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115건, 그중 20건 표시.
Genome-wide association studies and CRISPR/Cas9-mediated gene editing identify regulatory variants influencing eyebrow thickness in humans
Wu S,
Zhang M,
Yang X,
Peng F,
Zhang J,
Tan J,
Yang Y,
Wang L,
Hu Y,
Peng Q,
Li J,
Liu Y
외 24명 — 모두 보기
Guan Y,
Chen C,
Hamer MA,
Nijsten T,
Zeng C,
Adhikari K,
Gallo C,
Poletti G,
Schuler-Faccini L,
Bortolini MC,
Canizales-Quinteros S,
Rothhammer F,
Bedoya G,
González-José R,
Li H,
Krutmann J,
Liu F,
Kayser M,
Ruiz-Linares A,
Tang K,
Xu S,
Zhang L,
Jin L,
Wang S
PLoS genetics · 2018 · PMID 30248107 · open access
페이지 2개
Common variants at 5q33.1 predispose to migraine in African-American children
Chang X,
Pellegrino R,
Garifallou J,
March M,
Snyder J,
Mentch F,
Li J,
Hou C,
Liu Y,
Sleiman PMA,
Hakonarson H
Journal of medical genetics · 2018 · PMID 30266756
페이지 2개
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology
Spracklen CN,
Karaderi T,
Yaghootkar H,
Schurmann C,
Fine RS,
Kutalik Z,
Preuss MH,
Lu Y,
Wittemans LBL,
Adair LS,
Allison M,
Amin N
외 92명 — 모두 보기
Auer PL,
Bartz TM,
Blüher M,
Boehnke M,
Borja JB,
Bork-Jensen J,
Broer L,
Chasman DI,
Chen YI,
Chirstofidou P,
Demirkan A,
van Duijn CM,
Feitosa MF,
Garcia ME,
Graff M,
Grallert H,
Grarup N,
Guo X,
Haesser J,
Hansen T,
Harris TB,
Highland HM,
Hong J,
Ikram MA,
Ingelsson E,
Jackson R,
Jousilahti P,
Kähönen M,
Kizer JR,
Kovacs P,
Kriebel J,
Laakso M,
Lange LA,
Lehtimäki T,
Li J,
Li-Gao R,
Lind L,
Luan J,
Lyytikäinen LP,
MacGregor S,
Mackey DA,
Mahajan A,
Mangino M,
Männistö S,
McCarthy MI,
McKnight B,
Medina-Gomez C,
Meigs JB,
Molnos S,
Mook-Kanamori D,
Morris AP,
de Mutsert R,
Nalls MA,
Nedeljkovic I,
North KE,
Pennell CE,
Pradhan AD,
Province MA,
Raitakari OT,
Raulerson CK,
Reiner AP,
Ridker PM,
Ripatti S,
Roberston N,
Rotter JI,
Salomaa V,
Sandoval-Zárate AA,
Sitlani CM,
Spector TD,
Strauch K,
Stumvoll M,
Taylor KD,
Thuesen B,
Tönjes A,
Uitterlinden AG,
Venturini C,
Walker M,
Wang CA,
Wang S,
Wareham NJ,
Willems SM,
Willems van Dijk K,
Wilson JG,
Wu Y,
Yao J,
Young KL,
Langenberg C,
Frayling TM,
Kilpeläinen TO,
Lindgren CM,
Loos RJF,
Mohlke KL
American journal of human genetics · 2019 · PMID 31178129
페이지 2개
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Zhang H,
Ahearn TU,
Lecarpentier J,
Barnes D,
Beesley J,
Qi G,
Jiang X,
O'Mara TA,
Zhao N,
Bolla MK,
Dunning AM,
Dennis J
외 261명 — 모두 보기
Wang Q,
Ful ZA,
