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661 matches for
Er J,
showing the first 20.
Interethnic analyses of blood pressure loci in populations of East Asian and European descent
Takeuchi F,
Akiyama M,
Matoba N,
Katsuya T,
Nakatochi M,
Tabara Y,
Narita A,
Saw WY,
Moon S,
Spracklen CN,
Chai JF,
Kim YJ
and 83 more — show all
Zhang L,
Wang C,
Li H,
Li H,
Wu JY,
Dorajoo R,
Nierenberg JL,
Wang YX,
He J,
Bennett DA,
Takahashi A,
Momozawa Y,
Hirata M,
Matsuda K,
Rakugi H,
Nakashima E,
Isono M,
Shirota M,
Hozawa A,
Ichihara S,
Matsubara T,
Yamamoto K,
Kohara K,
Igase M,
Han S,
Gordon-Larsen P,
Huang W,
Lee NR,
Adair LS,
Hwang MY,
Lee J,
Chee ML,
Sabanayagam C,
Zhao W,
Liu J,
Reilly DF,
Sun L,
Huo S,
Edwards TL,
Long J,
Chang LC,
Chen CH,
Yuan JM,
Koh WP,
Friedlander Y,
Kelly TN,
Bin Wei W,
Xu L,
Cai H,
Xiang YB,
Lin K,
Clarke R,
Walters RG,
Millwood IY,
Li L,
Chambers JC,
Kooner JS,
Elliott P,
van der Harst P,
Chen Z,
Sasaki M,
Shu XO,
Jonas JB,
He J,
Heng CK,
Chen YT,
Zheng W,
Zheng W,
Lin X,
Teo YY,
Tai ES,
Cheng CY,
Wong TY,
Sim X,
Mohlke KL,
Yamamoto M,
Kim BJ,
Miki T,
Nabika T,
Yokota M,
Kamatani Y,
Kubo M,
Kato N
International Genomics of Blood Pressure (iGEN-BP) Consortium
Nature communications · 2018 · PMID 30487518 · open access
12 pages+
Discovery of common and rare genetic risk variants for colorectal cancer
Huyghe JR,
Bien SA,
Harrison TA,
Kang HM,
Chen S,
Schmit SL,
Conti DV,
Qu C,
Jeon J,
Edlund CK,
Greenside P,
Wainberg M
and 188 more — show all
Schumacher FR,
Smith JD,
Levine DM,
Nelson SC,
Sinnott-Armstrong NA,
Albanes D,
Alonso MH,
Anderson K,
Arnau-Collell C,
Arndt V,
Bamia C,
Banbury BL,
Baron JA,
Berndt SI,
Bézieau S,
Bishop DT,
Boehm J,
Boeing H,
Brenner H,
Brezina S,
Buch S,
Buchanan DD,
Burnett-Hartman A,
Butterbach K,
Caan BJ,
Campbell PT,
Carlson CS,
Castellví-Bel S,
Chan AT,
Chang-Claude J,
Chanock SJ,
Chirlaque MD,
Cho SH,
Connolly CM,
Cross AJ,
Cuk K,
Curtis KR,
de la Chapelle A,
Doheny KF,
Duggan D,
Easton DF,
Elias SG,
Elliott F,
English DR,
Feskens EJM,
Figueiredo JC,
Fischer R,
FitzGerald LM,
Forman D,
Gala M,
Gallinger S,
Gauderman WJ,
Giles GG,
Gillanders E,
Gong J,
Goodman PJ,
Grady WM,
Grove JS,
Gsur A,
Gunter MJ,
Haile RW,
Hampe J,
Hampel H,
Harlid S,
Hayes RB,
Hofer P,
Hoffmeister M,
Hopper JL,
Hsu WL,
Huang WY,
Hudson TJ,
Hunter DJ,
Ibañez-Sanz G,
Idos GE,
Ingersoll R,
Jackson RD,
Jacobs EJ,
Jenkins MA,
Joshi AD,
Joshu CE,
Keku TO,
Key TJ,
Kim HR,
Kobayashi E,
Kolonel LN,
Kooperberg C,
Kühn T,
Küry S,
Kweon SS,
Larsson SC,
Laurie CA,
Le Marchand L,
Leal SM,
Lee SC,
Lejbkowicz F,
Lemire M,
Li CI,
