For researchers

Is your paper here?

2,676 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.

15 matches for He W.

Multivariate genome-wide analyses of the well-being spectrum
BIOS consortium · Social Science Genetic Association Consortium
Nature genetics · 2019 · PMID 30643256
12 pages+
rs2865116 rs7523829 rs285006 rs782214 rs71384258 rs113322852
Genetic insights into biological mechanisms governing human ovarian ageing
Biobank-based Integrative Omics Study (BIOS) Consortium · eQTLGen Consortium and 6 more consortia
Nature · 2021 · PMID 34349265
12 pages+
rs2844466 rs140353819 rs540836853 rs2736609 rs9438982 rs117146677
Association of Novel Loci With Keratoconus Susceptibility in a Multitrait Genome-Wide Association Study of the UK Biobank Database and Canadian Longitudinal Study on Aging
International Glaucoma Genetics Consortium
JAMA ophthalmology · 2022 · PMID 35446358
12 pages+
rs4311997 rs4472909 rs149805418 rs256869 rs76275213 rs12807097
Genetic architecture of the white matter connectome of the human brain
Science advances · 2023 · PMID 36800424 · open access
12 pages+
rs4843586 rs10992671 rs12695824 rs13325955 rs6722862 rs3785891
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
GEMO Study Collaborators · EMBRACE Collaborators and 3 more consortia
Nature communications · 2021 · PMID 33597508 · open access
6 pages
rs60882887 rs9901834 rs12470785 rs79183898 rs736596 rs7222250
Genetic Overlap Analysis Identifies a Shared Etiology between Migraine and Headache with Type 2 Diabetes
Genes · 2022 · PMID 36292730 · open access
4 pages
rs4902684 rs4809370 rs10814274 rs73050128
Large-scale GWAS of strabismus identifies risk loci and provides support for a link with maternal smoking
Lifelines Cohort Study
Nature communications · 2025 · PMID 40849414 · open access
4 pages
rs3778977 rs4908704 rs8070929 Exotropia
Identification of a variant associated with adult-type hypolactasia
Nature genetics · 2002 · PMID 11788828
3 pages
rs4988235 Lactose Intolerance (Lactase Persistence) Lesson: lactose tolerance and natural selection
Genome-wide association study of vitamin D levels in children: replication in the Western Australian Pregnancy Cohort (Raine) study
Genes and immunity · 2014 · PMID 25208829
3 pages
rs17467825 rs1007392 rs11023332
Wnt signaling and Dupuytren's disease
Dutch Dupuytren Study Group · German Dupuytren Study Group and 2 more consortia
The New England journal of medicine · 2011 · PMID 21732829
2 pages
rs11672517 Dupuytren's Disease
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
Association of intronic sequence variant in the gene encoding spleen tyrosine kinase with susceptibility to vascular dementia
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry · 2013 · PMID 23480133
2 pages
rs290227 Vascular Dementia
Genome-wide association and admixture analysis of glaucoma in the Women's Health Initiative
Human molecular genetics · 2014 · PMID 25027321
2 pages
rs151326733 rs555091
Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus
PLoS genetics · 2012 · PMID 22792070 · open access
1 page
rs4609139
Genome-wide association study of tuberculosis in the western Chinese Han and Tibetan population
MedComm · 2023 · PMID 37009413 · open access
1 page
rs75609205

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.