For researchers
Is your paper here?
2,655 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.
12 matches for
Yao Y.
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
Hu Y,
Stilp AM,
McHugh CP,
Rao S,
Jain D,
Zheng X,
Lane J,
Méric de Bellefon S,
Raffield LM,
Chen MH,
Yanek LR,
Wheeler M
and 67 more — show all
Yao Y,
Ren C,
Broome J,
Moon JY,
de Vries PS,
Hobbs BD,
Sun Q,
Surendran P,
Brody JA,
Blackwell TW,
Choquet H,
Ryan K,
Duggirala R,
Heard-Costa N,
Wang Z,
Chami N,
Preuss MH,
Min N,
Ekunwe L,
Lange LA,
Cushman M,
Faraday N,
Curran JE,
Almasy L,
Kundu K,
Smith AV,
Gabriel S,
Rotter JI,
Fornage M,
Lloyd-Jones DM,
Vasan RS,
Smith NL,
North KE,
Boerwinkle E,
Becker LC,
Lewis JP,
Abecasis GR,
Hou L,
O'Connell JR,
Morrison AC,
Beaty TH,
Kaplan R,
Correa A,
Blangero J,
Jorgenson E,
Psaty BM,
Kooperberg C,
Walton RT,
Kleinstiver BP,
Tang H,
Loos RJF,
Soranzo N,
Butterworth AS,
Nickerson D,
Rich SS,
Mitchell BD,
Johnson AD,
Auer PL,
Li Y,
Mathias RA,
Lettre G,
Pankratz N,
Laurie CC,
Laurie CA,
Bauer DE,
Conomos MP,
Reiner AP
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
American journal of human genetics · 2021 · PMID 33887194
12 pages+
Genome-wide association meta-analysis of 88,250 individuals highlights pleiotropic mechanisms of five ocular diseases in UK Biobank
Xue Z,
Yuan J,
Chen F,
Yao Y,
Xing S,
Yu X,
Li K,
Wang C,
Bao J,
Qu J,
Su J,
Chen H
EBioMedicine · 2022 · PMID 35841873 · open access
12 pages+
A sex- and site-specific relationship between body mass index and osteoarthritis: evidence from observational and genetic analyses
Zhang L,
Zhang W,
Wu X,
Cui H,
Yan P,
Yang C,
Zhao X,
Xiao J,
Xiao C,
Tang M,
Wang Y,
Chen L
and 10 more — show all
Osteoarthritis and cartilage · 2023 · PMID 36889626
12 pages+
Using human genetics to understand the phenotypic association between chronotype and breast cancer
Wu X,
Yang C,
Zou Y,
Jones SE,
Zhao X,
Zhang L,
Han Z,
Hao Y,
Xiao J,
Xiao C,
Zhang W,
Yan P
and 10 more — show all
Journal of sleep research · 2024 · PMID 37380357
12 pages+
Genetic landscape and functional exploration of kidney cancer predisposition in cross-ancestral populations
Dai H,
Chu X,
Du H,
Yang S,
Yao Y,
Yu X,
Zhao Y,
Dong P,
Lyu Z,
Wang W,
Li H,
Mi Z
and 19 more — show all
Sheng C,
Li X,
Zheng H,
Song F,
Song F,
Sun M,
Dai J,
Lan Q,
Rothman N,
Hu Z,
Wei Q,
Ye D,
Yao X,
Jia W,
Chanock SJ,
Shen H,
Purdue MP,
Li MJ,
Chen K
Nature communications · 2026 · PMID 42000752 · open access
12 pages+
Novel Risk Loci Associated With Genetic Risk for Bipolar Disorder Among Han Chinese Individuals: A Genome-Wide Association Study and Meta-analysis
Li HJ,
Zhang C,
Hui L,
