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2,663 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.
31 matches for
Tsao P,
showing the first 11.
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program
Klarin D,
Verma SS,
Judy R,
Dikilitas O,
Wolford BN,
Paranjpe I,
Levin MG,
Pan C,
Tcheandjieu C,
Spin JM,
Lynch J,
Assimes TL
and 41 more — show all
Åldstedt Nyrønning L,
Mattsson E,
Edwards TL,
Denny J,
Larson E,
Lee MTM,
Carrell D,
Zhang Y,
Jarvik GP,
Gharavi AG,
Harley J,
Mentch F,
Pacheco JA,
Hakonarson H,
Skogholt AH,
Thomas L,
Gabrielsen ME,
Hveem K,
Nielsen JB,
Zhou W,
Fritsche L,
Huang J,
Natarajan P,
Sun YV,
DuVall SL,
Rader DJ,
Cho K,
Chang KM,
Wilson PWF,
O'Donnell CJ,
Kathiresan S,
Scali ST,
Berceli SA,
Willer C,
Jones GT,
Bown MJ,
Nadkarni G,
Kullo IJ,
Ritchie M,
Damrauer SM,
Tsao PS
Veterans Affairs Million Veteran Program†
Circulation · 2020 · PMID 32981348 · open access
6 pages
High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease
Tcheandjieu C,
Xiao K,
Tejeda H,
Lynch JA,
Ruotsalainen S,
Bellomo T,
Palnati M,
Judy R,
Klarin D,
Kember RL,
Verma S,
Palotie A
and 8 more — show all
Regeneron Genetics Center · VA Million Veterans Program and 1 more consortia
Nature genetics · 2022 · PMID 35637384
6 pages
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
Tcheandjieu C,
Zhu X,
Hilliard AT,
Clarke SL,
Napolioni V,
Ma S,
Lee KM,
Fang H,
Chen F,
Lu Y,
Tsao NL,
Raghavan S
and 70 more — show all
Koyama S,
Gorman BR,
Vujkovic M,
Klarin D,
Levin MG,
Sinnott-Armstrong N,
Wojcik GL,
Plomondon ME,
Maddox TM,
Waldo SW,
Bick AG,
Pyarajan S,
Huang J,
Song R,
Ho YL,
Buyske S,
Kooperberg C,
Haessler J,
Loos RJF,
Do R,
Verbanck M,
Chaudhary K,
North KE,
Avery CL,
Graff M,
Haiman CA,
Le Marchand L,
Wilkens LR,
Bis JC,
Leonard H,
Shen B,
Lange LA,
Giri A,
Dikilitas O,
Kullo IJ,
Stanaway IB,
Jarvik GP,
Gordon AS,
Hebbring S,
Namjou B,
Kaufman KM,
Ito K,
Ishigaki K,
Kamatani Y,
Verma SS,
Ritchie MD,
Kember RL,
Baras A,
Lotta LA,
Kathiresan S,
Hauser ER,
Miller DR,
Lee JS,
Saleheen D,
Reaven PD,
Cho K,
Gaziano JM,
Natarajan P,
Huffman JE,
Voight BF,
Rader DJ,
Chang KM,
Lynch JA,
Damrauer SM,
Wilson PWF,
Tang H,
Sun YV,
Tsao PS,
O'Donnell CJ,
Assimes TL
Regeneron Genetics Center · CARDIoGRAMplusC4D Consortium and 2 more consortia
Nature medicine · 2022 · PMID 35915156
6 pages
A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program
Raghavan S,
Huang J,
Tcheandjieu C,
Huffman JE,
Litkowski E,
Liu C,
Ho YA,
Hunter-Zinck H,
Zhao H,
Marouli E,
North KE,
Lange E
and 12 more — show all
Lange LA,
Voight BF,
Gaziano JM,
Pyarajan S,
Hauser ER,
Tsao PS,
Wilson PWF,
Chang KM,
Cho K,
O'Donnell CJ,
Sun YV,
Assimes TL
VA Million Veteran Program
PLoS genetics · 2022 · PMID 35653334 · open access
5 pages
Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations
Kranzler HR,
Zhou H,
Kember RL,
Vickers Smith R,
Justice AC,
Damrauer S,
Tsao PS,
Klarin D,
Baras A,
Reid J,
Overton J,
Rader DJ
and 8 more — show all
Nature communications · 2019 · PMID 30940813 · open access
4 pages
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
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
Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic Loci
Bellomo TR,
Bone WP,
Chen BY,
Gawronski KAB,
Zhang D,
Park J,
Levin M,
Tsao N,
Klarin D,
Lynch J,
Assimes TL,
Gaziano JM
and 10 more — show all
Frontiers in genetics · 2021 · PMID 35186008 · 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
Genome-Wide Association Study of CKD Progression
Robinson-Cohen C,
Triozzi JL,
Rowan B,
He J,
Chen HC,
Zheng NS,
Wei WQ,
Wei WQ,
Wilson OD,
Hellwege JN,
Tsao PS,
Gaziano JM
and 8 more — show all
Journal of the American Society of Nephrology : JASN · 2023 · PMID 37261792
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.