Aittomäki K,
Andrulis IL,
Anton-Culver H,
Arndt V,
Aronson KJ,
Arun BK,
Auer PL,
Azzollini J,
Barrowdale D,
Becher H,
Beckmann MW,
Behrens S,
Benitez J,
Bermisheva M,
Bialkowska K,
Blanco A,
Blomqvist C,
Bogdanova NV,
Bojesen SE,
Bonanni B,
Bondavalli D,
Borg A,
Brauch H,
Brenner H,
Briceno I,
Broeks A,
Brucker SY,
Brüning T,
Burwinkel B,
Buys SS,
Byers H,
Caldés T,
Caligo MA,
Calvello M,
Campa D,
Castelao JE,
Chang-Claude J,
Chanock SJ,
Christiaens M,
Christiansen H,
Chung WK,
Claes KBM,
Clarke CL,
Cornelissen S,
Couch FJ,
Cox A,
Cross SS,
Czene K,
Daly MB,
Devilee P,
Diez O,
Domchek SM,
Dörk T,
Dwek M,
Eccles DM,
Ekici AB,
Evans DG,
Fasching PA,
Figueroa J,
Foretova L,
Fostira F,
Friedman E,
Frost D,
Gago-Dominguez M,
Gapstur SM,
Garber J,
García-Sáenz JA,
Gaudet MM,
Gayther SA,
Giles GG,
Godwin AK,
Goldberg MS,
Goldgar DE,
González-Neira A,
Greene MH,
Gronwald J,
Guénel P,
Häberle L,
Hahnen E,
Haiman CA,
Hake CR,
Hall P,
Hamann U,
Harkness EF,
Heemskerk-Gerritsen BAM,
Hillemanns P,
Hogervorst FBL,
Holleczek B,
Hollestelle A,
Hooning MJ,
Hoover RN,
Hopper JL,
Howell A,
Huebner H,
Hulick PJ,
Imyanitov EN,
Isaacs C,
Izatt L,
Jager A,
Jakimovska M,
Jakubowska A,
James P,
Janavicius R,
Janni W,
John EM,
Jones ME,
Jung A,
Kaaks R,
Kapoor PM,
Karlan BY,
Keeman R,
Khan S,
Khusnutdinova E,
Kitahara CM,
Ko YD,
Konstantopoulou I,
Koppert LB,
Koutros S,
Kristensen VN,
Laenkholm AV,
Lambrechts D,
Larsson SC,
Laurent-Puig P,
Lazaro C,
Lazarova E,
Lejbkowicz F,
Leslie G,
Lesueur F,
Lindblom A,
Lissowska J,
Lo WY,
Loud JT,
Lubinski J,
Lukomska A,
MacInnis RJ,
Mannermaa A,
Manoochehri M,
Manoukian S,
Margolin S,
Martinez ME,
Matricardi L,
McGuffog L,
McLean C,
Mebirouk N,
Meindl A,
Menon U,
Miller A,
Mingazheva E,
Montagna M,
Mulligan AM,
Mulot C,
Muranen TA,
Nathanson KL,
Neuhausen SL,
Nevanlinna H,
Neven P,
Newman WG,
Nielsen FC,
Nikitina-Zake L,
Nodora J,
Offit K,
Olah E,
Olopade OI,
Olsson H,
Orr N,
Papi L,
Papp J,
Park-Simon TW,
Parsons MT,
Peissel B,
Peixoto A,
Peshkin B,
Peterlongo P,
Peto J,
Phillips KA,
Piedmonte M,
Plaseska-Karanfilska D,
Prajzendanc K,
Prentice R,
Prokofyeva D,
Rack B,
Radice P,
Ramus SJ,
Rantala J,
Rashid MU,
Rennert G,
Rennert HS,
Risch HA,
Romero A,
Rookus MA,
Rübner M,
Rüdiger T,
Saloustros E,
Sampson S,
Sandler DP,
Sawyer EJ,
Scheuner MT,
Schmutzler RK,
Schneeweiss A,
Schoemaker MJ,
Schöttker B,
Schürmann P,
Senter L,
Sharma P,
Sherman ME,
Shu XO,
Singer CF,
