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Lee IT.
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
Ehret GB,
Ferreira T,
Chasman DI,
Jackson AU,
Schmidt EM,
Johnson T,
Thorleifsson G,
Luan J,
Donnelly LA,
Kanoni S,
Petersen AK,
Pihur V
and 301 more — show all
Strawbridge RJ,
Shungin D,
Hughes MF,
Meirelles O,
Kaakinen M,
Bouatia-Naji N,
Kristiansson K,
Shah S,
Kleber ME,
Guo X,
Lyytikäinen LP,
Fava C,
Eriksson N,
Nolte IM,
Magnusson PK,
Salfati EL,
Rallidis LS,
Theusch E,
Smith AJP,
Folkersen L,
Witkowska K,
Pers TH,
Joehanes R,
Kim SK,
Lataniotis L,
Jansen R,
Johnson AD,
Warren H,
Kim YJ,
Zhao W,
Wu Y,
Tayo BO,
Bochud M,
Absher D,
Adair LS,
Amin N,
Arking DE,
Axelsson T,
Baldassarre D,
Balkau B,
Bandinelli S,
Barnes MR,
Barroso I,
Bevan S,
Bis JC,
Bjornsdottir G,
Boehnke M,
Boerwinkle E,
Bonnycastle LL,
Boomsma DI,
Bornstein SR,
Brown MJ,
Burnier M,
Cabrera CP,
Chambers JC,
Chang IS,
Cheng CY,
Chines PS,
Chung RH,
Collins FS,
Connell JM,
Döring A,
Dallongeville J,
Danesh J,
de Faire U,
Delgado G,
Dominiczak AF,
Doney ASF,
Drenos F,
Edkins S,
Eicher JD,
Elosua R,
Enroth S,
Erdmann J,
Eriksson P,
Esko T,
Evangelou E,
Evans A,
Fall T,
Farrall M,
Felix JF,
Ferrières J,
Ferrucci L,
Fornage M,
Forrester T,
Franceschini N,
Duran OHF,
Franco-Cereceda A,
Fraser RM,
Ganesh SK,
Gao H,
Gertow K,
Gianfagna F,
Gigante B,
Giulianini F,
Goel A,
Goodall AH,
Goodarzi MO,
Gorski M,
Gräßler J,
Groves C,
Gudnason V,
Gyllensten U,
Hallmans G,
Hartikainen AL,
Hassinen M,
Havulinna AS,
Hayward C,
Hercberg S,
Herzig KH,
Hicks AA,
Hingorani AD,
Hirschhorn JN,
Hofman A,
Holmen J,
Holmen OL,
Hottenga JJ,
Howard P,
Hsiung CA,
Hunt SC,
Ikram MA,
Illig T,
Iribarren C,
Jensen RA,
Kähönen M,
Kang H,
Kathiresan S,
Keating BJ,
Khaw KT,
Kim YK,
Kim E,
Kivimaki M,
Klopp N,
Kolovou G,
Komulainen P,
Kooner JS,
Kosova G,
Krauss RM,
Kuh D,
Kutalik Z,
Kuusisto J,
Kvaløy K,
Lakka TA,
Lee NR,
Lee IT,
Lee WJ,
Levy D,
Li X,
Liang KW,
Lin H,
Lin L,
Lindström J,
Lobbens S,
Männistö S,
Müller G,
Müller-Nurasyid M,
Mach F,
Markus HS,
Marouli E,
McCarthy MI,
McKenzie CA,
Meneton P,
Menni C,
Metspalu A,
Mijatovic V,
Moilanen L,
Montasser ME,
Morris AD,
Morrison AC,
Mulas A,
Nagaraja R,
Narisu N,
Nikus K,
O'Donnell CJ,
O'Reilly PF,
Ong KK,
Paccaud F,
Palmer CD,
Parsa A,
Pedersen NL,
Penninx BW,
Perola M,
Peters A,
Poulter N,
Pramstaller PP,
Psaty BM,
Quertermous T,
Rao DC,
Rasheed A,
Rayner NWNWR,
Renström F,
Rettig R,
Rice KM,
Roberts R,
Rose LM,
Rossouw J,
Samani NJ,
Sanna S,
Saramies J,
Schunkert H,
Sebert S,
Sheu WH,
Shin YA,
Sim X,
Smit JH,
Smith AV,
Sosa MX,
Spector TD,
Stančáková A,
Stanton A,
Stirrups KE,
Stringham HM,
Sundstrom J,
Swift AJ,
Syvänen AC,
Tai ES,
Tanaka T,
Tarasov KV,
Teumer A,
Thorsteinsdottir U,
Tobin MD,