Li L,
Lieb W,
Lin Y,
Lindblom A,
Lindor NM,
Ling H,
Louie TL,
Männistö S,
Markowitz SD,
Martín V,
Masala G,
McNeil CE,
Melas M,
Milne RL,
Moreno L,
Murphy N,
Myte R,
Naccarati A,
Newcomb PA,
Offit K,
Ogino S,
Onland-Moret NC,
Pardini B,
Parfrey PS,
Pearlman R,
Perduca V,
Pharoah PDP,
Pinchev M,
Platz EA,
Prentice RL,
Pugh E,
Raskin L,
Rennert G,
Rennert HS,
Riboli E,
Rodríguez-Barranco M,
Romm J,
Sakoda LC,
Schafmayer C,
Schoen RE,
Seminara D,
Shah M,
Shelford T,
Shin MH,
Shulman K,
Sieri S,
Slattery ML,
Southey MC,
Stadler ZK,
Stegmaier C,
Su YR,
Tangen CM,
Thibodeau SN,
Thomas DC,
Thomas SS,
Toland AE,
Trichopoulou A,
Ulrich CM,
Van Den Berg DJ,
van Duijnhoven FJB,
Van Guelpen B,
van Kranen H,
Vijai J,
Visvanathan K,
Vodicka P,
Vodickova L,
Vymetalkova V,
Weigl K,
Weinstein SJ,
White E,
Win AK,
Wolf CR,
Wolk A,
Woods MO,
Wu AH,
Zaidi SH,
Zanke BW,
Zhang Q,
Zheng W,
Zheng W,
Scacheri PC,
Potter JD,
Bassik MC,
Kundaje A,
Casey G,
Moreno V,
Abecasis GR,
Nickerson DA,
Gruber SB,
Hsu L,
Peters U
Nature genetics · 2019 · PMID 30510241 · open access
12 pages+
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies
Morris AP,
Le TH,
Wu H,
Akbarov A,
van der Most PJ,
Hemani G,
Smith GD,
Mahajan A,
Gaulton KJ,
Nadkarni GN,
Valladares-Salgado A,
Wacher-Rodarte N
and 60 more — show all
Mychaleckyj JC,
Dueker ND,
Guo X,
Hai Y,
Haessler J,
Kamatani Y,
Stilp AM,
Zhu G,
Cook JP,
Ärnlöv J,
Blanton SH,
de Borst MH,
Bottinger EP,
Buchanan TA,
Cechova S,
Charchar FJ,
Chu PL,
Damman J,
Eales J,
Gharavi AG,
Giedraitis V,
Heath AC,
Ipp E,
Kiryluk K,
Kramer HJ,
Kubo M,
Larsson A,
Lindgren CM,
Lu Y,
Madden PAF,
Montgomery GW,
Papanicolaou GJ,
Raffel LJ,
Sacco RL,
Sanchez E,
Stark H,
Sundstrom J,
Taylor KD,
Xiang AH,
Zivkovic A,
Lind L,
Ingelsson E,
Martin NG,
Whitfield JB,
Cai J,
Laurie CC,
Okada Y,
Matsuda K,
Kooperberg C,
Chen YI,
Rundek T,
Rich SS,
Loos RJF,
Parra EJ,
Cruz M,
Rotter JI,
Snieder H,
Tomaszewski M,
Humphreys BD,
Franceschini N
Nature communications · 2019 · PMID 30604766 · open access
12 pages+
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk
Jansen IE,
Savage JE,
Watanabe K,
Bryois J,
Williams DM,
Steinberg S,
Sealock J,
Karlsson IK,
Hägg S,
Athanasiu L,
Voyle N,
Proitsi P
and 41 more — show all
Witoelar A,
Stringer S,
Aarsland D,
Almdahl IS,
Andersen F,
Bergh S,
Bettella F,
Bjornsson S,
Brækhus A,
Bråthen G,
de Leeuw C,
Desikan RS,
Djurovic S,
Dumitrescu L,
Fladby T,
Hohman TJ,
Jonsson PV,
Kiddle SJ,
Rongve A,
Saltvedt I,
Sando SB,
Selbæk G,
Shoai M,
Skene NG,
Snaedal J,
Stordal E,
Ulstein ID,
Wang Y,
White LR,
Hardy J,
Hjerling-Leffler J,
