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성함이나 학술지명, PMID로 찾아보십시오.
Li R에 대해
28건, 그중 20건 표시.
Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci
He M,
Xu M,
Zhang B,
Liang J,
Chen P,
Lee JY,
Johnson TA,
Li H,
Yang X,
Dai J,
Liang L,
Gui L
외 79명 — 모두 보기
Qi Q,
Huang J,
Li Y,
Adair LS,
Aung T,
Cai Q,
Cheng CY,
Cho MC,
Cho YS,
Chu M,
Cui B,
Gao YT,
Go MJ,
Gu D,
Gu W,
Guo H,
Hao Y,
Hong J,
Hu Z,
Hu Y,
Huang J,
Hwang JY,
Ikram MK,
Jin G,
Kang DH,
Khor CC,
Kim BJ,
Kim HT,
Kubo M,
Lee J,
Lee J,
Lee NR,
Li R,
Li J,
Liu J,
Longe J,
Lu W,
Lu X,
Miao X,
Okada Y,
Ong RT,
Qiu G,
Seielstad M,
Sim X,
Song H,
Takeuchi F,
Tanaka T,
Taylor PR,
Wang L,
Wang W,
Wang Y,
Wu C,
Wu Y,
Xiang YB,
Yamamoto K,
Yang H,
Liao M,
Yokota M,
Young T,
Zhang X,
Kato N,
Wang QK,
Zheng W,
Zheng W,
Hu FB,
Lin D,
Shen H,
Teo YY,
Mo Z,
Wong TY,
Lin X,
Mohlke KL,
Ning G,
Tsunoda T,
Han BG,
Shu XO,
Tai ES,
Wu T,
Qi L
Human molecular genetics · 2015 · PMID 25429064
페이지 12개+
Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
Heilmann-Heimbach S,
Herold C,
Hochfeld LM,
Hillmer AM,
Nyholt DR,
Hecker J,
Javed A,
Chew EG,
Pechlivanis S,
Drichel D,
Heng XT,
Del Rosario RC
외 24명 — 모두 보기
Fier HL,
Paus R,
Rueedi R,
Galesloot TE,
Moebus S,
Anhalt T,
Prabhakar S,
Li R,
Kanoni S,
Papanikolaou G,
Kutalik Z,
Deloukas P,
Philpott MP,
Waeber G,
Spector TD,
Vollenweider P,
Kiemeney LA,
Dedoussis G,
Richards JB,
Nothnagel M,
Martin NG,
Becker T,
Hinds DA,
Nöthen MM
Nature communications · 2017 · PMID 28272467 · open access
페이지 12개+
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
Lee JJ,
Wedow R,
Okbay A,
Kong E,
Maghzian O,
Zacher M,
Nguyen-Viet TA,
Bowers P,
Sidorenko J,
Karlsson Linnér R,
Fontana MA,
Kundu T
외 65명 — 모두 보기
Lee C,
Li H,
Li R,
Royer R,
Timshel PN,
Walters RK,
Willoughby EA,
Yengo L,
Alver M,
Bao Y,
Clark DW,
Day FR,
Furlotte NA,
Joshi PK,
Kemper KE,
Kleinman A,
Langenberg C,
Mägi R,
Trampush JW,
Verma SS,
Wu Y,
Lam M,
Zhao JH,
Zheng Z,
Boardman JD,
Campbell H,
Freese J,
Harris KM,
Hayward C,
Herd P,
Kumari M,
Lencz T,
Luan J,
Malhotra AK,
Metspalu A,
Milani L,
Ong KK,
Perry JRB,
Porteous DJ,
Ritchie MD,
Smart MC,
Smith BH,
Tung JY,
Wareham NJ,
Wilson JF,
Beauchamp JP,
Conley DC,
Esko T,
Lehrer SF,
Magnusson PKE,
Oskarsson S,
Pers TH,
Robinson MR,
Thom K,
Watson C,
Chabris CF,
Meyer MN,
Laibson DI,
Yang J,
Johannesson M,
Koellinger PD,
Turley P,
Visscher PM,
Benjamin DJ,
Cesarini D
23andMe Research Team · COGENT (Cognitive Genomics Consortium) 외 컨소시엄 1곳
Nature genetics · 2018 · PMID 30038396
페이지 12개+
A cross-platform approach identifies genetic regulators of human metabolism and health
Lotta LA,
Pietzner M,
Stewart ID,
Wittemans LBL,
Li C,
Bonelli R,
Raffler J,
Biggs EK,