Zhou DS,
Li Y,
Zhang CY,
Wang C,
Wang L,
Li W,
Yang Y,
Qu N,
Tang J
and 37 more — show all
He Y,
Zhou J,
Yang Z,
Li X,
Cai J,
Yang L,
Chen J,
Fan W,
Tang W,
Tang W,
Jia QF,
Liu W,
Zhuo C,
Song X,
Liu F,
Bai Y,
Zhong BL,
Zhang SF,
Chen J,
Xia B,
Lv L,
Liu Z,
Hu S,
Li XY,
Liu JW,
Cai X,
Yao YG,
Zhang Y,
Yan H,
Chang S,
Zhao JP,
Yue WH,
Luo XJ,
Chen X,
Xiao X,
Fang Y,
Li M
GeseDNA Research Team
JAMA psychiatry · 2021 · PMID 33263727
4 pages
Epidemiological and Genetic Analyses of Schizophrenia and Breast Cancer
Tang M,
Wu X,
Zhang W,
Cui H,
Zhang L,
Yan P,
Yang C,
Wang Y,
Chen L,
Xiao C,
Liu Y,
Zou Y
and 7 more — show all
Schizophrenia bulletin · 2024 · PMID 37467357
3 pages
Genome-Wide Association and Functional Studies Identify <i>SCML4</i> and <i>THSD7A</i> as Novel Susceptibility Genes for Coronary Artery Disease
Li Y,
Wang DW,
Chen Y,
Chen C,
Guo J,
Zhang S,
Sun Z,
Ding H,
Yao Y,
Zhou L,
Xu K,
Song C
and 30 more — show all
Yang F,
Zhao B,
Yan H,
Wang WJ,
Wu C,
Lu X,
Yang X,
Dong J,
Zheng G,
Tian S,
Cui Y,
Jin L,
Liu G,
Cui H,
Wang S,
Jiang F,
Wang C,
Erdmann J,
Zeng L,
Huang S,
Zhong J,
Ma Y,
Chen W,
Sun J,
Lei W,
Chen S,
Rao S,
Gu D,
Schunkert H,
Tian XL
Arteriosclerosis, thrombosis, and vascular biology · 2018 · PMID 29472232
2 pages
Common variants on 6q16.2, 12q24.31 and 16p13.3 are associated with major depressive disorder
Li X,
Luo Z,
Gu C,
Hall LS,
McIntosh AM,
Zeng Y,
Porteous DJ,
Hayward C,
Li M,
Yao YG,
Zhang C,
Luo XJ
23andMe Research Team7
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018 · PMID 29728651
1 page
Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study
Zhao SX,
Liu W,
Liang J,
Gao GQ,
Zhang XM,
Yao Y,
Wang HN,
Yuan FF,
Xue LQ,
Ma YR,
Zhang LL,
Ye XP
and 25 more — show all
Zhang QY,
Sun F,
Zhang RJ,
Yang SY,
Zhan M,
Du WH,
Liu BL,
Chen X,
Song ZY,
Li XS,
Li P,
Ru Y,
Zuo CL,
Li SX,
Han B,
Zhu H,
Qiao J,
Xuan M,
Su B,
Sun F,
Ma JH,
Chen JL,
Tian HM,
Chen SJ,
Song HD
China Consortium for the Genetics of Autoimmune Thyroid Disease
JAMA network open · 2019 · PMID 31050781 · open access
1 page
Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophrenia
Liu J,
Li S,
Li X,
Li W,
Yang Y,
Guo S,
Lv L,
Xiao X,
Yao YG,
Guan F,
Li M,
Luo XJ
BMC medicine · 2021 · PMID 34380480 · open access
1 page
Genome-wide association study reveals genetic architecture and evolution of human retinal pigmentation
Yuan J,
Zhang Y,
Yao Y,
Li S,
Liang J,
Dai W,
Yang J,
Liu M,
Zhang Q,
Zhou Y,
Li J,
Liu H
and 5 more — show all
Myopia Associated Genetics and Intervention Consortium
Science advances · 2026 · PMID 41477839 · 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.