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581 matches for
An J,
showing the first 20.
Genome-wide association analyses identified novel susceptibility loci for pulmonary embolism among Han Chinese population
Zhang Z,
Li H,
Weng H,
Zhou G,
Chen H,
Yang G,
Zhang P,
Zhang X,
Ji Y,
Ying K,
Liu B,
Xu Q
and 36 more — show all
Tang Y,
Zhu G,
Liu Z,
Xia S,
Yang X,
Dong L,
Zhu L,
Zeng M,
Yuan Y,
Yang Y,
Zhang N,
Xu X,
Pang W,
Zhang M,
Zhang Y,
Zhen K,
Wang D,
Lei J,
Wu S,
Shu S,
Zhang Y,
Zhang S,
Gao Q,
Huang Q,
Deng C,
Fu X,
Chen G,
Duan W,
Wan J,
Xie W,
Zhang P,
Wang S,
Yang P,
Zuo X,
Zhai Z,
Wang C
China pUlmonary Thromboembolism REgistry Study (CURES) investigators
BMC medicine · 2023 · PMID 37076872 · open access
2 pages
Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries
Surakka I,
Wu KH,
Hornsby W,
Wolford BN,
Shen F,
Zhou W,
Huffman JE,
Pandit A,
Hu Y,
Brumpton B,
Skogholt AH,
Gabrielsen ME
and 9 more — show all
TOPMed Stroke Working Group · Million Veteran Program (MVP) and 1 more consortia
Cell genomics · 2023 · PMID 37601974 · open access
2 pages
Genetic determinants of IgG antibody response to COVID-19 vaccination
Bian S,
Guo X,
Yang X,
Wei Y,
Yang Z,
Cheng S,
Yan J,
Chen Y,
Chen GB,
Du X,
Francis SS,
Shu Y
and 1 more — show all
American journal of human genetics · 2024 · PMID 38181733 · open access
2 pages
Integrative genomic analyses identify candidate causal genes for calcific aortic valve stenosis involving tissue-specific regulation
Thériault S,
Li Z,
Abner E,
Luan J,
Manikpurage HD,
Houessou U,
Zamani P,
Briend M,
Boudreau DK,
Gaudreault N,
Frenette L,
Argaud D
and 10 more — show all
Estonian Biobank Research Team
Nature communications · 2024 · PMID 38494474 · open access
2 pages
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
Wang H,
Chang TS,
Dombroski BA,
Cheng PL,
Patil V,
Valiente-Banuet L,
Farrell K,
Mclean C,
Molina-Porcel L,
Rajput A,
De Deyn PP,
Le Bastard N
and 49 more — show all
Gearing M,
Kaat LD,
Van Swieten JC,
Dopper E,
Ghetti BF,
Newell KL,
Troakes C,
de Yébenes JG,
Rábano-Gutierrez A,
Meller T,
Oertel WH,
Respondek G,
Stamelou M,
Arzberger T,
Roeber S,
Müller U,
Hopfner F,
Pastor P,
Brice A,
Durr A,
Le Ber I,
Beach TG,
Serrano GE,
Hazrati LN,
Litvan I,
Rademakers R,
Ross OA,
Galasko D,
Boxer AL,
Miller BL,
Seeley WW,
Van Deerlin VM,
Lee EB,
White CL 3rd,
Morris H,
de Silva R,
Crary JF,
Goate AM,
Friedman JS,
Leung YY,
Coppola G,
Naj AC,
Wang LS,
Dalgard C,
Dickson DW,
Höglinger GU,
Schellenberg GD,
Geschwind DH,
Lee WP
P. S. P. genetics study group
Molecular neurodegeneration · 2024 · PMID 39152475 · open access
2 pages
High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene
Rahimov F,
Nieminen P,
Kumari P,
Juuri E,
Nikopensius T,
Paraiso K,
German J,
Karvanen A,
Kals M,
Elnahas AG,
Karjalainen J,
Kurki M
and 16 more — show all
Palotie A,
Heliövaara A,
Esko T,
Jukarainen S,
Palta P,
Ganna A,
Patni AP,
Mar D,
Bomsztyk K,
Mathieu J,
Ruohola-Baker H,
