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2,649 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.
8 matches for
Ware JS.
Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities
Francis CM,
Futschik ME,
Huang J,
Bai W,
Sargurupremraj M,
Teumer A,
Breteler MMB,
Petretto E,
Ho ASR,
Amouyel P,
Engelter ST,
Bülow R
and 11 more — show all
Völker U,
Völzke H,
Dörr M,
Imtiaz MA,
Aziz NA,
Lohner V,
Ware JS,
Debette S,
Elliott P,
Dehghan A,
Matthews PM
Nature communications · 2022 · PMID 35922433 · open access
12 pages+
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy
Tadros R,
Zheng SL,
Grace C,
Jordà P,
Francis C,
West DM,
Jurgens SJ,
Thomson KL,
Harper AR,
Ormondroyd E,
Xu X,
Theotokis PI
and 50 more — show all
Buchan RJ,
McGurk KA,
Mazzarotto F,
Boschi B,
Pelo E,
Lee M,
Noseda M,
Varnava A,
Vermeer AMC,
Walsh R,
Amin AS,
van Slegtenhorst MA,
Roslin NM,
Strug LJ,
Salvi E,
Lanzani C,
de Marvao A,
Roberts JD,
Tremblay-Gravel M,
Giraldeau G,
Cadrin-Tourigny J,
L'Allier PL,
Garceau P,
Talajic M,
Gagliano Taliun SA,
Pinto YM,
Rakowski H,
Pantazis A,
Bai W,
Baksi J,
Halliday BP,
Prasad SK,
Barton PJR,
O'Regan DP,
Cook SA,
de Boer RA,
Christiaans I,
Michels M,
Kramer CM,
Ho CY,
Neubauer S,
Matthews PM,
Wilde AAM,
Tardif JC,
Olivotto I,
Adler A,
Goel A,
Ware JS,
Bezzina CR,
Watkins H
Hypergenes InterOmics Collaborators · HCMR Investigators
Nature genetics · 2025 · PMID 39966646 · open access
12 pages+
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Henry A,
Mo X,
Finan C,
Chaffin MD,
Speed D,
Issa H,
Denaxas S,
Ware JS,
Zheng SL,
Malarstig A,
Gratton J,
Bond I
and 169 more — show all
Roselli C,
Miller D,
Chopade S,
Schmidt AF,
Abner E,
Adams L,
Andersson C,
Aragam KG,
Ärnlöv J,
Asselin G,
Raja AA,
Backman JD,
Bartz TM,
Biddinger KJ,
Biggs ML,
Bloom HL,
Boersma E,
Brandimarto J,
Brown MR,
Brunak S,
Bruun MT,
Buckbinder L,
Bundgaard H,
Carey DJ,
Chasman DI,
Chen X,
Cook JP,
Czuba T,
de Denus S,
Dehghan A,
Delgado GE,
Doney AS,
Dörr M,
Dowsett J,
Dudley SC,
Engström G,
Erikstrup C,
Esko T,
Farber-Eger EH,
Felix SB,
Finer S,
Ford I,
Ghanbari M,
Ghasemi S,
Ghouse J,
Giedraitis V,
Giulianini F,
Gottdiener JS,
Gross S,
Guðbjartsson DF,
Gui H,
Gutmann R,
Hägg S,
Haggerty CM,
Hedman ÅK,
Helgadottir A,
Hemingway H,
Hillege H,
Hyde CL,
Aagaard Jensen B,
Jukema JW,
Kardys I,
Karra R,
Kavousi M,
Kizer JR,
Kleber ME,
Køber L,
Koekemoer A,
Kuchenbaecker K,
Lai YP,
Lanfear D,
Langenberg C,
Lin H,
Lind L,
Lindgren CM,
Liu PP,
London B,
Lowery BD,
Luan J,
Lubitz SA,
Magnusson P,
Margulies KB,
Marston NA,
Martin H,
März W,
Melander O,
Mordi IR,
Morley MP,
Morris AP,
Morrison AC,
Morton L,
Nagle MW,
Nelson CP,
Niessner A,
Niiranen T,
Noordam R,
Nowak C,
O'Donoghue ML,
Ostrowski SR,
Owens AT,
Palmer CNA,
Paré G,
Pedersen OB,