Smichkoska S,
Soucy P,
Southey MC,
Spinelli JJ,
Stone J,
Stoppa-Lyonnet D,
Swerdlow AJ,
Szabo CI,
Tamimi RM,
Tapper WJ,
Taylor JA,
Teixeira MR,
Terry M,
Thomassen M,
Thull DL,
Tischkowitz M,
Toland AE,
Tollenaar RAEM,
Tomlinson I,
Torres D,
Troester MA,
Truong T,
Tung N,
Untch M,
Vachon CM,
van den Ouweland AMW,
van der Kolk LE,
van Veen EM,
vanRensburg EJ,
Vega A,
Wappenschmidt B,
Weinberg CR,
Weitzel JN,
Wildiers H,
Winqvist R,
Wolk A,
Yang XR,
Yannoukakos D,
Zheng W,
Zheng W,
Zorn KK,
Milne RL,
Kraft P,
Simard J,
Pharoah PDP,
Michailidou K,
Antoniou AC,
Schmidt MK,
Chenevix-Trench G,
Easton DF,
Chatterjee N,
García-Closas M
kConFab Investigators · ABCTB Investigators 외 컨소시엄 2곳
Nature genetics · 2020 · PMID 32424353 · open access
페이지 2개
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23
Garnier S,
Harakalova M,
Weiss S,
Mokry M,
Regitz-Zagrosek V,
Hengstenberg C,
Cappola TP,
Isnard R,
Arbustini E,
Cook SA,
van Setten J,
Calis JJA
외 64명 — 모두 보기
Hakonarson H,
Morley MP,
Stark K,
Prasad SK,
Li J,
O'Regan DP,
Grasso M,
Müller-Nurasyid M,
Meitinger T,
Empana JP,
Strauch K,
Waldenberger M,
Marguiles KB,
Seidman CE,
Kararigas G,
Meder B,
Haas J,
Boutouyrie P,
Lacolley P,
Jouven X,
Erdmann J,
Blankenberg S,
Wichter T,
Ruppert V,
Tavazzi L,
Dubourg O,
Roizes G,
Dorent R,
de Groote P,
Fauchier L,
Trochu JN,
Aupetit JF,
Bilinska ZT,
Germain M,
Völker U,
Hemerich D,
Raji I,
Bacq-Daian D,
Proust C,
Remior P,
Gomez-Bueno M,
Lehnert K,
Maas R,
Olaso R,
Saripella GV,
Felix SB,
McGinn S,
Duboscq-Bidot L,
van Mil A,
Besse C,
Fontaine V,
Blanché H,
Ader F,
Keating B,
Curjol A,
Boland A,
Komajda M,
Cambien F,
Deleuze JF,
Dörr M,
Asselbergs FW,
Villard E,
Trégouët DA,
Charron P
European heart journal · 2021 · PMID 33677556
페이지 2개
Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported loci
Qu HQ,
Qu J,
Bradfield J,
Marchand L,
Glessner J,
Chang X,
March M,
Li J,
Connolly JJ,
Roizen JD,
Sleiman P,
Polychronakos C
외 1명 — 모두 보기
Communications biology · 2021 · PMID 34302048 · open access
페이지 2개
Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy
Ollila HM,
Sharon E,
Lin L,
Sinnott-Armstrong N,
Ambati A,
Yogeshwar SM,
Hillary RP,
Jolanki O,
Faraco J,
Einen M,
Luo G,
Zhang J
외 78명 — 모두 보기
Han F,
Yan H,
Dong XS,
Li J,
Zhang J,
Hong SC,
Kim TW,
Dauvilliers Y,
Barateau L,
Lammers GJ,
Fronczek R,
Mayer G,
Santamaria J,
Arnulf I,
Knudsen-Heier S,
Bredahl MKL,
Thorsby PM,
Plazzi G,
Pizza F,
