For researchers

Is your paper here?

2,683 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.

80 matches for Okada Y, showing the first 20.

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+
rs17105330 rs8079564 rs4813853 rs7015100 rs7522427 rs9907557
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis
BioBank Japan Project
Nature genetics · 2022 · PMID 36333501
12 pages+
rs6495979 rs73005423 rs798000 rs56750287 rs16903108 rs6681482
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs882985 rs56029033 rs600388 rs409770 rs62098013 rs17638867
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+
rs76181804 rs9290877 rs9594366 rs16856530 rs62283809 rs10854002
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+
rs12136984 rs12374612 rs324901 rs534415 rs1526193 rs7415357
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs12789028 rs11466334 rs12555274 rs13094957 rs76675804 rs2056857
Causal relevance of different blood pressure traits on risk of cardiovascular diseases: GWAS and Mendelian randomisation in 100,000 Chinese adults
China Kadoorie Biobank Collaborative Group
Nature communications · 2024 · PMID 39048560 · open access
12 pages+
rs10477399 rs9847595 rs6585252 rs75268076 rs62175706 rs67913572
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+
rs174582 rs72912510 rs56336338 rs56240036 rs11109717 rs4441044
Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases
Penn Medicine BioBank · Virtual Thyroid Biopsy Consortium and 4 more consortia
Nature genetics · 2026 · PMID 41644669 · open access
12 pages+
rs17242727 rs369835958 rs11221322 rs8089538 rs12448508 rs34393407
Genome-wide association analyses of gestational phenotypes identify context-specific genetic effects
Nature genetics · 2026 · PMID 42509370
12 pages+
rs6127091 rs147740307 rs181128092 rs138811940 rs4236051 rs75746803
Multi-ancestry genome-wide association analyses provide insights into the genetic basis of Hashimoto's thyroiditis
Biobank Japan Project
Nature genetics · 2026 · PMID 42527560 · open access
12 pages+
rs736374 rs723291 rs11073337 rs11154825 rs3892710 rs12345171
Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population
Nature genetics · 2019 · PMID 30718926
10 pages
rs79407053 rs2908279 rs9505085 rs2844623 rs201597274 rs76550717
Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity
SUMMIT Consortium · BioBank Japan Project
American journal of human genetics · 2016 · PMID 27588450 · open access
8 pages
rs35716097 rs5020545 rs62435145 rs57989581 rs8096658 rs1511299
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
8 pages
rs139120857 rs5942972 rs7063103 rs62603531 rs151113194 rs762517
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
Nature communications · 2024 · PMID 38233393 · open access
8 pages
rs4328011 rs139036121 rs5933079 rs181497961 rs111410539 rs5933443
Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population
Nature genetics · 2012 · PMID 22446963
7 pages
rs12529514 rs2233434 rs10821944 rs11900673 rs657075 rs3781913
Seven new loci associated with age-related macular degeneration
AMD Gene Consortium
Nature genetics · 2013 · PMID 23455636 · open access
7 pages
rs1864163 rs920915 rs8135665 rs8017304 rs9542236 rs13081855
GWAS for systemic sclerosis identifies six novel susceptibility loci including one in the Fcγ receptor region
Nature communications · 2024 · PMID 38296975 · open access
7 pages
rs2021408 rs844663 rs10912594 rs11851053 rs10892286 rs5029949
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations
KidneyGen Consortium · CKDGen Consortium and 1 more consortia
Nature genetics · 2012 · PMID 22797727
6 pages
rs17730281 rs11868441 rs10767873 rs2074356 rs17730436 rs11864909
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes
Nature communications · 2016 · PMID 26818947 · open access
6 pages
rs1116357 rs1575972 rs9309245 rs67156297 rs7107784 rs78627331

Showing 20 of 80 · 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.