For researchers

Is your paper here?

2,685 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 Momozawa Y, 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+
rs2240920 rs1949804 rs2836768 rs77636220 rs17303831 rs4357030
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
InterAct Consortium
PloS one · 2018 · PMID 29912962 · open access
12 pages+
rs4886640 rs7125196 rs259983 rs11725969 rs1894400 rs34063670
Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect
Schizophrenia bulletin · 2019 · PMID 30285260
12 pages+
rs66492629 rs1837495 rs9859557 rs7807720 rs6670165 rs12139672
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+
rs58244401 rs6590816 rs6712094 rs2270860 rs1004467 rs4684242
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
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases
Nature genetics · 2020 · PMID 32514122
12 pages+
rs729949 rs7763637 rs60984983 rs75024669 rs80202727 rs9921081
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction
Nature genetics · 2021 · PMID 33398198 · open access
12 pages+
rs2018336 rs2038542 rs10412482 rs7618603 rs2074840 rs2672843
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+
rs62391632 rs66819623 rs10882167 rs12664587 rs8141610 rs56233426
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+
rs10500790 rs2629755 rs6902225 rs13387570 rs223449 rs9639575
Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration
Human molecular genetics · 2023 · PMID 37384397
12 pages+
rs11242483 rs10814514 rs1057703 rs6737318 rs34731055 rs7115856
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
Biobank Japan Project
Nature genetics · 2023 · PMID 37945903
12 pages+
rs10886810 rs1037137 rs11892008 rs6151589 rs4713343 rs2485662
Genome-wide analysis of heart failure yields insights into disease heterogeneity and enables prognostic prediction in the Japanese population
BioBank Japan Project
Nature communications · 2025 · PMID 41184235 · open access
12 pages+
rs1541596 rs73193820 rs3764351 rs7188250 rs59788391 rs2261787
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
CHARGE Neurology Working Group · COGENT-Kidney Consortium and 2 more consortia
American journal of human genetics · 2018 · PMID 29455858
7 pages
rs115234772 rs62319742 rs148772934 rs138973557 rs148753653 rs12135881
Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population
Journal of the American Society of Nephrology : JASN · 2019 · PMID 30975718
7 pages
rs6928986 rs6975977 rs35747824 rs7206790 rs2079742 rs13041834
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
Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population
Nature communications · 2023 · PMID 37236969 · open access
5 pages
rs75031349 rs137884934 rs682888 rs10901793 rs71467682
Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese
Nature communications · 2019 · PMID 31417091 · open access
4 pages
rs2467146 rs658839 rs7028900 rs17011903
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 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

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.