Moresco M,
Crowe C,
Van den Eeden SK,
Lecendreux M,
Bourgin P,
Kanbayashi T,
Martínez-Orozco FJ,
Peraita-Adrados R,
Benetó A,
Montplaisir J,
Desautels A,
Huang YS,
Jennum P,
Nevsimalova S,
Kemlink D,
Iranzo A,
Overeem S,
Wierzbicka A,
Geisler P,
Sonka K,
Honda M,
Högl B,
Stefani A,
Coelho FM,
Mantovani V,
Feketeova E,
Wadelius M,
Eriksson N,
Smedje H,
Hallberg P,
Hesla PE,
Rye D,
Pelin Z,
Ferini-Strambi L,
Bassetti CL,
Mathis J,
Khatami R,
Aran A,
Nampoothiri S,
Olsson T,
Kockum I,
Partinen M,
Perola M,
Kornum BR,
Rueger S,
Winkelmann J,
Miyagawa T,
Toyoda H,
Khor SS,
Shimada M,
Tokunaga K,
Rivas M,
Pritchard JK,
Risch N,
Kutalik Z,
O'Hara R,
Hallmayer J,
Ye CJ,
Mignot EJ
FinnGen
Nature communications · 2023 · PMID 37188663 · open access
페이지 2개
Genome-wide association meta-analysis of human olfactory identification discovers sex-specific and sex-differential genetic variants
Förster F,
Emmert D,
Horn K,
Pott J,
Frasnelli J,
Imtiaz MA,
Melas K,
Talevi V,
Chen H,
Engel C,
Filosi M,
Fornage M
외 11명 — 모두 보기
Gögele M,
Löffler M,
Mosley TH,
Pattaro C,
Pramstaller P,
Shrestha S,
Aziz NA,
Breteler MMB,
Wirkner K,
Scholz M,
Fuchsberger C
Nature communications · 2025 · PMID 40593737 · open access
페이지 2개
Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus
Han JW,
Zheng HF,
Cui Y,
Sun LD,
Ye DQ,
Hu Z,
Xu JH,
Cai ZM,
Huang W,
Zhao GP,
Xie HF,
Fang H
외 55명 — 모두 보기
Lu QJ,
Xu JH,
Li XP,
Pan YF,
Deng DQ,
Zeng FQ,
Ye ZZ,
Zhang XY,
Wang QW,
Hao F,
Ma L,
Zuo XB,
Zhou FS,
Du WH,
Cheng YL,
Yang JQ,
Shen SK,
Li J,
Sheng YJ,
Zuo XX,
Zhu WF,
Gao F,
Zhang PL,
Guo Q,
Li B,
Gao M,
Xiao FL,
Quan C,
Zhang C,
Zhang Z,
Zhu KJ,
Li Y,
Hu DY,
Lu WS,
Huang JL,
Liu SX,
Li H,
Ren YQ,
Wang ZX,
Yang CJ,
Wang PG,
Zhou WM,
Lv YM,
Zhang AP,
Zhang SQ,
Lin D,
Li Y,
Low HQ,
Shen M,
Zhai ZF,
Wang Y,
Zhang FY,
Yang S,
Liu JJ,
Zhang XJ
Nature genetics · 2009 · PMID 19838193
페이지 1개
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease
Lu X,
Wang L,
Chen S,
He L,
Yang X,
Shi Y,
Cheng J,
Zhang L,
Gu CC,
Huang J,
Wu T,
Ma Y
외 68명 — 모두 보기
Li J,
Cao J,
Chen J,
Ge D,
Fan Z,
Li Y,
Zhao L,
Li H,
Zhou X,
Chen L,
Liu D,
Chen J,
Duan X,
Hao Y,
Wang L,
Lu F,
Liu Z,
Yao C,
Shen C,
Pu X,
Yu L,
Fang X,
Xu L,
Mu J,
Wu X,
Zheng R,
Wu N,
Zhao Q,
Li Y,
Liu X,
Wang M,
Yu D,
Hu D,
Ji X,
Guo D,
Sun D,
Wang Q,
Yang Y,
Liu F,
Mao Q,
Liang X,
Ji J,
Chen P,
Mo X,
Li D,
Chai G,
Tang Y,
Li X,
Du Z,
Liu X,
Dou C,
Yang Z,
Meng Q,
Wang D,
Wang R,