Oliver-Williams C,
Auyeung VPW,
Luan J,
Wheeler E
외 22명 — 모두 보기
Paige E,
Surendran P,
Michelotti GA,
Scott RA,
Burgess S,
Zuber V,
Sanderson E,
Koulman A,
Imamura F,
Forouhi NG,
Khaw KT,
Griffin JL,
Wood AM,
Kastenmüller G,
Danesh J,
Butterworth AS,
Gribble FM,
Reimann F,
Bahlo M,
Fauman E,
Wareham NJ,
Langenberg C
MacTel Consortium
Nature genetics · 2021 · PMID 33414548
페이지 12개+
GWAS and ExWAS of blood mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia
Chong M,
Mohammadi-Shemirani P,
Perrot N,
Nelson W,
Morton R,
Narula S,
Lali R,
Khan I,
Khan M,
Judge C,
Machipisa T,
Cawte N
외 4명 — 모두 보기
eLife · 2022 · PMID 35023831 · open access
페이지 12개+
Multi-omic spatial effects on high-resolution AI-derived retinal thickness
Jackson VE,
Wu Y,
Bonelli R,
Owen JP,
Scott LW,
Farashi S,
Kihara Y,
Gantner ML,
Egan C,
Williams KM,
Ansell BRE,
Tufail A
외 2명 — 모두 보기
Nature communications · 2025 · PMID 39904976 · open access
페이지 12개+
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,
Stefansson K,
Uitterlinden AG,
Ralston SH,
Ioannidis JP,
Kiel DP,
Rivadeneira F
Nature genetics · 2012 · PMID 22504420 · open access
페이지 7개
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture
Zheng HF,
Forgetta V,
Hsu YH,
Estrada K,
Rosello-Diez A,
Leo PJ,
Dahia CL,
Park-Min KH,
Tobias JH,
Kooperberg C,
Kleinman A,
Styrkarsdottir U
외 146명 — 모두 보기
Liu CT,
Uggla C,
Evans DS,
Nielson CM,
Walter K,
Pettersson-Kymmer U,
McCarthy S,
Eriksson J,
Kwan T,
Jhamai M,
Trajanoska K,
Memari Y,
Min J,
Huang J,
Danecek P,
Wilmot B,
Li R,
Chou WC,
Mokry LE,
Moayyeri A,
Claussnitzer M,
Cheng CH,
Cheung W,
Medina-Gómez C,
Ge B,
Chen SH,
Choi K,
Oei L,
Fraser J,
Kraaij R,
Hibbs MA,
Gregson CL,
Paquette D,
Hofman A,
Wibom C,
Tranah GJ,
Marshall M,
Gardiner BB,
Cremin K,
Auer P,
Hsu L,
Ring S,
Tung JY,
Thorleifsson G,
Enneman AW,
van Schoor NM,
de Groot LC,
van der Velde N,
Melin B,
Kemp JP,
Christiansen C,
Sayers A,
Zhou Y,
Calderari S,
van Rooij J,
Carlson C,
Peters U,
Berlivet S,
Dostie J,
Uitterlinden AG,
Williams SR,
Farber C,
Grinberg D,
LaCroix AZ,
Haessler J,
Chasman DI,
Giulianini F,
Rose LM,
Ridker PM,
Eisman JA,
Nguyen TV,
Center JR,
Nogues X,
Nogues X,
Garcia-Giralt N,
Launer LL,
Gudnason V,
Mellström D,
Vandenput L,
Amin N,
van Duijn CM,
Karlsson MK,
Ljunggren Ö,
Svensson O,
Hallmans G,
Rousseau F,
Giroux S,
Bussière J,
Arp PP,
Koromani F,
Prince RL,
Lewis JR,
Langdahl BL,
Hermann AP,
Jensen JE,
Kaptoge S,
Khaw KT,
Reeve J,
Formosa MM,
Xuereb-Anastasi A,
Åkesson K,
McGuigan FE,
Garg G,
Olmos JM,
Zarrabeitia MT,
Riancho JA,
Ralston SH,
Alonso N,
Jiang X,
Goltzman D,
Pastinen T,
Grundberg E,
Gauguier D,
Orwoll ES,
Karasik D,
Davey-Smith G,
Smith AV,
Smith AV,
Siggeirsdottir K,