Tremoli E,
Uitterlinden AG,
Uusitupa M,
Vaez A,
Vaidya D,
van Duijn CM,
van Iperen EPA,
Vasan RS,
Verwoert GC,
Virtamo J,
Vitart V,
Voight BF,
Vollenweider P,
Wagner A,
Wain LV,
Wareham NJ,
Watkins H,
Weder AB,
Westra HJ,
Wilks R,
Wilsgaard T,
Wilson JF,
Wong TY,
Yang TP,
Yao J,
Yengo L,
Zhang W,
Zhao JH,
Zhu X,
Bovet P,
Cooper RS,
Mohlke KL,
Saleheen D,
Lee JY,
Elliott P,
Gierman HJ,
Willer CJ,
Franke L,
Hovingh GK,
Taylor KD,
Dedoussis G,
Sever P,
Wong A,
Lind L,
Assimes TL,
Njølstad I,
Schwarz PE,
Langenberg C,
Snieder H,
Caulfield MJ,
Melander O,
Laakso M,
Saltevo J,
Rauramaa R,
Tuomilehto J,
Ingelsson E,
Lehtimäki T,
Hveem K,
Palmas W,
März W,
Kumari M,
Salomaa V,
Chen YI,
Rotter JI,
Froguel P,
Jarvelin MR,
Lakatta EG,
Kuulasmaa K,
Franks PW,
Hamsten A,
Wichmann HE,
Palmer CNA,
Stefansson K,
Ridker PM,
Loos RJF,
Chakravarti A,
Deloukas P,
Morris AP,
Newton-Cheh C,
Munroe PB
CHARGE-EchoGen consortium · CHARGE-HF consortium and 1 more consortia
Nature genetics · 2016 · PMID 27618452 · open access
12 pages+
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+
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Surendran P,
Feofanova EV,
Lahrouchi N,
Ntalla I,
Karthikeyan S,
Cook J,
Chen L,
Mifsud B,
Yao C,
Kraja AT,
Cartwright JH,
Hellwege JN
and 269 more — show all
Giri A,
Tragante V,
Thorleifsson G,
Liu DJ,
Prins BP,
Stewart ID,
Cabrera CP,
Eales JM,
Akbarov A,
Auer PL,
Bielak LF,
Bis JC,
Braithwaite VS,
Brody JA,
Daw EW,
Warren HR,
Drenos F,
Nielsen SF,
Faul JD,
Fauman EB,
Fava C,
Ferreira T,
Foley CN,
Franceschini N,
Gao H,
Giannakopoulou O,
Giulianini F,
Gudbjartsson DF,
Guo X,
Harris SE,
Havulinna AS,
Helgadottir A,
Huffman JE,
Hwang SJ,
Kanoni S,
Kontto J,
Larson MG,
Li-Gao R,
Lindström J,
Lotta LA,
Lu Y,
Luan J,
Mahajan A,
Malerba G,
Masca NGD,
Mei H,
Menni C,
Mook-Kanamori DO,
Mosen-Ansorena D,
Müller-Nurasyid M,
Paré G,
Paul DS,
Perola M,
Poveda A,
Rauramaa R,
Richard M,
Richardson TG,
Sepúlveda N,
Sim X,
Smith AV,
Smith JA,
Staley JR,
Stanáková A,
Sulem P,
Thériault S,
Thorsteinsdottir U,
Trompet S,
Varga TV,
Velez Edwards DR,
Veronesi G,
Weiss S,
Willems SM,
Yao J,
Young R,
Yu B,
Zhang W,
Zhao JH,
Zhao W,
Zhao W,
Evangelou E,
Aeschbacher S,
Asllanaj E,
Blankenberg S,
Bonnycastle LL,
Bork-Jensen J,
Brandslund I,
Braund PS,
Burgess S,
Cho K,
Christensen C,
Connell J,
Mutsert R,
Dominiczak AF,
Dörr M,
Eiriksdottir G,
Farmaki AE,
Gaziano JM,
Grarup N,
Grove ML,
Hallmans G,
Hansen T,
Have CT,
Heiss G,
Jørgensen ME,
Jousilahti P,
Kajantie E,
Kamat M,
Käräjämäki A,
Karpe F,
Koistinen HA,
Kovesdy CP,
Kuulasmaa K,
Laatikainen T,
Lannfelt L,
Lee IT,
Lee WJ,
Linneberg A,
Martin LW,
Moitry M,
Nadkarni G,
Neville MJ,
Palmer CNA,
Papanicolaou GJ,
Pedersen O,
Peters J,
Poulter N,
Rasheed A,
