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54 matches for
Million Veteran Program,
showing the first 14.
Genome-wide association study of peripheral artery disease in the Million Veteran Program
Klarin D,
Lynch J,
Aragam K,
Chaffin M,
Assimes TL,
Huang J,
Lee KM,
Shao Q,
Huffman JE,
Natarajan P,
Arya S,
Small A
and 24 more — show all
Sun YV,
Vujkovic M,
Freiberg MS,
Wang L,
Chen J,
Saleheen D,
Lee JS,
Miller DR,
Reaven P,
Alba PR,
Patterson OV,
DuVall SL,
Boden WE,
Beckman JA,
Gaziano JM,
Concato J,
Rader DJ,
Cho K,
Chang KM,
Wilson PWF,
O'Donnell CJ,
Kathiresan S,
Tsao PS,
Damrauer SM
VA Million Veteran Program
Nature medicine · 2019 · PMID 31285632 · open access
3 pages
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience
Jurgens SJ,
Rämö JT,
Kramarenko DR,
Wijdeveld LFJM,
Haas J,
Chaffin MD,
Garnier S,
Gaziano L,
Weng LC,
Lipov A,
Zheng SL,
Henry A
and 46 more — show all
Huffman JE,
Challa S,
Rühle F,
Verdugo CD,
Krijger Juárez C,
Kany S,
van Orsouw CA,
Biddinger K,
Poel E,
Elliott AL,
Wang X,
Francis C,
Ruan R,
Koyama S,
Beekman L,
Zimmerman DS,
Deleuze JF,
Villard E,
Trégouët DA,
Isnard R,
Boomsma DI,
de Geus EJC,
Tadros R,
Pinto YM,
Wilde AAM,
Hottenga JJ,
Sinisalo J,
Niiranen T,
Walsh R,
Schmidt AF,
Choi SH,
Chang KM,
Tsao PS,
Matthews PM,
Ware JS,
Lumbers RT,
van der Crabben S,
Laukkanen J,
Palotie A,
Amin AS,
Charron P,
Meder B,
Ellinor PT,
Daly M,
Aragam KG,
Bezzina CR
FinnGen · VA Million Veteran Program and 1 more consortia
Nature genetics · 2024 · PMID 39572784 · open access
3 pages
Genome-wide gene-sleep interaction study identifies novel lipid loci in 732,564 participants
Noordam R,
Wang W,
Nagarajan P,
Wang H,
Brown MR,
Bentley AR,
Hui Q,
Kraja AT,
Morrison JL,
O'Connel JR,
Lee S,
Schwander K
and 137 more — show all
Bartz TM,
de Las Fuentes L,
Feitosa MF,
Guo X,
Hanfei X,
Harris SE,
Huang Z,
Kals M,
Lefevre C,
Mangino M,
Milaneschi Y,
van der Most PJ,
Pacheco NL,
Palmer ND,
Rao V,
Rauramaa R,
Sun Q,
Tabara Y,
Vojinovic D,
Wang Y,
Weiss S,
Yang Q,
Zhao W,
Zhu W,
Ansari MAY,
Aschard H,
Anugu P,
Assimes TL,
Attia J,
Baker LD,
Ballantyne C,
Bazzano L,
Boerwinkle E,
Cade B,
Chen HH,
Chen W,
Ida Chen YD,
Chen Z,
Cho K,
De Anda-Duran I,
Dimitrov L,
Do A,
Edwards T,
Faquih T,
Hingorani A,
Fisher-Hoch SP,
Gaziano JM,
Gharib SA,
Giri A,
Ghanbari M,
Grabe HJ,
Graff M,
Charles Gu C,
He J,
Heikkinen S,
Hixson J,
Ho YL,
Hood MM,
Houghton SC,
Karvonen-Gutierrez CA,
Kawaguchi T,
Kilpeläinen TO,
Komulainen P,
Lin HJ,
Linchangco GV Jr,
Luik AI,
Ma J,
Meigs JB,
McCormick JB,
Menni C,
Nolte IM,
Norris JM,
Petty LE,
Polikowsky HG,
Raffield LM,
Rich SS,
Riha RL,
Russ TC,
Ruiz-Narvaez EA,
Sitlani CM,
Smith JA,
Snieder H,
Sofer T,
Shen B,
Tang J,
Taylor KD,
Teder-Laving M,
Triatin R,
Tsai MY,
Völzke H,
Westerman KE,
Xia R,
Yao J,
Young KL,
Zhang R,
Zonderman AB,
Zhu X,
Below JE,
Cox SR,
Evans M,
Fornage M,
Fox ER,
Franceschini N,
Harlow SD,
Holliday E,
Ikram MA,
Kelly T,
Lakka TA,
Lawlor DA,
Li C,
Liu CT,
Mägi R,
Manning AK,
Matsuda F,
Morrison AC,
Nauck M,
North KE,
Penninx BW,
Province MA,
Psaty BM,
Rotter JI,
Spector TD,
Wagenknecht LE,
van Dijk KW,
Jaquish CE,
Wilson PW,
Peyser PA,
Munroe PB,
de Vries PS,
Gauderman WJ,
Sun YV,
Chen H,
Miller CL,
Winkler TW,
Rao DC,
Redline S,
van Heemst D
Lifelines Cohort Study · Million Veteran Program
Atherosclerosis · 2026 · PMID 41325697
3 pages
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism
Lindström S,
Wang L,
Smith EN,
Gordon W,
van Hylckama Vlieg A,
de Andrade M,
Brody JA,
Pattee JW,
Haessler J,
Brumpton BM,
Chasman DI,
Suchon P
and 45 more — show all
Chen MH,
Turman C,
Germain M,
Wiggins KL,
MacDonald J,
Braekkan SK,
Armasu SM,
Pankratz N,
Jackson RD,
Nielsen JB,
Giulianini F,
Puurunen MK,
Ibrahim M,
Heckbert SR,
Damrauer SM,
Natarajan P,
Klarin D,
de Vries PS,
Sabater-Lleal M,
Huffman JE,
Bammler TK,
Frazer KA,
McCauley BM,
Taylor K,
Pankow JS,
Reiner AP,
Gabrielsen ME,
