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.

33 matches for VA Million Veteran Program, showing the first 20.

Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program
Global Lipids Genetics Consortium · Myocardial Infarction Genetics (MIGen) Consortium and 2 more consortia
Nature genetics · 2018 · PMID 30275531 · open access
12 pages+
rs11706108 rs576907609 rs11720145 rs56149994 rs1521516 rs17532301
Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program
Nature communications · 2019 · PMID 31451708 · open access
12 pages+
rs7253870 rs8073120 rs1719983 rs2023463 rs72938846 rs112785404
Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis
HPAP Consortium · Regeneron Genetics Center and 1 more consortia
Nature genetics · 2020 · PMID 32541925 · open access
12 pages+
rs12519500 rs10993072 rs12187734 rs34143602 rs6716394 rs10916780
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
VA Million Veteran Program
Cell · 2020 · PMID 32888493
12 pages+
rs12153091 rs7724386 rs9426736 rs1322774 rs4876400 rs17754
The Polygenic and Monogenic Basis of Blood Traits and Diseases
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
rs3809789 rs56197624 rs11153279 rs1610660 rs831070 rs61986598
Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals
VA Million Veteran Program
Nature communications · 2020 · PMID 33082346 · open access
12 pages+
rs11191487 rs9375328 rs11012750 rs12632110 rs40590 rs1385108
Urate, Blood Pressure, and Cardiovascular Disease: Evidence From Mendelian Randomization and Meta-Analysis of Clinical Trials
VA Million Veteran Program
Hypertension (Dallas, Tex. : 1979) · 2021 · PMID 33356394 · open access
12 pages+
rs1384291 rs11669336 rs9672635 rs7795876 rs195485 rs12214118
Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes
Lifelines Cohort Study · VA Million Veteran Program
Nature communications · 2021 · PMID 33972514 · open access
12 pages+
rs144830380 rs61953500 rs2834963 rs77653204 rs3760353 rs13109814
Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals
VA Million Veteran Program
Nature communications · 2021 · PMID 34272381 · open access
12 pages+
rs2007458 rs7963577 rs12449763 rs2158812 rs216364 rs2991341
The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs111859808 rs17209803 rs74705598 rs10082867 rs12358424 rs78186330
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs12787013 rs17036665 rs17040476 rs174348 rs17617811 rs17712993
Genomics and phenomics of body mass index reveals a complex disease network
VA Million Veteran Program
Nature communications · 2022 · PMID 36581621 · open access
12 pages+
rs2749808 rs4745062 rs10933311 rs11070956 rs34246968 rs12514473
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs290490 rs3742636 rs74387263 rs10758321 rs11023938 rs116257126
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis
DBDS Genomic Consortium · Regeneron Genetics Center and 3 more consortia
Nature genetics · 2024 · PMID 38632349 · open access
12 pages+
rs7496289 rs11211482 rs554146 rs10517369 rs11815438 rs113469203
Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
12 pages+
rs13115816 rs144564964 rs34731601 rs4648884 rs4925094 rs62134679
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 association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries
VA Million Veteran Program · International AMD Genomics Consortium (IAMDGC)
Nature genetics · 2024 · PMID 39623103
12 pages+
rs7182946 rs6073957 rs7663219 rs444189 rs11569415 rs9973159
Exome-wide association study of plasma lipids in >300,000 individuals
Charge Diabetes Working Group · EPIC-InterAct Consortium and 3 more consortia
Nature genetics · 2017 · PMID 29083408 · open access
11 pages
rs10861661 rs201596848 rs900399 rs7157785 rs3927680 rs7946
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
A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulation
VA Million Veteran Program
Communications biology · 2024 · PMID 38582945 · open access
7 pages
rs79742895 rs2093985 rs11590557 rs74882680 rs114065856 rs141208202

Showing 20 of 33 · 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.