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.

13 matches for Wei Y.

Genetic basis of pregnancy-associated decreased platelet counts and gestational thrombocytopenia
Blood · 2024 · PMID 38064665 · open access
12 pages+
rs1991433 rs3975148 rs75322672 rs836848 rs842680 rs4819833
Developing an optimal stratification model for colorectal cancer screening and reducing racial disparities in multi-center population-based studies
Genome medicine · 2024 · PMID 38872215 · open access
12 pages+
rs2003311 rs11699816 rs1321456 rs4493936 rs114363880 rs2048123439
Genome-wide association studies of thyroid-related hormones, dysfunction, and autoimmunity among 85,421 Chinese pregnancies
Nature communications · 2024 · PMID 39266554 · open access
12 pages+
rs61865882 rs6757890 rs61515378 rs9398215 rs231770 rs1348003
Genetic architecture and risk prediction of gestational diabetes mellitus in Chinese pregnancies
Nature communications · 2025 · PMID 40325049 · open access
12 pages+
rs72554664 rs182573065 rs61160304 rs146844151 rs2971667 rs732360
Genome-wide association analyses of gestational phenotypes identify context-specific genetic effects
Nature genetics · 2026 · PMID 42509370
12 pages+
rs4802032 rs74678088 rs1977352 rs3826887 rs7332154 rs56805858
Novel Association of Genetic Markers Affecting CYP2A6 Activity and Lung Cancer Risk
Cancer research · 2016 · PMID 27488534
10 pages
rs113029345 rs76935404 rs10425738 rs11878604 rs7247903 rs2316205
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations
Ovarian Cancer Association Consortium (OCAC) · PRACTICAL Consortium and 3 more consortia
Cancer research · 2016 · PMID 27197191
6 pages
rs11844632 rs4808075 rs56084662 rs11571833 rs186507655 rs148883465
A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis
Nature genetics · 2011 · PMID 22138694
2 pages
rs17095830 Ankylosing Spondylitis
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis
Nature communications · 2017 · PMID 28425483 · open access
2 pages
rs9501251 Primary Biliary Cholangitis
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer
Nature genetics · 2014 · PMID 24880342 · open access
1 page
rs13314271
Genome-wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis
Hepatology (Baltimore, Md.) · 2019 · PMID 30854688 · open access
1 page
rs1794280
Genetic determinants of IgG antibody response to COVID-19 vaccination
American journal of human genetics · 2024 · PMID 38181733 · open access
1 page
rs10947290
Genome-wide association study identified novel loci and gene-environment interaction for refractive error in children
NPJ genomic medicine · 2025 · PMID 40410244 · open access
1 page
rs17074027

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.