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21 matches for
Yu H,
showing the first 20.
Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia
Li Z,
Chen J,
Yu H,
He L,
Xu Y,
Zhang D,
Yi Q,
Li C,
Li X,
Shen J,
Song Z,
Ji W
and 26 more — show all
Wang M,
Zhou J,
Chen B,
Liu Y,
Wang J,
Wang P,
Yang P,
Wang Q,
Feng G,
Liu B,
Sun W,
Li B,
He G,
Li W,
Wan C,
Xu Q,
Li W,
Wen Z,
Liu K,
Huang F,
Ji J,
Ripke S,
Yue W,
Sullivan PF,
O'Donovan MC,
Shi Y
Nature genetics · 2017 · PMID 28991256
12 pages+
Korea4K: whole genome sequences of 4,157 Koreans with 107 phenotypes derived from extensive health check-ups
Jeon S,
Choi H,
Jeon Y,
Choi WH,
Choi H,
An K,
Ryu H,
Bhak J,
Lee H,
Kwon Y,
Ha S,
Kim YJ
and 18 more — show all
Blazyte A,
Kim C,
Kim Y,
Kang Y,
Woo YJ,
Lee C,
Seo J,
Yoon C,
Bolser D,
Biro O,
Shin ES,
Kim BC,
Kim SY,
Park JH,
Jeon J,
Jung D,
Lee S,
Bhak J
GigaScience · 2024 · PMID 38626723 · open access
12 pages+
Exome-wide association study of plasma lipids in >300,000 individuals
Liu DJ,
Peloso GM,
Yu H,
Butterworth AS,
Wang X,
Mahajan A,
Saleheen D,
Emdin C,
Alam D,
Alves AC,
Amouyel P,
Di Angelantonio E
and 215 more — show all
Arveiler D,
Assimes TL,
Auer PL,
Baber U,
Ballantyne CM,
Bang LE,
Benn M,
Bis JC,
Boehnke M,
Boerwinkle E,
Bork-Jensen J,
Bottinger EP,
Brandslund I,
Brown M,
Busonero F,
Caulfield MJ,
Chambers JC,
Chasman DI,
Chen YE,
Chen YI,
Chowdhury R,
Christensen C,
Chu AY,
Connell JM,
Cucca F,
Cupples LA,
Damrauer SM,
Davies G,
Deary IJ,
Dedoussis G,
Denny JC,
Dominiczak A,
Dubé MP,
Ebeling T,
Eiriksdottir G,
Esko T,
Farmaki AE,
Feitosa MF,
Ferrario M,
Ferrieres J,
Ford I,
Fornage M,
Franks PW,
Frayling TM,
Frikke-Schmidt R,
Fritsche LG,
Frossard P,
Fuster V,
Ganesh SK,
Gao W,
Garcia ME,
Gieger C,
Giulianini F,
Goodarzi MO,
Grallert H,
Grarup N,
Groop L,
Grove ML,
Gudnason V,
Hansen T,
Harris TB,
Hayward C,
Hirschhorn JN,
Holmen OL,
Huffman J,
Huo Y,
Hveem K,
Jabeen S,
Jackson AU,
Jakobsdottir J,
Jarvelin MR,
Jensen GB,
Jørgensen ME,
Jukema JW,
Justesen JM,
Kamstrup PR,
Kanoni S,
Karpe F,
Kee F,
Khera AV,
Klarin D,
Koistinen HA,
Kooner JS,
Kooperberg C,
Kuulasmaa K,
Kuusisto J,
Laakso M,
Lakka T,
Langenberg C,
Langsted A,
Launer LJ,
Lauritzen T,
Liewald DCM,
Lin LA,
Linneberg A,
Loos RJF,
Lu Y,
Lu X,
Mägi R,
Malarstig A,
Manichaikul A,
Manning AK,
Mäntyselkä P,
Marouli E,
Masca NGD,
Maschio A,
Meigs JB,
Melander O,
Metspalu A,
Morris AP,
Morrison AC,
Mulas A,
Müller-Nurasyid M,
Munroe PB,
Neville MJ,
Nielsen JB,
Nielsen SF,
Nordestgaard BG,