Yang J,
Schunkert H,
Samani NJ,
Kathiresan S,
Reilly MP,
Erdmann J,
Peng X,
Wu X,
Liu D,
Yang Y,
Chen R,
Qiang B,
Gu D
Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Consortium
Nature genetics · 2012 · PMID 22751097
페이지 1개
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association
Desch KC,
Ozel AB,
Siemieniak D,
Kalish Y,
Shavit JA,
Thornburg CD,
Sharathkumar AA,
McHugh CP,
Laurie CC,
Crenshaw A,
Mirel DB,
Kim Y
외 10명 — 모두 보기
Proceedings of the National Academy of Sciences of the United States of America · 2013 · PMID 23267103
페이지 1개
Genome-wide association study of B cell non-Hodgkin lymphoma identifies 3q27 as a susceptibility locus in the Chinese population
Tan DE,
Foo JN,
Bei JX,
Chang J,
Peng R,
Zheng X,
Wei L,
Huang Y,
Lim WY,
Li J,
Cui Q,
Chew SH
외 15명 — 모두 보기
Ebstein RP,
Kuperan P,
Lim ST,
Tao M,
Tan SH,
Wong A,
Wong GC,
Tan SY,
Ng SB,
Zeng YX,
Khor CC,
Lin D,
Seow AL,
Jia WH,
Liu J
Nature genetics · 2013 · PMID 23749188
페이지 1개
Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity
Pei YF,
Zhang L,
Liu Y,
Li J,
Shen H,
Liu YZ,
Tian Q,
He H,
Wu S,
Ran S,
Han Y,
Hai R
외 5명 — 모두 보기
Human molecular genetics · 2014 · PMID 24064335
페이지 1개
A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23
Li Y,
Zhang K,
Chen H,
Sun F,
Xu J,
Wu Z,
Li P,
Zhang L,
Du Y,
Luan H,
Li X,
Wu L
외 64명 — 모두 보기
Li H,
Wu H,
Li X,
Li X,
Zhang X,
Gong L,
Dai L,
Sun L,
Zuo X,
Xu J,
Gong H,
Li Z,
Tong S,
Wu M,
Li X,
Xiao W,
Wang G,
Zhu P,
Shen M,
Liu S,
Zhao D,
Liu W,
Wang Y,
Huang C,
Jiang Q,
Liu G,
Liu B,
Hu S,
Zhang W,
Zhang Z,
You X,
Li M,
Hao W,
Zhao C,
Leng X,
Bi L,
Wang Y,
Zhang F,
Shi Q,
Qi W,
Zhang X,
Jia Y,
Su J,
Li Q,
Hou Y,
Wu Q,
Xu D,
Zheng W,
Zhang M,
Wang Q,
Fei Y,
Zhang X,
Li J,
Jiang Y,
Tian X,
Zhao L,
Wang L,
Zhou B,
Li Y,
Zhao Y,
Zeng X,
Ott J,
Wang J,
Zhang F
Nature genetics · 2013 · PMID 24097066
페이지 1개
A genome-wide association study identifies common variants influencing serum uric acid concentrations in a Chinese population
Yang B,
Mo Z,
Wu C,
Yang H,
Yang X,
He Y,
Gui L,
Zhou L,
Guo H,
Zhang X,
Yuan J,
Dai X
외 17명 — 모두 보기
Li J,
Qiu G,
Huang S,
Deng Q,
Feng Y,
Guan L,
Hu D,
Zhang X,
Wang T,
Zhu J,
Min X,
Lang M,
Li D,
Hu FB,
Lin D,
Wu T,
He M
BMC medical genomics · 2014 · PMID 24513273 · open access
페이지 1개
Genetic variants in PLG, LPA, and SIGLEC 14 as well as smoking contribute to plasma plasminogen levels
Ma Q,
Ozel AB,
Ramdas S,
McGee B,
Khoriaty R,
Siemieniak D,
