For researchers

Is your paper here?

2,657 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.

25 matches for Ota M, showing the first 20.

Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci
Human molecular genetics · 2015 · PMID 25429064
12 pages+
rs7184046 rs3755206 rs3771381 rs1865760 rs11970475 rs10448080
Interethnic analyses of blood pressure loci in populations of East Asian and European descent
International Genomics of Blood Pressure (iGEN-BP) Consortium
Nature communications · 2018 · PMID 30487518 · open access
12 pages+
rs6590816 rs6712094 rs2270860 rs1004467 rs4684242 rs4980389
Identification of type 2 diabetes loci in 433,540 East Asian individuals
Nature · 2020 · PMID 32499647 · open access
12 pages+
rs201018682 rs61021634 rs8038760 rs75990271 rs1328412 rs56687477
The trans-ancestral genomic architecture of glycemic traits
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
rs118164457 rs7063597 rs3752435 rs4317621 rs4731113 rs4674280
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+
rs114876144 rs145437104 rs3134988 rs7575245 rs269781 rs4741016
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+
rs11196296 rs3825801 rs7819706 rs1473781 rs6876198 rs3743140
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+
rs11570441 rs11656344 rs11030613 rs11769128 rs11955611 rs11991223
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs1203894 rs139149176 rs141307757 rs61876142 rs138348096 rs2007537
Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction
BioBank Japan Project
Nature genetics · 2023 · PMID 36653681 · open access
11 pages
rs2629755 rs6902225 rs13387570 rs223449 rs4757877 rs17042175
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
rs6813195 rs17106184 rs849135 rs2261181 rs9936385 rs4458523
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
DBDS Genomic Consortium · FinnGen Study and 3 more consortia
Nature genetics · 2023 · PMID 36914876
8 pages
rs2226158 rs71575922 rs1903068 rs3858429 rs4540228 rs57281976
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs12012576 rs139120857 rs5942972 rs7063103 rs62603531 rs151113194
Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians
Nature genetics · 2011 · PMID 21572416
4 pages
rs35444 rs17249754 rs6825911 Blood Pressure
Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals
Communications biology · 2019 · PMID 30993211 · open access
4 pages
rs1549287 rs16856823 rs4966024 rs11202346
Genome-Wide Association Study in Asians Identifies Novel Loci for High Myopia and Highlights a Nervous System Role in Its Pathogenesis
Ophthalmology · 2020 · PMID 32428537
3 pages
rs2246661 rs12032649 rs76903431
Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility
Writing Committee for the Normal Tension Glaucoma Genetic Study Group of Japan Glaucoma Society
Ophthalmology · 2010 · PMID 20363506
2 pages
rs3213787 Glaucoma
Meta-analysis identifies common variants associated with body mass index in east Asians
Genetic Investigation of ANthropometric Traits (GIANT) Consortium
Nature genetics · 2012 · PMID 22344219 · open access
2 pages
rs9356744 rs261967
New susceptibility loci associated with kidney disease in type 1 diabetes
DCCT/EDIC Research Group
PLoS genetics · 2012 · PMID 23028342 · open access
2 pages
rs12437854 rs7583877
A meta-analysis of genome-wide association studies for adiponectin levels in East Asians identifies a novel locus near WDR11-FGFR2
Human molecular genetics · 2014 · PMID 24105470
2 pages
rs10937273 Adiponectin Levels
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
BIOS-consortium · CARDIo GRAMplusCD and 2 more consortia
Nature genetics · 2015 · PMID 26390057
2 pages
rs9687065 rs1563788

Showing 20 of 25 · page 1 of 2

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.