For researchers

Is your paper here?

2,665 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.

24 matches for Han Y, showing the first 20.

Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
SpiroMeta Consortium
Nature genetics · 2017 · PMID 28604730 · open access
12 pages+
rs2004038 rs34878803 rs13213986 rs7383287 rs11632038 rs17400427
Genome-wide analysis highlights contribution of immune system pathways to the genetic architecture of asthma
Nature communications · 2020 · PMID 32296059 · open access
12 pages+
rs625228 rs906364 rs10178845 rs7636495 rs1051334 rs17669032
Multi-ancestry GWAS meta-analyses of lung cancer reveal susceptibility loci and elucidate smoking-independent genetic risk
VA Million Veteran Program
Nature communications · 2024 · PMID 39366959 · open access
12 pages+
rs4946259 rs7868253 rs398278 rs67824503 rs28557075 rs2271920
Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum
Genes & Health Research Team · Estonian Biobank Research Team and 3 more consortia
Nature genetics · 2025 · PMID 40229599 · open access
12 pages+
rs114087689 rs9643050 rs192776885 rs35118298 rs10866828 rs11956571
A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer
Breast and Prostate Cancer Cohort Consortium (BPC3) · PRACTICAL (Prostate Cancer Association Group to Investigate Cancer-Associated Alterations in the Genome) Consortium and 2 more consortia
Nature genetics · 2014 · PMID 25217961 · open access
10 pages
rs1041449 rs17599629 rs9287719 rs56232506 rs17694493 rs76934034
Novel Association of Genetic Markers Affecting CYP2A6 Activity and Lung Cancer Risk
Cancer research · 2016 · PMID 27488534
10 pages
rs113029345 rs76935404 rs10425738 rs11878604 rs7247903 rs2316205
An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs
PBC Consortia · Canadian PBC Consortium and 5 more consortia
Journal of hepatology · 2021 · PMID 34033851 · open access
10 pages
rs12942330 rs4709148 rs34655300 rs589446 rs11742270 rs859767
A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population
Genes & nutrition · 2015 · PMID 26584805
6 pages
rs11827215 rs509360 rs174534 rs174528 rs174577 rs7925523
Genome-wide meta-analysis across East Asian and European populations provides insights into the molecular basis of lung cancer
Genome medicine · 2026 · PMID 42152146 · open access
6 pages
rs1039766 rs12822733 rs4887067 rs13167280 rs4291686 rs36108040
Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease
Journal of the American Heart Association · 2019 · PMID 31070104 · open access
5 pages
rs12126607 rs2364368 rs71503800 rs12003835 rs11860711
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus
Spanish Scleroderma Group
Nature genetics · 2010 · PMID 20383147
3 pages
rs10488631 rs3821236 Systemic Sclerosis
International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways
Canadian-US PBC Consortium · Italian PBC Genetics Study Group and 1 more consortia
Nature communications · 2015 · PMID 26394269 · open access
3 pages
rs526231 rs6933404 Primary Biliary Cholangitis
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium · TOPMed Hematology & Hemostasis Working Group
PLoS genetics · 2019 · PMID 31869403 · open access
3 pages
rs2562181 rs35837297 rs11863726
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer
Nature genetics · 2022 · PMID 35915169
3 pages
rs11607355 rs2413932 rs12348845
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
Two Novel Susceptibility Loci for Prostate Cancer in Men of African Ancestry
PRACTICAL/ELLIPSE Consortium
Journal of the National Cancer Institute · 2017 · PMID 29117387 · open access
2 pages
rs75823044 rs78554043
Genome-wide analysis identifies novel susceptibility loci for myocardial infarction
INVENT Consortium · CHARGE Consortium Hemostasis Working Group and 2 more consortia
European heart journal · 2021 · PMID 33532862
2 pages
rs6694258 rs12897285
Multi-ancestry genome-wide association meta-analysis of hepatocellular carcinoma identifies 15 risk loci including MAP3K9, DHRS1, MTTP, and 8q24.21
HGG advances · 2026 · PMID 42357869 · open access
2 pages
rs924204 rs12983038
Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity
Human molecular genetics · 2014 · PMID 24064335
1 page
rs62033400
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer
Nature genetics · 2014 · PMID 24880342 · open access
1 page
rs13314271

Showing 20 of 24 · 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.