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.

53 matches for Lin H, showing the first 20.

Whole genome sequencing based analysis of inflammation biomarkers in the Trans-Omics for Precision Medicine (TOPMed) consortium
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Inflammation Working Group
Human molecular genetics · 2024 · PMID 38747556
11 pages
rs553202904 rs12495098 rs181704186 rs519064 rs144007943 rs6588153
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
Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling
CARDIoGRAM Consortium · CHARGE Inflammation Working Group and 1 more consortia
The Journal of clinical investigation · 2013 · PMID 23999434
9 pages
rs12999542 rs13019803 rs2302612 rs11693697 rs13029918 rs1014286
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
9 pages
rs3133370 rs2206656 rs4784256 rs196807 rs9505301 rs2410767
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation
Regeneron Genetics Center · Geisinger-Regeneron DiscovEHR Collaboration and 2 more consortia
Nature genetics · 2022 · PMID 35654975
8 pages
rs3935942 rs1626329 rs6059896 rs168144 rs74816838 rs3810367
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
COGS–Cancer Research UK GWAS–ELLIPSE (part of GAME-ON) Initiative · Australian Prostate Cancer Bioresource and 3 more consortia
Nature genetics · 2013 · PMID 23535732
7 pages
rs3850699 rs1894292 rs2273669 rs1270884 rs11650494 rs1218582
GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals
Scientific reports · 2017 · PMID 29213071 · open access
7 pages
rs73017364 rs12035622 rs55863869 rs35760656 rs12271931 rs12626657
Genetic loci associated with heart rate variability and their effects on cardiac disease risk
Nature communications · 2017 · PMID 28613276 · open access
6 pages
rs12980262 rs1812835 rs2529471 rs4899412 rs12974991 rs12974440
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function
The Journal of clinical investigation · 2017 · PMID 28394258
5 pages
rs6702619 rs17696696 rs7127129 rs2649 rs11207426
Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft
PLoS genetics · 2019 · PMID 31609978 · open access
5 pages
rs4646211 rs6791526 rs730570 rs17820943 rs730643
Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population
Nature communications · 2023 · PMID 37236969 · open access
5 pages
rs71467682 rs75031349 rs137884934 rs682888 rs10901793
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6
Genome biology · 2018 · PMID 30012220 · open access
4 pages
rs11588271 rs116202356 rs3746435 rs11848785
Identifying expression and DNA methylation biomarkers for lung adenocarcinoma risk in East Asia
Journal of the National Cancer Institute · 2026 · PMID 41581221 · open access
4 pages
rs9367106 rs11196089 rs2760995 rs4268071
Genome-wide association study of diabetic retinopathy in a Taiwanese population
Ophthalmology · 2011 · PMID 21310492
3 pages
rs17376456 rs12219125 Diabetic Retinopathy
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
Nature genetics · 2012 · PMID 22544366
3 pages
rs10821415 rs10824026 rs7164883
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
Genome-wide association study of PR interval in Hispanics/Latinos identifies novel locus at <i>ID2</i>
Heart (British Cardiac Society) · 2018 · PMID 29127183
3 pages
rs45567533 rs13105921 rs146974314
Genome-wide gene-sleep interaction study identifies novel lipid loci in 732,564 participants
Lifelines Cohort Study · Million Veteran Program
Atherosclerosis · 2026 · PMID 41325697
3 pages
rs150607032 rs190975828 rs192018195
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
Identification of new susceptibility loci for IgA nephropathy in Han Chinese
Nature communications · 2015 · PMID 26028593 · open access
2 pages
rs2074038 IgA Nephropathy

Showing 20 of 53 · page 2 of 3

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.