For researchers

Is your paper here?

2,657 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 Hu Q.

Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort
Nature genetics · 2022 · PMID 35115689
12 pages+
rs11153022 rs138925568 rs151169359 rs2527084 rs35515607 rs10931443
Genetic architecture of bone marrow fat fraction implies its involvement in osteoporosis risk
Nature communications · 2025 · PMID 40796918 · open access
12 pages+
rs79260952 rs117210562 rs11712037 rs10753536 rs10761756 rs6415470
Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci
Clinical and translational medicine · 2021 · PMID 33634981 · open access
11 pages
rs58275387 rs9929808 rs73530508 rs9204 rs9530695 rs73365860
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
Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease
CARDIoGRAMplusC4D Consortium
Nature genetics · 2017 · PMID 28714974 · open access
1 page
rs17517928
Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex
Blood advances · 2017 · PMID 29296818
1 page
rs11980379
UACA locus is associated with breast cancer chemoresistance and survival
NPJ breast cancer · 2022 · PMID 35322040 · open access
1 page
rs720251
Genetic Association Studies in Hepatocellular Carcinoma: Systematic Meta-Analyses, a Comprehensive Field Synopsis, and Epidemiological Evidence
MedComm · 2026 · PMID 42656915 · open access
1 page
Research roundup — September 2026
Genetic Evidence That Stroke Causally Increases Circulating PDGFB Levels: a Two-Sample Mendelian Randomization Study
Journal of molecular neuroscience : MN · 2026 · PMID 42700318
1 page
Research roundup — September 2026

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.