Visel A,
Fakhouri WD,
Schutte BC,
Cornell RA,
Rice DP
FinnGen · Estonian Biobank Research Team
Nature communications · 2024 · PMID 39500877 · open access
2 pages
Population-specific reference panel improves imputation quality for genome-wide association studies conducted on the Japanese population
Flanagan J,
Liu X,
Ortega-Reyes D,
Tomizuka K,
Matoba N,
Akiyama M,
Koido M,
Ishigaki K,
Ashikawa K,
Takata S,
Shi M,
Aoi T
and 8 more — show all
Biobank Japan Project
Communications biology · 2024 · PMID 39702642 · open access
2 pages
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Zhang X,
Brody JA,
Graff M,
Highland HM,
Chami N,
Xu H,
Wang Z,
Ferrier KR,
Chittoor G,
Josyula NS,
Meyer M,
Gupta S
and 113 more — show all
Li X,
Li Z,
Allison MA,
Becker DM,
Bielak LF,
Bis JC,
Boorgula MP,
Bowden DW,
Broome JG,
Buth EJ,
Carlson CS,
Chang KM,
Chavan S,
Chiu YF,
Chuang LM,
Conomos MP,
DeMeo DL,
Du M,
Duggirala R,
Eng C,
Fohner AE,
Freedman BI,
Garrett ME,
Guo X,
Haiman C,
Heavner BD,
Hidalgo B,
Hixson JE,
Ho YL,
Hobbs BD,
Hu D,
Hui Q,
Hwu CM,
Jackson RD,
Jain D,
Kalyani RR,
Kardia SLR,
Kelly TN,
Lange EM,
LeNoir M,
Li C,
Le Marchand L,
McDonald MN,
McHugh CP,
Morrison AC,
Naseri T,
O'Connell J,
O'Donnell CJ,
Palmer ND,
Pankow JS,
Perry JA,
Peters U,
Preuss MH,
Rao DC,
Regan EA,
Reupena SM,
Roden DM,
Rodriguez-Santana J,
Sitlani CM,
Smith JA,
Tiwari HK,
Vasan RS,
Wang Z,
Weeks DE,
Wessel J,
Wiggins KL,
Wilkens LR,
Wilson PWF,
Yanek LR,
Yoneda ZT,
Zhao W,
Zhao W,
Zöllner S,
Arnett DK,
Ashley-Koch AE,
Barnes KC,
Blangero J,
Boerwinkle E,
Burchard EG,
Carson AP,
Chasman DI,
Ida Chen YD,
Curran JE,
Fornage M,
Gordeuk VR,
He J,
Heckbert SR,
Hou L,
Irvin MR,
Kooperberg C,
Minster RL,
Mitchell BD,
Nouraie M,
Psaty BM,
Raffield LM,
Reiner AP,
Rich SS,
Rotter JI,
Benjamin Shoemaker M,
Smith NL,
Taylor KD,
Telen MJ,
Weiss ST,
Zhang Y,
Heard-Costa N,
Sun YV,
Lin X,
Cupples LA,
Lange LA,
Liu CT,
Loos RJF,
North KE,
Justice AE
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Nature communications · 2025 · PMID 40216759 · open access
2 pages
A type 1 diabetes genetic risk score discriminates between type 1 diabetes and type 2 diabetes in a Chinese population
Hu J,
Jiang G,
Qin J,
Luo S,
Fan B,
Xie Z,
Wan R,
Li X,
Tam CHT,
Wang Z,
Ding J,
Xia Y
and 16 more — show all
Yang Y,
Lin J,
Yu G,
Jin P,
Lim CKP,
Luk AOY,
So WY,
Chan JCN,
Wang C,
Huang J,
Weedon MN,
Hagopian WA,
Oram RA,
Ma RCW,
Xiao Y,
Zhou Z
Hong Kong Diabetes Biobank Study Group
Diabetologia · 2025 · PMID 40569436 · open access
2 pages
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer's disease
Rajabli F,
Benchek P,
Tosto G,
Kushch N,
Sha J,
Bazemore K,
Zhu C,
Lee WP,
Haut J,
Hamilton-Nelson KL,
Wheeler NR,
Zhao Y
and 274 more — show all
Farrell JJ,
Grunin MA,
Leung YY,
Kuksa PP,
Li D,
da Fonseca EL,
Mez JB,
Palmer EL,
Pillai J,
Sherva RM,
Song YE,
Zhang X,
Ikeuchi T,
Iqbal T,
Pathak O,
Valladares O,
Reyes-Dumeyer D,
Kuzma AB,
Abner E,
Adams LD,
