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2,657 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.
14 matches for
Levin M.
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Thibord F,
Klarin D,
Brody JA,
Chen MH,
Levin MG,
Chasman DI,
Goode EL,
Hveem K,
Teder-Laving M,
Martinez-Perez A,
Aïssi D,
Daian-Bacq D
and 76 more — show all
Ito K,
Natarajan P,
Lutsey PL,
Nadkarni GN,
de Vries PS,
Cuellar-Partida G,
Wolford BN,
Pattee JW,
Kooperberg C,
Braekkan SK,
Li-Gao R,
Saut N,
Sept C,
Germain M,
Judy RL,
Wiggins KL,
Ko D,
O'Donnell CJ,
Taylor KD,
Giulianini F,
De Andrade M,
Nøst TH,
Boland A,
Empana JP,
Koyama S,
Gilliland T,
Do R,
Huffman JE,
Wang X,
Wang X,
Zhou W,
Manuel Soria J,
Carlos Souto J,
Pankratz N,
Haessler J,
Hindberg K,
Rosendaal FR,
Turman C,
Olaso R,
Kember RL,
Bartz TM,
Lynch JA,
Heckbert SR,
Armasu SM,
Brumpton B,
Smadja DM,
Jouven X,
Komuro I,
Clapham KR,
Loos RJF,
Willer CJ,
Sabater-Lleal M,
Pankow JS,
Reiner AP,
Morelli VM,
Ridker PM,
Vlieg AVH,
Deleuze JF,
Kraft P,
Rader DJ,
Min Lee K,
Psaty BM,
Heidi Skogholt A,
Emmerich J,
Suchon P,
Rich SS,
Vy HMT,
Tang W,
Jackson RD,
Hansen JB,
Morange PE,
Kabrhel C,
Trégouët DA,
Damrauer SM,
Johnson AD,
Smith NL
Global Biobank Meta-Analysis Initiative; Estonian Biobank Research Team; 23andMe Research Team; Biobank Japan; CHARGE Hemostasis Working Group
Circulation · 2022 · PMID 36154123
12 pages+
CXCL12 drives natural variation in coronary artery anatomy across diverse populations
Rios Coronado PE,
Zhou J,
Fan X,
Zanetti D,
Naftaly JA,
Prabala P,
Martínez Jaimes AM,
Farah EN,
Kundu S,
Deshpande SS,
Evergreen I,
Kho PF
and 18 more — show all
Ma Q,
Hilliard AT,
Abramowitz S,
Pyarajan S,
Dochtermann D,
Damrauer SM,
Chang KM,
Levin MG,
Winn VD,
Paşca AM,
Plomondon ME,
Waldo SW,
Tsao PS,
Kundaje A,
Chi NC,
Clarke SL,
Red-Horse K,
Assimes TL
Million Veteran Program
Cell · 2025 · PMID 40049164
12 pages+
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum
Lee DSM,
Cardone KM,
Zhang DY,
Tsao NL,
Abramowitz S,
Sharma P,
DePaolo JS,
Conery M,
Aragam KG,
Biddinger K,
Dikilitas O,
Hoffman-Andrews L
and 23 more — show all
Judy RL,
Khan A,
Kullo IJ,
Puckelwartz MJ,
Reza N,
Satterfield BA,
Singhal P,
Arany Z,
Cappola TP,
Carruth ED,
Day SM,
Do R,
Haggerty CM,
Joseph J,
McNally EM,
Nadkarni G,
Owens AT,
Rader DJ,
Ritchie MD,
Sun YV,
Voight BF,
Levin MG,
Damrauer SM
Penn Medicine Biobank
Nature genetics · 2025 · PMID 40195560
12 pages+
Cross-population GWAS and proteomics improve risk prediction and reveal mechanisms in atrial fibrillation
Yuan S,
Chen J,
Ruan X,
Li Y,
Abramowitz SA,
Wang L,
Jiang F,
Xiong Y,
Levin MG,
Voight BF,
Gill D,
Burgess S
and 5 more — show all