Ordovas JM,
Mehran R,
O'Donnell CJ,
Orho-Melander M,
Molony CM,
Muntendam P,
Padmanabhan S,
Palmer CNA,
Pasko D,
Patel AP,
Pedersen O,
Perola M,
Peters A,
Pisinger C,
Pistis G,
Polasek O,
Poulter N,
Psaty BM,
Rader DJ,
Rasheed A,
Rauramaa R,
Reilly DF,
Reiner AP,
Renström F,
Rich SS,
Ridker PM,
Rioux JD,
Robertson NR,
Roden DM,
Rotter JI,
Rudan I,
Salomaa V,
Samani NJ,
Sanna S,
Sattar N,
Schmidt EM,
Scott RA,
Sever P,
Sevilla RS,
Shaffer CM,
Sim X,
Sivapalaratnam S,
Small KS,
Smith AV,
Smith BH,
Somayajula S,
Southam L,
Spector TD,
Speliotes EK,
Starr JM,
Stirrups KE,
Stitziel N,
Strauch K,
Stringham HM,
Surendran P,
Tada H,
Tall AR,
Tang H,
Tardif JC,
Taylor KD,
Trompet S,
Tsao PS,
Tuomilehto J,
Tybjaerg-Hansen A,
van Zuydam NR,
Varbo A,
Varga TV,
Virtamo J,
Waldenberger M,
Wang N,
Wareham NJ,
Warren HR,
Weeke PE,
Weinstock J,
Wessel J,
Wilson JG,
Wilson PWF,
Xu M,
Yaghootkar H,
Young R,
Zeggini E,
Zhang H,
Zheng NS,
Zhang W,
Zhang Y,
Zhou W,
Zhou Y,
Zoledziewska M,
Howson JMM,
Danesh J,
McCarthy MI,
Cowan CA,
Abecasis G,
Deloukas P,
Musunuru K,
Willer CJ,
Kathiresan S
Charge Diabetes Working Group · EPIC-InterAct Consortium and 3 more consortia
Nature genetics · 2017 · PMID 29083408 · open access
11 pages
Identification of nine new susceptibility loci for endometrial cancer
O'Mara TA,
Glubb DM,
Amant F,
Annibali D,
Ashton K,
Attia J,
Auer PL,
Beckmann MW,
Black A,
Bolla MK,
Brauch H,
Brenner H
and 114 more — show all
Brinton L,
Buchanan DD,
Burwinkel B,
Chang-Claude J,
Chanock SJ,
Chen C,
Chen MM,
Cheng THT,
Clarke CL,
Clendenning M,
Cook LS,
Couch FJ,
Cox A,
Crous-Bous M,
Czene K,
Day F,
Dennis J,
Depreeuw J,
Doherty JA,
Dörk T,
Dowdy SC,
Dürst M,
Ekici AB,
Fasching PA,
Fridley BL,
Friedenreich CM,
Fritschi L,
Fung J,
García-Closas M,
Gaudet MM,
Giles GG,
Goode EL,
Gorman M,
Haiman CA,
Hall P,
Hankison SE,
Healey CS,
Hein A,
Hillemanns P,
Hodgson S,
Hoivik EA,
Holliday EG,
Hopper JL,
Hunter DJ,
Jones A,
Krakstad C,
Kristensen VN,
Lambrechts D,
Marchand LL,
Liang X,
Lindblom A,
Lissowska J,
Long J,
Lu L,
Magliocco AM,
Martin L,
McEvoy M,
Meindl A,
Michailidou K,
Milne RL,
Mints M,
Montgomery GW,
Nassir R,
Olsson H,
Orlow I,
Otton G,
Palles C,
Perry JRB,
Peto J,
Pooler L,
Prescott J,
Proietto T,
Rebbeck TR,
Risch HA,
Rogers PAW,
Rübner M,
Runnebaum I,
Sacerdote C,
Sarto GE,
Schumacher F,
Scott RJ,
Setiawan VW,
Shah M,
Sheng X,
Shu XO,
Southey MC,
Swerdlow AJ,
Tham E,
Trovik J,
Turman C,
Tyrer JP,
Vachon C,
VanDen Berg D,
Vanderstichele A,
Wang Z,
Webb PM,
