For researchers

Is your paper here?

2,682 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+
rs17303831 rs4357030 rs3205718 rs4805566 rs7243785 rs2076463
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+
rs4445669 rs9298749 rs10957494 rs77819282 rs1045476 rs28502438
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
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+
rs62432759 rs1051447 rs10102889 rs10272546 rs948493 rs9397738
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+
rs188917216 rs34861762 rs4897160 rs2941487 rs148015593 rs12484809
GWAS of mosaic loss of chromosome Y highlights genetic effects on blood cell differentiation
Nature communications · 2019 · PMID 31624269 · open access
12 pages+
rs2646425 rs527504 rs2811487 rs10948011 rs55727837 rs12668837
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+
rs55902013 rs3858704 rs6587520 rs2269997 rs9381634 rs62010554
Identification of type 2 diabetes loci in 433,540 East Asian individuals
Nature · 2020 · PMID 32499647 · open access
12 pages+
rs60573766 rs149265787 rs186568031 rs117267808 rs4711389 rs75536691
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases
Nature genetics · 2020 · PMID 32514122
12 pages+
rs80005921 rs138213721 rs8107030 rs10965247 rs77792157 rs61275591
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+
rs78393402 rs79935131 rs8032549 rs8034838 rs8080418 rs9650988
The Polygenic and Monogenic Basis of Blood Traits and Diseases
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
rs7895133 rs978266 rs1048310 rs11206773 rs115593871 rs116369005
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+
rs10882167 rs8141610 rs56233426 rs11710845 rs1412829 rs61870251
A cross-population atlas of genetic associations for 220 human phenotypes
FinnGen
Nature genetics · 2021 · PMID 34594039
12 pages+
rs7842144 rs79512156 rs80157433 rs886997 rs9425339 rs958050
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+
rs7856817 rs11626768 rs180705493 rs2811468 rs532566544 rs5752963
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+
rs79495865 rs1871045 rs80102379 rs7819706 rs1473781 rs6876198
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+
rs2096884 rs7948776 rs8006022 rs8088446 rs8101705 rs8177375
Discerning asthma endotypes through comorbidity mapping
Nature communications · 2022 · PMID 36344522 · open access
12 pages+
rs28607030 rs7110818 rs78728108 rs1233493 rs10975413 rs340928
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs10065698 rs1028212 rs1079558 rs10863958 rs2357475 rs10918790
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
12 pages+
rs13387570 rs223449 rs9639575 rs4757877 rs17042175 rs74154539

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.