Nature communications · 2025 · PMID 40645996 · open access
12 pages+
Genome-wide analysis of heart failure yields insights into disease heterogeneity and enables prognostic prediction in the Japanese population
Enzan N,
Miyazawa K,
Koyama S,
Kurosawa R,
Ieki H,
Yoshida H,
Takechi F,
Fukuyama M,
Osako R,
Tomizuka K,
Liu X,
Ozaki K
and 18 more — show all
Onouchi Y,
Matsuda K,
Momozawa Y,
Aburatani H,
Kamatani Y,
Yamaguchi T,
Akazawa H,
Node K,
Ellinor PT,
Levin MG,
Damrauer SM,
Voight BF,
Joseph J,
Sun YV,
Terao C,
Ninomiya T,
Komuro I,
Ito K
BioBank Japan Project
Nature communications · 2025 · PMID 41184235 · open access
12 pages+
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction
Small AM,
Yang TY,
Itoh S,
Thériault S,
Dufresne L,
Kurosawa R,
Komuro I,
Matsuda K,
Vy HMT,
Farber-Eger EH,
Shaffer LL,
Boulier KM
and 89 more — show all
Corey KM,
Ramaker ME,
Laporte F,
Schott JJ,
Le Scouarnec S,
Singh SA,
Sonawane AR,
Smith HA,
Rafaels N,
Ghouse J,
Raja AA,
Ostrowski SR,
Sørensen E,
Mikkelsen C,
Pedersen OB,
Erikstrup C,
Ullum H,
Sveinbjornsson G,
Gudbjartsson DF,
Abner E,
Lee J,
Ganna A,
Nowak-Göttl U,
Finer S,
Schumacher J,
Maj C,
Al-Kassou B,
Nickenig G,
Trenkwalder T,
Dreβen M,
Krane M,
Nöthen MM,
Moksnes MR,
Brumpton BM,
Knight S,
Knowlton KU,
Nadauld L,
Debiec R,
Musameh MD,
Braund PS,
Nelson CP,
Czuba T,
Melander O,
Selvaraj MS,
Koyama S,
Bhukar R,
Ruan Y,
Ljungberg J,
Damrauer SM,
Levin MG,
Franke A,
Berger K,
Ruff CT,
Melloni GEM,
Kamanu FK,
Ito K,
Do R,
Loos RJF,
Schunkert H,
Wells QS,
Shah SH,
Le Tourneau T,
Messika-Zeitoun D,
Gignoux C,
Bundgaard H,
Larsson SC,
Michaëlsson K,
Holm H,
Helgadottir A,
Esko T,
van Heel DA,
Mathieu P,
Samani NJ,
Smith JG,
Söderberg S,
Rader DJ,
Marston NA,
Sabatine MS,
Pasaniuc B,
Cho K,
Wilson PWF,
O'Donnell CJ,
Stefansson K,
Bossé Y,
Aikawa E,
Engert JC,
Peloso GM,
Natarajan P,
Thanassoulis G
Colorado Center for Personalized Medicine · DBDS Genomic Consortium and 2 more consortia
Nature genetics · 2026 · PMID 41419686 · open access
12 pages+
Multi-population GWAS meta-analysis identifies bladder cancer susceptibility loci and highlights genetic regulation of smoking-related risk
Prokunina-Olsson L,
Florez-Vargas O,
Levin MG,
Dutta D,
Breeze CE,
Hurwitz LM,
Yan W,
Lamy P,
Papenberg BW,
Wang K,
Lee CH,
Milne RL
and 45 more — show all
Gu J,
Um CY,
Joseph V,
Furberg H,
Le Calvez-Kelm F,
Lori A,
Choudhury PP,
Afshar N,
Kogevinas M,
Offit K,
Vermeulen SH,
López de Maturana E,
Albanes D,
Purdue MP,
Cortessis VK,
Karagas MR,
Kooperberg C,
Bjurlin M,
Tadesse DA,
Moore SC,
Huang WY,
Haiman CA,
Stern MC,
Eliassen AH,
Mucci LA,
Aben KK,
Galesloot TE,
Verma A,
Yoshino S,
Hikino K,
Terao C,
Rafnar T,
Matsuda K,
Shuin T,
Garcia-Closas M,
