For researchers

Is your paper here?

2,675 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.

35 matches for Damrauer SM, showing the first 15.

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
rs168144 rs74816838 rs3810367 rs201082887 rs2763195 rs3935942
GWAS identifies genetic loci, lifestyle factors and circulating biomarkers that are risk factors for sarcoidosis
Nature communications · 2025 · PMID 40075078 · open access
8 pages
rs6761132 rs11202051 rs546039326 rs77029323 rs1140310 rs17041517
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease
INVENT Consortium · Veterans Affairs’ Million Veteran Program
Nature genetics · 2019 · PMID 31676865 · open access
7 pages
rs9411377 rs6083037 rs10747514 rs7051718 rs16867574 rs57328376
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
Regeneron Genetics Center · CARDIoGRAMplusC4D Consortium and 2 more consortia
Nature medicine · 2022 · PMID 35915156
7 pages
rs56210063 rs78532451 rs17101521 rs1867073 rs7622417 rs2715879
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs12012576 rs139120857 rs5942972 rs7063103 rs62603531 rs151113194
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program
Veterans Affairs Million Veteran Program†
Circulation · 2020 · PMID 32981348 · open access
6 pages
rs10808546 rs35254673 rs4401144 rs118039278 rs73149487 Abdominal Aortic Aneurysm
Stroke genetics informs drug discovery and risk prediction across ancestries
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
rs76110445 rs12415501 rs60401382 rs72934589 Cardioembolic Stroke
Genome-wide association study of peripheral artery disease in the Million Veteran Program
VA Million Veteran Program
Nature medicine · 2019 · PMID 31285632 · open access
3 pages
rs138294113 rs4722172 rs7476
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure
Regeneron Genetics Center
Nature communications · 2022 · PMID 36376295 · open access
3 pages
rs10738604 rs981150 rs17513625
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism
Million Veteran Program · CHARGE Hemostasis Working Group
Blood · 2019 · PMID 31420334
2 pages
rs4524 rs191945075
Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies
VA Million Veteran Program
American journal of human genetics · 2019 · PMID 31564439
1 page
rs17097556
Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic Loci
Frontiers in genetics · 2021 · PMID 35186008 · open access
1 page
rs1531817
Genome-wide and phenome-wide analysis of ideal cardiovascular health in the VA Million Veteran Program
Veterans Affairs’ Million Veteran Program
PloS one · 2022 · PMID 35613103 · open access
1 page
rs244417
Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism
Nature communications · 2023 · PMID 37286573 · open access
1 page
rs10737681
Meta-analysis of uveal melanoma genome-wide association studies identifies novel risk loci and population effect size heterogeneity
HGG advances · 2025 · PMID 40495383 · open access
1 page
rs11707457

Showing 15 of 35 · page 2 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.