Wentzensen N,
Werner HMJ,
Winham SJ,
Wolk A,
Xia L,
Xiang YB,
Yang HP,
Yu H,
Zheng W,
Zheng W,
Pharoah PDP,
Dunning AM,
Kraft P,
De Vivo I,
Tomlinson I,
Easton DF,
Spurdle AB,
Thompson DJ
Nature communications · 2018 · PMID 30093612 · open access
6 pages
Ethnic similarities in genetic polymorphisms associated with atrial fibrillation: Far East Asian vs European populations
Hong M,
Ebana Y,
Shim J,
Choi EK,
Lim HE,
Hwang I,
Yu HT,
Kim TH,
Uhm JS,
Joung B,
Oh S,
Lee MH
and 3 more — show all
European journal of clinical investigation · 2021 · PMID 33990960
6 pages
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer
Wolpin BM,
Rizzato C,
Kraft P,
Kooperberg C,
Petersen GM,
Wang Z,
Arslan AA,
Beane-Freeman L,
Bracci PM,
Buring J,
Canzian F,
Duell EJ
and 106 more — show all
Gallinger S,
Giles GG,
Goodman GE,
Goodman PJ,
Jacobs EJ,
Kamineni A,
Klein AP,
Kolonel LN,
Kulke MH,
Li D,
Malats N,
Olson SH,
Risch HA,
Sesso HD,
Visvanathan K,
White E,
Zheng W,
Zheng W,
Abnet CC,
Albanes D,
Andreotti G,
Austin MA,
Barfield R,
Basso D,
Berndt SI,
Boutron-Ruault MC,
Brotzman M,
Büchler MW,
Bueno-de-Mesquita HB,
Bugert P,
Burdette L,
Campa D,
Caporaso NE,
Capurso G,
Chung C,
Cotterchio M,
Costello E,
Elena J,
Funel N,
Gaziano JM,
Giese NA,
Giovannucci EL,
Goggins M,
Gorman MJ,
Gross M,
Haiman CA,
Hassan M,
Helzlsouer KJ,
Henderson BE,
Holly EA,
Hu N,
Hunter DJ,
Innocenti F,
Jenab M,
Kaaks R,
Key TJ,
Khaw KT,
Klein EA,
Kogevinas M,
Krogh V,
Kupcinskas J,
Kurtz RC,
LaCroix A,
Landi MT,
Landi S,
Le Marchand L,
Mambrini A,
Mannisto S,
Milne RL,
Nakamura Y,
Oberg AL,
Owzar K,
Patel AV,
Peeters PH,
Peters U,
Pezzilli R,
Piepoli A,
Porta M,
Real FX,
Riboli E,
Rothman N,
Scarpa A,
Shu XO,
Silverman DT,
Soucek P,
Sund M,
Talar-Wojnarowska R,
Taylor PR,
Theodoropoulos GE,
Thornquist M,
Tjønneland A,
Tobias GS,
Trichopoulos D,
Vodicka P,
Wactawski-Wende J,
Wentzensen N,
Wu C,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Hoover R,
Hartge P,
Fuchs C,
Chanock SJ,
Stolzenberg-Solomon RS,
Amundadottir LT
Nature genetics · 2014 · PMID 25086665 · open access
5 pages
Genome-wide association study on plasma levels of midregional-proadrenomedullin and C-terminal-pro-endothelin-1
Verweij N,
Mahmud H,
Mateo Leach I,
de Boer RA,
Brouwers FP,
Yu H,
Asselbergs FW,
Struck J,
Bakker SJ,
Gansevoort RT,
Munroe PB,
Hillege HL
and 4 more — show all
Hypertension (Dallas, Tex. : 1979) · 2013 · PMID 23381795
4 pages
Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer
Klein AP,
Wolpin BM,
Risch HA,