Rasmussen KL,
Rayner NW,
Mägi R,
Renström F,
Rettig R,
Rossouw J,
Schreiner PJ,
Sever PS,
Sigurdsson EL,
Skaaby T,
Sun YV,
Sundstrom J,
Thorgeirsson G,
Esko T,
Trabetti E,
Tsao PS,
Tuomi T,
Turner ST,
Tzoulaki I,
Vaartjes I,
Vergnaud AC,
Willer CJ,
Wilson PWF,
Witte DR,
Yonova-Doing E,
Zhang H,
Aliya N,
Almgren P,
Amouyel P,
Asselbergs FW,
Barnes MR,
Blakemore AI,
Boehnke M,
Bots ML,
Bottinger EP,
Buring JE,
Chambers JC,
Chen YI,
Chowdhury R,
Conen D,
Correa A,
Davey Smith G,
Boer RA,
Deary IJ,
Dedoussis G,
Deloukas P,
Di Angelantonio E,
Elliott P,
Felix SB,
Ferrières J,
Ford I,
Fornage M,
Franks PW,
Franks S,
Frossard P,
Gambaro G,
Gaunt TR,
Groop L,
Gudnason V,
Harris TB,
Hayward C,
Hennig BJ,
Herzig KH,
Ingelsson E,
Tuomilehto J,
Järvelin MR,
Jukema JW,
Kardia SLR,
Kee F,
Kooner JS,
Kooperberg C,
Launer LJ,
Lind L,
Loos RJF,
Majumder AAS,
Laakso M,
McCarthy MI,
Melander O,
Mohlke KL,
Murray AD,
Nordestgaard BG,
Orho-Melander M,
Packard CJ,
Padmanabhan S,
Palmas W,
Polasek O,
Porteous DJ,
Prentice AM,
Province MA,
Relton CL,
Rice K,
Ridker PM,
Rolandsson O,
Rosendaal FR,
Rotter JI,
Rudan I,
Salomaa V,
Samani NJ,
Sattar N,
Sheu WH,
Smith BH,
Soranzo N,
Spector TD,
Starr JM,
Sebert S,
Taylor KD,
Lakka TA,
Timpson NJ,
Tobin MD,
van der Harst P,
van der Meer P,
Ramachandran VS,
Verweij N,
Virtamo J,
Völker U,
Weir DR,
Zeggini E,
Charchar FJ,
Wareham NJ,
Langenberg C,
Tomaszewski M,
Butterworth AS,
Caulfield MJ,
Danesh J,
Edwards TL,
Holm H,
Hung AM,
Lindgren CM,
Liu C,
Manning AK,
Morris AP,
Morrison AC,
O'Donnell CJ,
Psaty BM,
Saleheen D,
Stefansson K,
Boerwinkle E,
Chasman DI,
Levy D,
Newton-Cheh C,
Munroe PB,
Howson JMM
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · 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
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
Liu C,
Kraja AT,
Smith JA,
Brody JA,
Franceschini N,
Bis JC,
Rice K,
Morrison AC,
Lu Y,
Weiss S,
Guo X,
Palmas W
and 83 more — show all
Martin LW,
Chen YD,
Surendran P,
Drenos F,
Cook JP,
Auer PL,
Chu AY,
Giri A,
Zhao W,
Jakobsdottir J,
Lin LA,
Stafford JM,
Amin N,
Mei H,
Yao J,
Voorman A,
Larson MG,
Grove ML,
Smith AV,
Hwang SJ,
Chen H,
Huan T,
Kosova G,
Stitziel NO,
Kathiresan S,
Samani N,
Schunkert H,
Deloukas P,
Li M,
Fuchsberger C,
Pattaro C,
Gorski M,
Kooperberg C,
Papanicolaou GJ,
Rossouw JE,
Faul JD,
Kardia SL,
Bouchard C,
Raffel LJ,
Uitterlinden AG,
Franco OH,
Vasan RS,
O'Donnell CJ,
Taylor KD,
Liu K,
Bottinger EP,
Gottesman O,
Daw EW,
Giulianini F,
Ganesh S,
Salfati E,
Harris TB,
Launer LJ,
Dörr M,
Felix SB,
Rettig R,
Völzke H,
Kim E,
Lee WJ,
Lee IT,
Sheu WH,
Tsosie KS,
Edwards DR,
Liu Y,
Correa A,
Weir DR,
Völker U,
Ridker PM,
Boerwinkle E,
Gudnason V,
Reiner AP,
van Duijn CM,
Borecki IB,
Edwards TL,
Chakravarti A,
