For researchers
Is your paper here?
2,663 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
38 matches for
Wang T,
showing the first 20.
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels
Spracklen CN,
Chen P,
Kim YJ,
Wang X,
Cai H,
Li S,
Long J,
Wu Y,
Wang YX,
Takeuchi F,
Wu JY,
Jung KJ
and 103 more — show all
Hu C,
Akiyama K,
Zhang Y,
Moon S,
Johnson TA,
Li H,
Dorajoo R,
He M,
Cannon ME,
Roman TS,
Salfati E,
Lin KH,
Guo X,
Sheu WHH,
Absher D,
Adair LS,
Assimes TL,
Aung T,
Cai Q,
Chang LC,
Chen CH,
Chien LH,
Chuang LM,
Chuang SC,
Du S,
Fan Q,
Fann CSJ,
Feranil AB,
Friedlander Y,
Gordon-Larsen P,
Gu D,
Gui L,
Guo Z,
Heng CK,
Hixson J,
Hou X,
Hsiung CA,
Hu Y,
Hwang MY,
Hwu CM,
Isono M,
Juang JJ,
Khor CC,
Kim YK,
Koh WP,
Kubo M,
Lee IT,
Lee SJ,
Lee WJ,
Liang KW,
Lim B,
Lim SH,
Liu J,
Nabika T,
Pan WH,
Peng H,
Quertermous T,
Sabanayagam C,
Sandow K,
Shi J,
Sun L,
Tan PC,
Tan SP,
Taylor KD,
Teo YY,
Toh SA,
Tsunoda T,
van Dam RM,
Wang A,
Wang F,
Wang J,
Wei WB,
Xiang YB,
Yao J,
Yuan JM,
Zhang R,
Zhao W,
Chen YI,
Rich SS,
Rotter JI,
Wang TD,
Wu T,
Lin X,
Han BG,
Tanaka T,
Cho YS,
Katsuya T,
Jia W,
Jee SH,
Chen YT,
Kato N,
Jonas JB,
Cheng CY,
Shu XO,
He J,
Zheng W,
Zheng W,
Wong TY,
Huang W,
Kim BJ,
Tai ES,
Mohlke KL,
Sim X
Human molecular genetics · 2017 · PMID 28334899
12 pages+
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
and 41 more — show all
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
12 pages+
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function
Wyss AB,
Sofer T,
Lee MK,
Terzikhan N,
Nguyen JN,
Lahousse L,
Latourelle JC,
Smith AV,
Bartz TM,
Feitosa MF,
Gao W,
Ahluwalia TS
and 91 more — show all
Tang W,
Oldmeadow C,
Duan Q,
de Jong K,
Wojczynski MK,
Wang XQ,
Noordam R,
Hartwig FP,
Jackson VE,
Wang T,
Obeidat M,
Hobbs BD,
Huan T,
Gui H,
Parker MM,
Hu D,
Mogil LS,
Kichaev G,
Jin J,
Graff M,
Harris TB,
Kalhan R,
Heckbert SR,
Paternoster L,
Burkart KM,
Liu Y,
Holliday EG,
Wilson JG,
Vonk JM,
Sanders JL,
Barr RG,
de Mutsert R,
Menezes AMB,
Adams HHH,
van den Berge M,
Joehanes R,
Levin AM,
Liberto J,
Launer LJ,
Morrison AC,
Sitlani CM,
Celedón JC,
Kritchevsky SB,
Scott RJ,
Christensen K,
Rotter JI,
Bonten TN,
Wehrmeister FC,
Bossé Y,
Xiao S,
Oh S,
Franceschini N,
Brody JA,
Kaplan RC,
Lohman K,
McEvoy M,
Province MA,
Rosendaal FR,
Taylor KD,
Nickle DC,
Williams LK,
Burchard EG,
Wheeler HE,
Wheeler HE,
Sin DD,
Gudnason V,
North KE,
Fornage M,
Psaty BM,
Myers RH,
O'Connor G,
Hansen T,
Laurie CC,
Cassano PA,
Sung J,
Kim WJ,
Attia JR,
Lange L,
Boezen HM,
Thyagarajan B,
Rich SS,
Mook-Kanamori DO,
Horta BL,
Uitterlinden AG,
Im HK,
Cho MH,
Brusselle GG,
Gharib SA,
Dupuis J,
Manichaikul A,
London SJ
Nature communications · 2018 · PMID 30061609 · open access
12 pages+
Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups
Wang YF,
Zhang Y,
Lin Z,
Zhang H,
Wang TY,
Cao Y,
Morris DL,
Sheng Y,
Yin X,
Zhong SL,
Gu X,
Lei Y
and 23 more — show all
He J,
Wu Q,
Shen JJ,
Yang J,
Lam TH,
Lin JH,
Mai ZM,
Guo M,
Tang Y,
Chen Y,
Song Q,
Ban B,
Mok CC,
Cui Y,
Lu L,
Shen N,
Sham PC,
Lau CS,
Smith DK,
Vyse TJ,
Zhang X,
Lau YL,
Yang W