Real FX,
Kiemeney LA,
Chanock SJ,
Malats N,
Silverman DT,
Dyrskjot L,
Rothman N,
Damrauer SM,
Koutros S,
Damrauer JS
UROMOL Consortium
Nature communications · 2026 · PMID 42706231 · open access
12 pages+
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease
Klarin D,
Busenkell E,
Judy R,
Lynch J,
Levin M,
Haessler J,
Aragam K,
Chaffin M,
Haas M,
Lindström S,
Assimes TL,
Huang J
and 30 more — show all
Min Lee K,
Shao Q,
Huffman JE,
Kabrhel C,
Huang Y,
Sun YV,
Vujkovic M,
Saleheen D,
Miller DR,
Reaven P,
DuVall S,
Boden WE,
Pyarajan S,
Reiner AP,
Trégouët DA,
Henke P,
Kooperberg C,
Gaziano JM,
Concato J,
Rader DJ,
Cho K,
Chang KM,
Wilson PWF,
Smith NL,
O'Donnell CJ,
Tsao PS,
Kathiresan S,
Obi A,
Damrauer SM,
Natarajan P
INVENT Consortium · Veterans Affairs’ Million Veteran Program
Nature genetics · 2019 · PMID 31676865 · open access
7 pages
GWAS identifies genetic loci, lifestyle factors and circulating biomarkers that are risk factors for sarcoidosis
Yuan S,
Chen J,
Geng J,
Zhao SS,
Yarmolinsky J,
Arkema EV,
Abramowitz S,
Levin MG,
Tsilidis KK,
Burgess S,
Damrauer SM,
Larsson SC
Nature communications · 2025 · PMID 40075078 · open access
7 pages
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
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
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure
Levin MG,
Tsao NL,
Singhal P,
Liu C,
Vy HMT,
Paranjpe I,
Backman JD,
Bellomo TR,
Bone WP,
Biddinger KJ,
Hui Q,
Dikilitas O
and 31 more — show all
Satterfield BA,
Yang Y,
Morley MP,
Bradford Y,
Burke M,
Reza N,
Charest B,
Judy RL,
Puckelwartz MJ,
Hakonarson H,
Khan A,
Kottyan LC,
Kullo I,
Luo Y,
McNally EM,
Rasmussen-Torvik LJ,
Day SM,
Do R,
Phillips LS,
Ellinor PT,
Nadkarni GN,
Ritchie MD,
Arany Z,
Cappola TP,
Margulies KB,
Aragam KG,
Haggerty CM,
Joseph J,
Sun YV,
Voight BF,
Damrauer SM
Regeneron Genetics Center
Nature communications · 2022 · PMID 36376295 · open access
3 pages
Identification of novel locus associated with coronary artery aneurysms and validation of loci for susceptibility to Kawasaki disease
Hoggart C,
Shimizu C,
Galassini R,
Wright VJ,
Shailes H,
Bellos E,
Herberg JA,
Pollard AJ,
O'Connor D,
Choi SW,
Seaby EG,
Menikou S
and 12 more — show all
Hibberd M,
Sallah N,
Burgner D,
Brogan P,
Patel H,
Kim J,
Tremoulet AH,
Salo E,
van Stijn D,
Kuijpers T,
Burns JC,
Levin M
International Kawasaki Disease Genetics Consortium · UK Kawasaki Disease Genetics Consortium and 1 more consortia
European journal of human genetics : EJHG · 2021 · PMID 33772158 · open access
2 pages
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
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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.