Rotter JI,
Psaty BM,
Loos RJ,
Fornage M,
Ehret GB,
Newton-Cheh C,
Levy D,
Chasman DI
CHD Exome+ Consortium · ExomeBP Consortium and 4 more consortia
Nature genetics · 2016 · PMID 27618448
9 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
Multi-omics analysis identifies CpGs near G6PC2 mediating the effects of genetic variants on fasting glucose
Chung RH,
Chiu YF,
Wang WC,
Hwu CM,
Hung YJ,
Lee IT,
Chuang LM,
Quertermous T,
Rotter JI,
Chen YI,
Chang IS,
Hsiung CA
Diabetologia · 2021 · PMID 33842983
3 pages
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
Bentley AR,
Sung YJ,
Brown MR,
Winkler TW,
Kraja AT,
Ntalla I,
Schwander K,
Chasman DI,
Lim E,
Deng X,
Guo X,
Liu J
and 290 more — show all
Lu Y,
Cheng CY,
Sim X,
Vojinovic D,
Huffman JE,
Musani SK,
Li C,
Feitosa MF,
Richard MA,
Noordam R,
Baker J,
Chen G,
Aschard H,
Bartz TM,
Ding J,
Dorajoo R,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Zhao W,
Graff M,
Alver M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Evangelou E,
Gao C,
Goel A,
Hagemeijer Y,
Harris SE,
Hartwig FP,
He M,
Horimoto ARVR,
Hsu FC,
Hung YJ,
Jackson AU,
Kasturiratne A,
Komulainen P,
Kühnel B,
Leander K,
Lin KH,
Luan J,
Lyytikäinen LP,
Matoba N,
Nolte IM,
Pietzner M,
Prins B,
Riaz M,
Robino A,
Said MA,
Schupf N,
Scott RA,
Sofer T,
Stancáková A,
Takeuchi F,
Tayo BO,
van der Most PJ,
Varga TV,
Wang TD,
Wang Y,
Ware EB,
Wen W,
Xiang YB,
Yanek LR,
Zhang W,
Zhao JH,
Adeyemo A,
Afaq S,
Amin N,
Amini M,
Arking DE,
Arzumanyan Z,
Aung T,
Ballantyne C,
Barr RG,
Bielak LF,
Boerwinkle E,
Bottinger EP,
Broeckel U,
Brown M,
Cade BE,
Campbell A,
Canouil M,
Charumathi S,
Chen YI,
Christensen K,
Concas MP,
Connell JM,
de las Fuentes L,
de Silva HJ,
de Vries PS,
Doumatey A,
Duan Q,
Eaton CB,
Eppinga RN,
Faul JD,
Floyd JS,
Forouhi NG,
Forrester T,
Friedlander Y,
Gandin I,
Gao H,
Ghanbari M,
Gharib SA,
Gigante B,
Giulianini F,
Grabe HJ,
Gu CC,
Harris TB,
Heikkinen S,
Heng CK,
Hirata M,
Hixson JE,
Ikram MA,
Jia Y,
Joehanes R,
Johnson C,
Jonas JB,
Justice AE,
Katsuya T,
Khor CC,
Kilpeläinen TO,
Koh WP,
Kolcic I,
Kooperberg C,
Krieger JE,
Kritchevsky SB,
Kubo M,
Kuusisto J,
Lakka TA,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lewis CE,
Li Y,
Liang J,
Lin S,
Liu CT,
Liu J,
Liu K,
Loh M,
Lohman KK,
Louie T,
Luzzi A,
Mägi R,
Mahajan A,
Manichaikul AW,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mohlke KL,
Momozawa Y,
Morris AP,
Murray AD,
Nalls MA,
Nauck M,
Nelson CP,
North KE,
O'Connell JR,
Palmer ND,
Papanicolau GJ,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Poulter N,
Raitakari OT,
Reiner AP,
Renström F,
Rice TK,
Rich SS,
Robinson JG,
Rose LM,
Rosendaal FR,
Rudan I,
Schmidt CO,
Schreiner PJ,
Scott WR,
Sever P,
Shi Y,
Sidney S,