Nature communications · 2021 · PMID 33536424 · open access
12 pages+
The trans-ancestral genomic architecture of glycemic traits
Chen J,
Spracklen CN,
Marenne G,
Varshney A,
Corbin LJ,
Luan J,
Willems SM,
Wu Y,
Zhang X,
Horikoshi M,
Boutin TS,
Mägi R
and 393 more — show all
Waage J,
Li-Gao R,
Chan KHK,
Yao J,
Anasanti MD,
Chu AY,
Claringbould A,
Heikkinen J,
Hong J,
Hottenga JJ,
Huo S,
Kaakinen MA,
Louie T,
März W,
Moreno-Macias H,
Ndungu A,
Nelson SC,
Nolte IM,
North KE,
Raulerson CK,
Ray D,
Rohde R,
Rybin D,
Schurmann C,
Sim X,
Southam L,
Stewart ID,
Wang CA,
Wang Y,
Wu P,
Zhang W,
Ahluwalia TS,
Appel EVR,
Bielak LF,
Brody JA,
Burtt NP,
Cabrera CP,
Cade BE,
Chai JF,
Chai X,
Chang LC,
Chen CH,
Chen BH,
Chitrala KN,
Chiu YF,
de Haan HG,
Delgado GE,
Demirkan A,
Duan Q,
Engmann J,
Fatumo SA,
Gayán J,
Giulianini F,
Gong JH,
Gustafsson S,
Hai Y,
Hartwig FP,
He J,
Heianza Y,
Huang T,
Huerta-Chagoya A,
Hwang MY,
Jensen RA,
Kawaguchi T,
Kentistou KA,
Kim YJ,
Kleber ME,
Kooner IK,
Lai S,
Lange LA,
Langefeld CD,
Lauzon M,
Li M,
Ligthart S,
Liu J,
Loh M,
Long J,
Lyssenko V,
Mangino M,
Marzi C,
Montasser ME,
Nag A,
Nakatochi M,
Noce D,
Noordam R,
Pistis G,
Preuss M,
Raffield L,
Rasmussen-Torvik LJ,
Rich SS,
Robertson NR,
Rueedi R,
Ryan K,
Sanna S,
Saxena R,
Schraut KE,
Sennblad B,
Setoh K,
Smith AV,
Sparsø T,
Strawbridge RJ,
Takeuchi F,
Tan J,
Trompet S,
van den Akker E,
van der Most PJ,
Verweij N,
Vogel M,
Wang H,
Wang C,
Wang N,
Warren HR,
Wen W,
Wilsgaard T,
Wong A,
Wood AR,
Xie T,
Zafarmand MH,
Zhao JH,
Zhao W,
Amin N,
Arzumanyan Z,
Astrup A,
Bakker SJL,
Baldassarre D,
Beekman M,
Bergman RN,
Bertoni A,
Blüher M,
Bonnycastle LL,
Bornstein SR,
Bowden DW,
Cai Q,
Campbell A,
Campbell H,
Chang YC,
de Geus EJC,
Dehghan A,
Du S,
Eiriksdottir G,
Farmaki AE,
Frånberg M,
Fuchsberger C,
Gao Y,
Gjesing AP,
Goel A,
Han S,
Hartman CA,
Herder C,
Hicks AA,
Hsieh CH,
Hsueh WA,
Ichihara S,
Igase M,
Ikram MA,
Johnson WC,
Jørgensen ME,
Joshi PK,
Kalyani RR,
Kandeel FR,
Katsuya T,
Khor CC,
Kiess W,
Kolcic I,
Kuulasmaa T,
Kuusisto J,
Läll K,
Lam K,
Lawlor DA,
Lee NR,
Lemaitre RN,
Li H,
Lin SY,
Lindström J,
Linneberg A,
Liu J,
Lorenzo C,
Matsubara T,
Matsuda F,
Mingrone G,
Mooijaart S,
Moon S,
Nabika T,
Nadkarni GN,
Nadler JL,
Nelis M,
Neville MJ,
Norris JM,
Ohyagi Y,
Peters A,
Peyser PA,
Polasek O,
Qi Q,
Raven D,
Reilly DF,
Reiner A,
Rivideneira F,
Roll K,
Rudan I,
Sabanayagam C,
Sandow K,
Sattar N,
Schürmann A,
Shi J,
Stringham HM,
Taylor KD,
Teslovich TM,
Thuesen B,
Timmers PRHJ,
Tremoli E,
Tsai MY,
Uitterlinden A,
van Dam RM,
van Heemst D,
van Hylckama Vlieg A,
van Vliet-Ostaptchouk JV,
Vangipurapu J,
Vestergaard H,
Wang T,
Willems van Dijk K,
Zemunik T,
Abecasis GR,
Adair LS,
Aguilar-Salinas CA,
Alarcón-Riquelme ME,
An P,
Aviles-Santa L,
Becker DM,
Beilin LJ,
Bergmann S,
Bisgaard H,
Black C,
Boehnke M,
Boerwinkle E,
Böhm BO,
Bønnelykke K,
Boomsma DI,
Bottinger EP,
Buchanan TA,
Canouil M,
Caulfield MJ,
Chambers JC,
Chasman DI,
Chen YI,
Cheng CY,
Collins FS,
Correa A,
Cucca F,
de Silva HJ,
Dedoussis G,
Elmståhl S,
Evans MK,
Ferrannini E,
Ferrucci L,
Florez JC,
Franks PW,