Harris TB,
Zillikens MC,
van Meurs JB,
Thorsteinsdottir U,
Maurano MT,
Timpson NJ,
Soranzo N,
Durbin R,
Wilson SG,
Ntzani EE,
Brown MA,
Stefansson K,
Hinds DA,
Spector T,
Cupples LA,
Ohlsson C,
Greenwood CM,
Jackson RD,
Rowe DW,
Loomis CA,
Evans DM,
Ackert-Bicknell CL,
Joyner AL,
Duncan EL,
Kiel DP,
Rivadeneira F,
Richards JB
AOGC Consortium · UK10K Consortium
Nature · 2015 · PMID 26367794
페이지 7개
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Verhoeven VJ,
Hysi PG,
Wojciechowski R,
Fan Q,
Guggenheim JA,
Höhn R,
MacGregor S,
Hewitt AW,
Nag A,
Cheng CY,
Yonova-Doing E,
Zhou X
외 96명 — 모두 보기
Ikram MK,
Buitendijk GH,
McMahon G,
Kemp JP,
Pourcain BS,
Simpson CL,
Mäkelä KM,
Lehtimäki T,
Kähönen M,
Paterson AD,
Hosseini SM,
Wong HS,
Xu L,
Jonas JB,
Pärssinen O,
Wedenoja J,
Yip SP,
Ho DW,
Pang CP,
Chen LJ,
Burdon KP,
Craig JE,
Klein BE,
Klein R,
Haller T,
Metspalu A,
Khor CC,
Tai ES,
Aung T,
Vithana E,
Tay WT,
Barathi VA,
Chen P,
Li R,
Liao J,
Zheng Y,
Ong RT,
Döring A,
Evans DM,
Timpson NJ,
Verkerk AJ,
Meitinger T,
Raitakari O,
Hawthorne F,
Spector TD,
Karssen LC,
Pirastu M,
Murgia F,
Ang W,
Mishra A,
Montgomery GW,
Pennell CE,
Cumberland PM,
Cotlarciuc I,
Mitchell P,
Wang JJ,
Schache M,
Janmahasatian S,
Igo RP Jr,
Lass JH,
Chew E,
Iyengar SK,
Gorgels TG,
Rudan I,
Hayward C,
Wright AF,
Polasek O,
Vatavuk Z,
Wilson JF,
Fleck B,
Zeller T,
Mirshahi A,
Müller C,
Uitterlinden AG,
Rivadeneira F,
Vingerling JR,
Hofman A,
Oostra BA,
Amin N,
Bergen AA,
Teo YY,
Rahi JS,
Vitart V,
Williams C,
Baird PN,
Wong TY,
Oexle K,
Pfeiffer N,
Mackey DA,
Young TL,
van Duijn CM,
Saw SM,
Bailey-Wilson JE,
Stambolian D,
Klaver CC,
Hammond CJ
Consortium for Refractive Error and Myopia (CREAM) · Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group 외 컨소시엄 2곳
Nature genetics · 2013 · PMID 23396134
페이지 6개
A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy
Yu XQ,
Li M,
Zhang H,
Low HQ,
Wei X,
Wang JQ,
Sun LD,
Sim KS,
Li Y,
Foo JN,
Wang W,
Li ZJ
외 13명 — 모두 보기
Yin XY,
Tang XQ,
Fan L,
Chen J,
Li RS,
Wan JX,
Liu ZS,
Lou TQ,
Zhu L,
Huang XJ,
Zhang XJ,
Liu ZH,
Liu JJ
Nature genetics · 2011 · PMID 22197929
페이지 5개
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer
Wolpin BM,
Rizzato C,
Kraft P,
Kooperberg C,
Petersen GM,
Wang Z,
Arslan AA,
Beane-Freeman L,
Bracci PM,
Buring J,
Canzian F,
Duell EJ
외 106명 — 모두 보기
Gallinger S,
Giles GG,
Goodman GE,
Goodman PJ,
Jacobs EJ,
Kamineni A,
Klein AP,
Kolonel LN,
Kulke MH,
Li D,
Malats N,
Olson SH,
Risch HA,
Sesso HD,
Visvanathan K,
White E,
Zheng W,
Zheng W,
Abnet CC,
Albanes D,
Andreotti G,
Austin MA,
Barfield R,
Basso D,
Berndt SI,
Boutron-Ruault MC,
Brotzman M,
Büchler MW,
Bueno-de-Mesquita HB,
Bugert P,
Burdette L,
Campa D,
