For researchers

Is your paper here?

2,663 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.

61 matches for Han J, showing the first 20.

Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer
Nature genetics · 2008 · PMID 18264098
3 pages
rs721048 rs5945572 Prostate Cancer
A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation
PLoS genetics · 2008 · PMID 18483556 · open access
3 pages
rs8033165 rs12203592 Sun Sensitivity, Freckling and Skin Cancer Risk
Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma
Nature genetics · 2012 · PMID 22941191 · open access
3 pages
rs4336470 rs17065417 Neuroblastoma
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia
Nature genetics · 2013 · PMID 23770605 · open access
3 pages
rs13401811 rs17483466 rs11636802
A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences
Cancer discovery · 2015 · PMID 26034056
3 pages
rs116041037 rs72725879 rs10896449
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Nature communications · 2016 · PMID 26833246 · open access
3 pages
rs6738627 rs4788099 rs693839
HLA-C*01 is a Risk Factor for Crohn's Disease
Inflammatory bowel diseases · 2016 · PMID 26891255
3 pages
rs114985235 rs6478109 rs140068907
Genome-wide meta-analysis identifies eight new susceptibility loci for cutaneous squamous cell carcinoma
Nature communications · 2020 · PMID 32041948 · open access
3 pages
rs6791479 rs10399947 Cutaneous Squamous Cell Carcinoma
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy
Nature genetics · 2023 · PMID 37337107
3 pages
rs2075836 rs57917667 rs75413466
Variants conferring risk of atrial fibrillation on chromosome 4q25
Nature · 2007 · PMID 17603472
2 pages
rs10033464 Atrial Fibrillation
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction
Nature genetics · 2009 · PMID 19198610
2 pages
rs4857855 rs12619285
Genome-wide association study of tanning phenotype in a population of European ancestry
The Journal of investigative dermatology · 2009 · PMID 19340012
2 pages
rs35391 Eye Color and Pigmentation
Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32
Nature genetics · 2010 · PMID 20639881 · open access
2 pages
rs10484561 Follicular Lymphoma
Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma
Human molecular genetics · 2011 · PMID 21700618
2 pages
rs12210050 rs7335046
Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia
Nature genetics · 2012 · PMID 23143601
2 pages
rs4488809 rs7086803
A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus
Nature communications · 2014 · PMID 24920014 · open access
2 pages
rs2069757 Hodgkin Lymphoma
Clinical Pharmacogenetics Implementation Consortium (CPIC) guidelines for human leukocyte antigen B (HLA-B) genotype and allopurinol dosing: 2015 update
Clinical Pharmacogenetics Implementation Consortium
Clinical pharmacology and therapeutics · 2016 · PMID 26094938
2 pages
Gout Drug-Induced Stevens–Johnson Syndrome and Toxic Epidermal Necrolysis
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma
GenoMEL Consortium · Essen-Heidelberg Investigators and 4 more consortia
Nature genetics · 2015 · PMID 26237428 · open access
2 pages
rs498136 Cutaneous Malignant Melanoma
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
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

Showing 20 of 61 · page 2 of 4

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.