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2,657 papers hold this site up. Every variant and condition page names
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17 matches for
Hang D.
Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases
Li YR,
Li J,
Zhao SD,
Bradfield JP,
Mentch FD,
Maggadottir SM,
Hou C,
Abrams DJ,
Chang D,
Gao F,
Guo Y,
Wei Z
and 54 more — show all
Connolly JJ,
Cardinale CJ,
Bakay M,
Glessner JT,
Li D,
Kao C,
Thomas KA,
Qiu H,
Chiavacci RM,
Kim CE,
Wang F,
Snyder J,
Richie MD,
Flatø B,
Førre Ø,
Denson LA,
Thompson SD,
Becker ML,
Guthery SL,
Latiano A,
Perez E,
Resnick E,
Russell RK,
Wilson DC,
Silverberg MS,
Annese V,
Lie BA,
Punaro M,
Dubinsky MC,
Monos DS,
Strisciuglio C,
Staiano A,
Miele E,
Kugathasan S,
Ellis JA,
Munro JE,
Sullivan KE,
Wise CA,
Chapel H,
Cunningham-Rundles C,
Grant SF,
Orange JS,
Sleiman PM,
Behrens EM,
Griffiths AM,
Satsangi J,
Finkel TH,
Keinan A,
Prak ET,
Polychronakos C,
Baldassano RN,
Li H,
Keating BJ,
Hakonarson H
Nature medicine · 2015 · PMID 26301688
12 pages+
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+
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Nalls MA,
Blauwendraat C,
Vallerga CL,
Heilbron K,
Bandres-Ciga S,
Chang D,
Tan M,
Kia DA,
Noyce AJ,
Xue A,
Bras J,
Young E
and 39 more — show all
von Coelln R,
Simón-Sánchez J,
Schulte C,
Sharma M,
Krohn L,
Pihlstrøm L,
Siitonen A,
Iwaki H,
Leonard H,
Faghri F,
Gibbs JR,
Hernandez DG,
Scholz SW,
Botia JA,
Martinez M,
Corvol JC,
Lesage S,
Jankovic J,
Shulman LM,
Sutherland M,
Tienari P,
Majamaa K,
Toft M,
Andreassen OA,
Bangale T,
Brice A,
Yang J,
Gan-Or Z,
Gasser T,
Heutink P,
Shulman JM,
Wood NW,
Hinds DA,
Hardy JA,
Morris HR,
Gratten J,
Visscher PM,
Graham RR,
Singleton AB
23andMe Research Team · System Genomics of Parkinson's Disease Consortium and 1 more consortia
The Lancet. Neurology · 2019 · PMID 31701892
12 pages+
Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci
Yin X,
Chan LS,
Bose D,
Jackson AU,
VandeHaar P,
Locke AE,
Fuchsberger C,
Stringham HM,
Welch R,
Yu K,
Fernandes Silva L,
Service SK
and 25 more — show all
Zhang D,
Hector EC,
Young E,
Ganel L,
Das I,
Abel H,
Erdos MR,
Bonnycastle LL,
Kuusisto J,
Stitziel NO,
Hall IM,
Wagner GR,
Kang J,
Morrison J,
Burant CF,
Collins FS,
Ripatti S,
Palotie A,
Freimer NB,
Mohlke KL,
Scott LJ,
Wen X,
Fauman EB,
Laakso M,
Boehnke M
FinnGen
Nature communications · 2022 · PMID 35347128 · open access
12 pages+
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum
Lee DSM,
Cardone KM,
Zhang DY,
Tsao NL,
Abramowitz S,
Sharma P,
DePaolo JS,
Conery M,
Aragam KG,
Biddinger K,
Dikilitas O,
Hoffman-Andrews L
and 23 more — show all
Judy RL,
Khan A,
Kullo IJ,
Puckelwartz MJ,
Reza N,
Satterfield BA,
Singhal P,
Arany Z,
Cappola TP,
Carruth ED,
Day SM,
Do R,
Haggerty CM,
Joseph J,
McNally EM,
Nadkarni G,
Owens AT,
Rader DJ,
Ritchie MD,
Sun YV,
Voight BF,
Levin MG,
Damrauer SM
Penn Medicine Biobank
Nature genetics · 2025 · PMID 40195560
12 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
A genome-wide association study of metabolic traits in human urine
Suhre K,
Wallaschofski H,
Raffler J,
Friedrich N,
Haring R,
Michael K,
Wasner C,
Krebs A,
Kronenberg F,
Chang D,
Meisinger C,
Wichmann HE
and 12 more — show all
Hoffmann W,
Völzke H,
Völker U,
Teumer A,
Biffar R,
Kocher T,
Felix SB,
Illig T,
Kroemer HK,
Gieger C,
Römisch-Margl W,
Nauck M
Nature genetics · 2011 · PMID 21572414
3 pages
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci
Chang D,
Nalls MA,
Hallgrímsdóttir IB,
Hunkapiller J,
van der Brug M,
Cai F,
Kerchner GA,
Ayalon G,
Bingol B,
Sheng M,
Hinds D,
Behrens TW
and 3 more — show all
International Parkinson's Disease Genomics Consortium · 23andMe Research Team
Nature genetics · 2017 · PMID 28892059
3 pages
Multiplex genomewide association analysis of breast milk fatty acid composition extends the phenotypic association and potential selection of <i>FADS1</i> variants to arachidonic acid, a critical infant micronutrient
Mychaleckyj JC,
