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Is your paper here?
2,673 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
67 matches for
He H,
showing the first 20.
A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12
Shi Y,
Li L,
Hu Z,
Li S,
Wang S,
Liu J,
Wu C,
He L,
Zhou J,
Li Z,
Hu T,
Chen Y
and 72 more — show all
Jia Y,
Wang S,
Wu L,
Cheng X,
Yang Z,
Yang R,
Li X,
Huang K,
Zhang Q,
Zhou H,
Tang F,
Chen Z,
Shen J,
Jiang J,
Ding H,
Xing H,
Zhang S,
Qu P,
Song X,
Lin Z,
Deng D,
Xi L,
Lv W,
Han X,
Tao G,
Yan L,
Han Z,
Li Z,
Miao X,
Pan S,
Shen Y,
Wang H,
Liu D,
Gong E,
Li Z,
Zhou L,
Luan X,
Wang C,
Song Q,
Wu S,
Xu H,
Shen J,
Qiang F,
Ma G,
Liu L,
Chen X,
Liu J,
Wu J,
Shen Y,
Wen Y,
Chu M,
Yu J,
Hu X,
Fan Y,
He H,
Jiang Y,
Lei Z,
Liu C,
Chen J,
Zhang Y,
Yi C,
Chen S,
Li W,
Wang D,
Wang Z,
Di W,
Shen K,
Lin D,
Shen H,
Feng Y,
Xie X,
Ma D
Nature genetics · 2013 · PMID 23817570
2 pages
Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease
Kottyan LC,
Davis BP,
Sherrill JD,
Liu K,
Rochman M,
Kaufman K,
Weirauch MT,
Vaughn S,
Lazaro S,
Rupert AM,
Kohram M,
Stucke EM
and 17 more — show all
Kemme KA,
Magnusen A,
He H,
Dexheimer P,
Chehade M,
Wood RA,
Pesek RD,
Vickery BP,
Fleischer DM,
Lindbad R,
Sampson HA,
Mukkada VA,
Putnam PE,
Abonia JP,
Martin LJ,
Harley JB,
Rothenberg ME
Nature genetics · 2014 · PMID 25017104 · open access
2 pages
Genetic and functional insights into the fractal structure of the heart
Meyer HV,
Dawes TJW,
Serrani M,
Bai W,
Tokarczuk P,
Cai J,
de Marvao A,
Henry A,
Lumbers RT,
Gierten J,
Thumberger T,
Wittbrodt J
and 8 more — show all
Nature · 2020 · PMID 32814899
2 pages
Exome-Wide Association Analysis Suggests LRP2BP as a Susceptibility Gene for Endothelial Injury in Systemic Sclerosis in the Han Chinese Population
Pu W,
Wu W,
Liu Q,
Ma Y,
Tu W,
Zuo X,
Guo G,
Jiang S,
Zhao Y,
Zuo X,
Wang Q,
Yang L
and 32 more — show all
Xiao R,
Chu H,
Wang L,
Sun L,
Cui J,
Yu L,
Li H,
Li Y,
Shi Y,
Zhang J,
Zhang H,
Liang M,
Chen D,
Ding Y,
Chen X,
Chen Y,
Zhang R,
Zhao H,
Li Y,
Qi Q,
Bai P,
Zhao L,
Reveille JD,
Mayes MD,
Jin L,
Lee EB,
Zhang X,
Xu J,
Zhang Z,
Zhou X,
Zou H,
Wang J
The Journal of investigative dermatology · 2021 · PMID 33069728
2 pages
Association of Single-Nucleotide Variants in the Human Leukocyte Antigen and Other Loci With Childhood Hodgkin Lymphoma
Chen C,
Song N,
Dong Q,
Sun X,
Mulder HL,
Easton J,
Zhang J,
Yasui Y,
Bhatia S,
Armstrong GT,
Wang H,
Ness KK
and 3 more — show all
JAMA network open · 2022 · PMID 35939300 · open access
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
The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population
Terao C,
Yamada R,
Ohmura K,
Takahashi M,
Kawaguchi T,
Kochi Y,
Okada Y,
Nakamura Y,
Yamamoto K,
Melchers I,
Lathrop M,
Mimori T
and 1 more — show all
