For researchers

Is your paper here?

2,673 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.

23 matches for Kanai 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+
rs2033732 rs2235056 rs10062657 rs10840099 rs3121672 rs2240920
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
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+
rs6779998 rs4441471 rs6574652 rs74748843 rs7966357 rs6473252
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+
rs11781985 rs72782806 rs861536 rs10438961 rs6707386 rs98270
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases
Nature genetics · 2020 · PMID 32514122
12 pages+
rs12483725 rs72480748 rs373205748 rs12506083 rs12253987 rs2378519
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+
rs6897196 rs75211492 rs76738175 rs922 rs10423120 rs10493441
The Polygenic and Monogenic Basis of Blood Traits and Diseases
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
rs4700436 rs6595714 rs72843867 rs7356611 rs7810260 rs79709502
Genetic analyses identify widespread sex-differential participation bias
FinnGen Study · 23andMe Research Team and 1 more consortia
Nature genetics · 2021 · PMID 33888908
12 pages+
rs1368546 rs77966298 rs10468280 rs73186025 rs80028017 rs10964391
A cross-population atlas of genetic associations for 220 human phenotypes
FinnGen
Nature genetics · 2021 · PMID 34594039
12 pages+
rs2369280 rs3751297 rs549283835 rs62110225 rs76494985 rs10198975
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+
rs10928512 rs187479321 rs6493583 rs72729623 rs115726216 rs144242131
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+
rs1887200 rs11904581 rs6139109 rs1442883 rs973730 rs6020177
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
rs2276133 rs7748159 rs9266669 rs7636138 rs11880613 rs2728099
Nuclear genetic control of mtDNA copy number and heteroplasmy in humans
Nature · 2023 · PMID 37587338 · open access
12 pages+
rs3859187 rs2436537 rs578069621 rs11871678 rs11979102 rs8066387
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
PGC-MDD Working Group · China Kadoorie Biobank Collaborative Group and 3 more consortia
Nature genetics · 2024 · PMID 38177345 · open access
12 pages+
rs324901 rs534415 rs1526193 rs7415357 rs72786643 rs3091404
Causal relevance of different blood pressure traits on risk of cardiovascular diseases: GWAS and Mendelian randomisation in 100,000 Chinese adults
China Kadoorie Biobank Collaborative Group
Nature communications · 2024 · PMID 39048560 · open access
12 pages+
rs9322356 rs78236399 rs13116214 rs2853795 rs835445 rs11191454
Genome-wide association analyses of gestational phenotypes identify context-specific genetic effects
Nature genetics · 2026 · PMID 42509370
12 pages+
rs3211908 rs78117616 rs148479079 rs60290423 rs147339781 rs4931170
Multi-ancestry genome-wide association analyses provide insights into the genetic basis of Hashimoto's thyroiditis
Biobank Japan Project
Nature genetics · 2026 · PMID 42527560 · open access
12 pages+
rs736374 rs723291 rs11073337 rs11154825 rs3892710 rs12345171
Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population
Nature genetics · 2019 · PMID 30718926
9 pages
rs113547729 rs16884025 rs3751237 rs79407053 rs2908279 rs9505085
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
Nature communications · 2024 · PMID 38233393 · open access
8 pages
rs5931180 rs12382607 rs4328011 rs139036121 rs5933079 rs181497961
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs762517 rs12012576 rs139120857 rs5942972 rs7063103 rs62603531

Showing 20 of 23 · 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.