For researchers

Is your paper here?

2,645 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 Sakaue S.

Transethnic Meta-Analysis of Genome-Wide Association Studies Identifies Three New Loci and Characterizes Population-Specific Differences for Coronary Artery Disease
Circulation. Genomic and precision medicine · 2020 · PMID 32469254
12 pages+
rs2269997 rs9381634 rs62010554 rs3008629 rs7214227 rs34914832
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases
Nature genetics · 2020 · PMID 32514122
12 pages+
rs9733843 rs150626020 rs12483725 rs72480748 rs373205748 rs12506083
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
VA Million Veteran Program
Cell · 2020 · PMID 32888493
12 pages+
rs11656414 rs76756213 rs189129074 rs191751273 rs2425157 rs56078345
The Polygenic and Monogenic Basis of Blood Traits and Diseases
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
rs1023243 rs151336 rs187856913 rs370025470 rs5765229 rs12223916
Cerebral small vessel disease genomics and its implications across the lifespan
International Network against Thrombosis (INVENT) Consortium · International Headache Genomics Consortium (IHGC)
Nature communications · 2020 · PMID 33293549 · open access
12 pages+
rs4843553 rs11685652 rs7157599 rs73923006 rs6797002 rs7603972
A cross-population atlas of genetic associations for 220 human phenotypes
FinnGen
Nature genetics · 2021 · PMID 34594039
12 pages+
rs12946693 rs11191447 rs12902050 rs62576695 rs73200263 rs9573566
The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs12633551 rs557901815 rs10185855 rs117777720 rs570553136 rs188503412
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+
rs293428 rs9738836 rs12372134 rs12528442 rs3217863 rs11082403
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis
BioBank Japan Project
Nature genetics · 2022 · PMID 36333501
12 pages+
rs6930468 rs12519914 rs7171617 rs55762233 rs1188620266 rs4687070
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
10 pages
rs12374612 rs324901 rs534415 rs1526193 rs7415357 rs72786643
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs151113194 rs762517 rs12012576 rs139120857 rs5942972 rs7063103
Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data
Nature communications · 2019 · PMID 31235808 · open access
5 pages
rs28822480 rs6495046 rs9831002 rs2046850 rs7852129
Whole-genome sequencing reveals rare and structural variants contributing to psoriasis and identifies CERCAM as a risk gene
Biobank Japan Project
Cell genomics · 2025 · PMID 40848718 · open access
3 pages
rs28383305 rs9380151 rs12036815

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.