Li HD,
Guan Y,
Brody LC,
Mills JL,
Molloy AM,
Ginsburg D
외 2명 — 모두 보기
Blood · 2014 · PMID 25208887
페이지 1개
Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk
Lindström S,
Thompson DJ,
Paterson AD,
Li J,
Gierach GL,
Scott C,
Stone J,
Douglas JA,
dos-Santos-Silva I,
Fernandez-Navarro P,
Verghase J,
Smith P
외 33명 — 모두 보기
Brown J,
Luben R,
Wareham NJ,
Loos RJ,
Heit JA,
Pankratz VS,
Norman A,
Goode EL,
Cunningham JM,
deAndrade M,
Vierkant RA,
Czene K,
Fasching PA,
Baglietto L,
Southey MC,
Giles GG,
Shah KP,
Chan HP,
Helvie MA,
Beck AH,
Knoblauch NW,
Hazra A,
Hunter DJ,
Kraft P,
Pollan M,
Figueroa JD,
Couch FJ,
Hopper JL,
Hall P,
Easton DF,
Boyd NF,
Vachon CM,
Tamimi RM
Nature communications · 2014 · PMID 25342443 · open access
페이지 1개
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women
Wang Z,
Seow WJ,
Shiraishi K,
Hsiung CA,
Matsuo K,
Liu J,
Chen K,
Yamji T,
Yang Y,
Chang IS,
Wu C,
Hong YC
외 138명 — 모두 보기
Burdett L,
Wyatt K,
Chung CC,
Li SA,
Yeager M,
Hutchinson A,
Hu W,
Caporaso N,
Landi MT,
Chatterjee N,
Song M,
Fraumeni JF Jr,
Kohno T,
Yokota J,
Kunitoh H,
Ashikawa K,
Momozawa Y,
Daigo Y,
Mitsudomi T,
Yatabe Y,
Hida T,
Hu Z,
Dai J,
Ma H,
Jin G,
Song B,
Wang Z,
Cheng S,
Yin Z,
Li X,
Ren Y,
Guan P,
Chang J,
Tan W,
Chen CJ,
Chang GC,
Tsai YH,
Su WC,
Chen KY,
Huang MS,
Chen YM,
Zheng H,
Li H,
Cui P,
Guo H,
Xu P,
Liu L,
Iwasaki M,
Shimazu T,
Tsugane S,
Zhu J,
Jiang G,
Fei K,
Park JY,
Kim YH,
Sung JS,
Park KH,
Kim YT,
Jung YJ,
Kang CH,
Park IK,
Kim HN,
Jeon HS,
Choi JE,
Choi YY,
Kim JH,
Oh IJ,
Kim YC,
Sung SW,
Kim JS,
Yoon HI,
Kweon SS,
Shin MH,
Seow A,
Chen Y,
Lim WY,
Liu J,
Wong MP,
Lee VH,
Bassig BA,
Tucker M,
Berndt SI,
Chow WH,
Ji BT,
Wang J,
Xu J,
Sihoe AD,
Ho JC,
Chan JK,
Wang JC,
Lu D,
Zhao X,
Zhao Z,
Wu J,
Chen H,
Jin L,
Wei F,
Wu G,
An SJ,
Zhang XC,
Su J,
Wu YL,
Gao YT,
Xiang YB,
He X,
Li J,
Zheng W,
Shu XO,
Cai Q,
Klein R,
Pao W,
Lawrence C,
Hosgood HD 3rd,
Hsiao CF,
Chien LH,
Chen YH,
Chen CH,
Wang WC,
Chen CY,
Wang CL,
Yu CJ,
Chen HL,
Su YC,
Tsai FY,
Chen YS,
Li YJ,
Yang TY,
Lin CC,
Yang PC,
Wu T,
Lin D,
Zhou B,
Yu J,
Shen H,
Kubo M,
Chanock SJ,
Rothman N,
Lan Q
Human molecular genetics · 2016 · PMID 26732429
페이지 1개
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Day FR,
Thompson DJ,
Helgason H,
Chasman DI,
Finucane H,
Sulem P,
Ruth KS,
Whalen S,
Sarkar AK,
Albrecht E,
Altmaier E,
Amini M
외 204명 — 모두 보기
Barbieri CM,
Boutin T,
Campbell A,
Demerath E,
Giri A,
