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145 matches for
He J,
showing the first 20.
Genetic diversity fuels gene discovery for tobacco and alcohol use
Saunders GRB,
Wang X,
Chen F,
Jang SK,
Liu M,
Wang C,
Gao S,
Jiang Y,
Khunsriraksakul C,
Otto JM,
Addison C,
Akiyama M
and 205 more — show all
Albert CM,
Aliev F,
Alonso A,
Arnett DK,
Ashley-Koch AE,
Ashrani AA,
Barnes KC,
Barr RG,
Bartz TM,
Becker DM,
Bielak LF,
Benjamin EJ,
Bis JC,
Bjornsdottir G,
Blangero J,
Bleecker ER,
Boardman JD,
Boerwinkle E,
Boomsma DI,
Boorgula MP,
Bowden DW,
Brody JA,
Cade BE,
Chasman DI,
Chavan S,
Chen YI,
Chen Z,
Cheng I,
Cho MH,
Choquet H,
Cole JW,
Cornelis MC,
Cucca F,
Curran JE,
de Andrade M,
Dick DM,
Docherty AR,
Duggirala R,
Eaton CB,
Ehringer MA,
Esko T,
Faul JD,
Fernandes Silva L,
Fiorillo E,
Fornage M,
Freedman BI,
Gabrielsen ME,
Garrett ME,
Gharib SA,
Gieger C,
Gillespie N,
Glahn DC,
Gordon SD,
Gu CC,
Gu D,
Gudbjartsson DF,
Guo X,
Haessler J,
Hall ME,
Haller T,
Harris KM,
He J,
Herd P,
Hewitt JK,
Hickie I,
Hidalgo B,
Hokanson JE,
Hopfer C,
Hottenga J,
Hou L,
Huang H,
Hung YJ,
Hunter DJ,
Hveem K,
Hwang SJ,
Hwu CM,
Iacono W,
Irvin MR,
Jee YH,
Johnson EO,
Joo YY,
Jorgenson E,
Justice AE,
Kamatani Y,
Kaplan RC,
Kaprio J,
Kardia SLR,
Keller MC,
Kelly TN,
Kooperberg C,
Korhonen T,
Kraft P,
Krauter K,
Kuusisto J,
Laakso M,
Lasky-Su J,
Lee WJ,
Lee JJ,
Levy D,
Li L,
Li K,
Li Y,
Lin K,
Lind PA,
Liu C,
Lloyd-Jones DM,
Lutz SM,
Ma J,
Mägi R,
Manichaikul A,
Martin NG,
Mathur R,
Matoba N,
McArdle PF,
McGue M,
McQueen MB,
Medland SE,
Metspalu A,
Meyers DA,
Millwood IY,
Mitchell BD,
Mohlke KL,
Moll M,
Montasser ME,
Morrison AC,
Mulas A,
Nielsen JB,
North KE,
Oelsner EC,
Okada Y,
Orrù V,
Palmer ND,
Palviainen T,
Pandit A,
Park SL,
Peters U,
Peters A,
Peyser PA,
Polderman TJC,
Rafaels N,
Redline S,
Reed RM,
Reiner AP,
Rice JP,
Rich SS,
Richmond NE,
Roan C,
Rotter JI,
Rueschman MN,
Runarsdottir V,
Saccone NL,
Schwartz DA,
Shadyab AH,
Shi J,
Shringarpure SS,
Sicinski K,
Skogholt AH,
Smith JA,
Smith NL,
Sotoodehnia N,
Stallings MC,
Stefansson H,
Stefansson K,
Stitzel JA,
Sun X,
Syed M,
Tal-Singer R,
Taylor AE,
Taylor KD,
Telen MJ,
Thai KK,
Tiwari H,
Turman C,
Tyrfingsson T,
Wall TL,
Walters RG,
Weir DR,
Weiss ST,
White WB,
Whitfield JB,
Wiggins KL,
Willemsen G,
Willer CJ,
Winsvold BS,
Xu H,
Yanek LR,
Yin J,
Young KL,
Young KA,
Yu B,
Zhao W,
Zhou W,
Zöllner S,
Zuccolo L,
Batini C,
Bergen AW,
Bierut LJ,
David SP,
Gagliano Taliun SA,
Hancock DB,
Jiang B,
Munafò MR,
Thorgeirsson TE,
Liu DJ,
Vrieze S
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries
Fernandez-Rozadilla C,
Timofeeva M,
Chen Z,
Law P,
Thomas M,
Schmit S,
Díez-Obrero V,
Hsu L,
Fernandez-Tajes J,
Palles C,
Sherwood K,
Briggs S
and 198 more — show all
Svinti V,
Donnelly K,
Farrington S,
Blackmur J,
Vaughan-Shaw P,
