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Is your paper here?
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.
5 matches for
Tanck MW.
Genetic analyses across cardiovascular traits: leveraging genetic correlations to empower locus discovery and prediction in common cardiovascular diseases
Jordà P,
Lai Y,
Jeuken A,
Lemieux Perreault LP,
Goulet E,
Lahrouchi N,
Nozza A,
Tanck MW,
Guerra P,
Cadrin-Tourigny J,
de Denus S,
Bezzina CR
and 5 more — show all
NPJ genomic medicine · 2025 · PMID 41022758 · 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
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
Barc J,
Tadros R,
Glinge C,
Chiang DY,
Jouni M,
Simonet F,
Jurgens SJ,
Baudic M,
Nicastro M,
Potet F,
Offerhaus JA,
Walsh R
and 134 more — show all
Choi SH,
Verkerk AO,
Mizusawa Y,
Anys S,
Minois D,
Arnaud M,
Duchateau J,
Wijeyeratne YD,
Muir A,
Papadakis M,
Castelletti S,
Torchio M,
Ortuño CG,
Lacunza J,
Giachino DF,
Cerrato N,
Martins RP,
Campuzano O,
Van Dooren S,
Thollet A,
Kyndt F,
Mazzanti A,
Clémenty N,
Bisson A,
Corveleyn A,
Stallmeyer B,
Dittmann S,
Saenen J,
Noël A,
Honarbakhsh S,
Rudic B,
Marzak H,
Rowe MK,
Federspiel C,
Le Page S,
Placide L,
Milhem A,
Barajas-Martinez H,
Beckmann BM,
Krapels IP,
Steinfurt J,
Winkel BG,
Jabbari R,
Shoemaker MB,
Boukens BJ,
Škorić-Milosavljević D,
Bikker H,
Manevy F,
Lichtner P,
Ribasés M,
Meitinger T,
Müller-Nurasyid M,
Veldink JH,
van den Berg LH,
Van Damme P,
Cusi D,
Lanzani C,
Rigade S,
Charpentier E,
Baron E,
Bonnaud S,
Lecointe S,
Donnart A,
Le Marec H,
Chatel S,
Karakachoff M,
Bézieau S,
London B,
Tfelt-Hansen J,
Roden D,
Odening KE,
Cerrone M,
Chinitz LA,
Volders PG,
van de Berg MP,
Laurent G,
Faivre L,
Antzelevitch C,
Kääb S,
Arnaout AA,
Dupuis JM,
Pasquie JL,
Billon O,
Roberts JD,
Jesel L,
Borggrefe M,
Lambiase PD,
Mansourati J,
Loeys B,
Leenhardt A,
Guicheney P,
Maury P,
Schulze-Bahr E,
Robyns T,
Breckpot J,
Babuty D,
Priori SG,
Napolitano C,
de Asmundis C,
Brugada P,
Brugada R,
Arbelo E,
Brugada J,
Mabo P,
Behar N,
Giustetto C,
Molina MS,
Gimeno JR,
Hasdemir C,
Schwartz PJ,
Crotti L,
McKeown PP,
Sharma S,
Behr ER,
Haissaguerre M,
Sacher F,
Rooryck C,
Tan HL,
Remme CA,
Postema PG,
Delmar M,
Ellinor PT,
Lubitz SA,
Gourraud JB,
Tanck MW,
George AL Jr,
MacRae CA,
Burridge PW,
Dina C,
Probst V,
Wilde AA,
Schott JJ,
Redon R,
Bezzina CR
KORA-Study Group · Nantes Referral Center for inherited cardiac arrhythmia
Nature genetics · 2022 · PMID 35210625
5 pages
Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci
Ishikawa T,
Masuda T,
Hachiya T,
Dina C,
Simonet F,
Nagata Y,
Tanck MWT,
Sonehara K,
Glinge C,
Tadros R,
Khongphatthanayothin A,
Lu TP
and 26 more — show all
Higuchi C,
Nakajima T,
Hayashi K,
Aizawa Y,
Nakano Y,
Nogami A,
Morita H,
Ohno S,
Aiba T,
Krijger Juárez C,
Mauleekoonphairoj J,
Poovorawan Y,
Gourraud JB,
Shimizu W,
Probst V,
Horie M,
Wilde AAM,
Redon R,
Juang JJ,
Nademanee K,
Bezzina CR,
Barc J,
Tanaka T,
Okada Y,
Schott JJ,
Makita N
European heart journal · 2024 · PMID 38747976
3 pages
Large genome-wide association study identifies three novel risk variants for restless legs syndrome
Didriksen M,
Nawaz MS,
Dowsett J,
Bell S,
Erikstrup C,
Pedersen OB,
Sørensen E,
Jennum PJ,
Burgdorf KS,
Burchell B,
Butterworth AS,
Soranzo N
and 22 more — show all
Rye DB,
Trotti LM,
Saini P,
Stefansdottir L,
Magnusson SH,
Thorleifsson G,
Sigmundsson T,
Sigurdsson AP,
Van Den Hurk K,
Quee F,
Tanck MWT,
Ouwehand WH,
Roberts DJ,
Earley EJ,
Busch MP,
Mast AE,
Page GP,
Danesh J,
Di Angelantonio E,
Stefansson H,
Ullum H,
Stefansson K
Communications biology · 2020 · PMID 33239738 · 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.