Sullivan PF,
van der Flier WM,
Dobson R,
Davis LK,
Stefansson H,
Stefansson K,
Pedersen NL,
Ripke S,
Andreassen OA,
Posthuma D
Nature genetics · 2019 · PMID 30617256
12 pages+
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
Liu M,
Jiang Y,
Wedow R,
Li Y,
Brazel DM,
Chen F,
Datta G,
Davila-Velderrain J,
McGuire D,
Tian C,
Zhan X,
Choquet H
and 111 more — show all
Docherty AR,
Faul JD,
Foerster JR,
Fritsche LG,
Gabrielsen ME,
Gordon SD,
Haessler J,
Hottenga JJ,
Huang H,
Jang SK,
Jansen PR,
Ling Y,
Mägi R,
Matoba N,
McMahon G,
Mulas A,
Orrù V,
Palviainen T,
Pandit A,
Reginsson GW,
Skogholt AH,
Smith JA,
Taylor AE,
Turman C,
Willemsen G,
Young H,
Young KA,
Zajac GJM,
Zhao W,
Zhou W,
Bjornsdottir G,
Boardman JD,
Boehnke M,
Boomsma DI,
Chen C,
Cucca F,
Davies GE,
Eaton CB,
Ehringer MA,
Esko T,
Fiorillo E,
Gillespie NA,
Gudbjartsson DF,
Haller T,
Harris KM,
Heath AC,
Hewitt JK,
Hickie IB,
Hokanson JE,
Hopfer CJ,
Hunter DJ,
Iacono WG,
Johnson EO,
Kamatani Y,
Kardia SLR,
Keller MC,
Kellis M,
Kooperberg C,
Kraft P,
Krauter KS,
Laakso M,
Lind PA,
Loukola A,
Lutz SM,
Madden PAF,
Martin NG,
McGue M,
McQueen MB,
Medland SE,
Metspalu A,
Mohlke KL,
Nielsen JB,
Okada Y,
Peters U,
Polderman TJC,
Posthuma D,
Reiner AP,
Rice JP,
Rimm E,
Rose RJ,
Runarsdottir V,
Stallings MC,
Stančáková A,
Stefansson H,
Thai KK,
Tindle HA,
Tyrfingsson T,
Wall TL,
Weir DR,
Weisner C,
Whitfield JB,
Winsvold BS,
Yin J,
Zuccolo L,
Bierut LJ,
Hveem K,
Lee JJ,
Munafò MR,
Saccone NL,
Willer CJ,
Cornelis MC,
David SP,
Hinds DA,
Jorgenson E,
Kaprio J,
Stitzel JA,
Stefansson K,
Thorgeirsson TE,
Abecasis G,
Liu DJ,
Vrieze S
23andMe Research Team · HUNT All-In Psychiatry
Nature genetics · 2019 · PMID 30643251 · open access
12 pages+
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity
Kilpeläinen TO,
Bentley AR,
Noordam R,
Sung YJ,
Schwander K,
Winkler TW,
Jakupović H,
Chasman DI,
Manning A,
Ntalla I,
Aschard H,
Brown MR
and 217 more — show all
de las Fuentes L,
Franceschini N,
Guo X,
Vojinovic D,
Aslibekyan S,
Feitosa MF,
Kho M,
Musani SK,
Richard M,
Wang H,
Wang Z,
Bartz TM,
Bielak LF,
Campbell A,
Dorajoo R,
Fisher V,
Hartwig FP,
Horimoto ARVR,
Li C,
Lohman KK,
Marten J,
Sim X,
Smith AV,
Tajuddin SM,
Alver M,
Amini M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Evangelou E,
Gao C,
Graff M,
Harris SE,
He M,
Hsu FC,
Jackson AU,
Zhao JH,
Kraja AT,
Kühnel B,
Laguzzi F,
Lyytikäinen LP,
Nolte IM,
Rauramaa R,
Riaz M,
Robino A,
Rueedi R,
Stringham HM,
Takeuchi F,
van der Most PJ,
Varga TV,
Verweij N,
Ware EB,
Wen W,
Li X,
Yanek LR,
Amin N,
Arnett DK,
Boerwinkle E,
Brumat M,
Cade B,
