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.

58 matches for Huang J, showing the first 18.

A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis
Nature genetics · 2011 · PMID 22138694
2 pages
rs17095830 Ankylosing Spondylitis
Common variants at 12q14 and 12q24 are associated with hippocampal volume
Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504421 · open access
2 pages
rs17178006 rs6581612
Genome-wide association study in Han Chinese identifies three novel loci for human height
Human genetics · 2013 · PMID 23456168
2 pages
rs3816804 rs3751599
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations
SUNLIGHT Consortium · GEFOS Consortium
PLoS genetics · 2013 · PMID 24068962 · open access
2 pages
rs7481584 rs7336933
Two new susceptibility loci 1q24.2 and 11p11.2 confer risk to severe acne
Nature communications · 2014 · PMID 24399259
2 pages
rs7531806 Severe Acne
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2
Cohorts for Heart and Aging Research in Genome Epidemiology (CHARGE) Consortium Neurology Working Group · CARDIoGRAM Consortium and 1 more consortia
Arteriosclerosis, thrombosis, and vascular biology · 2014 · PMID 24578379
2 pages
rs9399599 rs3136739
A novel common variant in DCST2 is associated with length in early life and height in adulthood
Early Genetics and Lifecourse Epidemiology (EAGLE) Consortium · Genetic Investigation of ANthropometric Traits (GIANT) Consortium and 1 more consortia
Human molecular genetics · 2015 · PMID 25281659 · open access
2 pages
rs1380294 rs905938
Genetic studies of body mass index yield new insights for obesity biology
LifeLines Cohort Study · ADIPOGen Consortium and 12 more consortia
Nature · 2015 · PMID 25673413
2 pages
rs16851483 rs2121279
Performance of genetic risk factors in prediction of trichloroethylene induced hypersensitivity syndrome
Scientific reports · 2015 · PMID 26190474 · open access
2 pages
rs2857281 Trichloroethylene-Induced Hypersensitivity Syndrome
Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia
Nature communications · 2016 · PMID 26956414 · open access
2 pages
rs9270750 rs72742684
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps
UK10K Consortium
Nature genetics · 2016 · PMID 27668658
2 pages
rs3130725 rs113373353
A type 1 diabetes genetic risk score discriminates between type 1 diabetes and type 2 diabetes in a Chinese population
Hong Kong Diabetes Biobank Study Group
Diabetologia · 2025 · PMID 40569436 · open access
2 pages
rs9269173 rs72848653
Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus
Nature genetics · 2009 · PMID 19838193
1 page
rs1167796
Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression
The American journal of psychiatry · 2010 · PMID 20713499
1 page
rs6484218
Genetic predictors of fibrin D-dimer levels in healthy adults
Circulation · 2011 · PMID 21502573
1 page
rs12029080
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease
Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Consortium
Nature genetics · 2012 · PMID 22751097
1 page
rs9268402
Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes
Aging · 2018 · PMID 29615537 · open access
1 page
rs17489268
Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies
VA Million Veteran Program
American journal of human genetics · 2019 · PMID 31564439
1 page
rs17097556

Showing 18 of 58 · page 3 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.