Frayling TM,
Froguel P,
Gigante B,
Goodarzi MO,
Gordon-Larsen P,
Grallert H,
Grarup N,
Grimsgaard S,
Groop L,
Gudnason V,
Guo X,
Hamsten A,
Hansen T,
Hayward C,
Heckbert SR,
Horta BL,
Huang W,
Ingelsson E,
James PS,
Jarvelin MR,
Jonas JB,
Jukema JW,
Kaleebu P,
Kaplan R,
Kardia SLR,
Kato N,
Keinanen-Kiukaanniemi SM,
Kim BJ,
Kivimaki M,
Koistinen HA,
Kooner JS,
Körner A,
Kovacs P,
Kuh D,
Kumari M,
Kutalik Z,
Laakso M,
Lakka TA,
Launer LJ,
Leander K,
Li H,
Lin X,
Lind L,
Lindgren C,
Liu S,
Loos RJF,
Magnusson PKE,
Mahajan A,
Metspalu A,
Mook-Kanamori DO,
Mori TA,
Munroe PB,
Njølstad I,
O'Connell JR,
Oldehinkel AJ,
Ong KK,
Padmanabhan S,
Palmer CNA,
Palmer ND,
Pedersen O,
Pennell CE,
Porteous DJ,
Pramstaller PP,
Province MA,
Psaty BM,
Qi L,
Raffel LJ,
Rauramaa R,
Redline S,
Ridker PM,
Rosendaal FR,
Saaristo TE,
Sandhu M,
Saramies J,
Schneiderman N,
Schwarz P,
Scott LJ,
Selvin E,
Sever P,
Shu XO,
Slagboom PE,
Small KS,
Smith BH,
Snieder H,
Sofer T,
Sørensen TIA,
Spector TD,
Stanton A,
Steves CJ,
Stumvoll M,
Sun L,
Tabara Y,
Tai ES,
Timpson NJ,
Tönjes A,
Tuomilehto J,
Tusie T,
Uusitupa M,
van der Harst P,
van Duijn C,
Vitart V,
Vollenweider P,
Vrijkotte TGM,
Wagenknecht LE,
Walker M,
Wang YX,
Wareham NJ,
Watanabe RM,
Watkins H,
Wei WB,
Wickremasinghe AR,
Willemsen G,
Wilson JF,
Wong TY,
Wu JY,
Xiang AH,
Yanek LR,
Yengo L,
Yokota M,
Zeggini E,
Zheng W,
Zonderman AB,
Rotter JI,
Gloyn AL,
McCarthy MI,
Dupuis J,
Meigs JB,
Scott RA,
Prokopenko I,
Leong A,
Liu CT,
Parker SCJ,
Mohlke KL,
Langenberg C,
Wheeler E,
Morris AP,
Barroso I
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease
Cadby G,
Giles C,
Melton PE,
Huynh K,
Mellett NA,
Duong T,
Nguyen A,
Cinel M,
Smith A,
Olshansky G,
Wang T,
Brozynska M
and 32 more — show all
Inouye M,
McCarthy NS,
Ariff A,
Hung J,
Hui J,
Beilby J,
Dubé MP,
Watts GF,
Shah S,
Wray NR,
Lim WLF,
Chatterjee P,
Martins I,
Laws SM,
Porter T,
Vacher M,
Bush AI,
Rowe CC,
Villemagne VL,
Ames D,
Masters CL,
Taddei K,
Arnold M,
Kastenmüller G,
Nho K,
Saykin AJ,
Han X,
Kaddurah-Daouk R,
Martins RN,
Blangero J,
Meikle PJ,
Moses EK
Nature communications · 2022 · PMID 35668104 · open access
12 pages+
Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals
Tahir UA,
Katz DH,
Avila-Pachecho J,
Bick AG,
Pampana A,
Robbins JM,
Yu Z,
Chen ZZ,
Benson MD,
Cruz DE,
Ngo D,
Deng S
and 27 more — show all
Shi X,
Zheng S,
Eisman AS,
Farrell L,
Hall ME,
Correa A,
Tracy RP,
Durda P,
Taylor KD,
Liu Y,
Johnson WC,
Guo X,
Yao J,
Chen YI,
Manichaikul AW,
Ruberg FL,
Blaner WS,
Jain D,
Bouchard C,
Sarzynski MA,
Rich SS,
Rotter JI,
Wang TJ,
Wilson JG,
Clish CB,
Natarajan P,
Gerszten RE
NHLBI Trans-Omics for Precision Medicine 1 Consortium
Nature communications · 2022 · PMID 35995766 · open access
12 pages+
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
Zhao W,
Rasheed A,
Tikkanen E,
Lee JJ,
Butterworth AS,
Howson JMM,
Assimes TL,
Chowdhury R,
Orho-Melander M,
Damrauer S,
Small A,
Asma S
and 78 more — show all
Imamura M,
Yamauch T,
Chambers JC,
Chen P,
Sapkota BR,
Shah N,
Jabeen S,
Surendran P,
Lu Y,
Zhang W,
Imran A,
Abbas S,
Majeed F,
Trindade K,
Qamar N,
