For researchers

Is your paper here?

2,671 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.

9 matches for Ji H.

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
rs2021408 rs844663 rs10912594 rs11851053 rs10892286 rs5029949
Genetic determinants and an epistasis of <i>LILRA3</i> and HLA-B*52 in Takayasu arteritis
Proceedings of the National Academy of Sciences of the United States of America · 2018 · PMID 30498034
3 pages
rs1713450 rs4817988 Takayasu Arteritis
IgG4-related disease in the Japanese population: a whole-genome sequencing study
Japanese IgG4-Related Disease Working Consortium
The Lancet. Rheumatology · 2026 · PMID 41197642
3 pages
rs894063168 rs66917126 IgG4-Related Disease
Genome-Wide Association Study Identifies TLL1 Variant Associated With Development of Hepatocellular Carcinoma After Eradication of Hepatitis C Virus Infection
Japanese Genome-Wide Association Study Group for Viral Hepatitis
Gastroenterology · 2017 · PMID 28163062
2 pages
rs17047200 Liver Cancer Risk After Hepatitis C Is Cured
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
Genome-wide approach identifies a novel gene-maternal pre-pregnancy BMI interaction on preterm birth
Nature communications · 2017 · PMID 28598419 · open access
2 pages
rs8029754 rs11161721
Radiogenomics Consortium Genome-Wide Association Study Meta-Analysis of Late Toxicity After Prostate Cancer Radiotherapy
Journal of the National Cancer Institute · 2020 · PMID 31095341 · open access
2 pages
rs10969913 rs17055178
Genome-wide association study identifies 8p21.3 associated with persistent hepatitis B virus infection among Chinese
Nature communications · 2016 · PMID 27244555 · open access
1 page
rs7000921
A variant at 9q34.11 is associated with HLA-DQB1*06:02 negative essential hypersomnia
Journal of human genetics · 2018 · PMID 30266950
1 page
rs10988217

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.