For researchers

Is your paper here?

2,661 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.

21 matches for Chen F, showing the first 20.

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
23andMe Research Team · HUNT All-In Psychiatry
Nature genetics · 2019 · PMID 30643251 · open access
12 pages+
rs4650206 rs8192726 rs3025312 rs17234745 rs7833370 rs6545765
Genome-wide association meta-analysis of 88,250 individuals highlights pleiotropic mechanisms of five ocular diseases in UK Biobank
EBioMedicine · 2022 · PMID 35841873 · open access
12 pages+
rs12602519 rs3924761 rs12950511 rs7118248 rs6650097 rs11992725
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs10813745 rs587204 rs655559 rs4963744 rs61875182 rs10185713
Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes
CHIMGEN Consortium
Nature genetics · 2023 · PMID 37337106
12 pages+
rs4767461 rs10850725 rs74712405 rs10479662 rs6478240 rs7636254
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 rs78416326
Cross-ancestry genome-wide association studies of brain imaging phenotypes
CHIMGEN Consortium
Nature genetics · 2024 · PMID 38811844
12 pages+
rs9327011 rs1163297 rs12030374 rs919445 rs3744349 rs60865161
Cross-ancestry and sex-stratified genome-wide association analyses of amygdala and subnucleus volumes
CHIMGEN Consortium
Nature genetics · 2025 · PMID 40097784
12 pages+
rs12565378 rs35166705 rs56390130 rs62329462 rs12679702 rs150434736
Development and validation of a multiancestry and multitrait polygenic risk score for lung cancer
Nature communications · 2026 · PMID 42364979 · open access
12 pages+
rs62329691 rs7243964 rs4803381 rs1138373 rs705698 rs7638643
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium
Molecular psychiatry · 2020 · PMID 30617275 · open access
7 pages
rs6692219 rs11971186 rs1937455 rs6738833 rs13026471 rs6883351
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
Regeneron Genetics Center · CARDIoGRAMplusC4D Consortium and 2 more consortia
Nature medicine · 2022 · PMID 35915156
6 pages
rs7884019 rs56210063 rs78532451 rs1867073 rs7622417 rs2715879
Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer
Nature communications · 2018 · PMID 29422604 · open access
4 pages
rs13303010 rs1517037 rs4795218 rs2941471
Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese
American journal of human genetics · 2012 · PMID 23103227
2 pages
rs2494938 rs2285947
Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese
PLoS genetics · 2013 · PMID 23341777 · open access
2 pages
rs12296850 Lung Squamous Cell Carcinoma
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
NABEC Consortium · UKBEC Consortium and 2 more consortia
Nature genetics · 2013 · PMID 23583978 · open access
2 pages
rs348495 rs10261878
Genome-wide association of body fat distribution in African ancestry populations suggests new loci
PLoS genetics · 2013 · PMID 23966867 · open access
2 pages
rs6931262 rs2075064
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations
Asian Genetic Epidemiology Network Consortium
American journal of human genetics · 2013 · PMID 23972371
2 pages
rs17428471 rs17080102
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2
Cohorts for Heart and Aging Research in Genome Epidemiology (CHARGE) Consortium Neurology Working Group · CARDIoGRAM Consortium and 1 more consortia
Arteriosclerosis, thrombosis, and vascular biology · 2014 · PMID 24578379
2 pages
rs9399599 rs3136739
Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke
Genomics and Randomized Trials Network · Framingham Heart Study
PLoS genetics · 2014 · PMID 24651765 · open access
2 pages
rs9296404 rs1047891
A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese
Nature genetics · 2011 · PMID 21725308
1 page
rs753955
A genome-wide association study identifies susceptibility loci of silica-related pneumoconiosis in Han Chinese
Human molecular genetics · 2014 · PMID 24986923
1 page
rs73329476

Showing 20 of 21 · 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.