Mallick NH,
Yaqoob Z,
Saghir T,
Rizvi SNH,
Memon A,
Rasheed SZ,
Memon FU,
Mehmood K,
Ahmed N,
Qureshi IH,
Tanveer-Us-Salam,
Iqbal W,
Malik U,
Mehra N,
Kuo JZ,
Sheu WH,
Guo X,
Hsiung CA,
Juang JJ,
Taylor KD,
Hung YJ,
Lee WJ,
Quertermous T,
Lee IT,
Hsu CC,
Bottinger EP,
Ralhan S,
Teo YY,
Wang TD,
Alam DS,
Di Angelantonio E,
Epstein S,
Nielsen SF,
Nordestgaard BG,
Tybjaerg-Hansen A,
Young R,
Benn M,
Frikke-Schmidt R,
Kamstrup PR,
Jukema JW,
Sattar N,
Smit R,
Chung RH,
Liang KW,
Anand S,
Sanghera DK,
Ripatti S,
Loos RJF,
Kooner JS,
Tai ES,
Rotter JI,
Chen YI,
Frossard P,
Maeda S,
Kadowaki T,
Reilly M,
Pare G,
Melander O,
Salomaa V,
Rader DJ,
Danesh J,
Voight BF,
Saleheen D
CHD Exome+ Consortium · EPIC-CVD Consortium and 2 more consortia
Nature genetics · 2017 · PMID 28869590 · open access
11 pages
Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women
Fan W,
Kan H,
Liu HY,
Wang TL,
He YN,
Zhang M,
Li YX,
Li YJ,
Meng W,
Li Q,
Hu AQ,
Zheng YJ
mSystems · 2021 · PMID 34282934 · open access
11 pages
Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling
Ho JE,
Chen WY,
Chen MH,
Larson MG,
McCabe EL,
Cheng S,
Ghorbani A,
Coglianese E,
Emilsson V,
Johnson AD,
Walter S,
Franceschini N
and 12 more — show all
O'Donnell CJ,
Dehghan A,
Lu C,
Levy D,
Newton-Cheh C,
Lin H,
Felix JF,
Schreiter ER,
Vasan RS,
Januzzi JL,
Lee RT,
Wang TJ
CARDIoGRAM Consortium · CHARGE Inflammation Working Group and 1 more consortia
The Journal of clinical investigation · 2013 · PMID 23999434
9 pages
A genome-wide association study of neonatal metabolites
He Q,
Liu H,
Lu L,
Zhang Q,
Wang Q,
Wang B,
Wu X,
Guan L,
Mao J,
Xue Y,
Zhang C,
Cao X
and 9 more — show all
Cell genomics · 2024 · PMID 39389019 · open access
9 pages
Common variants associated with general and MMR vaccine-related febrile seizures
Feenstra B,
Pasternak B,
Geller F,
Carstensen L,
Wang T,
Huang F,
Eitson JL,
Hollegaard MV,
Svanström H,
Vestergaard M,
Hougaard DM,
Schoggins JW
and 3 more — show all
Nature genetics · 2014 · PMID 25344690 · open access
8 pages
Genome-wide association study of PR interval
Pfeufer A,
van Noord C,
Marciante KD,
Arking DE,
Larson MG,
Smith AV,
Tarasov KV,
Müller M,
Sotoodehnia N,
Sinner MF,
Verwoert GC,
Li M
and 53 more — show all
Kao WH,
Köttgen A,
Coresh J,
Bis JC,
Psaty BM,
Rice K,
Rotter JI,
Rivadeneira F,
Hofman A,
Kors JA,
Stricker BH,
Uitterlinden AG,
van Duijn CM,
Beckmann BM,
Sauter W,
Gieger C,
Lubitz SA,
Newton-Cheh C,
Wang TJ,
Magnani JW,
Schnabel RB,
Chung MK,
Barnard J,
Smith JD,
Van Wagoner DR,
Vasan RS,
Aspelund T,
Eiriksdottir G,
Harris TB,
Launer LJ,
Najjar SS,
Lakatta E,
Schlessinger D,
Uda M,
Abecasis GR,
Müller-Myhsok B,
Ehret GB,
Boerwinkle E,
Chakravarti A,
Soliman EZ,
Lunetta KL,
Perz S,
Wichmann HE,
Meitinger T,
Levy D,
Gudnason V,
Ellinor PT,
Sanna S,
Kääb S,
Witteman JC,
Alonso A,
Benjamin EJ,
Heckbert SR
Nature genetics · 2010 · PMID 20062060 · open access
6 pages
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
Wain LV,
Verwoert GC,
O'Reilly PF,
Shi G,
Johnson T,
Johnson AD,
Bochud M,
Rice KM,
Henneman P,
Smith AV,
Ehret GB,
Amin N
and 214 more — show all
