For researchers
Is your paper here?
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.
26 matches for
Lubitz S,
showing the first 6.
Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse
Roselli C,
Yu M,
Nauffal V,
Georges A,
Yang Q,
Love K,
Weng LC,
Delling FN,
Maurya SR,
Schrölkamp M,
Tfelt-Hansen J,
Hagège A
and 42 more — show all
Jeunemaitre X,
Debette S,
Amouyel P,
Guan W,
Muehlschlegel JD,
Body SC,
Shah S,
Samad Z,
Kyryachenko S,
Haynes C,
Rienstra M,
Le Tourneau T,
Probst V,
Roussel R,
Wijdh-Den Hamer IJ,
Siland JE,
Knowlton KU,
Jacques Schott J,
Levine RA,
Benjamin EJ,
Vasan RS,
Horne BD,
Muhlestein JB,
Benfari G,
Enriquez-Sarano M,
Natale A,
Mohanty S,
Trivedi C,
Shoemaker MB,
Yoneda ZT,
Wells QS,
Baker MT,
Farber-Eger E,
Michelena HI,
Lundby A,
Norris RA,
Slaugenhaupt SA,
Dina C,
Lubitz SA,
Bouatia-Naji N,
Ellinor PT,
Milan DJ
European heart journal · 2022 · PMID 35245370
2 pages
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
Benjamin EJ,
Rice KM,
Arking DE,
Pfeufer A,
van Noord C,
Smith AV,
Schnabel RB,
Bis JC,
Boerwinkle E,
Sinner MF,
Dehghan A,
Lubitz SA
and 44 more — show all
D'Agostino RB Sr,
Lumley T,
Ehret GB,
Heeringa J,
Aspelund T,
Newton-Cheh C,
Larson MG,
Marciante KD,
Soliman EZ,
Rivadeneira F,
Wang TJ,
Eiríksdottir G,
Levy D,
Psaty BM,
Li M,
Chamberlain AM,
Hofman A,
Vasan RS,
Harris TB,
Rotter JI,
Kao WH,
Agarwal SK,
Stricker BH,
Wang K,
Launer LJ,
Smith NL,
Chakravarti A,
Uitterlinden AG,
Wolf PA,
Sotoodehnia N,
Köttgen A,
van Duijn CM,
Meitinger T,
Mueller M,
Perz S,
Steinbeck G,
Wichmann HE,
Lunetta KL,
Heckbert SR,
Gudnason V,
Alonso A,
Kääb S,
Ellinor PT,
Witteman JC
Nature genetics · 2009 · PMID 19597492 · open access
1 page
Common variants in KCNN3 are associated with lone atrial fibrillation
Ellinor PT,
Lunetta KL,
Glazer NL,
Pfeufer A,
Alonso A,
Chung MK,
Sinner MF,
de Bakker PI,
Mueller M,
Lubitz SA,
Fox E,
Darbar D
and 50 more — show all
Smith NL,
Smith JD,
Schnabel RB,
Soliman EZ,
Rice KM,
Van Wagoner DR,
Beckmann BM,
van Noord C,
Wang K,
Ehret GB,
Rotter JI,
Hazen SL,
Steinbeck G,
Smith AV,
Launer LJ,
Harris TB,
Makino S,
Nelis M,
Milan DJ,
Perz S,
Esko T,
Köttgen A,
Moebus S,
Newton-Cheh C,
Li M,
Möhlenkamp S,
Wang TJ,
Kao WH,
Vasan RS,
Nöthen MM,
MacRae CA,
Stricker BH,
Hofman A,
Uitterlinden AG,
Levy D,
Boerwinkle E,
Metspalu A,
Topol EJ,
Chakravarti A,
Gudnason V,
Psaty BM,
Roden DM,
Meitinger T,
Wichmann HE,
Witteman JC,
Barnard J,
Arking DE,
Benjamin EJ,
Heckbert SR,
Kääb S
Nature genetics · 2010 · PMID 20173747 · open access
1 page
Heritability of Atrial Fibrillation
Weng LC,
Choi SH,
Klarin D,
Smith JG,
Loh PR,
Chaffin M,
Roselli C,
Hulme OL,
Lunetta KL,
Dupuis J,
Benjamin EJ,
Newton-Cheh C
and 3 more — show all
Circulation. Cardiovascular genetics · 2017 · PMID 29237688
1 page
ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals
Bihlmeyer NA,
Brody JA,
Smith AV,
Warren HR,
Lin H,
Isaacs A,
Liu CT,
Marten J,
Radmanesh F,
Hall LM,
Grarup N,
Mei H
and 88 more — show all
Müller-Nurasyid M,
Huffman JE,
Verweij N,
Guo X,
Yao J,
Li-Gao R,
van den Berg M,
Weiss S,
Prins BP,
van Setten J,
Haessler J,
Lyytikäinen LP,
Li M,
Alonso A,
Soliman EZ,
Bis JC,
Austin T,
Chen YI,
Psaty BM,
Harrris TB,
Launer LJ,
Padmanabhan S,
Dominiczak A,
Huang PL,
Xie Z,
Ellinor PT,
Kors JA,
Campbell A,
Murray AD,
Nelson CP,
Tobin MD,
Bork-Jensen J,
Hansen T,
Pedersen O,
Linneberg A,
Sinner MF,
Peters A,
Waldenberger M,
Meitinger T,
Perz S,
Kolcic I,
Rudan I,
de Boer RA,
van der Meer P,
Lin HJ,
Taylor KD,
de Mutsert R,
Trompet S,
Jukema JW,
Maan AC,
Stricker BHC,
Rivadeneira F,
Uitterlinden A,
Völker U,
Homuth G,
Völzke H,
Felix SB,
Mangino M,
Spector TD,
Bots ML,
Perez M,
Raitakari OT,
Kähönen M,
Mononen N,
Gudnason V,
Munroe PB,
Lubitz SA,
van Duijn CM,
Newton-Cheh CH,
Hayward C,
Rosand J,
Samani NJ,
Kanters JK,
Wilson JG,
Kääb S,
Polasek O,
van der Harst P,
Heckbert SR,
Rotter JI,
Mook-Kanamori DO,
Eijgelsheim M,
Dörr M,
Jamshidi Y,
Asselbergs FW,
Kooperberg C,
Lehtimäki T,
Arking DE,
Sotoodehnia N
Circulation. Genomic and precision medicine · 2018 · PMID 29874175 · open access
1 page
Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass
Khurshid S,
Lazarte J,
Pirruccello JP,
Weng LC,
Choi SH,
Hall AW,
Wang X,
Friedman SF,
Nauffal V,
Biddinger KJ,
Aragam KG,
Batra P
and 4 more — show all
Nature communications · 2023 · PMID 36944631 · 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.