For researchers

Is your paper here?

2,681 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.

43 matches for Yamamoto K, showing the first 20.

Genetics of rheumatoid arthritis contributes to biology and drug discovery
RACI consortium · GARNET consortium
Nature · 2014 · PMID 24390342 · open access
12 pages+
rs9653442 rs71508903 rs9372120 rs72634030 rs11933540 rs2561477
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 rs13072744 rs3755206 rs3771381 rs1865760 rs11970475
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+
rs3735567 rs12403994 rs60054445 rs201018682 rs61021634 rs8038760
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases
Nature genetics · 2020 · PMID 32514122
12 pages+
rs60984983 rs75024669 rs80202727 rs9921081 rs193457 rs2283159
Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus
Japanese Research Committee on Idiopathic Osteonecrosis of the Femoral Head
Annals of the rheumatic diseases · 2021 · PMID 33272962 · open access
12 pages+
rs116785379 rs12120358 rs76107698 rs2039982 rs4143303 rs218174
A cross-population atlas of genetic associations for 220 human phenotypes
FinnGen
Nature genetics · 2021 · PMID 34594039
12 pages+
rs6069681 rs6686367 rs76537328 rs7669911 rs7846033 rs8070734
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+
rs57634870 rs11196296 rs3825801 rs79495865 rs1871045 rs80102379
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+
rs6058896 rs649523 rs6552828 rs3806325 rs7162940 rs7219047
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis
BioBank Japan Project
Nature genetics · 2022 · PMID 36333501
12 pages+
rs4341355 rs10872479 rs6495979 rs73005423 rs798000 rs56750287
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs74627567 rs7851052 rs79190780 rs10849893 rs117526461 rs1109772
A genome-wide association analysis reveals new pathogenic pathways in gout
FAST Study Group · Japan Gout Genomics Consortium and 3 more consortia
Nature genetics · 2024 · PMID 39406924
12 pages+
rs59328845 rs640304 rs7632 rs2048159 rs2894421 rs35297160
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
Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population
Nature genetics · 2012 · PMID 22446963
7 pages
rs12529514 rs2233434 rs10821944 rs11900673 rs657075 rs3781913
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations
KidneyGen Consortium · CKDGen Consortium and 1 more consortia
Nature genetics · 2012 · PMID 22797727
6 pages
rs17730281 rs11868441 rs10767873 rs2074356 rs17730436 rs11864909
Subtype-specific gout susceptibility loci and enrichment of selection pressure on <i>ABCG2</i> and <i>ALDH2</i> identified by subtype genome-wide meta-analyses of clinically defined gout patients
Japan Gout Genomics Consortium (Japan Gout)
Annals of the rheumatic diseases · 2020 · PMID 32238385 · open access
6 pages
rs76741582 rs116873087 rs548944057 rs145954970 rs76499759 rs2817188
A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci
Human molecular genetics · 2010 · PMID 20189936
5 pages
rs7833986 rs9825379 rs7571816 rs5742692 rs7678436
Identification of nine novel loci associated with white blood cell subtypes in a Japanese population
PLoS genetics · 2011 · PMID 21738478 · open access
5 pages
rs11018874 rs9373124 rs12988934 rs2516399 rs7275212
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
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population
Journal of human genetics · 2011 · PMID 21900946
4 pages
rs3893464 rs4313034 rs4248154 Graves' Disease

Showing 20 of 43 · page 1 of 3

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.