Larson MG,
Mooser V,
Hadley D,
Dörr M,
Bis JC,
Aspelund T,
Esko T,
Janssens AC,
Zhao JH,
Heath S,
Laan M,
Fu J,
Pistis G,
Luan J,
Arora P,
Lucas G,
Pirastu N,
Pichler I,
Jackson AU,
Webster RJ,
Zhang F,
Peden JF,
Schmidt H,
Tanaka T,
Campbell H,
Igl W,
Milaneschi Y,
Hottenga JJ,
Vitart V,
Chasman DI,
Trompet S,
Bragg-Gresham JL,
Alizadeh BZ,
Chambers JC,
Guo X,
Lehtimäki T,
Kühnel B,
Lopez LM,
Polašek O,
Boban M,
Nelson CP,
Morrison AC,
Pihur V,
Ganesh SK,
Hofman A,
Kundu S,
Mattace-Raso FU,
Rivadeneira F,
Sijbrands EJ,
Uitterlinden AG,
Hwang SJ,
Vasan RS,
Wang TJ,
Bergmann S,
Vollenweider P,
Waeber G,
Laitinen J,
Pouta A,
Zitting P,
McArdle WL,
Kroemer HK,
Völker U,
Völzke H,
Glazer NL,
Taylor KD,
Harris TB,
Alavere H,
Haller T,
Keis A,
Tammesoo ML,
Aulchenko Y,
Barroso I,
Khaw KT,
Galan P,
Hercberg S,
Lathrop M,
Eyheramendy S,
Org E,
Org E,
Sõber S,
Lu X,
Nolte IM,
Penninx BW,
Corre T,
Masciullo C,
Sala C,
Groop L,
Voight BF,
Melander O,
O'Donnell CJ,
Salomaa V,
d'Adamo AP,
Fabretto A,
Faletra F,
Ulivi S,
Del Greco F,
Facheris M,
Collins FS,
Bergman RN,
Beilby JP,
Hung J,
Musk AW,
Mangino M,
Shin SY,
Soranzo N,
Watkins H,
Goel A,
Hamsten A,
Gider P,
Loitfelder M,
Zeginigg M,
Hernandez D,
Najjar SS,
Navarro P,
Wild SH,
Corsi AM,
Singleton A,
de Geus EJ,
Willemsen G,
Willemsen G,
Parker AN,
Rose LM,
Buckley B,
Stott D,
Orru M,
Uda M,
van der Klauw MM,
Zhang W,
Li X,
Scott J,
Chen YD,
Burke GL,
Kähönen M,
Viikari J,
Döring A,
Meitinger T,
Davies G,
Starr JM,
Emilsson V,
Plump A,
Lindeman JH,
Hoen PA,
König IR,
Felix JF,
Clarke R,
Hopewell JC,
Ongen H,
Breteler M,
Debette S,
Destefano AL,
Fornage M,
Mitchell GF,
Smith NL,
Holm H,
Stefansson K,
Thorleifsson G,
Thorsteinsdottir U,
Samani NJ,
Preuss M,
Rudan I,
Hayward C,
Deary IJ,
Wichmann HE,
Raitakari OT,
Palmas W,
Kooner JS,
Stolk RP,
Jukema JW,
Wright AF,
Boomsma DI,
Bandinelli S,
Gyllensten UB,
Wilson JF,
Ferrucci L,
Schmidt R,
Farrall M,
Spector TD,
Palmer LJ,
Tuomilehto J,
Pfeufer A,
Gasparini P,
Siscovick D,
Altshuler D,
Loos RJ,
Toniolo D,
Snieder H,
Gieger C,
Meneton P,
Wareham NJ,
Oostra BA,
Metspalu A,
Launer L,
Rettig R,
Strachan DP,
Beckmann JS,
Witteman JC,
Erdmann J,
van Dijk KW,
Boerwinkle E,
Boehnke M,
Ridker PM,
Jarvelin MR,
Chakravarti A,
Abecasis GR,
Gudnason V,
Newton-Cheh C,
Levy D,
Munroe PB,
Psaty BM,
Caulfield MJ,
Rao DC,
Tobin MD,
Elliott P,
van Duijn CM
LifeLines Cohort Study · EchoGen consortium and 6 more consortia
Nature genetics · 2011 · PMID 21909110 · open access
6 pages
Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations
Hong J,
Hatchell KE,
Bradfield JP,
Bjonnes A,
Chesi A,
Lai CQ,
Langefeld CD,
Lu L,
Lu Y,
Lutsey PL,
Musani SK,
Nalls MA
and 48 more — show all
Robinson-Cohen C,
Roizen JD,
Saxena R,
Tucker KL,
Ziegler JT,
Arking DE,
Bis JC,
Boerwinkle E,
Bottinger EP,
Bowden DW,
Gilsanz V,
Houston DK,
Kalkwarf HJ,
Kelly A,
Lappe JM,
Liu Y,
Michos ED,
Oberfield SE,
Palmer ND,
Rotter JI,
Sapkota B,
Shepherd JA,
Wilson JG,
Basu S,
de Boer IH,
Divers J,
Freedman BI,
Grant SFA,
Hakanarson H,
Harris TB,
Kestenbaum BR,
Kritchevsky SB,
Loos RJF,
Norris JM,
