For researchers

Is your paper here?

2,663 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.

9 matches for Gamazon ER.

Mapping the proteo-genomic convergence of human diseases
Science (New York, N.Y.) · 2021 · PMID 34648354
12 pages+
rs79344818 rs893184 rs118065662 rs3815026 rs1917342 rs2070631
Rare and common genetic determinants of metabolic individuality and their effects on human health
Nature medicine · 2022 · PMID 36357675 · open access
12 pages+
rs9332172 rs13149149 rs1043011 rs11188148 rs191860149 rs1163548
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+
rs9594366 rs16856530 rs62283809 rs10854002 rs2276133 rs7748159
Large-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits
DIAMANTE Hispanic/Latino Consortium · Global Hispanic Lipids Consortium
Nature communications · 2025 · PMID 40210677 · open access
12 pages+
rs58458113 rs58223766 rs117525671 rs75594955 rs188287950 rs117961479
Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs
Scientific reports · 2016 · PMID 26780889 · open access
3 pages
rs8102280 rs138534124 rs2238675
Genetic analysis in African ancestry populations reveals genetic contributors to lung cancer susceptibility
American journal of human genetics · 2025 · PMID 40829600
2 pages
rs141174940 rs181801863
Novel genetic predictors of venous thromboembolism risk in African Americans
Blood · 2016 · PMID 26888256
1 page
rs1998081
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
ADRA2A and IRX1 are putative risk genes for Raynaud's phenomenon
Genes & Health Research Team
Nature communications · 2023 · PMID 37828025 · open access
1 page
rs12653958

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.