For researchers

Is your paper here?

2,675 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.

58 matches for Chen H, showing the first 20.

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
Wellcome Trust Case Control Consortium
Nature genetics · 2008 · PMID 18372903
5 pages
rs12779790 rs864745 rs7961581 rs7578597 rs10923931
Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study
International Consortium on Lithium Genetics (ConLi+Gen)
JAMA psychiatry · 2018 · PMID 29121268
5 pages
rs66486766 rs324899 rs6942227 rs209474 rs6728642
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
The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study
23andMe Research Team, China Kadoorie Biobank Collaborative Group, and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
JAMA psychiatry · 2021 · PMID 34586374 · open access
4 pages
rs1950829 rs4936272 rs17410557 rs112176860
GWAS of Chronic Spontaneous Urticaria Reveals Genetic Overlap with Autoimmune Diseases, Not Atopic Diseases
The Journal of investigative dermatology · 2023 · PMID 35933036
4 pages
rs61986182 rs73075571 rs117754460 rs434124
The largest genome-wide association study for breast cancer in Taiwanese Han population
Breast cancer research and treatment · 2024 · PMID 37851288
4 pages
rs147358466 rs76893106 rs9613774 rs12173562
Identifying expression and DNA methylation biomarkers for lung adenocarcinoma risk in East Asia
Journal of the National Cancer Institute · 2026 · PMID 41581221 · open access
4 pages
rs11196089 rs2760995 rs4268071 rs9367106
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes
DIAGRAM Consortium · GIANT Consortium and 3 more consortia
Diabetes · 2011 · PMID 21873549 · open access
3 pages
rs6235 rs11558471 rs1549318
Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium
HGG advances · 2022 · PMID 35399580 · open access
3 pages
rs6817771 rs9922708 rs3751813
Impact of polygenic risk score for triglyceride trajectory and diabetic complications in subjects with type 2 diabetes based on large electronic medical record data from Taiwan: a case control study
Journal of endocrinological investigation · 2024 · PMID 38795312
3 pages
rs75662937 rs61346349 rs2854116
Genome-wide gene-sleep interaction study identifies novel lipid loci in 732,564 participants
Lifelines Cohort Study · Million Veteran Program
Atherosclerosis · 2026 · PMID 41325697
3 pages
rs150607032 rs190975828 rs192018195
Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC
Nature genetics · 2010 · PMID 20526339
2 pages
rs2236313 Vitiligo
Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia
Nature genetics · 2012 · PMID 23143601
2 pages
rs4488809 rs7086803
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
Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B
Hepatology (Baltimore, Md.) · 2015 · PMID 25802187
2 pages
rs2856718 rs2853953
Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese
Nature communications · 2018 · PMID 30287856 · open access
2 pages
rs6114027 Tuberculosis
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
Genome-wide association study identified novel loci and gene-environment interaction for refractive error in children
NPJ genomic medicine · 2025 · PMID 40410244 · open access
2 pages
rs17074027 rs6925312
Genome-wide association meta-analysis of human olfactory identification discovers sex-specific and sex-differential genetic variants
Nature communications · 2025 · PMID 40593737 · open access
2 pages
rs41286168 rs669453
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

Showing 20 of 58 · 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.