Norwood AF,
Ordovas JM,
Pankow JS,
Psaty BM,
Sanghera DK,
Wagenknecht LE,
Zemel BS,
Meigs J,
Dupuis J,
Florez JC,
Wang T,
Liu CT,
Engelman CD,
Billings LK
The Journal of clinical endocrinology and metabolism · 2018 · PMID 29325163
6 pages
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
Sotoodehnia N,
Isaacs A,
de Bakker PI,
Dörr M,
Newton-Cheh C,
Nolte IM,
van der Harst P,
Müller M,
Eijgelsheim M,
Alonso A,
Hicks AA,
Padmanabhan S
and 91 more — show all
Hayward C,
Smith AV,
Polasek O,
Giovannone S,
Fu J,
Magnani JW,
Marciante KD,
Pfeufer A,
Gharib SA,
Teumer A,
Li M,
Bis JC,
Rivadeneira F,
Aspelund T,
Köttgen A,
Johnson T,
Rice K,
Sie MP,
Wang YA,
Klopp N,
Fuchsberger C,
Wild SH,
Mateo Leach I,
Estrada K,
Völker U,
Wright AF,
Asselbergs FW,
Qu J,
Chakravarti A,
Sinner MF,
Kors JA,
Petersmann A,
Harris TB,
Soliman EZ,
Munroe PB,
Psaty BM,
Oostra BA,
Cupples LA,
Perz S,
de Boer RA,
Uitterlinden AG,
Völzke H,
Spector TD,
Liu FY,
Boerwinkle E,
Dominiczak AF,
Rotter JI,
van Herpen G,
Levy D,
Wichmann HE,
van Gilst WH,
Witteman JC,
Kroemer HK,
Kao WH,
Heckbert SR,
Meitinger T,
Hofman A,
Campbell H,
Folsom AR,
van Veldhuisen DJ,
Schwienbacher C,
O'Donnell CJ,
Volpato CB,
Caulfield MJ,
Connell JM,
Launer L,
Lu X,
Franke L,
Fehrmann RS,
te Meerman G,
Groen HJ,
Weersma RK,
van den Berg LH,
Wijmenga C,
Ophoff RA,
Navis G,
Rudan I,
Snieder H,
Wilson JF,
Pramstaller PP,
Siscovick DS,
Wang TJ,
Gudnason V,
van Duijn CM,
Felix SB,
Fishman GI,
Jamshidi Y,
Stricker BH,
Samani NJ,
Kääb S,
Arking DE
Nature genetics · 2010 · PMID 21076409 · open access
5 pages
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Ehret GB,
Munroe PB,
Rice KM,
Bochud M,
Johnson AD,
Chasman DI,
Smith AV,
Tobin MD,
Verwoert GC,
Hwang SJ,
Pihur V,
Vollenweider P
and 336 more — show all
O'Reilly PF,
Amin N,
Bragg-Gresham JL,
Teumer A,
Glazer NL,
Launer L,
Zhao JH,
Aulchenko Y,
Heath S,
Sõber S,
Parsa A,
Luan J,
Arora P,
Dehghan A,
Zhang F,
Lucas G,
Hicks AA,
Jackson AU,
Peden JF,
Tanaka T,
Wild SH,
Rudan I,
Igl W,
Milaneschi Y,
Parker AN,
Fava C,
Chambers JC,
Fox ER,
Kumari M,
Go MJ,
van der Harst P,
Kao WH,
Sjögren M,
Vinay DG,
Alexander M,
Tabara Y,
Shaw-Hawkins S,
Whincup PH,
Liu Y,
Shi G,
Kuusisto J,
Tayo B,
Seielstad M,
Sim X,
Nguyen KD,
Lehtimäki T,
Matullo G,
Wu Y,
Gaunt TR,
Onland-Moret NC,
Cooper MN,
Platou CG,
Org E,
Org E,
Hardy R,
Dahgam S,
Palmen J,
Vitart V,
Braund PS,
Kuznetsova T,
Kuznetsova T,
Uiterwaal CS,
Adeyemo A,
Palmas W,
Campbell H,
Ludwig B,
Tomaszewski M,
Tzoulaki I,
Palmer ND,
Aspelund T,
Garcia M,
Chang YP,
O'Connell JR,
Steinle NI,
Grobbee DE,
Arking DE,
Kardia SL,
Morrison AC,
Hernandez D,
Najjar S,
McArdle WL,
Hadley D,
Brown MJ,
Connell JM,
Hingorani AD,
Day IN,
Lawlor DA,
Beilby JP,
Lawrence RW,
Clarke R,
Hopewell JC,
Ongen H,
Dreisbach AW,
Li Y,
Young JH,
Bis JC,
Kähönen M,
Viikari J,
Adair LS,
Lee NR,
Chen MH,
Olden M,
Pattaro C,
Bolton JA,
Köttgen A,
Bergmann S,
Mooser V,
Chaturvedi N,
Frayling TM,
Islam M,
Jafar TH,
Erdmann J,
Kulkarni SR,
Bornstein SR,
Grässler J,
Groop L,
Voight BF,
Kettunen J,
Howard P,
Taylor A,
Guarrera S,
Ricceri F,
Emilsson V,