Adams PM,
Aguirre A,
Albert MS,
Albin RL,
Allen M,
Alvarez L,
Apostolova LG,
Arnold SE,
Asthana S,
Atwood CS,
Auerbach S,
Ayres G,
Baldwin CT,
Barber RC,
Barnes LL,
Barral S,
Beach TG,
Becker JT,
Beecham GW,
Beekly D,
Benitez BA,
Bennett D,
Bertelson J,
Bird TD,
Blacker D,
Boeve BF,
Bowen JD,
Boxer A,
Brewer J,
Burke JR,
Burns JM,
Buxbaum JD,
Cairns NJ,
Cantwell LB,
Cao C,
Carlson CS,
Carlsson CM,
Carney RM,
Carrasquillo MM,
Chasse S,
Chesselet MF,
Chin NA,
Chui HC,
Chung J,
Craft S,
Crane PK,
Cribbs DH,
Crocco EA,
Cruchaga C,
Cuccaro ML,
Cullum M,
Darby E,
Davis B,
De Jager PL,
DeCarli C,
DeToledo J,
Dick M,
Dickson DW,
Dombroski BA,
Doody RS,
Duara R,
Ertekin-Taner N,
Evans DA,
Faber KM,
Fairchild TJ,
Fallon KB,
Fardo DW,
Farlow MR,
Fernandez-Hernandez V,
Ferris S,
Friedland RP,
Foroud TM,
Frosch MP,
Fulton-Howard B,
Galasko DR,
Gamboa A,
Gearing M,
Geschwind DH,
Ghetti B,
Gilbert JR,
Go RCP,
Goate AM,
Grabowski TJ,
Graff-Radford NR,
Green RC,
Growdon JH,
Hakonarson H,
Hall J,
Hamilton RL,
Harari O,
Hardy J,
Harrell LE,
Head E,
Henderson VW,
Hernandez M,
Hohman T,
Honig LS,
Huebinger RM,
Huentelman MJ,
Hulette CM,
Hyman BT,
Hynan LS,
Ibanez L,
Jarvik GP,
Jayadev S,
Jin LW,
Johnson K,
Johnson L,
Kamboh MI,
Karydas AM,
Katz MJ,
Kauwe JS,
Kaye JA,
Keene CD,
Khaleeq A,
Kikuchi M,
Kim R,
Knebl J,
Kowall NW,
Kramer JH,
Kukull WA,
LaFerla FM,
Lah JJ,
Larson EB,
Lerner A,
Leverenz JB,
Levey AI,
Lieberman AP,
Lipton RB,
Logue M,
Lopez OL,
Lunetta KL,
Lyketsos CG,
Mains D,
Margaret FE,
Marson DC,
Martin ER,
Martiniuk F,
Mash DC,
Masliah E,
Massman P,
Masurkar A,
McCormick WC,
McCurry SM,
McDavid AN,
McDonough S,
McKee AC,
Mesulam M,
Miller BL,
Miller CA,
Miller JW,
Montine TJ,
Monuki ES,
Morris JC,
Mukherjee S,
Myers AJ,
Nguyen T,
Obisesan T,
O'Bryant S,
Olichney JM,
Ory M,
Palmer R,
Parisi JE,
Paulson HL,
Pavlik V,
Paydarfar D,
Perez V,
Peskind E,
Petersen RC,
Petrovitch H,
Pierce A,
Polk M,
Poon WW,
Potter H,
Qu L,
Quiceno M,
Quinn JF,
Raj A,
Raskind M,
Reiman EM,
Reisberg B,
Reisch JS,
Ringman JM,
Roberson ED,
Rodriguear M,
Rogaeva E,
Rosen HJ,
Rosenberg RN,
Royall DR,
Sabbagh M,
Sadovnick AD,
Sager MA,
Sano M,
Saykin AJ,
Schneider JA,
Schneider LS,
Seeley WW,
Slifer SH,
Small S,
Smith AG,
Smith JP,
Sonnen JA,
Spina S,
George-Hyslop PS,
Starks TD,
Stern RA,
Stevens AB,
Strittmatter SM,
Sultzer D,
Swerdlow RH,
Tanzi RE,
Tilson JL,
Trojanowski JQ,
Troncoso JC,
Tsolaki M,
Tsuang DW,
Van Deerlin VM,
van Eldik LJ,
Vance JM,
Vardarajan BN,
Vassar R,
Vinters HV,
Vonsattel JP,
Weintraub S,
Welsh-Bohmer KA,
Whitehead PL,
Wijsman EM,
Wilhelmsen KC,
Williams B,
Williamson J,
Wilms H,
Wingo TS,
Wisniewski T,
Woltjer RL,
Woon M,
Wright CB,
Wu CK,
Younkin SG,
Yu CE,
Yu L,
Zhu X,
Kunkle BW,
Bush WS,
Miyashita A,
Byrd GS,
Wang LS,
Farrer LA,
Haines JL,
Mayeux R,
Pericak-Vance MA,
Schellenberg GD,
Jun GR,
Reitz C,
Naj AC
Alzheimer’s Disease Genetics Consortium (ADGC)
Genome biology · 2025 · PMID 40676597 · open access
