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661 matches for
Er J,
showing the first 20.
Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits
Zhou H,
Sealock JM,
Sanchez-Roige S,
Clarke TK,
Levey DF,
Cheng Z,
Li B,
Polimanti R,
Kember RL,
Smith RV,
Thygesen JH,
Morgan MY
and 15 more — show all
Atkinson SR,
Thursz MR,
Nyegaard M,
Nyegaard M,
Mattheisen M,
Børglum AD,
Johnson EC,
Justice AC,
Palmer AA,
McQuillin A,
Davis LK,
Edenberg HJ,
Agrawal A,
Kranzler HR,
Gelernter J
Nature neuroscience · 2020 · PMID 32451486 · open access
12 pages+
Identification of type 2 diabetes loci in 433,540 East Asian individuals
Spracklen CN,
Horikoshi M,
Kim YJ,
Lin K,
Bragg F,
Moon S,
Suzuki K,
Tam CHT,
Tabara Y,
Kwak SH,
Takeuchi F,
Long J
and 101 more — show all
Lim VJY,
Chai JF,
Chen CH,
Nakatochi M,
Yao J,
Choi HS,
Iyengar AK,
Perrin HJ,
Brotman SM,
van de Bunt M,
Gloyn AL,
Below JE,
Boehnke M,
Bowden DW,
Chambers JC,
Mahajan A,
McCarthy MI,
Ng MCY,
Petty LE,
Zhang W,
Morris AP,
Adair LS,
Akiyama M,
Bian Z,
Chan JCN,
Chang LC,
Chee ML,
Chen YI,
Chen YT,
Chen Z,
Chuang LM,
Du S,
Gordon-Larsen P,
Gross M,
Guo X,
Guo Y,
Han S,
Howard AG,
Huang W,
Hung YJ,
Hwang MY,
Hwu CM,
Ichihara S,
Isono M,
Jang HM,
Jiang G,
Jonas JB,
Kamatani Y,
Katsuya T,
Kawaguchi T,
Khor CC,
Kohara K,
Lee MS,
Lee NR,
Li L,
Liu J,
Luk AO,
Lv J,
Okada Y,
Pereira MA,
Sabanayagam C,
Shi J,
Shin DM,
So WY,
Takahashi A,
Tomlinson B,
Tsai FJ,
van Dam RM,
Xiang YB,
Yamamoto K,
Yamauchi T,
Yoon K,
Yu C,
Yuan JM,
Zhang L,
Zheng W,
Zheng W,
Igase M,
Cho YS,
Rotter JI,
Wang YX,
Sheu WHH,
Yokota M,
Wu JY,
Cheng CY,
Wong TY,
Shu XO,
Kato N,
Park KS,
Tai ES,
Matsuda F,
Koh WP,
Ma RCW,
Maeda S,
Millwood IY,
Lee J,
Kadowaki T,
Walters RG,
Kim BJ,
Mohlke KL,
Sim X
Nature · 2020 · PMID 32499647 · open access
12 pages+
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
Chen MH,
Raffield LM,
Mousas A,
Sakaue S,
Huffman JE,
Moscati A,
Trivedi B,
Jiang T,
Akbari P,
Vuckovic D,
Bao EL,
Zhong X
and 98 more — show all
Manansala R,
Laplante V,
Chen M,
Lo KS,
Qian H,
Lareau CA,
Beaudoin M,
Hunt KA,
Akiyama M,
Bartz TM,
Ben-Shlomo Y,
Beswick A,
Bork-Jensen J,
Bottinger EP,
Brody JA,
van Rooij FJA,
Chitrala K,
Cho K,
Choquet H,
Correa A,
Danesh J,
Di Angelantonio E,
Dimou N,
Ding J,
Elliott P,
Esko T,
Evans MK,
Floyd JS,
Broer L,
Grarup N,
Guo MH,
Greinacher A,
Haessler J,
Hansen T,
Howson JMM,
Huang QQ,
Huang W,
Jorgenson E,
Kacprowski T,
Kähönen M,
Kamatani Y,
Kanai M,
Karthikeyan S,
Koskeridis F,
Lange LA,
Lehtimäki T,
Lerch MM,
Linneberg A,