Perola M,
Pigeyre M,
Psaty BM,
Rice KM,
Ridker PM,
Romaine SPR,
Rotter JI,
Ruff CT,
Sabatine MS,
Sallah N,
Salomaa V,
Sattar N,
Shalaby AA,
Shekhar A,
Smelser DT,
Smith NL,
Sørensen E,
Srinivasan S,
Stefansson K,
Sveinbjörnsson G,
Svensson P,
Tammesoo ML,
Tardif JC,
Teder-Laving M,
Teumer A,
Thorgeirsson G,
Thorsteinsdottir U,
Torp-Pedersen C,
Tragante V,
Trompet S,
Uitterlinden AG,
Ullum H,
van der Harst P,
van Heel D,
van Setten J,
van Vugt M,
Veluchamy A,
Verschuuren M,
Verweij N,
Vissing CR,
Völker U,
Voors AA,
Wallentin L,
Wang Y,
Weeke PE,
Wiggins KL,
Williams LK,
Yang Y,
Yu B,
Zannad F,
Zheng C,
Asselbergs FW,
Cappola TP,
Dubé MP,
Dunn ME,
Lang CC,
Samani NJ,
Shah S,
Vasan RS,
Smith JG,
Holm H,
Shah S,
Ellinor PT,
Hingorani AD,
Wells Q,
Lumbers RT
Genes & Health Research Team · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2025 · PMID 40038546 · open access
12 pages+
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
Tadros R,
Francis C,
Xu X,
Vermeer AMC,
Harper AR,
Huurman R,
Kelu Bisabu K,
Walsh R,
Hoorntje ET,
Te Rijdt WP,
Buchan RJ,
van Velzen HG
and 58 more — show all
van Slegtenhorst MA,
Vermeulen JM,
Offerhaus JA,
Bai W,
de Marvao A,
Lahrouchi N,
Beekman L,
Karper JC,
Veldink JH,
Kayvanpour E,
Pantazis A,
Baksi AJ,
Whiffin N,
Mazzarotto F,
Sloane G,
Suzuki H,
Schneider-Luftman D,
Elliott P,
Richard P,
Ader F,
Villard E,
Lichtner P,
Meitinger T,
Tanck MWT,
van Tintelen JP,
Thain A,
McCarty D,
Hegele RA,
Roberts JD,
Amyot J,
Dubé MP,
Cadrin-Tourigny J,
Giraldeau G,
L'Allier PL,
Garceau P,
Tardif JC,
Boekholdt SM,
Lumbers RT,
Asselbergs FW,
Barton PJR,
Cook SA,
Prasad SK,
O'Regan DP,
van der Velden J,
Verweij KJH,
Talajic M,
Lettre G,
Pinto YM,
Meder B,
Charron P,
de Boer RA,
Christiaans I,
Michels M,
Wilde AAM,
Watkins H,
Matthews PM,
Ware JS,
Bezzina CR
Nature genetics · 2021 · PMID 33495596 · open access
10 pages
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity
Harper AR,
Goel A,
Grace C,
Thomson KL,
Petersen SE,
Xu X,
Waring A,
Ormondroyd E,
Kramer CM,
Ho CY,
Neubauer S,
Tadros R
and 4 more — show all
HCMR Investigators
Nature genetics · 2021 · PMID 33495597
7 pages
Environmental and genetic predictors of human cardiovascular ageing
Shah M,
de A Inácio MH,
Lu C,
Schiratti PR,
Zheng SL,
Clement A,
de Marvao A,
Bai W,
King AP,
Ware JS,
Wilkins MR,
Mielke J
and 6 more — show all
Nature communications · 2023 · PMID 37604819 · 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
Genetic and functional insights into the fractal structure of the heart
Meyer HV,
Dawes TJW,
Serrani M,
Bai W,
Tokarczuk P,
Cai J,
de Marvao A,
Henry A,
Lumbers RT,
Gierten J,
Thumberger T,
Wittbrodt J
and 8 more — show all
Nature · 2020 · PMID 32814899
2 pages
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.