For researchers

Is your paper here?

2,681 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.

78 matches for 23andMe, showing the first 20.

Genetic analyses identify widespread sex-differential participation bias
FinnGen Study · 23andMe Research Team and 1 more consortia
Nature genetics · 2021 · PMID 33888908
12 pages+
rs10040110 rs6718702 rs7652179 rs2213635 rs3771602 rs66830472
A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects
23andMe Research Team
Nature communications · 2021 · PMID 34127677 · open access
12 pages+
rs17608087 rs2686878 rs17172647 rs4814857 rs9842371 rs1014607
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
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals
23andMe Research Team · Social Science Genetic Association Consortium
Nature genetics · 2022 · PMID 35361970 · open access
12 pages+
rs6500680 rs6916517 rs73047060 rs7397905 rs75564433 rs7750668
Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways
23andMe Research Team
Nature genetics · 2022 · PMID 35835914
12 pages+
rs7592105 rs79099448 rs801732 rs12458228 rs12750136 rs1839246
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Global Biobank Meta-Analysis Initiative; Estonian Biobank Research Team; 23andMe Research Team; Biobank Japan; CHARGE Hemostasis Working Group
Circulation · 2022 · PMID 36154123
12 pages+
rs6632109 rs8049403 rs2048528 rs1518760 rs78475244 rs76668186
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs6058896 rs649523 rs6552828 rs3806325 rs7162940 rs7219047
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs6020572 rs6075408 rs6081332 rs6136498 rs6433950 rs7044210
A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma
23andMe Research Team
Nature communications · 2022 · PMID 36496446 · open access
12 pages+
rs12142181 rs7498985 rs9878566 rs251465 rs10830255 rs6989943
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
GenOMICC Investigators · SCOURGE Consortium and 2 more consortia
Nature · 2023 · PMID 37198478 · open access
12 pages+
rs186910 rs2478868 rs1123573 rs111837807 rs7528026 rs17713054
Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci
23andMe Research Team · International Glaucoma Genetics Consortium
Nature genetics · 2023 · PMID 37386247 · open access
12 pages+
rs1392874 rs11530219 rs851400 rs7581865 rs9559369 rs2317385
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
23andMe Research Team · Estonian Biobank Research Team
Nature communications · 2023 · PMID 37794016 · open access
12 pages+
rs4312054 rs6023002 rs705699 rs117137535 rs11236813 rs56308324
Multi-ancestry genome-wide association meta-analysis of Parkinson's disease
23andMe Research Team · Global Parkinson’s Genetics Program (GP2)
Nature genetics · 2024 · PMID 38155330 · open access
12 pages+
rs78327649 rs246815 rs6592142 rs6803771 rs11177328 rs8327
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+
rs1526193 rs7415357 rs72786643 rs3091404 rs9351533 rs12886138
Multi-ancestry genome-wide meta-analysis identifies novel basal cell carcinoma loci and shared genetic effects with squamous cell carcinoma
23andMe Research Team
Communications biology · 2024 · PMID 38182794 · open access
12 pages+
rs71396949 rs12833418 rs2797304 rs2359795 rs6741117 rs7582362
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
23andMe Research Team · D.E.S.I.R. study group
Nature genetics · 2024 · PMID 38839884 · open access
12 pages+
rs61815846 rs3096648 rs12957682 rs35895933 rs9463138 rs72772738
A genome-wide association analysis reveals new pathogenic pathways in gout
FAST Study Group · Japan Gout Genomics Consortium and 3 more consortia
Nature genetics · 2024 · PMID 39406924
12 pages+
rs59328845 rs640304 rs7632 rs2048159 rs2894421 rs35297160
Large-scale genome-wide analyses of stuttering
23andMe Research Team
Nature genetics · 2025 · PMID 40721530 · open access
12 pages+
rs192857772 rs35713684 rs76347047 rs62337988 rs58120907 rs558002155
Genome-wide association study and polygenic risk prediction of hypothyroidism
DBDS Genomic Consortium · Estonian Biobank Research Team and 1 more consortia
Nature genetics · 2025 · PMID 41238958 · open access
12 pages+
rs8022931 rs221811 rs411365 rs4390668 rs6678625 rs1559539
Multi-ancestry genome-wide association analyses of refractive error augment genetic discovery and polygenic prediction
Estonian Biobank Research Team · 23andMe Research Team
Nature genetics · 2026 · PMID 42009823 · open access
12 pages+
rs73150901 rs7561939 rs9608575 rs585101 rs78223756 rs2678662

Showing 20 of 78 · page 2 of 4

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.