He C,
Hottenga JJ,
Karlsson R,
Kolcic I,
Loh PR,
Lunetta KL,
Mangino M,
Marco B,
McMahon G,
Medland SE,
Nolte IM,
Noordam R,
Nutile T,
Paternoster L,
Perjakova N,
Porcu E,
Rose LM,
Schraut KE,
Segrè AV,
Smith AV,
Stolk L,
Teumer A,
Andrulis IL,
Bandinelli S,
Beckmann MW,
Benitez J,
Bergmann S,
Bochud M,
Boerwinkle E,
Bojesen SE,
Bolla MK,
Brand JS,
Brauch H,
Brenner H,
Broer L,
Brüning T,
Buring JE,
Campbell H,
Catamo E,
Chanock S,
Chenevix-Trench G,
Corre T,
Couch FJ,
Cousminer DL,
Cox A,
Crisponi L,
Czene K,
Davey Smith G,
de Geus EJCN,
de Mutsert R,
De Vivo I,
Dennis J,
Devilee P,
Dos-Santos-Silva I,
Dunning AM,
Eriksson JG,
Fasching PA,
Fernández-Rhodes L,
Ferrucci L,
Flesch-Janys D,
Franke L,
Gabrielson M,
Gandin I,
Giles GG,
Grallert H,
Gudbjartsson DF,
Guénel P,
Hall P,
Hallberg E,
Hamann U,
Harris TB,
Hartman CA,
Heiss G,
Hooning MJ,
Hopper JL,
Hu F,
Hunter DJ,
Ikram MA,
Im HK,
Järvelin MR,
Joshi PK,
Karasik D,
Kellis M,
Kutalik Z,
LaChance G,
Lambrechts D,
Langenberg C,
Launer LJ,
Laven JSE,
Lenarduzzi S,
Li J,
Lind PA,
Lindstrom S,
Liu Y,
Luan J,
Mägi R,
Mannermaa A,
Mbarek H,
McCarthy MI,
Meisinger C,
Meitinger T,
Menni C,
Metspalu A,
Michailidou K,
Milani L,
Milne RL,
Montgomery GW,
Mulligan AM,
Nalls MA,
Navarro P,
Nevanlinna H,
Nyholt DR,
Oldehinkel AJ,
O'Mara TA,
Padmanabhan S,
Palotie A,
Pedersen N,
Peters A,
Peto J,
Pharoah PDP,
Pouta A,
Radice P,
Rahman I,
Ring SM,
Robino A,
Rosendaal FR,
Rudan I,
Rueedi R,
Ruggiero D,
Sala CF,
Schmidt MK,
Scott RA,
Shah M,
Sorice R,
Southey MC,
Sovio U,
Stampfer M,
Steri M,
Strauch K,
Tanaka T,
Tikkanen E,
Timpson NJ,
Traglia M,
Truong T,
Tyrer JP,
Uitterlinden AG,
Edwards DRV,
Vitart V,
Völker U,
Vollenweider P,
Wang Q,
Widen E,
van Dijk KW,
Willemsen G,
Winqvist R,
Wolffenbuttel BHR,
Zhao JH,
Zoledziewska M,
Zygmunt M,
Alizadeh BZ,
Boomsma DI,
Ciullo M,
Cucca F,
Esko T,
Franceschini N,
Gieger C,
Gudnason V,
Hayward C,
Kraft P,
Lawlor DA,
Magnusson PKE,
Martin NG,
Mook-Kanamori DO,
Nohr EA,
Polasek O,
Porteous D,
Price AL,
Ridker PM,
Snieder H,
Spector TD,
Stöckl D,
Toniolo D,
Ulivi S,
Visser JA,
Völzke H,
Wareham NJ,
Wilson JF,
Spurdle AB,
Thorsteindottir U,
Pollard KS,
Easton DF,
Tung JY,
Chang-Claude J,
Hinds D,
Murray A,
Murabito JM,
Stefansson K,
Ong KK,
Perry JRB
LifeLines Cohort Study · InterAct Consortium 외 컨소시엄 4곳
Nature genetics · 2017 · PMID 28436984
페이지 1개
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