For researchers

Is your paper here?

2,663 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.

43 matches for Chen G, showing the first 20.

Evaluating genetic risk for prostate cancer among Japanese and Latinos
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2012 · PMID 22923026
2 pages
rs6983561 rs10505483
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
Two new susceptibility loci 1q24.2 and 11p11.2 confer risk to severe acne
Nature communications · 2014 · PMID 24399259
2 pages
rs7531806 Severe Acne
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis
Nature communications · 2017 · PMID 28425483 · open access
2 pages
rs9501251 Primary Biliary Cholangitis
Association Study and Fine-Mapping Major Histocompatibility Complex Analysis of Pemphigus Vulgaris in a Han Chinese Population
The Journal of investigative dermatology · 2018 · PMID 29857070
2 pages
rs11218708 Pemphigus Vulgaris
Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease
Nature communications · 2018 · PMID 30111768 · open access
2 pages
rs149066340 rs143654430
Genome-wide association analyses identified novel susceptibility loci for pulmonary embolism among Han Chinese population
China pUlmonary Thromboembolism REgistry Study (CURES) investigators
BMC medicine · 2023 · PMID 37076872 · open access
2 pages
rs35801946 rs4843804
Genetic determinants of IgG antibody response to COVID-19 vaccination
American journal of human genetics · 2024 · PMID 38181733 · open access
2 pages
rs10947290 rs35986240
Large-scale blood pressure GWAS accounting for gene-depression interactions in 564,680 individuals from diverse populations
Biobank Japan Project · Lifelines Cohort Study,
HGG advances · 2026 · PMID 41520179 · open access
2 pages
rs145132348 rs757194
A genome-wide association study identifies two new risk loci for Graves' disease
China Consortium for Genetics of Autoimmune Thyroid Disease
Nature genetics · 2011 · PMID 21841780
1 page
rs12101261
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
Gene Environment Interaction and Breast Cancer in Germany (GENICA) Consortium
Nature genetics · 2011 · PMID 22037553
1 page
rs10069690
Genome-wide meta-analyses of smoking behaviors in African Americans
Translational psychiatry · 2012 · PMID 22832964 · open access
1 page
rs2036527
A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11
Australian Breast Cancer Tissue Bank Investigators · Familial Breast Cancer Study and 1 more consortia
Human molecular genetics · 2012 · PMID 22976474
1 page
rs9383938
Genome-wide association study of age at menarche in African-American women
Human molecular genetics · 2013 · PMID 23599027
1 page
rs10441737
Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations
China Consortium for Genetics of Autoimmune Thyroid Disease
Human molecular genetics · 2014 · PMID 24852370
1 page
rs2622590
Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study
Lancet (London, England) · 2016 · PMID 26806518 · open access
1 page
rs74795342
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity
Nature communications · 2017 · PMID 28232668 · open access
1 page
rs12229892
Two novel genetic variants in the STK38L and RAB27A genes are associated with glioma susceptibility
International journal of cancer · 2019 · PMID 30714141
1 page
rs10842893

Showing 20 of 43 · page 2 of 3

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.