Shu XO,
Long J,
Cai Q,
Guo X,
Lu Y,
Broderick P,
Studd J,
Huyghe J,
Harrison T,
Conti D,
Dampier C,
Devall M,
Schumacher F,
Melas M,
Rennert G,
Obón-Santacana M,
Martín-Sánchez V,
Moratalla-Navarro F,
Oh JH,
Kim J,
Jee SH,
Jung KJ,
Kweon SS,
Shin MH,
Shin A,
Ahn YO,
Kim DH,
Oze I,
Wen W,
Matsuo K,
Matsuda K,
Tanikawa C,
Ren Z,
Gao YT,
Jia WH,
Hopper J,
Jenkins M,
Win AK,
Pai R,
Figueiredo J,
Haile R,
Gallinger S,
Woods M,
Newcomb P,
Duggan D,
Cheadle J,
Kaplan R,
Maughan T,
Kerr R,
Kerr D,
Kirac I,
Böhm J,
Mecklin LP,
Jousilahti P,
Knekt P,
Aaltonen L,
Rissanen H,
Pukkala E,
Eriksson J,
Cajuso T,
Hänninen U,
Kondelin J,
Palin K,
Tanskanen T,
Renkonen-Sinisalo L,
Zanke B,
Männistö S,
Albanes D,
Weinstein S,
Ruiz-Narvaez E,
Palmer J,
Buchanan D,
Platz E,
Visvanathan K,
Ulrich C,
Siegel E,
Brezina S,
Gsur A,
Campbell P,
Chang-Claude J,
Hoffmeister M,
Brenner H,
Slattery M,
Potter J,
Tsilidis K,
Schulze M,
Gunter M,
Murphy N,
Castells A,
Castellví-Bel S,
Moreira L,
Arndt V,
Shcherbina A,
Stern M,
Pardamean B,
Bishop T,
Giles G,
Southey M,
Idos G,
McDonnell K,
Abu-Ful Z,
Greenson J,
Shulman K,
Lejbkowicz F,
Offit K,
Su YR,
Steinfelder R,
Keku T,
van Guelpen B,
Hudson T,
Hampel H,
Pearlman R,
Berndt S,
Hayes R,
Martinez ME,
Thomas S,
Corley D,
Pharoah P,
Larsson S,
Yen Y,
Lenz HJ,
White E,
Li L,
Doheny K,
Pugh E,
Shelford T,
Chan A,
Cruz-Correa M,
Lindblom A,
Hunter D,
Joshi A,
Schafmayer C,
Scacheri P,
Kundaje A,
Nickerson D,
Schoen R,
Hampe J,
Stadler Z,
Vodicka P,
Vodickova L,
Vymetalkova V,
Papadopoulos N,
Edlund C,
Gauderman W,
Thomas D,
Shibata D,
Toland A,
Markowitz S,
Kim A,
Chanock S,
van Duijnhoven F,
Feskens E,
Sakoda L,
Gago-Dominguez M,
Wolk A,
Naccarati A,
Pardini B,
FitzGerald L,
Lee SC,
Ogino S,
Bien S,
Kooperberg C,
Li C,
Lin Y,
Prentice R,
Qu C,
Bézieau S,
Tangen C,
Mardis E,
Yamaji T,
Sawada N,
Iwasaki M,
Haiman C,
Le Marchand L,
Wu A,
Qu C,
McNeil C,
Coetzee G,
Hayward C,
Deary I,
Harris S,
Theodoratou E,
Reid S,
Walker M,
Ooi LY,
Moreno V,
Casey G,
Gruber S,
Tomlinson I,
Zheng W,
Dunlop M,
Houlston R,
Peters U
Nature genetics · 2023 · PMID 36539618
12 pages+
Genome-wide analysis of heart failure yields insights into disease heterogeneity and enables prognostic prediction in the Japanese population
Enzan N,
Miyazawa K,
Koyama S,
Kurosawa R,
Ieki H,
Yoshida H,
Takechi F,
Fukuyama M,
Osako R,
Tomizuka K,
Liu X,
Ozaki K
and 18 more — show all
Onouchi Y,
Matsuda K,
Momozawa Y,
Aburatani H,
Kamatani Y,
Yamaguchi T,
Akazawa H,
Node K,
Ellinor PT,
Levin MG,
Damrauer SM,
Voight BF,
Joseph J,
Sun YV,
Terao C,
Ninomiya T,
Komuro I,
Ito K
BioBank Japan Project
Nature communications · 2025 · PMID 41184235 · open access
12 pages+
Multi-ancestry genome-wide association and integrated multi-omics analyses of endometriosis and its clinical manifestations
