For researchers

Is your paper here?

2,676 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.

90 matches for Wang J, showing the first 20.

Genome-wide association study in East Asians suggests UHMK1 as a novel bone mineral density susceptibility gene
Bone · 2016 · PMID 27424934
2 pages
rs9371538 Spine Bone Mineral Density
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
NT5C2 germline variants alter thiopurine metabolism and are associated with acquired NT5C2 relapse mutations in childhood acute lymphoblastic leukaemia
Leukemia · 2018 · PMID 30201983
2 pages
rs79050301 rs10949482
Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese
Nature communications · 2018 · PMID 30287856 · open access
2 pages
rs6114027 Tuberculosis
A Genome-Wide Association Study Identifies Two Novel Susceptible Regions for Squamous Cell Carcinoma of the Head and Neck
Cancer research · 2020 · PMID 32276964
2 pages
rs13211972 rs1265081
Exome-Wide Association Analysis Suggests LRP2BP as a Susceptibility Gene for Endothelial Injury in Systemic Sclerosis in the Han Chinese Population
The Journal of investigative dermatology · 2021 · PMID 33069728
2 pages
rs76285340 rs45471499
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Lifelines Cohort Study · Regeneron Genetics Center
Kidney international · 2021 · PMID 33137338
2 pages
rs56012466 rs141809766
Deep Learning of the Retina Enables Phenome- and Genome-Wide Analyses of the Microvasculature
Circulation · 2022 · PMID 34743558
2 pages
rs17547627 rs75048985
Genome-wide association study of HBV-related hepatocellular carcinoma identifies a functional variant at the FAM114A1 locus
Journal of genetics and genomics = Yi chuan xue bao · 2026 · PMID 41241147
2 pages
rs55718051 HBV-Related Hepatocellular Carcinoma
A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese
Nature genetics · 2011 · PMID 21725308
1 page
rs753955
Assessment of genetic determinants of the association of γ' fibrinogen in relation to cardiovascular disease
Arteriosclerosis, thrombosis, and vascular biology · 2011 · PMID 21757653
1 page
rs7681423
Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6
Genes, brain, and behavior · 2012 · PMID 22554406
1 page
rs2835872
New susceptibility loci in MYL2, C12orf51 and OAS1 associated with 1-h plasma glucose as predisposing risk factors for type 2 diabetes in the Korean population
Journal of human genetics · 2013 · PMID 23575436
1 page
rs11066453
A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23
Nature genetics · 2013 · PMID 24097066
1 page
rs4282438
Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families
Drug and alcohol dependence · 2014 · PMID 24962325
1 page
rs2168784
Meta analysis identifies a novel susceptibility locus associated with heel bone strength in the Korean population
Bone · 2016 · PMID 26686025
1 page
rs2446422
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women
Human molecular genetics · 2016 · PMID 26732429
1 page
rs7741164
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma
ANZRAG Consortium
Nature genetics · 2016 · PMID 26752265 · open access
1 page
rs1333037
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference
Scientific reports · 2016 · PMID 26785701 · open access
1 page
rs10051787
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
Nature genetics · 2016 · PMID 27064256
1 page
rs3739821

Showing 20 of 90 · page 4 of 5

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.