Plump A,
Barroso I,
Khaw KT,
Weder AB,
Hunt SC,
Sun YV,
Bergman RN,
Collins FS,
Bonnycastle LL,
Scott LJ,
Stringham HM,
Peltonen L,
Perola M,
Vartiainen E,
Brand SM,
Staessen JA,
Wang TJ,
Burton PR,
Soler Artigas M,
Dong Y,
Snieder H,
Wang X,
Zhu H,
Lohman KK,
Rudock ME,
Heckbert SR,
Smith NL,
Wiggins KL,
Doumatey A,
Shriner D,
Veldre G,
Viigimaa M,
Kinra S,
Prabhakaran D,
Tripathy V,
Langefeld CD,
Rosengren A,
Thelle DS,
Corsi AM,
Singleton A,
Forrester T,
Hilton G,
McKenzie CA,
Salako T,
Iwai N,
Kita Y,
Ogihara T,
Ohkubo T,
Okamura T,
Ueshima H,
Umemura S,
Eyheramendy S,
Meitinger T,
Wichmann HE,
Cho YS,
Kim HL,
Lee JY,
Scott J,
Sehmi JS,
Zhang W,
Hedblad B,
Nilsson P,
Smith GD,
Wong A,
Narisu N,
Stančáková A,
Raffel LJ,
Yao J,
Kathiresan S,
O'Donnell CJ,
Schwartz SM,
Ikram MA,
Longstreth WT Jr,
Mosley TH,
Seshadri S,
Shrine NR,
Wain LV,
Morken MA,
Swift AJ,
Laitinen J,
Prokopenko I,
Zitting P,
Cooper JA,
Humphries SE,
Danesh J,
Rasheed A,
Goel A,
Hamsten A,
Watkins H,
Bakker SJ,
van Gilst WH,
Janipalli CS,
Mani KR,
Yajnik CS,
Hofman A,
Mattace-Raso FU,
Oostra BA,
Demirkan A,
Isaacs A,
Rivadeneira F,
Lakatta EG,
Orru M,
Scuteri A,
Ala-Korpela M,
Kangas AJ,
Lyytikäinen LP,
Soininen P,
Tukiainen T,
Würtz P,
Ong RT,
Dörr M,
Kroemer HK,
Völker U,
Völzke H,
Galan P,
Hercberg S,
Lathrop M,
Zelenika D,
Deloukas P,
Mangino M,
Spector TD,
Zhai G,
Meschia JF,
Nalls MA,
Sharma P,
Terzic J,
Kumar MV,
Denniff M,
Zukowska-Szczechowska E,
Wagenknecht LE,
Fowkes FG,
Charchar FJ,
Schwarz PE,
Hayward C,
Guo X,
Rotimi C,
Bots ML,
Brand E,
Samani NJ,
Polasek O,
Talmud PJ,
Nyberg F,
Kuh D,
Laan M,
Hveem K,
Palmer LJ,
van der Schouw YT,
Casas JP,
Mohlke KL,
Vineis P,
Raitakari O,
Ganesh SK,
Wong TY,
Tai ES,
Cooper RS,
Laakso M,
Rao DC,
Harris TB,
Morris RW,
Dominiczak AF,
Kivimaki M,
Marmot MG,
Miki T,
Saleheen D,
Chandak GR,
Coresh J,
Navis G,
Salomaa V,
Han BG,
Zhu X,
Kooner JS,
Melander O,
Ridker PM,
Bandinelli S,
Gyllensten UB,
Wright AF,
Wilson JF,
Ferrucci L,
Farrall M,
Tuomilehto J,
Pramstaller PP,
Elosua R,
Soranzo N,
Sijbrands EJ,
Altshuler D,
Loos RJ,
Shuldiner AR,
Gieger C,
Meneton P,
Uitterlinden AG,
Wareham NJ,
Gudnason V,
Rotter JI,
Rettig R,
Uda M,
Strachan DP,
Witteman JC,
Hartikainen AL,
Beckmann JS,
Boerwinkle E,
Vasan RS,
Boehnke M,
Larson MG,
Järvelin MR,
Psaty BM,
Abecasis GR,
Chakravarti A,
Elliott P,
van Duijn CM,
Newton-Cheh C,
Levy D,
Caulfield MJ,
Johnson T
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index
Wen W,
Zheng W,
Zheng W,
Okada Y,
Takeuchi F,
Tabara Y,
Hwang JY,
Dorajoo R,
Li H,
Tsai FJ,
Yang X,
He J
and 98 more — show all
Wu Y,
He M,
Zhang Y,
Liang J,
Guo X,
Sheu WH,
Delahanty R,
Guo X,
Kubo M,
Yamamoto K,
Ohkubo T,
Go MJ,
Liu JJ,
Gan W,
Chen CC,
Gao Y,
Li S,
Lee NR,
Wu C,
Zhou X,
Song H,
Yao J,
Lee IT,
Long J,
Tsunoda T,
Akiyama K,
Takashima N,
Cho YS,
Ong RT,
Lu L,
Chen CH,
Tan A,
Rice TK,
Adair LS,
Gui L,
Allison M,
Lee WJ,
Cai Q,
Isomura M,
Umemura S,
Kim YJ,
Seielstad M,
Hixson J,
Xiang YB,
Isono M,
Kim BJ,
Sim X,
Lu W,
Nabika T,
Lee J,
Lim WY,
Gao YT,
Takayanagi R,
Kang DH,
Wong TY,
Hsiung CA,
Wu IC,
Juang JM,
Shi J,
