For researchers

Is your paper here?

2,649 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.

30 matches for Akiyama M, showing the first 20.

Genome-wide association study identifies 112 new loci for body mass index in the Japanese population
Nature genetics · 2017 · PMID 28892062
12 pages+
rs139913 rs2540034 rs11130319 rs2033732 rs2235056 rs10062657
Elucidating the genetic architecture of reproductive ageing in the Japanese population
Nature communications · 2018 · PMID 29773799 · open access
12 pages+
rs9393800 rs707938 rs1799949 rs291269 rs1516883 rs144048300
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation
Lifelines Cohort Study
Nature communications · 2018 · PMID 30367059 · open access
12 pages+
rs6785807 rs4445669 rs9298749 rs10957494 rs77819282 rs1045476
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+
rs11044991 rs8084192 rs3774427 rs751985 rs6590811 rs62501779
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
12 pages+
rs34468415 rs12671694 rs6504021 rs78241494 rs2980423 rs1268168
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
German Chronic Kidney Disease Study · Lifelines Cohort Study and 1 more consortia
Nature genetics · 2019 · PMID 31578528 · open access
12 pages+
rs34888828 rs62585312 rs2760215 rs60388273 rs17550549 rs11781985
GWAS of mosaic loss of chromosome Y highlights genetic effects on blood cell differentiation
Nature communications · 2019 · PMID 31624269 · open access
12 pages+
rs527504 rs2811487 rs10948011 rs55727837 rs12668837 rs9299129
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
Identification of type 2 diabetes loci in 433,540 East Asian individuals
Nature · 2020 · PMID 32499647 · open access
12 pages+
rs12907887 rs73085586 rs13086331 rs117737118 rs147689733 rs3135911
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases
Nature genetics · 2020 · PMID 32514122
12 pages+
rs8113007 rs3805495 rs9733843 rs150626020 rs12483725 rs72480748
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+
rs3213794 rs10208769 rs11104870 rs11878568 rs11712552 rs36035825
The Polygenic and Monogenic Basis of Blood Traits and Diseases
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
rs34230287 rs62525616 rs10901250 rs56998314 rs12034342 rs2064431
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
NEIGHBORHOOD consortium · ANZRAG consortium and 5 more consortia
Nature communications · 2021 · PMID 33627673 · open access
12 pages+
rs1412829 rs61870251 rs34175429 rs938604 rs1893261 rs62521288
A cross-population atlas of genetic associations for 220 human phenotypes
FinnGen
Nature genetics · 2021 · PMID 34594039
12 pages+
rs8112217 rs2367585 rs527393 rs34619169 rs11218946 rs11039165
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+
rs149939015 rs76511906 rs2291428 rs73729085 rs2250751 rs3735018
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+
rs3768301 rs72830009 rs7100404 rs7076754 rs835576 rs151215
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+
rs6564905 rs4674101 rs6123837 rs12149514 rs451992 rs12266147
Discerning asthma endotypes through comorbidity mapping
Nature communications · 2022 · PMID 36344522 · open access
12 pages+
rs10975413 rs340928 rs17312661 rs75125788 rs157577 rs3001425
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs13035558 rs817493 rs10853676 rs2859263 rs77636063 rs11209838
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+
rs1658436 rs4414666 rs17254069 rs280875 rs2218471 rs13090630

Showing 20 of 30 · 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.