Stolzenberg-Solomon RZ,
Mocci E,
Zhang M,
Canzian F,
Childs EJ,
Hoskins JW,
Jermusyk A,
Zhong J,
Chen F
and 112 more — show all
Albanes D,
Andreotti G,
Arslan AA,
Babic A,
Bamlet WR,
Beane-Freeman L,
Berndt SI,
Blackford A,
Borges M,
Borgida A,
Bracci PM,
Brais L,
Brennan P,
Brenner H,
Bueno-de-Mesquita B,
Buring J,
Campa D,
Capurso G,
Cavestro GM,
Chaffee KG,
Chung CC,
Cleary S,
Cotterchio M,
Dijk F,
Duell EJ,
Foretova L,
Fuchs C,
Funel N,
Gallinger S,
M Gaziano JM,
Gazouli M,
Giles GG,
Giovannucci E,
Goggins M,
Goodman GE,
Goodman PJ,
Hackert T,
Haiman C,
Hartge P,
Hasan M,
Hegyi P,
Helzlsouer KJ,
Herman J,
Holcatova I,
Holly EA,
Hoover R,
Hung RJ,
Jacobs EJ,
Jamroziak K,
Janout V,
Kaaks R,
Khaw KT,
Klein EA,
Kogevinas M,
Kooperberg C,
Kulke MH,
Kupcinskas J,
Kurtz RJ,
Laheru D,
Landi S,
Lawlor RT,
Lee IM,
LeMarchand L,
Lu L,
Malats N,
Mambrini A,
Mannisto S,
Milne RL,
Mohelníková-Duchoňová B,
Neale RE,
Neoptolemos JP,
Oberg AL,
Olson SH,
Orlow I,
Pasquali C,
Patel AV,
Peters U,
Pezzilli R,
Porta M,
Real FX,
Rothman N,
Scelo G,
Sesso HD,
Severi G,
Shu XO,
Silverman D,
Smith JP,
Soucek P,
Sund M,
Talar-Wojnarowska R,
Tavano F,
Thornquist MD,
Tobias GS,
Van Den Eeden SK,
Vashist Y,
Visvanathan K,
Vodicka P,
Wactawski-Wende J,
Wang Z,
Wentzensen N,
White E,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Zheng W,
Zheng W,
Kraft P,
Li D,
Chanock S,
Obazee O,
Petersen GM,
Amundadottir LT
Nature communications · 2018 · PMID 29422604 · open access
4 pages
Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study
Yu H,
Yan H,
Wang L,
Li J,
Tan L,
Deng W,
Chen Q,
Yang G,
Zhang F,
Lu T,
Yang J,
Li K
and 12 more — show all
Lv L,
Tan Q,
Zhang H,
Xiao X,
Li M,
Ma X,
Yang F,
Li L,
Wang C,
Li T,
Zhang D,
Yue W
Chinese Antipsychotics Pharmacogenomics Consortium
The lancet. Psychiatry · 2018 · PMID 29503163
4 pages
GWAS of Chronic Spontaneous Urticaria Reveals Genetic Overlap with Autoimmune Diseases, Not Atopic Diseases
Zhang L,
Qiu L,
Wu J,
Qi Y,
Gao X,
He C,
Qi R,
Wang H,
Yao X,
Zhu H,
Li Y,
Hao S
and 33 more — show all
Lu Q,
Long H,
Lian S,
Zhu W,
Zhang H,
Lai W,
Su X,
Lu R,
Guo Z,
Li J,
Li M,
Liu Q,
Wang H,
He L,
Nong X,
Li F,
Li Y,
Yao C,
Xu J,
Tang H,
Wang D,
Li Z,
Yu H,
Xiao S,
An J,
Pu X,
Yu S,
Zhang J,
Chen X,
Wang H,
Huang W,
Chen H,
Xiao T
The Journal of investigative dermatology · 2023 · PMID 35933036
4 pages
Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer
Amundadottir L,
Kraft P,
Stolzenberg-Solomon RZ,
Fuchs CS,
Petersen GM,
Arslan AA,
Bueno-de-Mesquita HB,
