For researchers

Is your paper here?

2,673 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.

28 matches for Lin Y, showing the first 20.

Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma
Nature communications · 2016 · PMID 27539887 · open access
12 pages+
rs10425559 rs73635312 rs61824911 rs12916300 rs141115006 rs10093547
Discovery of common and rare genetic risk variants for colorectal cancer
Nature genetics · 2019 · PMID 30510241 · open access
12 pages+
rs12144319 rs116353863 rs117079142 rs11884596 rs12708491 rs4901473
Your height affects your health: genetic determinants and health-related outcomes in Taiwan
BMC medicine · 2022 · PMID 35831902 · open access
12 pages+
rs1246647183 rs62424499 rs17790804 rs80328976 rs1824305 rs28723025
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries
Nature genetics · 2023 · PMID 36539618
12 pages+
rs9614460 rs1554865 rs966816 rs1445012 rs9271363 rs7859362
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
rs2276133 rs7748159 rs9266669 rs7636138 rs11880613 rs2728099
Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Science China. Life sciences · 2019 · PMID 30591961
6 pages
rs12504231 rs7047871 rs11078446 rs17737857 rs4467035 rs201143466
Cross-definition GWAS of IBS in 2.8 million individuals reveals cardiometabolic and triglyceride-linked mechanisms
Colorado Center for Personalized Medicine · Estonian Biobank Research Team and 3 more consortia
Gut · 2026 · PMID 42425734
6 pages
rs2195110 rs72700810 rs10184811 rs12221193 rs35947881 Irritable Bowel Syndrome
Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft
PLoS genetics · 2019 · PMID 31609978 · open access
5 pages
rs730570 rs17820943 rs730643 rs4646211 rs6791526
Genetic architectures of proximal and distal colorectal cancer are partly distinct
Gut · 2021 · PMID 33632709 · open access
5 pages
rs73161913 rs62131228 rs6014965 rs61975764 rs80158569
Genomewide association study of leprosy
The New England journal of medicine · 2009 · PMID 20018961
4 pages
rs602875 rs40457 rs42490 Leprosy
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci
International MS Genetics Consortium
Nature genetics · 2009 · PMID 19525953
3 pages
rs2300747 rs17445836 Multiple Sclerosis
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
EMBRACE · GEMO Study Collaborators and 6 more consortia
Nature genetics · 2015 · PMID 25581431 · open access
3 pages
rs10088218 rs8170 rs9303542
Novel Common Genetic Susceptibility Loci for Colorectal Cancer
Journal of the National Cancer Institute · 2019 · PMID 29917119
3 pages
rs10911251 rs3824999 rs17094983
Genome-wide meta-analysis identifies eight new susceptibility loci for cutaneous squamous cell carcinoma
Nature communications · 2020 · PMID 32041948 · open access
3 pages
rs10399947 rs6791479 Cutaneous Squamous Cell Carcinoma
Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans
Arthritis & rheumatology (Hoboken, N.J.) · 2014 · PMID 24782177
2 pages
rs12525220 rs1854853
Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study
Nature communications · 2015 · PMID 26151496 · open access
2 pages
rs9263688 rs7768644
Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population
American journal of human genetics · 2011 · PMID 21640322
1 page
rs9318086
A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population
Human molecular genetics · 2013 · PMID 23406873
1 page
rs4455882
A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations
Nature genetics · 2013 · PMID 23708190
1 page
rs1531070
Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity
Human molecular genetics · 2014 · PMID 24064335
1 page
rs62033400

Showing 20 of 28 · 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.