Caporaso NE,
Capurso G,
Chung C,
Cotterchio M,
Costello E,
Elena J,
Funel N,
Gaziano JM,
Giese NA,
Giovannucci EL,
Goggins M,
Gorman MJ,
Gross M,
Haiman CA,
Hassan M,
Helzlsouer KJ,
Henderson BE,
Holly EA,
Hu N,
Hunter DJ,
Innocenti F,
Jenab M,
Kaaks R,
Key TJ,
Khaw KT,
Klein EA,
Kogevinas M,
Krogh V,
Kupcinskas J,
Kurtz RC,
LaCroix A,
Landi MT,
Landi S,
Le Marchand L,
Mambrini A,
Mannisto S,
Milne RL,
Nakamura Y,
Oberg AL,
Owzar K,
Patel AV,
Peeters PH,
Peters U,
Pezzilli R,
Piepoli A,
Porta M,
Real FX,
Riboli E,
Rothman N,
Scarpa A,
Shu XO,
Silverman DT,
Soucek P,
Sund M,
Talar-Wojnarowska R,
Taylor PR,
Theodoropoulos GE,
Thornquist M,
Tjønneland A,
Tobias GS,
Trichopoulos D,
Vodicka P,
Wactawski-Wende J,
Wentzensen N,
Wu C,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Hoover R,
Hartge P,
Fuchs C,
Chanock SJ,
Stolzenberg-Solomon RS,
Amundadottir LT
Nature genetics · 2014 · PMID 25086665 · open access
페이지 5개
The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype
Stanaway IB,
Hall TO,
Rosenthal EA,
Palmer M,
Naranbhai V,
Knevel R,
Namjou-Khales B,
Carroll RJ,
Kiryluk K,
Gordon AS,
Linder J,
Howell KM
외 28명 — 모두 보기
Mapes BM,
Lin FTJ,
Joo YY,
Hayes MG,
Gharavi AG,
Pendergrass SA,
Ritchie MD,
de Andrade M,
Croteau-Chonka DC,
Raychaudhuri S,
Weiss ST,
Lebo M,
Amr SS,
Carrell D,
Larson EB,
Chute CG,
Rasmussen-Torvik LJ,
Roy-Puckelwartz MJ,
Sleiman P,
Hakonarson H,
Li R,
Karlson EW,
Peterson JF,
Kullo IJ,
Chisholm R,
Denny JC,
Jarvik GP,
Crosslin DR
eMERGE Network
Genetic epidemiology · 2019 · PMID 30298529 · open access
페이지 5개
Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer
Klein AP,
Wolpin BM,
Risch HA,
Stolzenberg-Solomon RZ,
Mocci E,
Zhang M,
Canzian F,
Childs EJ,
Hoskins JW,
Jermusyk A,
Zhong J,
Chen F
외 112명 — 모두 보기
Albanes D,
Andreotti G,
Arslan AA,
Babic A,
Bamlet WR,
Beane-Freeman L,
Berndt SI,
Blackford A,
Borges M,
Borgida A,
Bracci PM,
Brais L,
Brennan P,
Brenner H,
Bueno-de-Mesquita B,
Buring J,
Campa D,
Capurso G,
Cavestro GM,
Chaffee KG,
Chung CC,
Cleary S,
Cotterchio M,
Dijk F,
Duell EJ,
Foretova L,
Fuchs C,
Funel N,
Gallinger S,
M Gaziano JM,
Gazouli M,
Giles GG,
Giovannucci E,
Goggins M,
Goodman GE,
Goodman PJ,
Hackert T,
Haiman C,
Hartge P,
Hasan M,
Hegyi P,
Helzlsouer KJ,
Herman J,
Holcatova I,
Holly EA,
Hoover R,
Hung RJ,
Jacobs EJ,
Jamroziak K,
Janout V,
Kaaks R,
Khaw KT,
Klein EA,
Kogevinas M,
Kooperberg C,
Kulke MH,
Kupcinskas J,
Kurtz RJ,
Laheru D,
Landi S,
Lawlor RT,
Lee IM,
LeMarchand L,
Lu L,
Malats N,
Mambrini A,
Mannisto S,
Milne RL,
Mohelníková-Duchoňová B,
Neale RE,
Neoptolemos JP,
Oberg AL,
Olson SH,
Orlow I,
Pasquali C,
Patel AV,
Peters U,
Pezzilli R,
Porta M,
Real FX,
Rothman N,
Scelo G,