Koller D,
He J,
Løkhammer S,
Aranda S,
Qiu D,
Davtian D,
Chen Q,
Xu Z,
Mao Z,
Friligkou E,
Karaca S,
Cormand B
and 5 more — show all
Nature genetics · 2026 · PMID 42056605
12 pages+
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
Barrett JC,
Hansoul S,
Nicolae DL,
Cho JH,
Duerr RH,
Rioux JD,
Brant SR,
Silverberg MS,
Taylor KD,
Barmada MM,
Bitton A,
Dassopoulos T
and 49 more — show all
Datta LW,
Green T,
Griffiths AM,
Kistner EO,
Murtha MT,
Regueiro MD,
Rotter JI,
Schumm LP,
Steinhart AH,
Targan SR,
Xavier RJ,
Libioulle C,
Sandor C,
Lathrop M,
Belaiche J,
Dewit O,
Gut I,
Heath S,
Laukens D,
Mni M,
Rutgeerts P,
Van Gossum A,
Zelenika D,
Franchimont D,
Hugot JP,
de Vos M,
Vermeire S,
Louis E,
Cardon LR,
Anderson CA,
Drummond H,
Nimmo E,
Ahmad T,
Prescott NJ,
Onnie CM,
Fisher SA,
Marchini J,
Ghori J,
Bumpstead S,
Gwilliam R,
Tremelling M,
Deloukas P,
Mansfield J,
Jewell D,
Satsangi J,
Mathew CG,
Parkes M,
Georges M,
Daly MJ
NIDDK IBD Genetics Consortium · Belgian-French IBD Consortium and 1 more consortia
Nature genetics · 2008 · PMID 18587394
11 pages
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Surendran P,
Drenos F,
Young R,
Warren H,
Cook JP,
Manning AK,
Grarup N,
Sim X,
Barnes DR,
Witkowska K,
Staley JR,
Tragante V
and 198 more — show all
Tukiainen T,
Yaghootkar H,
Masca N,
Freitag DF,
Ferreira T,
Giannakopoulou O,
Tinker A,
Harakalova M,
Mihailov E,
Liu C,
Kraja AT,
Fallgaard Nielsen S,
Rasheed A,
Samuel M,
Zhao W,
Bonnycastle LL,
Jackson AU,
Narisu N,
Swift AJ,
Southam L,
Marten J,
Huyghe JR,
Stančáková A,
Fava C,
Ohlsson T,
Matchan A,
Stirrups KE,
Bork-Jensen J,
Gjesing AP,
Kontto J,
Perola M,
Shaw-Hawkins S,
Havulinna AS,
Zhang H,
Donnelly LA,
Groves CJ,
Rayner NW,
Neville MJ,
Robertson NR,
Yiorkas AM,
Herzig KH,
Kajantie E,
Zhang W,
Willems SM,
Lannfelt L,
Malerba G,
Soranzo N,
Trabetti E,
Verweij N,
Evangelou E,
Moayyeri A,
Vergnaud AC,
Nelson CP,
Poveda A,
Varga TV,
Caslake M,
de Craen AJ,
Trompet S,
Luan J,
Scott RA,
Harris SE,
Liewald DC,
Marioni R,
Menni C,
Farmaki AE,
Hallmans G,
Renström F,
Huffman JE,
Hassinen M,
Burgess S,
Vasan RS,
Felix JF,
Uria-Nickelsen M,
Malarstig A,
Reily DF,
Hoek M,
Vogt T,
Lin H,
Lieb W,
Traylor M,
Markus HF,
Highland HM,
Justice AE,
Marouli E,
Lindström J,
Uusitupa M,
Komulainen P,
Lakka TA,
Rauramaa R,
Polasek O,
Rudan I,
Rolandsson O,
Franks PW,
Dedoussis G,
Spector TD,
Jousilahti P,
Männistö S,
Deary IJ,
Starr JM,
Langenberg C,
Wareham NJ,
Brown MJ,
Dominiczak AF,
Connell JM,
Jukema JW,
Sattar N,
Ford I,
Packard CJ,
Esko T,
Mägi R,
Metspalu A,
de Boer RA,
van der Meer P,
van der Harst P,
Gambaro G,
Ingelsson E,
Lind L,
de Bakker PI,
Numans ME,
Brandslund I,
Christensen C,
Petersen ER,
Korpi-Hyövälti E,
Oksa H,
Chambers JC,
Kooner JS,
Blakemore AI,
Franks S,
Jarvelin MR,
Husemoen LL,
Linneberg A,
