For researchers

Is your paper here?

2,671 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 Kadowaki T.

Identification of type 2 diabetes loci in 433,540 East Asian individuals
Nature · 2020 · PMID 32499647 · open access
12 pages+
rs186568031 rs117267808 rs4711389 rs75536691 rs7787720 rs1955163
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases
Nature genetics · 2020 · PMID 32514122
12 pages+
rs10965247 rs77792157 rs61275591 rs192314256 rs3816157 rs187150787
A cross-population atlas of genetic associations for 220 human phenotypes
FinnGen
Nature genetics · 2021 · PMID 34594039
12 pages+
rs551625260 rs79231157 rs9475429 rs7100296 rs117629395 rs422249
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
12 pages+
rs7819706 rs1473781 rs6876198 rs3743140 rs3806155 rs7313668
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs11466334 rs12555274 rs13094957 rs76675804 rs2056857 rs72802365
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
CHD Exome+ Consortium · EPIC-CVD Consortium and 2 more consortia
Nature genetics · 2017 · PMID 28869590 · open access
11 pages
rs2421016 rs9505118 rs4689388 rs2706785 rs329122 rs2050188
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24509480 · open access
9 pages
rs17791513 rs6813195 rs17106184 rs849135 rs2261181 rs9936385
Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population
Nature genetics · 2019 · PMID 30718926
9 pages
rs79407053 rs2908279 rs9505085 rs2844623 rs201597274 rs76550717
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
SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations
Nature genetics · 2008 · PMID 18711366
3 pages
rs2237897 rs4712524 rs6769511
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
A cross-population compendium of gene-environment interactions
BioBank Japan Project
Nature · 2026 · PMID 41606330 · open access
2 pages
rs12507330 rs730154
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
DIAGRAM Consortium · MuTHER Consortium
Nature genetics · 2011 · PMID 22158537
1 page
rs9470794

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.