Canouil M,
Chen YI,
Concas MP,
Connell J,
de Mutsert R,
de Silva HJ,
de Vries PS,
Demirkan A,
Ding J,
Eaton CB,
Faul JD,
Friedlander Y,
Gabriel KP,
Ghanbari M,
Giulianini F,
Gu CC,
Gu D,
Harris TB,
He J,
Heikkinen S,
Heng CK,
Hunt SC,
Ikram MA,
Jonas JB,
Koh WP,
Komulainen P,
Krieger JE,
Kritchevsky SB,
Kutalik Z,
Kuusisto J,
Langefeld CD,
Langenberg C,
Launer LJ,
Leander K,
Lemaitre RN,
Lewis CE,
Liang J,
Liu J,
Mägi R,
Manichaikul A,
Meitinger T,
Metspalu A,
Milaneschi Y,
Mohlke KL,
Mosley TH Jr,
Murray AD,
Nalls MA,
Nang EK,
Nelson CP,
Nona S,
Norris JM,
Nwuba CV,
O'Connell J,
Palmer ND,
Papanicolau GJ,
Pazoki R,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Porteous DJ,
Poveda A,
Raitakari OT,
Rich SS,
Risch N,
Robinson JG,
Rose LM,
Rudan I,
Schreiner PJ,
Scott RA,
Sidney SS,
Sims M,
Smith JA,
Snieder H,
Sofer T,
Starr JM,
Sternfeld B,
Strauch K,
Tang H,
Taylor KD,
Tsai MY,
Tuomilehto J,
Uitterlinden AG,
van der Ende MY,
van Heemst D,
Voortman T,
Waldenberger M,
Wennberg P,
Wilson G,
Xiang YB,
Yao J,
Yu C,
Yuan JM,
Zhao W,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
de Faire U,
Deary IJ,
Elliott P,
Esko T,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Kato N,
Laakso M,
Lakka TA,
Lehtimäki T,
Magnusson PKE,
Oldehinkel AJ,
Penninx BWJH,
Samani NJ,
Shu XO,
van der Harst P,
Van Vliet-Ostaptchouk JV,
Vollenweider P,
Wagenknecht LE,
Wang YX,
Wareham NJ,
Weir DR,
Wu T,
Zheng W,
Zhu X,
Evans MK,
Franks PW,
Gudnason V,
Hayward C,
Horta BL,
Kelly TN,
Liu Y,
North KE,
Pereira AC,
Ridker PM,
Tai ES,
van Dam RM,
Fox ER,
Kardia SLR,
Liu CT,
Mook-Kanamori DO,
Province MA,
Redline S,
van Duijn CM,
Rotter JI,
Kooperberg CB,
Gauderman WJ,
Psaty BM,
Rice K,
Munroe PB,
Fornage M,
Cupples LA,
Rotimi CN,
Morrison AC,
Rao DC,
Loos RJF
Lifelines Cohort Study
Nature communications · 2019 · PMID 30670697 · open access
12 pages+
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use
Brazel DM,
Jiang Y,
Hughey JM,
Turcot V,
Zhan X,
Gong J,
Batini C,
Weissenkampen JD,
Liu M,
Barnes DR,
Bertelsen S,
Chou YL
and 59 more — show all
Erzurumluoglu AM,
Faul JD,
Haessler J,
Hammerschlag AR,
Hsu C,
Kapoor M,
Lai D,
Le N,
de Leeuw CA,
Loukola A,
Mangino M,
Melbourne CA,
Pistis G,
Qaiser B,
Rohde R,
Shao Y,
Stringham H,
Wetherill L,
Zhao W,
Agrawal A,
Bierut L,
Chen C,
Eaton CB,
Goate A,
Haiman C,
Heath A,
Iacono WG,
Martin NG,
Polderman TJ,
Reiner A,
Rice J,
Schlessinger D,
Scholte HS,
Smith JA,
Tardif JC,
Tindle HA,
van der Leij AR,
Boehnke M,
Chang-Claude J,
Cucca F,
David SP,
Foroud T,
Howson JMM,
Kardia SLR,
Kooperberg C,
Laakso M,
Lettre G,