Liu Y,
Lyytikäinen LP,
Manichaikul A,
Martin HC,
Matsuda K,
Mohlke KL,
Mononen N,
Murakami Y,
Nadkarni GN,
Nauck M,
Nikus K,
Ouwehand WH,
Pankratz N,
Pedersen O,
Preuss M,
Psaty BM,
Raitakari OT,
Roberts DJ,
Rich SS,
Rodriguez BAT,
Rosen JD,
Rotter JI,
Schubert P,
Spracklen CN,
Surendran P,
Tang H,
Tardif JC,
Trembath RC,
Ghanbari M,
Völker U,
Völzke H,
Watkins NA,
Zonderman AB,
Wilson PWF,
Li Y,
Butterworth AS,
Gauchat JF,
Chiang CWK,
Li B,
Loos RJF,
Astle WJ,
Evangelou E,
van Heel DA,
Sankaran VG,
Okada Y,
Soranzo N,
Johnson AD,
Reiner AP,
Auer PL,
Lettre G
VA Million Veteran Program
Cell · 2020 · PMID 32888493
12 pages+
The Polygenic and Monogenic Basis of Blood Traits and Diseases
Vuckovic D,
Bao EL,
Akbari P,
Lareau CA,
Mousas A,
Jiang T,
Chen MH,
Raffield LM,
Tardaguila M,
Huffman JE,
Ritchie SC,
Megy K
and 100 more — show all
Ponstingl H,
Penkett CJ,
Albers PK,
Wigdor EM,
Sakaue S,
Moscati A,
Manansala R,
Lo KS,
Qian H,
Akiyama M,
Bartz TM,
Ben-Shlomo Y,
Beswick A,
Bork-Jensen J,
Bottinger EP,
Brody JA,
van Rooij FJA,
Chitrala KN,
Wilson PWF,
Choquet H,
Danesh J,
Di Angelantonio E,
Dimou N,
Ding J,
Elliott P,
Esko T,
Evans MK,
Felix SB,
Floyd JS,
Broer L,
Grarup N,
Guo MH,
Guo Q,
Greinacher A,
Haessler J,
Hansen T,
Howson JMM,
Huang W,
Jorgenson E,
Kacprowski T,
Kähönen M,
Kamatani Y,
Kanai M,
Karthikeyan S,
Koskeridis F,
Lange LA,
Lehtimäki T,
Linneberg A,
Liu Y,
Lyytikäinen LP,
Manichaikul A,
Matsuda K,
Mohlke KL,
Mononen N,
Murakami Y,
Nadkarni GN,
Nikus K,
Pankratz N,
Pedersen O,
Preuss M,
Psaty BM,
Raitakari OT,
Rich SS,
Rodriguez BAT,
Rosen JD,
Rotter JI,
Schubert P,
Spracklen CN,
Surendran P,
Tang H,
Tardif JC,
Ghanbari M,
Völker U,
Völzke H,
Watkins NA,
Weiss S,
Cai N,
Kundu K,
Watt SB,
Walter K,
Zonderman AB,
Cho K,
Li Y,
Loos RJF,
Knight JC,
Georges M,
Stegle O,
Evangelou E,
Okada Y,
Roberts DJ,
Inouye M,
Johnson AD,
Auer PL,
Astle WJ,
Reiner AP,
Butterworth AS,
Ouwehand WH,
Lettre G,
Sankaran VG,
Soranzo N
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals
Xu K,
Li B,
McGinnis KA,
Vickers-Smith R,
Dao C,
Sun N,
Kember RL,
Zhou H,
Becker WC,
Gelernter J,
Kranzler HR,
Zhao H
and 1 more — show all
VA Million Veteran Program
Nature communications · 2020 · PMID 33082346 · open access
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+
Insights into the genetic architecture of the human face
White JD,
Indencleef K,
Naqvi S,
Eller RJ,
Hoskens H,
Roosenboom J,
Lee MK,
Li J,
Mohammed J,
Richmond S,
Quillen EE,
Norton HL
and 11 more — show all
Feingold E,
Swigut T,
Marazita ML,