Human Disease Genomics Working Group · RA Clinical and Genetic Study Consortium
Human molecular genetics · 2011 · PMID 21505073
1 page
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
Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis
Fakiola M,
Strange A,
Cordell HJ,
Miller EN,
Pirinen M,
Su Z,
Mishra A,
Mehrotra S,
Monteiro GR,
Band G,
Bellenguez C,
Dronov S
and 39 more — show all
Edkins S,
Freeman C,
Giannoulatou E,
Gray E,
Hunt SE,
Lacerda HG,
Langford C,
Pearson R,
Pontes NN,
Rai M,
Singh SP,
Smith L,
Sousa O,
Vukcevic D,
Bramon E,
Brown MA,
Casas JP,
Corvin A,
Duncanson A,
Jankowski J,
Markus HS,
Mathew CG,
Palmer CN,
Plomin R,
Rautanen A,
Sawcer SJ,
Trembath RC,
Viswanathan AC,
Wood NW,
Wilson ME,
Deloukas P,
Peltonen L,
Christiansen F,
Witt C,
Jeronimo SM,
Sundar S,
Spencer CC,
Blackwell JM,
Donnelly P
LeishGEN Consortium · Wellcome Trust Case Control Consortium 2
Nature genetics · 2013 · PMID 23291585 · open access
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
Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity
Pei YF,
Zhang L,
Liu Y,
Li J,
Shen H,
Liu YZ,
Tian Q,
He H,
Wu S,
Ran S,
Han Y,
Hai R
and 5 more — show all
Human molecular genetics · 2014 · PMID 24064335
1 page
A genome-wide association study yields five novel thyroid cancer risk loci
Gudmundsson J,
Thorleifsson G,
Sigurdsson JK,
Stefansdottir L,
Jonasson JG,
Gudjonsson SA,
Gudbjartsson DF,
Masson G,
Johannsdottir H,
Halldorsson GH,
Stacey SN,
Helgason H
and 28 more — show all
Sulem P,
Senter L,
He H,
Liyanarachchi S,
Ringel MD,
Aguillo E,
Panadero A,
Prats E,
Garcia-Castaño A,
De Juan A,
Rivera F,
Xu L,
Kiemeney LA,
Eyjolfsson GI,
Sigurdardottir O,
Olafsson I,
Kristvinsson H,
Netea-Maier RT,
Jonsson T,
Mayordomo JI,
Plantinga TS,
Hjartarson H,
Hrafnkelsson J,
Sturgis EM,
Thorsteinsdottir U,
Rafnar T,
de la Chapelle A,
Stefansson K
Nature communications · 2017 · PMID 28195142 · open access
1 page
Genetic variation in <i>CFH</i> predicts phenytoin-induced maculopapular exanthema in European-descent patients
McCormack M,
Gui H,
Ingason A,
Speed D,
Wright GEB,
Zhang EJ,
Secolin R,
Yasuda C,
Kwok M,
Wolking S,
Becker F,
Rau S
and 37 more — show all
Avbersek A,
Heggeli K,
Leu C,
Depondt C,
Sills GJ,
Marson AG,
Auce P,
Brodie MJ,
Francis B,
Johnson MR,
Koeleman BPC,
Striano P,
Coppola A,
Zara F,
Kunz WS,
Sander JW,
Lerche H,
Klein KM,
Weckhuysen S,
Krenn M,
Gudmundsson LJ,
Stefánsson K,
Krause R,
Shear N,
Ross CJD,
Delanty N,
Pirmohamed M,
Carleton BC,
Cendes F,
Lopes-Cendes I,
Liao WP,
O'Brien TJ,
Sisodiya SM,
Cherny S,
Kwan P,
Baum L,
Cavalleri GL
EPIGEN Consortium; · Canadian Pharmacogenomics Network for Drug Safety; and 2 more consortia
Neurology · 2018 · PMID 29288229 · open access
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.