For researchers

Is your paper here?

2,677 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.

23 matches for Hu C, showing the first 20.

Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels
Human molecular genetics · 2017 · PMID 28334899
12 pages+
rs2188380 rs2144300 rs11984636 rs3786247 rs11208004 rs2244608
Discovery of common and rare genetic risk variants for colorectal cancer
Nature genetics · 2019 · PMID 30510241 · open access
12 pages+
rs12144319 rs116353863 rs117079142 rs11884596 rs12708491 rs4901473
Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders
Translational psychiatry · 2021 · PMID 33479212 · open access
12 pages+
rs12265655 rs1367635 rs9926049 rs4936216 rs6449528 rs7716818
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
23andMe Research Team · Estonian Biobank Research Team
Nature communications · 2023 · PMID 37794016 · open access
12 pages+
rs4312054 rs6023002 rs705699 rs117137535 rs11236813 rs56308324
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
PGC-MDD Working Group · China Kadoorie Biobank Collaborative Group and 3 more consortia
Nature genetics · 2024 · PMID 38177345 · open access
12 pages+
rs324901 rs534415 rs1526193 rs7415357 rs72786643 rs3091404
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24509480 · open access
9 pages
rs6813195 rs17106184 rs849135 rs2261181 rs9936385 rs4458523
New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders
Nature human behaviour · 2019 · PMID 31358974
9 pages
rs2277499 rs10496076 rs71414193 rs57281063 rs227179 rs4794015
New insights into the genetic etiology of Alzheimer's disease and related dementias
EADB · GR@ACE and 7 more consortia
Nature genetics · 2022 · PMID 35379992 · open access
9 pages
rs3848143 rs62374257 rs3851179 rs6605556 rs7767350 rs6586028
Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility
Nature communications · 2015 · PMID 25903422 · open access
7 pages
rs34394770 rs8128234 rs7709212 rs3747517 rs842625 rs12564022
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes
Nature communications · 2016 · PMID 26818947 · open access
6 pages
rs1116357 rs1575972 rs9309245 rs67156297 rs7107784 rs78627331
Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study
Stroke · 2018 · PMID 29273593
6 pages
rs9614159 rs74388387 rs9907978 rs10782008 rs117353193 Moyamoya Disease
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
ABCTB Investigators · EMBRACE and 4 more consortia
Nature genetics · 2017 · PMID 29058716
5 pages
rs10995201 rs9397437 rs6562760 rs6678914 rs67397200
Detailed stratified GWAS analysis for severe COVID-19 in four European populations
COVICAT study group, Aachen Study (COVAS) · Norwegian SARS-CoV-2 Study group and 2 more consortia
Human molecular genetics · 2022 · PMID 35848942 · open access
5 pages
rs77534576 rs143334143 rs35731912 rs2269899 COVID-19 with Respiratory Failure Requiring Mechanical Ventilation
Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits
MAGIC consortium
Nature genetics · 2011 · PMID 21909109
3 pages
rs11216126 rs2286276 rs7232775
A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans
DIAGRAM Consortium · AGEN-T2D Consortium
Diabetes · 2013 · PMID 22961080 · open access
3 pages
rs10886471 rs10814916 rs12010175
Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis
International PSC Study Group
Nature communications · 2023 · PMID 36828809 · open access
3 pages
rs2523593 rs3094210 rs6905775
Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC
Nature genetics · 2010 · PMID 20526339
2 pages
rs2236313 Vitiligo
Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study
Nature communications · 2015 · PMID 26151496 · open access
2 pages
rs7768644 rs9263688
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
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer's disease
Alzheimer’s Disease Genetics Consortium (ADGC)
Genome biology · 2025 · PMID 40676597 · open access
2 pages
rs111486601 rs1898895

Showing 20 of 23 · page 1 of 2

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.