Choi BY,
Aung T,
Hu F,
Kim MK,
Lim WY,
Wang TD,
Shin MH,
Lee J,
Ji BT,
Lee YH,
Young TL,
Shin DH,
Chun BY,
Cho MC,
Han BG,
Hwu CM,
Assimes TL,
Absher D,
Yan X,
Kim E,
Kuo JZ,
Kwon S,
Taylor KD,
Chen YD,
Rotter JI,
Qi L,
Zhu D,
Wu T,
Mohlke KL,
Gu D,
Mo Z,
Wu JY,
Lin X,
Miki T,
Tai ES,
Lee JY,
Kato N,
Shu XO,
Tanaka T
Human molecular genetics · 2014 · PMID 24861553
4 pages
GWAS meta-analysis of cerebrospinal fluid Alzheimer's biomarkers reveals loci regulating lipids, brain volume and autophagy
Timsina J,
Jiang C,
McCartney DL,
Tao F,
Dalmasso MC,
Najar J,
Anastasi F,
Ohlei O,
Puerta Fuentes R,
Yang C,
Bradley J,
Western D
and 143 more — show all
Ali M,
Wang C,
Yang C,
Wu Y,
Liu M,
Budde J,
Williams J,
Mahoney R,
Castillo Morales A,
Hohman TJ,
Dumitrescu L,
Wang TC,
Tesi N,
Kern S,
Waern M,
Skoog I,
van Harten A,
Pijnenburg YAL,
van der Flier WM,
Sánchez-Juan P,
Rodriguez-Rodriguez E,
Kleineidam L,
Peters O,
Schneider A,
Küçükali F,
Bellenguez C,
Grenier-Boley B,
Heikkinen S,
de Rojas I,
Rujescu D,
Scherbaum N,
Hausner L,
Düzel E,
Grimmer T,
Wiltfang J,
Vandenberghe R,
Engelborghs S,
Heilmann-Heimbach S,
Schmid M,
Tegos T,
Scarmeas N,
Dols-Icardo O,
Moreno F,
Pérez-Tur J,
Bullido MJ,
Sánchez-Valle R,
Álvarez V,
García-González P,
Mir P,
Real LM,
Piñol-Ripoll G,
García-Alberca JM,
Seelaar H,
Ramakers I,
Papma J,
Hulsman M,
Laske C,
Teipel S,
Priller J,
Perneczky R,
Buerger K,
Nöthen MM,
Lewczuk P,
Kornhuber J,
Hampel H,
Giegling I,
Goldhardt O,
Diehl-Schmid J,
Andrade V,
Heneka MM,
Frölich L,
Vogelgsang J,
Graff C,
Thonberg H,
Ullgren A,
Papenberg G,
Deleuze JF,
Dufouil C,
Wagner M,
Jessen F,
Holstege H,
van Duijn C,
Lebouvier T,
Hannon O,
Leinonen V,
Soininen H,
Herukka SK,
Giedraitis V,
Löwenmark M,
Kilander L,
Genius P,
Rodríguez B,
Luckett ES,
Navarro A,
Cano A,
Marquié M,
Blennow K,
Zetterberg H,
Lleo A,
Boada M,
Ruiz A,
Lee VM,
Van Deerlin VM,
Deming Y,
Johnson SC,
Engelman CD,
Pastor P,
Alvarez I,
Peskind ER,
Heslegrave AJ,
Saykin AJ,
Nho K,
Schindler SE,
Morris JC,
Holtzman DM,
McDade E,
Renton AE,
Goate A,
Ibanez L,
Riemenschneider M,
Albert MS,
Laws SM,
Porter T,
O'Brien EK,
Shaw LM,
Tijms BM,
Ingelsson M,
Visser PJ,
Hiltunen M,
Sleegers K,
Ritchie CW,
Sims R,
Belloy M,
Lambert JC,
Vilor-Tejedor N,
Fernández MV,
Li QS,
Nagle MW,
Marioni RE,
Ramirez A,
Bertram L,
van der Lee SJ,
Cruchaga C
Nature communications · 2026 · PMID 42014397 · open access
4 pages
Genome-wide association study of blood pressure and hypertension
Levy D,
Ehret GB,
Rice K,
Verwoert GC,
Launer LJ,
Dehghan A,
Glazer NL,
Morrison AC,
Johnson AD,
Aspelund T,
Aulchenko Y,
Lumley T
and 32 more — show all
Köttgen A,
Vasan RS,
Rivadeneira F,
Eiriksdottir G,
Guo X,
Arking DE,
Mitchell GF,
Mattace-Raso FU,
Smith AV,
Taylor K,
Scharpf RB,
Hwang SJ,
Sijbrands EJ,
Bis J,
Harris TB,
Ganesh SK,
O'Donnell CJ,
Hofman A,
Rotter JI,
Coresh J,
Benjamin EJ,
Uitterlinden AG,
Heiss G,
Fox CS,
Witteman JC,
Boerwinkle E,
Wang TJ,
Gudnason V,
Larson MG,
Chakravarti A,
Psaty BM,
van Duijn CM
Nature genetics · 2009 · PMID 19430479
3 pages
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.