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.

14 matches for Gao J.

Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes
CHIMGEN Consortium
Nature genetics · 2023 · PMID 37337106
12 pages+
rs9498383 rs10888849 rs13243296 rs4767460 rs12174588 rs2927567
Cross-ancestry genome-wide association studies of brain imaging phenotypes
CHIMGEN Consortium
Nature genetics · 2024 · PMID 38811844
12 pages+
rs2286184 rs4962692 rs72640140 rs631929 rs4938399 rs2640
Cross-ancestry and sex-stratified genome-wide association analyses of amygdala and subnucleus volumes
CHIMGEN Consortium
Nature genetics · 2025 · PMID 40097784
12 pages+
rs13119968 rs61067594 rs12501273 rs111737209 rs7980920 rs372682919
Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer
Gastroenterology · 2019 · PMID 30529582
6 pages
rs7542665 rs201395236 rs113569514 rs3830041 rs77969132 rs1886450
Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians
American journal of human genetics · 2013 · PMID 23273568
5 pages
rs6705628 rs4852324 rs6804441 rs34330 rs729302
Development and evaluation of a polygenic risk score for lung cancer in never-smoking women: A large-scale prospective Chinese cohort study
International journal of cancer · 2024 · PMID 37846649
3 pages
rs11196063 rs11928222 rs9275164
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 study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations
Nature genetics · 2011 · PMID 22158540
2 pages
rs372883 Pancreatic Cancer
Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans
Arthritis & rheumatology (Hoboken, N.J.) · 2014 · PMID 24782177
2 pages
rs1854853 rs12525220
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
Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization
Genes · 2021 · PMID 34202464 · open access
2 pages
rs9919007 rs3118662
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Nature genetics · 2009 · PMID 19915575 · open access
1 page
rs393152
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
Identification of Novel Loci and New Risk Variant in Known Loci for Colorectal Cancer Risk in East Asians
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020 · PMID 31826910
1 page
rs10795668

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.