Sesso HD,
Severi G,
Shu XO,
Silverman D,
Smith JP,
Soucek P,
Sund M,
Talar-Wojnarowska R,
Tavano F,
Thornquist MD,
Tobias GS,
Van Den Eeden SK,
Vashist Y,
Visvanathan K,
Vodicka P,
Wactawski-Wende J,
Wang Z,
Wentzensen N,
White E,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Zheng W,
Zheng W,
Kraft P,
Li D,
Chanock S,
Obazee O,
Petersen GM,
Amundadottir LT
Nature communications · 2018 · PMID 29422604 · open access
페이지 4개
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
Ellinor PT,
Lunetta KL,
Albert CM,
Glazer NL,
Ritchie MD,
Smith AV,
Arking DE,
Müller-Nurasyid M,
Krijthe BP,
Lubitz SA,
Bis JC,
Chung MK
외 77명 — 모두 보기
Dörr M,
Ozaki K,
Roberts JD,
Smith JG,
Pfeufer A,
Sinner MF,
Lohman K,
Ding J,
Smith NL,
Smith JD,
Rienstra M,
Rice KM,
Van Wagoner DR,
Magnani JW,
Wakili R,
Clauss S,
Rotter JI,
Steinbeck G,
Launer LJ,
Davies RW,
Borkovich M,
Harris TB,
Lin H,
Völker U,
Völzke H,
Milan DJ,
Hofman A,
Boerwinkle E,
Chen LY,
Soliman EZ,
Voight BF,
Li G,
Chakravarti A,
Kubo M,
Tedrow UB,
Rose LM,
Ridker PM,
Conen D,
Tsunoda T,
Furukawa T,
Sotoodehnia N,
Xu S,
Kamatani N,
Levy D,
Nakamura Y,
Parvez B,
Mahida S,
Furie KL,
Rosand J,
Muhammad R,
Psaty BM,
Meitinger T,
Perz S,
Wichmann HE,
Witteman JC,
Kao WH,
Kathiresan S,
Roden DM,
Uitterlinden AG,
Rivadeneira F,
McKnight B,
Sjögren M,
Newman AB,
Liu Y,
Gollob MH,
Melander O,
Tanaka T,
Stricker BH,
Felix SB,
Alonso A,
Darbar D,
Barnard J,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Gudnason V,
Kääb S
Nature genetics · 2012 · PMID 22544366
페이지 3개
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
Li R,
Brockschmidt FF,
Kiefer AK,
Stefansson H,
Nyholt DR,
Song K,
Vermeulen SH,
Kanoni S,
Glass D,
Medland SE,
Dimitriou M,
Waterworth D
외 27명 — 모두 보기
Tung JY,
Geller F,
Heilmann S,
Hillmer AM,
Bataille V,
Eigelshoven S,
Hanneken S,
Moebus S,
Herold C,
den Heijer M,
Montgomery GW,
Deloukas P,
Eriksson N,
Heath AC,
Becker T,
Sulem P,
Mangino M,
Vollenweider P,
Spector TD,
Dedoussis G,
Martin NG,
Kiemeney LA,
Mooser V,
Stefansson K,
Hinds DA,
Nöthen MM,
Richards JB
PLoS genetics · 2012 · PMID 22693459 · open access
페이지 3개
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk
Ritchie MD,
Denny JC,
Zuvich RL,
Crawford DC,
Schildcrout JS,
Bastarache L,
Ramirez AH,
Mosley JD,
Pulley JM,
Basford MA,
Bradford Y,
Rasmussen LV
외 15명 — 모두 보기
Pathak J,
Chute CG,
Kullo IJ,
McCarty CA,
Chisholm RL,
Kho AN,
Carlson CS,
Larson EB,
Jarvik GP,
Sotoodehnia N,
Manolio TA,
Li R,
Masys DR,
Haines JL,
Roden DM
Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) QRS Group
Circulation · 2013 · PMID 23463857
페이지 3개
Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer
Childs EJ,
Mocci E,
Campa D,
Bracci PM,