2 pages
Genetic analysis in African ancestry populations reveals genetic contributors to lung cancer susceptibility
Betti MJ,
Jaworski J,
Zhao S,
Rao JS,
Ryan BM,
Schwartz AG,
Lusk CM,
McCoy L,
Wiencke JK,
Bruce MA,
Chanock S,
Gamazon ER
and 2 more — show all
American journal of human genetics · 2025 · PMID 40829600
2 pages
Genome-wide association study of HBV-related hepatocellular carcinoma identifies a functional variant at the FAM114A1 locus
Yu HP,
Xiang BD,
Qian J,
Liu H,
Li YF,
Lin Q,
Liu S,
Wei J,
Zhan S,
Jiang B,
Dai J,
Ma L
and 20 more — show all
Zhang L,
Liu Y,
Wen Q,
Gong W,
Li S,
Jiang Y,
Zheng J,
Zhu T,
Zhou Z,
Zeng X,
Wang Z,
Wang JA,
Guo R,
Yang Y,
Wei Q,
Zhou G,
Qiu XQ,
Tang W,
Wang M,
Zhang R
Journal of genetics and genomics = Yi chuan xue bao · 2026 · PMID 41241147
2 pages
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia
Hillmer AM,
Hanneken S,
Ritzmann S,
Becker T,
Freudenberg J,
Brockschmidt FF,
Flaquer A,
Freudenberg-Hua Y,
Jamra RA,
Metzen C,
Heyn U,
Schweiger N
and 13 more — show all
Betz RC,
Blaumeiser B,
Hampe J,
Schreiber S,
Schulze TG,
Hennies HC,
Schumacher J,
Propping P,
Ruzicka T,
Cichon S,
Wienker TF,
Kruse R,
Nothen MM
American journal of human genetics · 2005 · PMID 15902657
1 page
An SCN9A channelopathy causes congenital inability to experience pain
Cox JJ,
Reimann F,
Nicholas AK,
Thornton G,
Roberts E,
Springell K,
Karbani G,
Jafri H,
Mannan J,
Raashid Y,
Al-Gazali L,
Hamamy H
and 7 more — show all
Nature · 2006 · PMID 17167479
1 page
A genomewide association study of skin pigmentation in a South Asian population
Stokowski RP,
Pant PV,
Dadd T,
Fereday A,
Hinds DA,
Jarman C,
Filsell W,
Ginger RS,
Green MR,
van der Ouderaa FJ,
Cox DR
American journal of human genetics · 2007 · PMID 17999355
1 page
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21
Tenesa A,
Farrington SM,
Prendergast JG,
Porteous ME,
Walker M,
Haq N,
Barnetson RA,
Theodoratou E,
Cetnarskyj R,
Cartwright N,
Semple C,
Clark AJ
and 45 more — show all
Reid FJ,
Smith LA,
Kavoussanakis K,
Koessler T,
Pharoah PD,
Buch S,
Schafmayer C,
Tepel J,
Schreiber S,
Völzke H,
Schmidt CO,
Hampe J,
Chang-Claude J,
Hoffmeister M,
Brenner H,
Wilkening S,
Canzian F,
Capella G,
Moreno V,
Deary IJ,
Starr JM,
Tomlinson IP,
Kemp Z,
Howarth K,
Carvajal-Carmona L,
Webb E,
Broderick P,
Vijayakrishnan J,
Houlston RS,
Rennert G,
Ballinger D,
Rozek L,
Gruber SB,
Matsuda K,
Kidokoro T,
Nakamura Y,
Zanke BW,
Greenwood CM,
Rangrej J,
Kustra R,
Montpetit A,
Hudson TJ,
Gallinger S,
Campbell H,
Dunlop MG
Nature genetics · 2008 · PMID 18372901
1 page
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
cites your work, and links to the paper on PubMed — which is what a citation is.
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
inconsistent across databases; where two people share a form of a name we cannot
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
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.