For researchers

Is your paper here?

2,660 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 Feng Y.

Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
rs4515883 rs6743072 rs35073727 rs57631119 rs9380498 rs12187932
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
PGC-MDD Working Group · China Kadoorie Biobank Collaborative Group and 3 more consortia
Nature genetics · 2024 · PMID 38177345 · open access
12 pages+
rs534415 rs1526193 rs7415357 rs72786643 rs3091404 rs9351533
Multi-trait and multi-ancestry genetic analysis of comorbid lung diseases and traits improves genetic discovery and polygenic risk prediction
Nature genetics · 2026 · PMID 41565855
12 pages+
rs924150 rs8089099 rs4791806 rs41522747 rs340121 rs2609260
Novel genetic insight for psoriasis: integrative genome-wide analyses in 863 080 individuals and proteome-wide Mendelian randomization
Briefings in bioinformatics · 2024 · PMID 39883516 · open access
8 pages
rs34693947 rs6067293 rs6457109 rs74817271 rs62401434 rs2596546
Cross-definition GWAS of IBS in 2.8 million individuals reveals cardiometabolic and triglyceride-linked mechanisms
Colorado Center for Personalized Medicine · Estonian Biobank Research Team and 3 more consortia
Gut · 2026 · PMID 42425734
5 pages
rs2195110 rs72700810 rs10184811 rs12221193 Irritable Bowel Syndrome
Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium
HGG advances · 2022 · PMID 35399580 · open access
3 pages
rs6817771 rs9922708 rs3751813
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
NABEC Consortium · UKBEC Consortium and 2 more consortia
Nature genetics · 2013 · PMID 23583978 · open access
2 pages
rs348495 rs10261878
A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12
Nature genetics · 2013 · PMID 23817570
2 pages
rs13117307 Cervical Cancer
Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese
Nature communications · 2018 · PMID 30287856 · open access
2 pages
rs6114027 Tuberculosis
A genome-wide association study identifies common variants influencing serum uric acid concentrations in a Chinese population
BMC medical genomics · 2014 · PMID 24513273 · open access
1 page
rs4148152
Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer
Human molecular genetics · 2016 · PMID 28171663
1 page
rs12998806
Evaluation of the causal relationship between smoking and schizophrenia in East Asia
Schizophrenia (Heidelberg, Germany) · 2022 · PMID 36085329 · open access
1 page
rs553874586
Omitting post-alignment processing and merging batch-based imputation: an efficient workflow for NIPT data imputation and its application in maternal folate metabolism genotyping
Journal of human genetics · 2026 · PMID 42581209
1 page
Research roundup — September 2026

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.