Gallinger S,
Goggins M,
Li D,
Neale RE,
Olson SH,
Scelo G,
Amundadottir LT,
Bamlet WR
외 50명 — 모두 보기
Bijlsma MF,
Blackford A,
Borges M,
Brennan P,
Brenner H,
Bueno-de-Mesquita HB,
Canzian F,
Capurso G,
Cavestro GM,
Chaffee KG,
Chanock SJ,
Cleary SP,
Cotterchio M,
Foretova L,
Fuchs C,
Funel N,
Gazouli M,
Hassan M,
Herman JM,
Holcatova I,
Holly EA,
Hoover RN,
Hung RJ,
Janout V,
Key TJ,
Kupcinskas J,
Kurtz RC,
Landi S,
Lu L,
Malecka-Panas E,
Mambrini A,
Mohelnikova-Duchonova B,
Neoptolemos JP,
Oberg AL,
Orlow I,
Pasquali C,
Pezzilli R,
Rizzato C,
Saldia A,
Scarpa A,
Stolzenberg-Solomon RZ,
Strobel O,
Tavano F,
Vashist YK,
Vodicka P,
Wolpin BM,
Yu H,
Petersen GM,
Risch HA,
Klein AP
Nature genetics · 2015 · PMID 26098869 · open access
페이지 3개
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Lu Y,
Day FR,
Gustafsson S,
Buchkovich ML,
Na J,
Bataille V,
Cousminer DL,
Dastani Z,
Drong AW,
Esko T,
Evans DM,
Falchi M
외 247명 — 모두 보기
Feitosa MF,
Ferreira T,
Hedman ÅK,
Haring R,
Hysi PG,
Iles MM,
Justice AE,
Kanoni S,
Lagou V,
Li R,
Li X,
Locke A,
Lu C,
Mägi R,
Perry JR,
Pers TH,
Qi Q,
Sanna M,
Schmidt EM,
Scott WR,
Shungin D,
Teumer A,
Vinkhuyzen AA,
Walker RW,
Westra HJ,
Zhang M,
Zhang W,
Zhao JH,
Zhu Z,
Afzal U,
Ahluwalia TS,
Bakker SJ,
Bellis C,
Bonnefond A,
Borodulin K,
Buchman AS,
Cederholm T,
Choh AC,
Choi HJ,
Curran JE,
de Groot LC,
De Jager PL,
Dhonukshe-Rutten RA,
Enneman AW,
Eury E,
Evans DS,
Forsen T,
Friedrich N,
Fumeron F,
Garcia ME,
Gärtner S,
Han BG,
Havulinna AS,
Hayward C,
Hernandez D,
Hillege H,
Ittermann T,
Kent JW,
Kolcic I,
Laatikainen T,
Lahti J,
Mateo Leach I,
Lee CG,
Lee JY,
Liu T,
Liu Y,
Lobbens S,
Loh M,
Lyytikäinen LP,
Medina-Gomez C,
Michaëlsson K,
Nalls MA,
Nielson CM,
Oozageer L,
Pascoe L,
Paternoster L,
Polašek O,
Ripatti S,
Sarzynski MA,
Shin CS,
Narančić NS,
Spira D,
Srikanth P,
Steinhagen-Thiessen E,
Sung YJ,
Swart KM,
Taittonen L,
Tanaka T,
Tikkanen E,
van der Velde N,
van Schoor NM,
Verweij N,
Wright AF,
Yu L,
Zmuda JM,
Eklund N,
Forrester T,
Grarup N,
Jackson AU,
Kristiansson K,
Kuulasmaa T,
Kuusisto J,
Lichtner P,
Luan J,
Mahajan A,
Männistö S,
Palmer CD,
Ried JS,
Scott RA,
Stancáková A,
Wagner PJ,
Demirkan A,
Döring A,
Gudnason V,
Kiel DP,
Kühnel B,
Mangino M,
Mcknight B,
Menni C,
O'Connell JR,
Oostra BA,
Shuldiner AR,
Song K,
Vandenput L,
van Duijn CM,
Vollenweider P,
White CC,
Boehnke M,
Boettcher Y,
Cooper RS,
Forouhi NG,
Gieger C,
Grallert H,
Hingorani A,
Jørgensen T,
Jousilahti P,
Kivimaki M,
Kumari M,
Laakso M,
Langenberg C,
Linneberg A,
Luke A,
Mckenzie CA,
Palotie A,
Pedersen O,
Peters A,
Strauch K,
Tayo BO,
Wareham NJ,
Bennett DA,
Bertram L,
Blangero J,
Blüher M,
Bouchard C,
Campbell H,
Cho NH,
Cummings SR,
