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.

83 matches for Kamatani Y, showing the first 20.

Multiple loci are associated with white blood cell phenotypes
PLoS genetics · 2011 · PMID 21738480 · open access
3 pages
rs1449263 rs10980800 rs2517510
Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma
Nature communications · 2016 · PMID 27501781 · open access
3 pages
rs7216064 rs2495239 EGFR Mutation-Positive Lung Adenocarcinoma
GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes
Eurogout Consortium · Eurogout Consortium
Annals of the rheumatic diseases · 2017 · PMID 27899376 · open access
3 pages
rs11758351 rs1871744 rs4766566
GWAS identifies two novel colorectal cancer loci at 16q24.1 and 20q13.12
Carcinogenesis · 2018 · PMID 29471430
3 pages
rs4939567 rs4572213 rs6691195
12 new susceptibility loci for prostate cancer identified by genome-wide association study in Japanese population
Nature communications · 2019 · PMID 31562322 · open access
3 pages
rs10086908 rs73862213 rs75777376
Genetic variants of calcium and vitamin D metabolism in kidney stone disease
Nature communications · 2019 · PMID 31729369 · open access
3 pages
rs10917002 rs1170174 rs77648599
A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population
Human molecular genetics · 2011 · PMID 21750111
2 pages
rs3077 Chronic Hepatitis B
Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age
Human molecular genetics · 2014 · PMID 24688116 · open access
2 pages
rs2149954 Human Lifespan and Longevity
A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis
American journal of human genetics · 2015 · PMID 26211971
2 pages
rs4637667 Adolescent Idiopathic Scoliosis
A genome-wide association study identifies two novel susceptibility loci and trans population polygenicity associated with bipolar disorder
Molecular psychiatry · 2018 · PMID 28115744 · open access
2 pages
rs4926298 rs4332037
Genome-wide association study of cervical cancer suggests a role for ARRDC3 gene in human papillomavirus infection
Human molecular genetics · 2019 · PMID 30412241
2 pages
rs59661306 rs7457728
Genome-wide analysis identifies novel susceptibility loci for myocardial infarction
INVENT Consortium · CHARGE Consortium Hemostasis Working Group and 2 more consortia
European heart journal · 2021 · PMID 33532862
2 pages
rs6694258 rs12897285
Population-specific reference panel improves imputation quality for genome-wide association studies conducted on the Japanese population
Biobank Japan Project
Communications biology · 2024 · PMID 39702642 · open access
2 pages
rs202213319 rs117371763
Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count
Human molecular genetics · 2010 · PMID 20172861
1 page
rs2072910
Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus
Human molecular genetics · 2011 · PMID 21196492
1 page
rs2097677
Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese
PloS one · 2012 · PMID 22558069 · open access
1 page
rs4985726
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
European Alzheimer's Disease Initiative (EADI) · Genetic and Environmental Risk in Alzheimer's Disease and 2 more consortia
Nature genetics · 2013 · PMID 24162737
1 page
rs10498633
Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism
iPSYCH-SSI-Broad Group
Nature communications · 2017 · PMID 28537267 · open access
1 page
rs12700667
Splicing variant of <i>WDFY4</i> augments MDA5 signalling and the risk of clinically amyopathic dermatomyositis
Annals of the rheumatic diseases · 2018 · PMID 29331962
1 page
rs7919656
Genome-wide association study identifies gastric cancer susceptibility loci at 12q24.11-12 and 20q11.21
Cancer science · 2018 · PMID 30281874 · open access
1 page
rs7849280

Showing 20 of 83 · page 4 of 5

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.