Skaaby T,
Thuesen B,
Karpe F,
Tuomilehto J,
Doney AS,
Morris AD,
Palmer CN,
Holmen OL,
Hveem K,
Willer CJ,
Tuomi T,
Groop L,
Käräjämäki A,
Palotie A,
Ripatti S,
Salomaa V,
Alam DS,
Shafi Majumder AA,
Di Angelantonio E,
Chowdhury R,
McCarthy MI,
Poulter N,
Stanton AV,
Sever P,
Amouyel P,
Arveiler D,
Blankenberg S,
Ferrières J,
Kee F,
Kuulasmaa K,
Müller-Nurasyid M,
Veronesi G,
Virtamo J,
Deloukas P,
Elliott P,
Zeggini E,
Kathiresan S,
Melander O,
Kuusisto J,
Laakso M,
Padmanabhan S,
Porteous D,
Hayward C,
Scotland G,
Collins FS,
Mohlke KL,
Hansen T,
Pedersen O,
Boehnke M,
Stringham HM,
Frossard P,
Newton-Cheh C,
Tobin MD,
Nordestgaard BG,
Caulfield MJ,
Mahajan A,
Morris AP,
Tomaszewski M,
Samani NJ,
Saleheen D,
Asselbergs FW,
Lindgren CM,
Danesh J,
Wain LV,
Butterworth AS,
Howson JM,
Munroe PB
CHARGE-Heart Failure Consortium · EchoGen Consortium and 12 more consortia
Nature genetics · 2016 · PMID 27618447 · 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
Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population
Suzuki K,
Akiyama M,
Ishigaki K,
Kanai M,
Hosoe J,
Shojima N,
Hozawa A,
Kadota A,
Kuriki K,
Naito M,
Tanno K,
Ishigaki Y
and 20 more — show all
Hirata M,
Matsuda K,
Iwata N,
Ikeda M,
Sawada N,
Yamaji T,
Iwasaki M,
Ikegawa S,
Maeda S,
Murakami Y,
Wakai K,
Tsugane S,
Sasaki M,
Yamamoto M,
Okada Y,
Kubo M,
Kamatani Y,
Horikoshi M,
Yamauchi T,
Kadowaki T
Nature genetics · 2019 · PMID 30718926
9 pages
Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype
Ferreira MA,
Matheson MC,
Tang CS,
Granell R,
Ang W,
Hui J,
Kiefer AK,
Duffy DL,
Baltic S,
Danoy P,
Bui M,
Price L
and 22 more — show all
Sly PD,
Eriksson N,
Madden PA,
Abramson MJ,
Holt PG,
Heath AC,
Hunter M,
Musk B,
Robertson CF,
Le Souëf P,
Montgomery GW,
Henderson AJ,
Tung JY,
Dharmage SC,
Brown MA,
James A,
Thompson PJ,
Pennell C,
Martin NG,
Evans DM,
Hinds DA,
Hopper JL
Australian Asthma Genetics Consortium Collaborators
The Journal of allergy and clinical immunology · 2014 · PMID 24388013
8 pages
Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages
Chung J,
Wang X,
Maruyama T,
Ma Y,
Zhang X,
Mez J,
Sherva R,
Takeyama H,
Lunetta KL,
Farrer LA,
Jun GR
Alzheimer's Disease Neuroimaging Initiative
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2018 · PMID 29274321
8 pages
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation
Vujkovic M,
Ramdas S,
Lorenz KM,
Guo X,
Darlay R,
Cordell HJ,
He J,
Gindin Y,
Chung C,
Myers RP,
Schneider CV,
Park J
and 78 more — show all
Lee KM,
Serper M,
Carr RM,
Kaplan DE,
Haas ME,
MacLean MT,
Witschey WR,
Zhu X,
Tcheandjieu C,
Kember RL,
Kranzler HR,
Verma A,
Giri A,
Klarin DM,
Sun YV,
Huang J,
Huffman JE,
Creasy KT,
Hand NJ,
Liu CT,
Long MT,
Yao J,
Budoff M,
Tan J,
Li X,
Lin HJ,
Chen YI,
Taylor KD,
Chang RK,
Krauss RM,
Vilarinho S,
Brancale J,