Sims M,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Stringham HM,
Tan NYQ,
Tang H,
Taylor KD,
Teo YY,
Tham YC,
Tiemeier H,
Turner ST,
Uitterlinden AG,
van Heemst D,
Waldenberger M,
Wang H,
Wang L,
Wang L,
Wei WB,
Williams CA,
Wilson G Sr,
Wojczynski MK,
Yao J,
Young K,
Yu C,
Yuan JM,
Zhou J,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
Chambers JC,
Cooper RS,
de Faire U,
Deary IJ,
Elliott P,
Esko T,
Farrall M,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Horta BL,
Juang JJ,
Kamatani Y,
Kammerer CM,
Kato N,
Kooner JS,
Laakso M,
Laurie CC,
Lee IT,
Lehtimäki T,
Magnusson PKE,
Oldehinkel AJ,
Penninx BWJH,
Pereira AC,
Rauramaa R,
Redline S,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wang JS,
Wang YX,
Wareham NJ,
Watkins H,
Weir DR,
Wickremasinghe AR,
Wu T,
Zeggini E,
Zheng W,
Zheng W,
Bouchard C,
Evans MK,
Gudnason V,
Kardia SLR,
Liu Y,
Psaty BM,
Ridker PM,
van Dam RM,
Mook-Kanamori DO,
Fornage M,
Province MA,
Kelly TN,
Fox ER,
Hayward C,
van Duijn CM,
Tai ES,
Wong TY,
Loos RJF,
Franceschini N,
Rotter JI,
Zhu X,
Bierut LJ,
Gauderman WJ,
Rice K,
Munroe PB,
Morrison AC,
Rao DC,
Rotimi CN,
Cupples LA
COGENT-Kidney Consortium · EPIC-InterAct Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30926973 · open access
1 page
Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake
Williamson A,
Norris DM,
Yin X,
Broadaway KA,
Moxley AH,
Vadlamudi S,
Wilson EP,
Jackson AU,
Ahuja V,
Andersen MK,
Arzumanyan Z,
Bonnycastle LL
and 103 more — show all
Bornstein SR,
Bretschneider MP,
Buchanan TA,
Chang YC,
Chuang LM,
Chung RH,
Clausen TD,
Damm P,
Delgado GE,
de Mello VD,
Dupuis J,
Dwivedi OP,
Erdos MR,
Fernandes Silva L,
Frayling TM,
Gieger C,
Goodarzi MO,
Guo X,
Gustafsson S,
Hakaste L,
Hammar U,
Hatem G,
Herrmann S,
Højlund K,
Horn K,
Hsueh WA,
Hung YJ,
Hwu CM,
Jonsson A,
Kårhus LL,
Kleber ME,
Kovacs P,
Lakka TA,
Lauzon M,
Lee IT,
Lindgren CM,
Lindström J,
Linneberg A,
Liu CT,
Luan J,
Aly DM,
Mathiesen E,
Moissl AP,
Morris AP,
Narisu N,
Perakakis N,
Peters A,
Prasad RB,
Rodionov RN,
Roll K,
Rundsten CF,
Sarnowski C,
Savonen K,
Scholz M,
Sharma S,
Stinson SE,
Suleman S,
Tan J,
Taylor KD,
Uusitupa M,
Vistisen D,
Witte DR,
Walther R,
Wu P,
Xiang AH,
Zethelius B,
Ahlqvist E,
Bergman RN,
Chen YI,
Collins FS,
Fall T,
Florez JC,
Fritsche A,
Grallert H,
Groop L,
Hansen T,
Koistinen HA,
Komulainen P,
Laakso M,
Lind L,
Loeffler M,
März W,
Meigs JB,
Raffel LJ,
Rauramaa R,
Rotter JI,
Schwarz PEH,
Stumvoll M,
Sundström J,
Tönjes A,
Tuomi T,
Tuomilehto J,
Wagner R,
Barroso I,
Walker M,
Grarup N,
Boehnke M,
Wareham NJ,
Mohlke KL,
Wheeler E,
O'Rahilly S,
Fazakerley DJ,
Langenberg C
Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2023 · PMID 37291194 · open access
1 page
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