Madden P,
McGue M,
North K,
Posthuma D,
Spector T,
Stram D,
Tobin MD,
Weir DR,
Kaprio J,
Abecasis GR,
Liu DJ,
Vrieze S
CHD Exome+ Consortium · Consortium for Genetics of Smoking Behaviour
Biological psychiatry · 2019 · PMID 30679032
12 pages+
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
Justice AE,
Karaderi T,
Highland HM,
Young KL,
Graff M,
Lu Y,
Turcot V,
Auer PL,
Fine RS,
Guo X,
Schurmann C,
Lempradl A
and 268 more — show all
Marouli E,
Mahajan A,
Winkler TW,
Winkler TW,
Locke AE,
Medina-Gomez C,
Esko T,
Vedantam S,
Giri A,
Lo KS,
Alfred T,
Mudgal P,
Ng MCY,
Heard-Costa NL,
Feitosa MF,
Manning AK,
Willems SM,
Sivapalaratnam S,
Abecasis G,
Alam DS,
Allison M,
Amouyel P,
Arzumanyan Z,
Balkau B,
Bastarache L,
Bergmann S,
Bielak LF,
Blüher M,
Boehnke M,
Boeing H,
Boerwinkle E,
Böger CA,
Bork-Jensen J,
Bottinger EP,
Bowden DW,
Brandslund I,
Broer L,
Burt AA,
Butterworth AS,
Caulfield MJ,
Cesana G,
Chambers JC,
Chasman DI,
Chen YI,
Chowdhury R,
Christensen C,
Chu AY,
Collins FS,
Cook JP,
Cox AJ,
Crosslin DS,
Danesh J,
de Bakker PIW,
Denus S,
Mutsert R,
Dedoussis G,
Demerath EW,
Dennis JG,
Denny JC,
Di Angelantonio E,
Dörr M,
Drenos F,
Dubé MP,
Dunning AM,
Easton DF,
Elliott P,
Evangelou E,
Farmaki AE,
Feng S,
Ferrannini E,
Ferrieres J,
Florez JC,
Fornage M,
Fox CS,
Franks PW,
Friedrich N,
Gan W,
Gandin I,
Gasparini P,
Giedraitis V,
Girotto G,
Gorski M,
Grallert H,
Grarup N,
Grove ML,
Gustafsson S,
Haessler J,
Hansen T,
Hattersley AT,
Hayward C,
Heid IM,
Holmen OL,
Hovingh GK,
Howson JMM,
Hu Y,
Hung YJ,
Hveem K,
Ikram MA,
Ingelsson E,
Jackson AU,
Jarvik GP,
Jia Y,
Jørgensen T,
Jousilahti P,
Justesen JM,
Kahali B,
Karaleftheri M,
Kardia SLR,
Karpe F,
Kee F,
Kitajima H,
Komulainen P,
Kooner JS,
Kovacs P,
Krämer BK,
Kuulasmaa K,
Kuusisto J,
Laakso M,
Lakka TA,
Lamparter D,
Lange LA,
Langenberg C,
Larson EB,
Lee NR,
Lee WJ,
Lehtimäki T,
Lewis CE,
Li H,
Li J,
Li-Gao R,
Lin LA,
Lin X,
Lind L,
Lindström J,
Linneberg A,
Liu CT,
Liu DJ,
Luan J,
Lyytikäinen LP,
MacGregor S,
Mägi R,
Männistö S,
Marenne G,
Marten J,
Masca NGD,
McCarthy MI,
Meidtner K,
Mihailov E,
Moilanen L,
Moitry M,
Mook-Kanamori DO,
Morgan A,
Morris AP,
Müller-Nurasyid M,
Munroe PB,
Narisu N,
Nelson CP,
Neville M,
Ntalla I,
O'Connell JR,
Owen KR,
Pedersen O,
Peloso GM,
Pennell CE,
Perola M,
Perry JA,
Perry JRB,
Pers TH,
Ewing A,
Polasek O,
Raitakari OT,
Rasheed A,
Raulerson CK,
Rauramaa R,
Reilly DF,
Reiner AP,
Ridker PM,
Rivas MA,
Robertson NR,
Robino A,
Rudan I,
Ruth KS,
Saleheen D,
Salomaa V,
Samani NJ,
Schreiner PJ,
Schulze MB,
Scott RA,
Segura-Lepe M,
Sim X,
Slater AJ,
Small KS,