Nayak U,
Colgate ER,
Zhang D,
Carstensen T,
Ahmed S,
Ahmed T,
Mentzer AJ,
Alam M,
Kirkpatrick BD,
Haque R,
Faruque ASG
and 1 more — show all
Journal of medical genetics · 2018 · PMID 29514873 · open access
3 pages
Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer
Wu X,
Ye Y,
Kiemeney LA,
Sulem P,
Rafnar T,
Matullo G,
Seminara D,
Yoshida T,
Saeki N,
Andrew AS,
Dinney CP,
Czerniak B
and 36 more — show all
Zhang ZF,
Kiltie AE,
Bishop DT,
Vineis P,
Porru S,
Buntinx F,
Kellen E,
Zeegers MP,
Kumar R,
Rudnai P,
Gurzau E,
Koppova K,
Mayordomo JI,
Sanchez M,
Saez B,
Lindblom A,
de Verdier P,
Steineck G,
Mills GB,
Schned A,
Guarrera S,
Polidoro S,
Chang SC,
Lin J,
Chang DW,
Hale KS,
Majewski T,
Grossman HB,
Thorlacius S,
Thorsteinsdottir U,
Aben KK,
Witjes JA,
Stefansson K,
Amos CI,
Karagas MR,
Gu J
Nature genetics · 2009 · PMID 19648920
2 pages
Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency
Bronson PG,
Chang D,
Bhangale T,
Seldin MF,
Ortmann W,
Ferreira RC,
Urcelay E,
Pereira LF,
Martin J,
Plebani A,
Lougaris V,
Friman V
and 7 more — show all
Nature genetics · 2016 · PMID 27723758 · open access
2 pages
Genome-wide association study of cervical cancer suggests a role for ARRDC3 gene in human papillomavirus infection
Takeuchi F,
Kukimoto I,
Li Z,
Li S,
Li N,
Hu Z,
Takahashi A,
Inoue S,
Yokoi S,
Chen J,
Hang D,
Kuroda M
and 10 more — show all
Human molecular genetics · 2019 · PMID 30412241
2 pages
Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population
Shi Y,
Qu J,
Zhang D,
Zhao P,
Zhang Q,
Tam POS,
Sun L,
Zuo X,
Zhou X,
Xiao X,
Hu J,
Li Y
and 30 more — show all
Cai L,
Liu X,
Lu F,
Liao S,
Chen B,
He F,
Gong B,
Lin H,
Ma S,
Cheng J,
Zhang J,
Chen Y,
Zhao F,
Yang X,
Chen Y,
Yang C,
Lam DSC,
Li X,
Shi F,
Wu Z,
Lin Y,
Yang J,
Li S,
Ren Y,
Xue A,
Fan Y,
Li D,
Pang CP,
Zhang X,
Yang Z
American journal of human genetics · 2011 · PMID 21640322
1 page
A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population
Shi Y,
Gong B,
Chen L,
Zuo X,
Liu X,
Tam PO,
Zhou X,
Zhao P,
Lu F,
Qu J,
Sun L,
Zhao F
and 13 more — show all
Chen H,
Zhang Y,
Zhang D,
Lin Y,
Lin H,
Ma S,
Cheng J,
Yang J,
Huang L,
Zhang M,
Zhang X,
Pang CP,
Yang Z
Human molecular genetics · 2013 · PMID 23406873
1 page
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
Xie J,
Liu L,
Mladkova N,
Li Y,
Ren H,
Wang W,
Cui Z,
Lin L,
Hu X,
Yu X,
Xu J,
Liu G
and 108 more — show all
Caliskan Y,
Sidore C,
Balderes O,
Rosen RJ,
Bodria M,
Zanoni F,
Zhang JY,
Krithivasan P,
Mehl K,
Marasa M,
Khan A,
Ozay F,
Canetta PA,
Bomback AS,
Appel GB,
Sanna-Cherchi S,
Sampson MG,
Mariani LH,
Perkowska-Ptasinska A,
Durlik M,
Mucha K,
Moszczuk B,
Foroncewicz B,
Pączek L,
Habura I,
Ars E,
Ballarin J,
Mani LY,
Vogt B,
Ozturk S,
Yildiz A,
Seyahi N,
Arikan H,
Koc M,
Basturk T,
Karahan G,
Akgul SU,
Sever MS,
Zhang D,
Santoro D,
Bonomini M,
Londrino F,
Gesualdo L,
Reiterova J,
Tesar V,
Izzi C,
Savoldi S,
Spotti D,
Marcantoni C,
Messa P,
Galliani M,
Roccatello D,
Granata S,
Zaza G,
Lugani F,
Ghiggeri G,
Pisani I,
Allegri L,
Sprangers B,
Park JH,
Cho B,
Kim YS,
Kim DK,
Suzuki H,
Amoroso A,
Cattran DC,
Fervenza FC,
Pani A,
Hamilton P,
Harris S,
Gupta S,
Cheshire C,
Dufek S,
Issler N,
Pepper RJ,
Connolly J,
Powis S,
Bockenhauer D,
Stanescu HC,
Ashman N,
Loos RJF,
Kenny EE,
Wuttke M,
Eckardt KU,
Köttgen A,
Hofstra JM,
Coenen MJH,
Kiemeney LA,
Akilesh S,
Kretzler M,
Beck LH,
Stengel B,
Debiec H,
Ronco P,
Wetzels JFM,
Zoledziewska M,
Cucca F,
Ionita-Laza I,
Lee H,
Hoxha E,
Stahl RAK,
Brenchley P,
Scolari F,
Zhao MH,
Gharavi AG,
Kleta R,
Chen N,
Kiryluk K
Nature communications · 2020 · PMID 32231244 · open access
1 page
Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic Loci
Bellomo TR,
Bone WP,
Chen BY,
Gawronski KAB,
Zhang D,
Park J,
Levin M,
Tsao N,
Klarin D,
Lynch J,
Assimes TL,
Gaziano JM
and 10 more — show all
Frontiers in genetics · 2021 · PMID 35186008 · open access
1 page
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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.