hunter D,
Joshi A,
Schafmayer C,
Scacheri P,
Kundaje A,
Nickerson D,
Schoen R,
Hampe J,
Stadler Z,
Vodicka P,
Vodickova L,
Vymetalkova V,
Papadopoulos N,
Edlund C,
Gauderman W,
Thomas D,
Shibata D,
Toland A,
Markowitz S,
Kim A,
Chanock S,
van Duijnhoven F,
Feskens E,
Sakoda L,
Gago-Dominguez M,
Wolk A,
Naccarati A,
Pardini B,
FitzGerald L,
Lee SC,
Ogino S,
Bien S,
Kooperberg C,
Li C,
Lin Y,
Prentice R,
Qu C,
Bézieau S,
Tangen C,
Mardis E,
Yamaji T,
Sawada N,
Iwasaki M,
Haiman C,
Le Marchand L,
Wu A,
Qu C,
McNeil C,
Coetzee G,
Hayward C,
Deary I,
Harris S,
Theodoratou E,
Reid S,
Walker M,
Ooi LY,
Moreno V,
Casey G,
Gruber S,
Tomlinson I,
Zheng W,
Dunlop M,
Houlston R,
Peters U
Nature genetics · 2023 · PMID 36539618
페이지 12개+
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium
Ng MCY,
Graff M,
Lu Y,
Justice AE,
Mudgal P,
Liu CT,
Young K,
Yanek LR,
Feitosa MF,
Wojczynski MK,
Rand K,
Brody JA
외 101명 — 모두 보기
Cade BE,
Dimitrov L,
Duan Q,
Guo X,
Lange LA,
Nalls MA,
Okut H,
Tajuddin SM,
Tayo BO,
Vedantam S,
Bradfield JP,
Chen G,
Chen WM,
Chesi A,
Irvin MR,
Padhukasahasram B,
Smith JA,
Zheng W,
Zheng W,
Allison MA,
Ambrosone CB,
Bandera EV,
Bartz TM,
Berndt SI,
Bernstein L,
Blot WJ,
Bottinger EP,
Carpten J,
Chanock SJ,
Chen YI,
Conti DV,
Cooper RS,
Fornage M,
Freedman BI,
Garcia M,
Goodman PJ,
Hsu YH,
Hu J,
Huff CD,
Ingles SA,
John EM,
Kittles R,
Klein E,
Li J,
McKnight B,
Nayak U,
Nemesure B,
Ogunniyi A,
Olshan A,
Press MF,
Rohde R,
Rybicki BA,
Salako B,
Sanderson M,
Shao Y,
Siscovick DS,
Stanford JL,
Stevens VL,
Stram A,
Strom SS,
Vaidya D,
Witte JS,
Yao J,
Zhu X,
Ziegler RG,
Zonderman AB,
Adeyemo A,
Ambs S,
Cushman M,
Faul JD,
Hakonarson H,
Levin AM,
Nathanson KL,
Ware EB,
Weir DR,
Zhao W,
Zhi D,
Arnett DK,
Grant SFA,
Kardia SLR,
Oloapde OI,
Rao DC,
Rotimi CN,
Sale MM,
Williams LK,
Zemel BS,
Becker DM,
Borecki IB,
Evans MK,
Harris TB,
Hirschhorn JN,
Li Y,
Patel SR,
Psaty BM,
Rotter JI,
Wilson JG,
Bowden DW,
Cupples LA,
Haiman CA,
Loos RJF,
North KE
Bone Mineral Density in Childhood Study (BMDCS) Group
PLoS genetics · 2017 · PMID 28430825 · open access
페이지 11개
Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus
Medina-Gomez C,
Kemp JP,
Dimou NL,
Kreiner E,
Chesi A,
Zemel BS,
Bønnelykke K,
Boer CG,
Ahluwalia TS,
Bisgaard H,
Evangelou E,
Heppe DHM
외 22명 — 모두 보기
Bonewald LF,
Gorski JP,
Ghanbari M,
Demissie S,
Duque G,
Maurano MT,
Kiel DP,
Hsu YH,
C J van der Eerden B,
Ackert-Bicknell C,
Reppe S,
Gautvik KM,
Raastad T,
Karasik D,
van de Peppel J,
Jaddoe VWV,
Uitterlinden AG,
Tobias JH,