Gross M,
Helzlsouer K,
Jacobs EJ,
LaCroix A,
Zheng W
and 60 more — show all
Zheng W,
Albanes D,
Bamlet W,
Berg CD,
Berrino F,
Bingham S,
Buring JE,
Bracci PM,
Canzian F,
Clavel-Chapelon F,
Clipp S,
Cotterchio M,
de Andrade M,
Duell EJ,
Fox JW Jr,
Gallinger S,
Gaziano JM,
Giovannucci EL,
Goggins M,
González CA,
Hallmans G,
Hankinson SE,
Hassan M,
Holly EA,
Hunter DJ,
Hutchinson A,
Jackson R,
Jacobs KB,
Jenab M,
Kaaks R,
Klein AP,
Kooperberg C,
Kurtz RC,
Li D,
Lynch SM,
Mandelson M,
McWilliams RR,
Mendelsohn JB,
Michaud DS,
Olson SH,
Overvad K,
Patel AV,
Peeters PH,
Rajkovic A,
Riboli E,
Risch HA,
Shu XO,
Thomas G,
Tobias GS,
Trichopoulos D,
Van Den Eeden SK,
Virtamo J,
Wactawski-Wende J,
Wolpin BM,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Chanock SJ,
Hartge P,
Hoover RN
Nature genetics · 2009 · PMID 19648918
3 pages
Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer
Childs EJ,
Mocci E,
Campa D,
Bracci PM,
Gallinger S,
Goggins M,
Li D,
Neale RE,
Olson SH,
Scelo G,
Amundadottir LT,
Bamlet WR
and 50 more — show all
Bijlsma MF,
Blackford A,
Borges M,
Brennan P,
Brenner H,
Bueno-de-Mesquita HB,
Canzian F,
Capurso G,
Cavestro GM,
Chaffee KG,
Chanock SJ,
Cleary SP,
Cotterchio M,
Foretova L,
Fuchs C,
Funel N,
Gazouli M,
Hassan M,
Herman JM,
Holcatova I,
Holly EA,
Hoover RN,
Hung RJ,
Janout V,
Key TJ,
Kupcinskas J,
Kurtz RC,
Landi S,
Lu L,
Malecka-Panas E,
Mambrini A,
Mohelnikova-Duchonova B,
Neoptolemos JP,
Oberg AL,
Orlow I,
Pasquali C,
Pezzilli R,
Rizzato C,
Saldia A,
Scarpa A,
Stolzenberg-Solomon RZ,
Strobel O,
Tavano F,
Vashist YK,
Vodicka P,
Wolpin BM,
Yu H,
Petersen GM,
Risch HA,
Klein AP
Nature genetics · 2015 · PMID 26098869 · open access
3 pages
Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21
Zhang M,
Wang Z,
Obazee O,
Jia J,
Childs EJ,
Hoskins J,
Figlioli G,
Mocci E,
Collins I,
Chung CC,
Hautman C,
Arslan AA
and 112 more — show all
Beane-Freeman L,
Bracci PM,
Buring J,
Duell EJ,
Gallinger S,
Giles GG,
Goodman GE,
Goodman PJ,
Kamineni A,
Kolonel LN,
Kulke MH,
Malats N,
Olson SH,
Sesso HD,
Visvanathan K,
White E,
Zheng W,
Zheng W,
Abnet CC,
Albanes D,
Andreotti G,
Brais L,
Bueno-de-Mesquita HB,
Basso D,
Berndt SI,
Boutron-Ruault MC,
Bijlsma MF,
Brenner H,
Burdette L,
Campa D,
Caporaso NE,
Capurso G,
Cavestro GM,
Cotterchio M,
Costello E,
Elena J,
Boggi U,
Gaziano JM,
Gazouli M,
Giovannucci EL,
Goggins M,
Gross M,
Haiman CA,
Hassan M,
Helzlsouer KJ,
Hu N,
Hunter DJ,
Iskierka-Jazdzewska E,
Jenab M,
Kaaks R,
Key TJ,
Khaw KT,
Klein EA,
Kogevinas M,
