For researchers

Is your paper here?

2,662 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.

8 matches for Byun J.

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 rs116826541
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
Multi-trait and multi-ancestry genetic analysis of comorbid lung diseases and traits improves genetic discovery and polygenic risk prediction
Nature genetics · 2026 · PMID 41565855
12 pages+
rs924150 rs8089099 rs4791806 rs41522747 rs340121 rs2609260
Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes
Myositis Genetics Consortium
Genes and immunity · 2015 · PMID 26291516
9 pages
rs114388793 rs115146037 rs114012716 rs116088953 rs114771815 rs115902351
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
Identification of Functional and Expression Polymorphisms Associated With Risk for Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis
Vasculitis Clinical Research Consortium
Arthritis & rheumatology (Hoboken, N.J.) · 2017 · PMID 28029757 · open access
4 pages
rs62132293 rs7454108 rs35242582 ANCA-Associated Vasculitis
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

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.