Czerwinski SA,
Demuth I,
Eckardt R,
Eriksson JG,
Ferrucci L,
Franco OH,
Froguel P,
Gansevoort RT,
Hansen T,
Harris TB,
Hastie N,
Heliövaara M,
Hofman A,
Jordan JM,
Jula A,
Kähönen M,
Kajantie E,
Knekt PB,
Koskinen S,
Kovacs P,
Lehtimäki T,
Lind L,
Liu Y,
Orwoll ES,
Osmond C,
Perola M,
Pérusse L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Rivadeneira F,
Rudan I,
Salomaa V,
Sørensen TI,
Stumvoll M,
Tönjes A,
Towne B,
Tranah GJ,
Tremblay A,
Uitterlinden AG,
van der Harst P,
Vartiainen E,
Viikari JS,
Vitart V,
Vohl MC,
Völzke H,
Walker M,
Wallaschofski H,
Wild S,
Wilson JF,
Yengo L,
Bishop DT,
Borecki IB,
Chambers JC,
Cupples LA,
Dehghan A,
Deloukas P,
Fatemifar G,
Fox C,
Furey TS,
Franke L,
Han J,
Hunter DJ,
Karjalainen J,
Karpe F,
Kaplan RC,
Kooner JS,
McCarthy MI,
Murabito JM,
Morris AP,
Bishop JA,
North KE,
Ohlsson C,
Ong KK,
Prokopenko I,
Richards JB,
Schadt EE,
Spector TD,
Widén E,
Willer CJ,
Yang J,
Ingelsson E,
Mohlke KL,
Hirschhorn JN,
Pospisilik JA,
Zillikens MC,
Lindgren C,
Kilpeläinen TO,
Loos RJ
Nature communications · 2016 · PMID 26833246 · open access
페이지 3개
Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21
Zhang M,
Wang Z,
Obazee O,
Jia J,
Childs EJ,
Hoskins J,
Figlioli G,
Mocci E,
Collins I,
Chung CC,
Hautman C,
Arslan AA
외 112명 — 모두 보기
Beane-Freeman L,
Bracci PM,
Buring J,
Duell EJ,
Gallinger S,
Giles GG,
Goodman GE,
Goodman PJ,
Kamineni A,
Kolonel LN,
Kulke MH,
Malats N,
Olson SH,
Sesso HD,
Visvanathan K,
White E,
Zheng W,
Zheng W,
Abnet CC,
Albanes D,
Andreotti G,
Brais L,
Bueno-de-Mesquita HB,
Basso D,
Berndt SI,
Boutron-Ruault MC,
Bijlsma MF,
Brenner H,
Burdette L,
Campa D,
Caporaso NE,
Capurso G,
Cavestro GM,
Cotterchio M,
Costello E,
Elena J,
Boggi U,
Gaziano JM,
Gazouli M,
Giovannucci EL,
Goggins M,
Gross M,
Haiman CA,
Hassan M,
Helzlsouer KJ,
Hu N,
Hunter DJ,
Iskierka-Jazdzewska E,
Jenab M,
Kaaks R,
Key TJ,
Khaw KT,
Klein EA,
Kogevinas M,
Krogh V,
Kupcinskas J,
Kurtz RC,
Landi MT,
Landi S,
Le Marchand L,
Mambrini A,
Mannisto S,
Milne RL,
Neale RE,
Oberg AL,
Panico S,
Patel AV,
Peeters PH,
Peters U,
Pezzilli R,
Porta M,
Purdue M,
Quiros JR,
Riboli E,
Rothman N,
Scarpa A,
Scelo G,
Shu XO,
Silverman DT,
Soucek P,
Strobel O,
Sund M,
Małecka-Panas E,
Taylor PR,
Tavano F,
Travis RC,
Thornquist M,
Tjønneland A,
Tobias GS,
Trichopoulos D,
Vashist Y,
Vodicka P,
Wactawski-Wende J,
Wentzensen N,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Kooperberg C,
Risch HA,
Jacobs EJ,
Li D,
Fuchs C,
Hoover R,
Hartge P,
Chanock SJ,
Petersen GM,
Stolzenberg-Solomon RS,
Wolpin BM,
Kraft P,
Klein AP,
Canzian F,
Amundadottir LT
Oncotarget · 2016 · PMID 27579533 · open access
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