For researchers

Is your paper here?

2,660 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.

36 matches for Matsuda F, 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
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
CREAM Consortium · 23andMe Research Team and 1 more consortia
Nature genetics · 2018 · PMID 29808027 · open access
12 pages+
rs2162488 rs4332760 rs41393947 rs10879211 rs1346720 rs55684140
Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population
European journal of human genetics : EJHG · 2019 · PMID 30659259 · open access
12 pages+
rs6966061 rs2080346 rs2135116 rs4673546 rs61997624 rs2242508
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
Cerebral small vessel disease genomics and its implications across the lifespan
International Network against Thrombosis (INVENT) Consortium · International Headache Genomics Consortium (IHGC)
Nature communications · 2020 · PMID 33293549 · open access
12 pages+
rs17205972 rs7596872 rs55940034 rs2303655 rs55897749 rs72934583
The trans-ancestral genomic architecture of glycemic traits
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
rs118164457 rs7063597 rs3752435 rs4317621 rs4731113 rs4674280
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+
rs184980867 rs10248717 rs11672003 rs149590572 rs113920320 rs111589301
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+
rs4267865 rs57634870 rs11196296 rs3825801 rs79495865 rs7819706
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+
rs1551728 rs16832694 rs16942312 rs17093810 rs6666757 rs2032289
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis
BioBank Japan Project
Nature genetics · 2022 · PMID 36333501
12 pages+
rs4341355 rs6495979 rs73005423 rs798000 rs56750287 rs16903108
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs1533104 rs580585 rs1046521 rs1393202 rs183623967 rs35404821
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
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs12012576 rs139120857 rs5942972 rs7063103 rs62603531 rs151113194
GWAS for systemic sclerosis identifies six novel susceptibility loci including one in the Fcγ receptor region
Nature communications · 2024 · PMID 38296975 · open access
7 pages
rs844663 rs10912594 rs11851053 rs10892286 rs5029949 rs7355798
Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk
Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO) · Colorectal Transdisciplinary (CORECT) Study and 1 more consortia
Gastroenterology · 2016 · PMID 26965516
3 pages
rs2450115 rs4919687 rs6061231
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
Genetic determinants and an epistasis of <i>LILRA3</i> and HLA-B*52 in Takayasu arteritis
Proceedings of the National Academy of Sciences of the United States of America · 2018 · PMID 30498034
3 pages
rs1713450 rs4817988 Takayasu Arteritis
Genome-Wide Association Study in Asians Identifies Novel Loci for High Myopia and Highlights a Nervous System Role in Its Pathogenesis
Ophthalmology · 2020 · PMID 32428537
3 pages
rs2246661 rs12032649 rs76903431
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease
CHARGE consortium
Nature medicine · 2023 · PMID 37069360 · open access
3 pages
rs112407396 rs72485816 rs6011998
Whole-genome sequencing reveals rare and structural variants contributing to psoriasis and identifies CERCAM as a risk gene
Biobank Japan Project
Cell genomics · 2025 · PMID 40848718 · open access
3 pages
rs28383305 rs9380151 rs12036815

Showing 20 of 36 · 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.