Grant SFA,
Bagos PG,
Evans DM,
Rivadeneira F
Nature communications · 2017 · PMID 28743860 · open access
페이지 11개
Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression
Amare AT,
Vaez A,
Hsu YH,
Direk N,
Kamali Z,
Howard DM,
McIntosh AM,
McIntosh AM,
Tiemeier H,
Bültmann U,
Snieder H,
Hartman CA
Molecular psychiatry · 2020 · PMID 30626913 · open access
페이지 9개
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
Estrada K,
Styrkarsdottir U,
Evangelou E,
Hsu YH,
Duncan EL,
Ntzani EE,
Oei L,
Albagha OM,
Amin N,
Kemp JP,
Koller DL,
Li G
외 170명 — 모두 보기
Liu CT,
Minster RL,
Moayyeri A,
Vandenput L,
Willner D,
Xiao SM,
Yerges-Armstrong LM,
Zheng HF,
Alonso N,
Eriksson J,
Kammerer CM,
Kaptoge SK,
Leo PJ,
Thorleifsson G,
Wilson SG,
Wilson JF,
Aalto V,
Alen M,
Aragaki AK,
Aspelund T,
Center JR,
Dailiana Z,
Duggan DJ,
Garcia M,
Garcia-Giralt N,
Giroux S,
Hallmans G,
Hocking LJ,
Husted LB,
Jameson KA,
Khusainova R,
Kim GS,
Kooperberg C,
Koromila T,
Kruk M,
Laaksonen M,
Lacroix AZ,
Lee SH,
Leung PC,
Lewis JR,
Masi L,
Mencej-Bedrac S,
Nguyen TV,
Nogues X,
Nogues X,
Patel MS,
Prezelj J,
Rose LM,
Scollen S,
Siggeirsdottir K,
Smith AV,
Svensson O,
Trompet S,
Trummer O,
van Schoor NM,
Woo J,
Zhu K,
Balcells S,
Brandi ML,
Buckley BM,
Cheng S,
Christiansen C,
Cooper C,
Dedoussis G,
Ford I,
Frost M,
Goltzman D,
González-Macías J,
Kähönen M,
Karlsson M,
Khusnutdinova E,
Koh JM,
Kollia P,
Langdahl BL,
Leslie WD,
Lips P,
Ljunggren Ö,
Lorenc RS,
Marc J,
Mellström D,
Obermayer-Pietsch B,
Olmos JM,
Pettersson-Kymmer U,
Reid DM,
Riancho JA,
Ridker PM,
Rousseau F,
Slagboom PE,
Tang NL,
Urreizti R,
Van Hul W,
Viikari J,
Zarrabeitia MT,
Aulchenko YS,
Castano-Betancourt M,
Grundberg E,
Herrera L,
Ingvarsson T,
Johannsdottir H,
Kwan T,
Li R,
Luben R,
Medina-Gómez C,
Palsson ST,
Reppe S,
Rotter JI,
Sigurdsson G,
van Meurs JB,
Verlaan D,
Williams FM,
Wood AR,
Zhou Y,
Gautvik KM,
Pastinen T,
Raychaudhuri S,
Cauley JA,
Chasman DI,
Clark GR,
Cummings SR,
Danoy P,
Dennison EM,
Eastell R,
Eisman JA,
Gudnason V,
Hofman A,
Jackson RD,
Jones G,
Jukema JW,
Khaw KT,
Lehtimäki T,
Liu Y,
Lorentzon M,
McCloskey E,
Mitchell BD,
Nandakumar K,
Nicholson GC,
Oostra BA,
Peacock M,
Pols HA,
Prince RL,
Raitakari O,
Reid IR,
Robbins J,
Sambrook PN,
Sham PC,
Shuldiner AR,
Tylavsky FA,
van Duijn CM,
Wareham NJ,
Cupples LA,
Econs MJ,
Evans DM,
Harris TB,
Kung AW,
Psaty BM,
Reeve J,
Spector TD,
Streeten EA,
Zillikens MC,
Thorsteinsdottir U,
Ohlsson C,
Karasik D,
Richards JB,
Brown MA,
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