Smith BH,
Smith JA,
Southam L,
Spector TD,
Speliotes EK,
Stefansson K,
Steinthorsdottir V,
Stirrups KE,
Strauch K,
Stringham HM,
Stumvoll M,
Sun L,
Surendran P,
Swart KMA,
Tardif JC,
Taylor KD,
Teumer A,
Thompson DJ,
Thorleifsson G,
Thorsteinsdottir U,
Thuesen BH,
Tönjes A,
Torres M,
Tsafantakis E,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
van Duijn CM,
Vanhala M,
Varma R,
Vermeulen SH,
Vestergaard H,
Vitart V,
Vogt TF,
Vuckovic D,
Wagenknecht LE,
Walker M,
Wallentin L,
Wang F,
Wang CA,
Wang S,
Wareham NJ,
Warren HR,
Waterworth DM,
Wessel J,
White HD,
Willer CJ,
Wilson JG,
Wood AR,
Wu Y,
Yaghootkar H,
Yao J,
Yerges-Armstrong LM,
Young R,
Zeggini E,
Zhan X,
Zhang W,
Zhao JH,
Zhao W,
Zheng H,
Zhou W,
Zillikens MC,
Rivadeneira F,
Borecki IB,
Pospisilik JA,
Deloukas P,
Frayling TM,
Lettre G,
Mohlke KL,
Rotter JI,
Kutalik Z,
Hirschhorn JN,
Cupples LA,
Loos RJF,
North KE,
Lindgren CM
CHD Exome+ Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and 8 more consortia
Nature genetics · 2019 · PMID 30778226 · open access
12 pages+
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
Shrine N,
Guyatt AL,
Erzurumluoglu AM,
Jackson VE,
Hobbs BD,
Melbourne CA,
Batini C,
Fawcett KA,
Song K,
Sakornsakolpat P,
Li X,
Boxall R
and 99 more — show all
Reeve NF,
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German Chronic Kidney Disease Study · Lifelines Cohort Study and 1 more consortia
Nature genetics · 2019 · PMID 31578528 · open access
12 pages+
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
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23andMe Research Team
Nature communications · 2019 · PMID 31649266 · open access
12 pages+
Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans
Schlosser P,
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Nature genetics · 2020 · PMID 31959995
12 pages+
The genetic architecture of the human cerebral cortex
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Alzheimer’s Disease Neuroimaging Initiative · CHARGE Consortium and 5 more consortia
Science (New York, N.Y.) · 2020 · PMID 32193296
12 pages+
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration
Revez JA,
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Nature communications · 2020 · PMID 32242144 · open access
12 pages+
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Ntalla I,
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Hayward C,
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Nature communications · 2020 · PMID 32439900 · open access
12 pages+
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