Peeters H,
Hens G,
Shaffer JR,
Wysocka J,
Walsh S,
Weinberg SM,
Shriver MD,
Claes P
Nature genetics · 2021 · PMID 33288918 · open access
12 pages+
Cerebral small vessel disease genomics and its implications across the lifespan
Sargurupremraj M,
Suzuki H,
Jian X,
Sarnowski C,
Evans TE,
Bis JC,
Eiriksdottir G,
Sakaue S,
Terzikhan N,
Habes M,
Zhao W,
Zhao W
and 105 more — show all
Armstrong NJ,
Hofer E,
Yanek LR,
Hagenaars SP,
Kumar RB,
van den Akker EB,
McWhirter RE,
Trompet S,
Mishra A,
Saba Y,
Satizabal CL,
Beaudet G,
Petit L,
Tsuchida A,
Zago L,
Schilling S,
Sigurdsson S,
Gottesman RF,
Lewis CE,
Aggarwal NT,
Lopez OL,
Smith JA,
Valdés Hernández MC,
van der Grond J,
Wright MJ,
Knol MJ,
Dörr M,
Thomson RJ,
Bordes C,
Le Grand Q,
Duperron MG,
Smith AV,
Knopman DS,
Schreiner PJ,
Evans DA,
Rotter JI,
Beiser AS,
Maniega SM,
Beekman M,
Trollor J,
Stott DJ,
Vernooij MW,
Wittfeld K,
Niessen WJ,
Soumaré A,
Boerwinkle E,
Sidney S,
Turner ST,
Davies G,
Thalamuthu A,
Völker U,
van Buchem MA,
Bryan RN,
Dupuis J,
Bastin ME,
Ames D,
Teumer A,
Amouyel P,
Kwok JB,
Bülow R,
Deary IJ,
Schofield PR,
Brodaty H,
Jiang J,
Tabara Y,
Setoh K,
Miyamoto S,
Yoshida K,
Nagata M,
Kamatani Y,
Matsuda F,
Psaty BM,
Bennett DA,
De Jager PL,
Mosley TH,
Sachdev PS,
Schmidt R,
Warren HR,
Evangelou E,
Trégouët DA,
Ikram MA,
Wen W,
DeCarli C,
Srikanth VK,
Jukema JW,
Slagboom EP,
Kardia SLR,
Okada Y,
Mazoyer B,
Wardlaw JM,
Nyquist PA,
Mather KA,
Grabe HJ,
Schmidt H,
Van Duijn CM,
Gudnason V,
Longstreth WT Jr,
Launer LJ,
Lathrop M,
Seshadri S,
Tzourio C,
Adams HH,
Matthews PM,
Fornage M,
Debette S
International Network against Thrombosis (INVENT) Consortium · International Headache Genomics Consortium (IHGC)
Nature communications · 2020 · PMID 33293549 · open access
12 pages+
Causal Relationship and Shared Genetic Loci between Psoriasis and Type 2 Diabetes through Trans-Disease Meta-Analysis
Patrick MT,
Stuart PE,
Zhang H,
Zhao Q,
Yin X,
He K,
Zhou XJ,
Mehta NN,
Voorhees JJ,
Boehnke M,
Gudjonsson JE,
Nair RP
and 4 more — show all
The Journal of investigative dermatology · 2021 · PMID 33385400
12 pages+
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction
Conti DV,
Darst BF,
Moss LC,
Saunders EJ,
Sheng X,
Chou A,
Schumacher FR,
Olama AAA,
Benlloch S,
Dadaev T,
Brook MN,
Sahimi A
and 220 more — show all
Hoffmann TJ,
Takahashi A,
Matsuda K,
Momozawa Y,
Fujita M,
Muir K,
Lophatananon A,
Wan P,
Le Marchand L,
Wilkens LR,
Stevens VL,
Gapstur SM,
Carter BD,
Schleutker J,
Tammela TLJ,
Sipeky C,
Auvinen A,
Giles GG,
Southey MC,