Krogh V,
Kupcinskas J,
Kurtz RC,
Landi MT,
Landi S,
Le Marchand L,
Mambrini A,
Mannisto S,
Milne RL,
Neale RE,
Oberg AL,
Panico S,
Patel AV,
Peeters PH,
Peters U,
Pezzilli R,
Porta M,
Purdue M,
Quiros JR,
Riboli E,
Rothman N,
Scarpa A,
Scelo G,
Shu XO,
Silverman DT,
Soucek P,
Strobel O,
Sund M,
Małecka-Panas E,
Taylor PR,
Tavano F,
Travis RC,
Thornquist M,
Tjønneland A,
Tobias GS,
Trichopoulos D,
Vashist Y,
Vodicka P,
Wactawski-Wende J,
Wentzensen N,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Kooperberg C,
Risch HA,
Jacobs EJ,
Li D,
Fuchs C,
Hoover R,
Hartge P,
Chanock SJ,
Petersen GM,
Stolzenberg-Solomon RS,
Wolpin BM,
Kraft P,
Klein AP,
Canzian F,
Amundadottir LT
Oncotarget · 2016 · PMID 27579533 · open access
3 pages
Large-scale meta- and cross-trait analyses uncover shared genetic risk factors for IBS and psychiatric disorders
Ye W,
Ding H,
Peng B,
Wang X,
Cheng Y,
Zhang G,
Yu H,
Ullah K,
Chang X,
Wang X,
Wang Z
Frontiers in psychiatry · 2026 · PMID 42221328 · open access
3 pages
Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3
Hou S,
Du L,
Lei B,
Pang CP,
Zhang M,
Zhuang W,
Zhang M,
Huang L,
Gong B,
Wang M,
Zhang Q,
Hu K
and 17 more — show all
Zhou Q,
Qi J,
Wang C,
Tian Y,
Ye Z,
Liang L,
Yu H,
Li H,
Zhou Y,
Cao Q,
Liu Y,
Bai L,
Liao D,
Kijlstra A,
Xu J,
Yang Z,
Yang P
Nature genetics · 2014 · PMID 25108386
2 pages
Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B
Jiang DK,
Ma XP,
Yu H,
Cao G,
Ding DL,
Chen H,
Huang HX,
Gao YZ,
Wu XP,
Long XD,
Zhang H,
Zhang Y
and 29 more — show all
Gao Y,
Chen TY,
Ren WH,
Zhang P,
Shi Z,
Jiang W,
Wan B,
Saiyin H,
Yin J,
Zhou YF,
Zhai Y,
Lu PX,
Zhang H,
Gu X,
Tan A,
Wang JB,
Zuo XB,
Sun LD,
Liu JO,
Yi Q,
Mo Z,
Zhou G,
Liu Y,
Sun J,
Shugart YY,
Zheng SL,
Zhang XJ,
Xu J,
Yu L
Hepatology (Baltimore, Md.) · 2015 · PMID 25802187
2 pages
GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21
Wiemels JL,
Walsh KM,
de Smith AJ,
Metayer C,
Gonseth S,
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Estonian Biobank Research Team
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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
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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
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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
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How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
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