Nielsen JB,
Locke AE,
Jones MB,
Verweij N,
Baras A,
Reddy KR,
Neuschwander-Tetri BA,
Schwimmer JB,
Sanyal AJ,
Chalasani N,
Ryan KA,
Mitchell BD,
Gill D,
Wells AD,
Manduchi E,
Saiman Y,
Mahmud N,
Miller DR,
Reaven PD,
Phillips LS,
Muralidhar S,
DuVall SL,
Lee JS,
Assimes TL,
Pyarajan S,
Cho K,
Edwards TL,
Damrauer SM,
Wilson PW,
Gaziano JM,
O'Donnell CJ,
Khera AV,
Grant SFA,
Brown CD,
Tsao PS,
Saleheen D,
Lotta LA,
Bastarache L,
Anstee QM,
Daly AK,
Meigs JB,
Rotter JI,
Lynch JA,
Rader DJ,
Voight BF,
Chang KM
Regeneron Genetics Center · Geisinger-Regeneron DiscovEHR Collaboration and 2 more consortia
Nature genetics · 2022 · PMID 35654975
8 pages
Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population
Okada Y,
Terao C,
Ikari K,
Kochi Y,
Ohmura K,
Suzuki A,
Kawaguchi T,
Stahl EA,
Kurreeman FA,
Nishida N,
Ohmiya H,
Myouzen K
and 39 more — show all
Takahashi M,
Sawada T,
Nishioka Y,
Yukioka M,
Matsubara T,
Wakitani S,
Teshima R,
Tohma S,
Takasugi K,
Shimada K,
Murasawa A,
Honjo S,
Matsuo K,
Tanaka H,
Tajima K,
Suzuki T,
Iwamoto T,
Kawamura Y,
Tanii H,
Okazaki Y,
Sasaki T,
Gregersen PK,
Padyukov L,
Worthington J,
Siminovitch KA,
Lathrop M,
Taniguchi A,
Takahashi A,
Tokunaga K,
Kubo M,
Nakamura Y,
Kamatani N,
Mimori T,
Plenge RM,
Yamanaka H,
Momohara S,
Yamada R,
Matsuda F,
Yamamoto K
Nature genetics · 2012 · PMID 22446963
7 pages
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
Sung YJ,
Winkler TW,
de las Fuentes L,
Bentley AR,
Brown MR,
Kraja AT,
Schwander K,
Ntalla I,
Guo X,
Franceschini N,
Lu Y,
Cheng CY
and 286 more — show all
Sim X,
Vojinovic D,
Marten J,
Musani SK,
Li C,
Feitosa MF,
Kilpeläinen TO,
Richard MA,
Noordam R,
Aslibekyan S,
Aschard H,
Bartz TM,
Dorajoo R,
Liu Y,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Tayo BO,
Warren HR,
Zhao W,
Zhou Y,
Matoba N,
Sofer T,
Alver M,
Amini M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Gandin I,
Gao C,
Giulianini F,
Goel A,
Harris SE,
Hartwig FP,
Horimoto ARVR,
Hsu FC,
Jackson AU,
Kähönen M,
Kasturiratne A,
Kühnel B,
Leander K,
Lee WJ,
Lin KH,
'an Luan J,
McKenzie CA,
Meian H,
Nelson CP,
Rauramaa R,
Schupf N,
Scott RA,
Sheu WHH,
Stančáková A,
Takeuchi F,
van der Most PJ,
Varga TV,
Wang H,
Wang Y,
Ware EB,
Weiss S,
Wen W,
Yanek LR,
Zhang W,
Zhao JH,
Afaq S,
Alfred T,
Amin N,
Arking D,
Aung T,
Barr RG,
Bielak LF,
Boerwinkle E,
Bottinger EP,
Braund PS,
Brody JA,
Broeckel U,
Cabrera CP,
Cade B,
Caizheng Y,
Campbell A,
Canouil M,
Chakravarti A,
Chauhan G,
Christensen K,
Cocca M,
Collins FS,
Connell JM,
de Mutsert R,
de Silva HJ,
Debette S,
Dörr M,
Duan Q,
Eaton CB,
Ehret G,
Evangelou E,
Faul JD,
Fisher VA,
Forouhi NG,
Franco OH,
Friedlander Y,
Gao H,
Gigante B,
Graff M,
Gu CC,
Gu D,
Gupta P,
Hagenaars SP,
Harris TB,
He J,
Heikkinen S,
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