For researchers

Is your paper here?

2,657 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.

14 matches for Zhao X.

A sex- and site-specific relationship between body mass index and osteoarthritis: evidence from observational and genetic analyses
Osteoarthritis and cartilage · 2023 · PMID 36889626
12 pages+
rs2681781 rs4858223 rs11753081 rs10846921 rs3731695 rs12200892
Using human genetics to understand the phenotypic association between chronotype and breast cancer
Journal of sleep research · 2024 · PMID 37380357
12 pages+
rs115356840 rs139909 rs695459 rs61863443 rs7907439 rs1242507
Regulatory Genomic Circuitry of Brain Age by Integrative Functional Genomic Analyses
Genomics, proteomics & bioinformatics · 2025 · PMID 40795387 · open access
11 pages
rs742396 rs199491 rs2668639 rs62061820 rs112572874 rs62056934
Investigating the shared genetic architecture of uterine leiomyoma and breast cancer: A genome-wide cross-trait analysis
American journal of human genetics · 2022 · PMID 35803233
8 pages
rs851981 rs851982 rs9611271 rs12217370 rs851984 rs10789665
Genomewide association study of leprosy
The New England journal of medicine · 2009 · PMID 20018961
4 pages
rs602875 rs40457 rs42490 Leprosy
Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3
Nature genetics · 2011 · PMID 21151128
4 pages
rs13429458 rs10818854 rs12478601 Polycystic Ovary Syndrome
Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome
Nature genetics · 2012 · PMID 22885925
4 pages
rs3802457 rs1894116 rs2272046 rs6022786
Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia
Nature genetics · 2012 · PMID 23143601
2 pages
rs4488809 rs7086803
Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese
PLoS genetics · 2013 · PMID 23341777 · open access
2 pages
rs12296850 Lung Squamous Cell Carcinoma
Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization
Genes · 2021 · PMID 34202464 · open access
2 pages
rs3118662 rs9919007
A large-scale genome-wide cross-trait analysis for the effect of COVID-19 on female-specific cancers
iScience · 2023 · PMID 37636041 · open access
2 pages
rs9620778 rs71238846
A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese
Nature genetics · 2011 · PMID 21725308
1 page
rs753955
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women
Human molecular genetics · 2016 · PMID 26732429
1 page
rs7741164
G protein-coupled receptor kinase 5 regulates thrombin signaling in platelets via PAR-1
Blood advances · 2022 · PMID 34581777 · open access
1 page
rs773902

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.