Deleuze JF,
O'Donnell CJ,
Kim J,
McKnight B,
Kraft P,
Hansen JB,
Rosendaal FR,
Heit JA,
Psaty BM,
Tang W,
Kooperberg C,
Hveem K,
Ridker PM,
Morange PE,
Johnson AD,
Kabrhel C,
Trégouët DA,
Smith NL
Million Veteran Program · CHARGE Hemostasis Working Group
Blood · 2019 · PMID 31420334
2 pages
Cross-ancestry meta-analysis of opioid use disorder uncovers novel loci with predominant effects in brain regions associated with addiction
Kember RL,
Vickers-Smith R,
Xu H,
Toikumo S,
Niarchou M,
Zhou H,
Hartwell EE,
Crist RC,
Rentsch CT,
Davis LK,
Justice AC,
Sanchez-Roige S
and 3 more — show all
Million Veteran Program
Nature neuroscience · 2022 · PMID 36171425
2 pages
Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank
McDonald MN,
Lakshman Kumar P,
Srinivasasainagendra V,
Nair A,
Rocco AP,
Wilson AC,
Chiles JW,
Richman JS,
Pinson SA,
Dennis RA,
Jagadale V,
Brown CJ
and 4 more — show all
Nature genetics · 2022 · PMID 36411363
2 pages
Identification of Novel, Replicable Genetic Risk Loci for Suicidal Thoughts and Behaviors Among US Military Veterans
Kimbrel NA,
Ashley-Koch AE,
Qin XJ,
Lindquist JH,
Garrett ME,
Dennis MF,
Hair LP,
Huffman JE,
Jacobson DA,
Madduri RK,
Trafton JA,
Coon H
and 9 more — show all
Million Veteran Program Suicide Exemplar Workgroup, the International Suicide Genetics Consortium, the Veterans Affairs Mid-Atlantic Mental Illness Research, Education, and Clinical Center Workgroup, and the Veterans Affairs Million Veteran Program
JAMA psychiatry · 2023 · PMID 36515925
2 pages
Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure
Rasooly D,
Peloso GM,
Pereira AC,
Dashti H,
Giambartolomei C,
Wheeler E,
Aung N,
Ferolito BR,
Pietzner M,
Farber-Eger EH,
Wells QS,
Kosik NM
and 22 more — show all
Gaziano L,
Posner DC,
Bento AP,
Hui Q,
Liu C,
Aragam K,
Wang Z,
Charest B,
Huffman JE,
Wilson PWF,
Phillips LS,
Whittaker J,
Munroe PB,
Petersen SE,
Cho K,
Leach AR,
Magariños MP,
Gaziano JM,
Langenberg C,
Sun YV,
Joseph J,
Casas JP
VA Million Veteran Program
Nature communications · 2023 · PMID 37429843 · open access
2 pages
Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries
Surakka I,
Wu KH,
Hornsby W,
Wolford BN,
Shen F,
Zhou W,
Huffman JE,
Pandit A,
Hu Y,
Brumpton B,
Skogholt AH,
Gabrielsen ME
and 9 more — show all
TOPMed Stroke Working Group · Million Veteran Program (MVP) and 1 more consortia
Cell genomics · 2023 · PMID 37601974 · open access
2 pages
Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies
Fang H,
Hui Q,
Lynch J,
Honerlaw J,
Assimes TL,
Huang J,
Vujkovic M,
Damrauer SM,
Pyarajan S,
Gaziano JM,
DuVall SL,
O'Donnell CJ
and 6 more — show all
VA Million Veteran Program
American journal of human genetics · 2019 · PMID 31564439
1 page
Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction
Saw J,
Yang ML,
Trinder M,
Tcheandjieu C,
Xu C,
Starovoytov A,
Birt I,
Mathis MR,
Hunker KL,
Schmidt EM,
Jackson L,
Fendrikova-Mahlay N
and 15 more — show all
Zawistowski M,
Brummett CM,
Zoellner S,
Katz A,
Coleman DM,
Swan K,
Swan K,
O'Donnell CJ,
Zhou X,
Li JZ,
Gornik HL,
Assimes TL,
Stanley JC,
Brunham LR,
Ganesh SK
Million Veteran Program
Nature communications · 2020 · PMID 32887874 · open access
1 page
Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program
Peloso GM,
Tcheandjieu C,
McGeary JE,
Posner DC,
Ho YL,
Zhou JJ,
Hilliard AT,
Joseph J,
O'Donnell CJ,
Efird JT,
Crawford DC,
Wu WC
and 4 more — show all
VA Million Veteran Program COVID-19 Science Initiative
Frontiers in genetics · 2021 · PMID 35222515 · open access
1 page
Genome-wide and phenome-wide analysis of ideal cardiovascular health in the VA Million Veteran Program
Huang RDL,
Nguyen XT,
Peloso GM,
Trinder M,
Posner DC,
Aragam KG,
Ho YL,
Lynch JA,
Damrauer SM,
Chang KM,
Tsao PS,
Natarajan P
and 7 more — show all
Veterans Affairs’ Million Veteran Program
PloS one · 2022 · PMID 35613103 · open access
1 page
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.