MacInnis RJ,
Cybulski C,
Wokołorczyk D,
Lubiński J,
Neal DE,
Donovan JL,
Hamdy FC,
Martin RM,
Nordestgaard BG,
Nielsen SF,
Weischer M,
Bojesen SE,
Røder MA,
Iversen P,
Batra J,
Chambers S,
Moya L,
Horvath L,
Clements JA,
Tilley W,
Risbridger GP,
Gronberg H,
Aly M,
Szulkin R,
Eklund M,
Nordström T,
Pashayan N,
Dunning AM,
Ghoussaini M,
Travis RC,
Key TJ,
Riboli E,
Park JY,
Sellers TA,
Lin HY,
Albanes D,
Weinstein SJ,
Mucci LA,
Giovannucci E,
Lindstrom S,
Kraft P,
Hunter DJ,
Penney KL,
Turman C,
Tangen CM,
Goodman PJ,
Thompson IM Jr,
Hamilton RJ,
Fleshner NE,
Finelli A,
Parent MÉ,
Stanford JL,
Ostrander EA,
Geybels MS,
Koutros S,
Freeman LEB,
Stampfer M,
Wolk A,
Håkansson N,
Andriole GL,
Hoover RN,
Machiela MJ,
Sørensen KD,
Borre M,
Blot WJ,
Zheng W,
Zheng W,
Yeboah ED,
Mensah JE,
Lu YJ,
Zhang HW,
Feng N,
Mao X,
Wu Y,
Zhao SC,
Sun Z,
Thibodeau SN,
McDonnell SK,
Schaid DJ,
West CML,
Burnet N,
Barnett G,
Maier C,
Schnoeller T,
Luedeke M,
Kibel AS,
Drake BF,
Cussenot O,
Cancel-Tassin G,
Menegaux F,
Truong T,
Koudou YA,
John EM,
Grindedal EM,
Maehle L,
Khaw KT,
Ingles SA,
Stern MC,
Vega A,
Gómez-Caamaño A,
Fachal L,
Rosenstein BS,
Kerns SL,
Ostrer H,
Teixeira MR,
Paulo P,
Brandão A,
Watya S,
Lubwama A,
Bensen JT,
Fontham ETH,
Mohler J,
Taylor JA,
Kogevinas M,
Llorca J,
Castaño-Vinyals G,
Cannon-Albright L,
Teerlink CC,
Huff CD,
Strom SS,
Multigner L,
Blanchet P,
Brureau L,
Kaneva R,
Slavov C,
Mitev V,
Leach RJ,
Weaver B,
Brenner H,
Cuk K,
Holleczek B,
Saum KU,
Klein EA,
Hsing AW,
Kittles RA,
Murphy AB,
Logothetis CJ,
Kim J,
Neuhausen SL,
Steele L,
Ding YC,
Isaacs WB,
Nemesure B,
Hennis AJM,
Carpten J,
Pandha H,
Michael A,
De Ruyck K,
De Meerleer G,
Ost P,
Xu J,
Razack A,
Lim J,
Teo SH,
Newcomb LF,
Lin DW,
Fowke JH,
Neslund-Dudas C,
Rybicki BA,
Gamulin M,
Lessel D,
Kulis T,
Usmani N,
Singhal S,
Parliament M,
Claessens F,
Joniau S,
Van den Broeck T,
Gago-Dominguez M,
Castelao JE,
Martinez ME,
Larkin S,
Townsend PA,
Aukim-Hastie C,
Bush WS,
Aldrich MC,
Crawford DC,
Srivastava S,
Cullen JC,
Petrovics G,
Casey G,
Roobol MJ,
Jenster G,
van Schaik RHN,
Hu JJ,
Sanderson M,
Varma R,
McKean-Cowdin R,
Torres M,
Mancuso N,
Berndt SI,
Van Den Eeden SK,
Easton DF,
Chanock SJ,
Cook MB,
Wiklund F,
Nakagawa H,
Witte JS,
Eeles RA,
Kote-Jarai Z,
Haiman CA
Nature genetics · 2021 · PMID 33398198 · open access
12 pages+
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
and 22 more — show all
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
12 pages+
Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders
Yao X,
Glessner JT,
Li J,
Qi X,
Hou X,
Zhu C,
Li X,
March ME,
Yang L,
Mentch FD,
Hain HS,
Meng X
and 3 more — show all
Translational psychiatry · 2021 · PMID 33479212 · open access
12 pages+
A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus
Hardcastle AJ,
Liskova P,
Bykhovskaya Y,
McComish BJ,
Davidson AE,
Inglehearn CF,
Li X,
Choquet H,
Habeeb M,
Lucas SEM,
Sahebjada S,
Pontikos N
and 50 more — show all
Lopez KER,
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American journal of human genetics · 2021 · PMID 33713608
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Nature genetics · 2021 · PMID 34059833 · open access
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Nature genetics · 2021 · PMID 34127860 · open access
12 pages+
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Guo X,
Jeong A,
Jung J,
Kasela S,
Katrinli S
and 97 more — show all
Kuo PL,
Matias-Garcia PR,
Mishra PP,
Nygaard M,
Palviainen T,
Patki A,
Raffield LM,
Ratliff SM,
Richardson TG,
Robinson O,
Soerensen M,
Sun D,
Tsai PC,
van der Zee MD,
Walker RM,
Wang X,
Wang Y,
Xia R,
Xu Z,
Yao J,
Zhao W,
Correa A,
Boerwinkle E,
Dugué PA,
Durda P,
Elliott HR,
Gieger C,
de Geus EJC,
Harris SE,
Hemani G,
Imboden M,
Kähönen M,
Kardia SLR,
Kresovich JK,
Li S,
Lunetta KL,
Mangino M,
Mason D,
McIntosh AM,
Mengel-From J,
Moore AZ,
Murabito JM,
Ollikainen M,
Pankow JS,
Pedersen NL,
Peters A,
Polidoro S,
Porteous DJ,
Raitakari O,
Rich SS,
Sandler DP,
Sillanpää E,
Smith AK,
Southey MC,
Strauch K,
Tiwari H,
Tanaka T,
Tillin T,
Uitterlinden AG,
Van Den Berg DJ,
van Dongen J,
Wilson JG,
Wright J,
Yet I,
Arnett D,
Bandinelli S,
Bell JT,
Binder AM,
Boomsma DI,
Chen W,
Christensen K,
Conneely KN,
Elliott P,
Ferrucci L,
Fornage M,
Hägg S,
Hayward C,
Irvin M,
Kaprio J,
Lawlor DA,
Lehtimäki T,
Lohoff FW,
Milani L,
Milne RL,
Probst-Hensch N,
Reiner AP,
Ritz B,
Rotter JI,
Smith JA,
Taylor JA,
van Meurs JBJ,
Vineis P,
Waldenberger M,
Deary IJ,
Relton CL,
Horvath S,
Marioni RE
Genetics of DNA Methylation Consortium · NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Genome biology · 2021 · PMID 34187551 · open access
12 pages+
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Because a study that needed 622 people is a different kind of study from one that
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My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
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My paper is not here. Does that mean you rejected it?
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