For researchers
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.
4 matches for
Steinbeck G.
Common variants at ten loci modulate the QT interval duration in the QTSCD Study
Pfeufer A,
Sanna S,
Arking DE,
Müller M,
Gateva V,
Fuchsberger C,
Ehret GB,
Orrú M,
Pattaro C,
Köttgen A,
Perz S,
Usala G
and 32 more — show all
Barbalic M,
Li M,
Pütz B,
Scuteri A,
Prineas RJ,
Sinner MF,
Gieger C,
Najjar SS,
Kao WH,
Mühleisen TW,
Dei M,
Happle C,
Möhlenkamp S,
Crisponi L,
Erbel R,
Jöckel KH,
Naitza S,
Steinbeck G,
Marroni F,
Hicks AA,
Lakatta E,
Müller-Myhsok B,
Pramstaller PP,
Wichmann HE,
Schlessinger D,
Boerwinkle E,
Meitinger T,
Uda M,
Coresh J,
Kääb S,
Abecasis GR,
Chakravarti A
Nature genetics · 2009 · PMID 19305409
4 pages
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
Ellinor PT,
Lunetta KL,
Albert CM,
Glazer NL,
Ritchie MD,
Smith AV,
Arking DE,
Müller-Nurasyid M,
Krijthe BP,
Lubitz SA,
Bis JC,
Chung MK
and 77 more — show all
Dörr M,
Ozaki K,
Roberts JD,
Smith JG,
Pfeufer A,
Sinner MF,
Lohman K,
Ding J,
Smith NL,
Smith JD,
Rienstra M,
Rice KM,
Van Wagoner DR,
Magnani JW,
Wakili R,
Clauss S,
Rotter JI,
Steinbeck G,
Launer LJ,
Davies RW,
Borkovich M,
Harris TB,
Lin H,
Völker U,
Völzke H,
Milan DJ,
Hofman A,
Boerwinkle E,
Chen LY,
Soliman EZ,
Voight BF,
Li G,
Chakravarti A,
Kubo M,
Tedrow UB,
Rose LM,
Ridker PM,
Conen D,
Tsunoda T,
Furukawa T,
Sotoodehnia N,
Xu S,
Kamatani N,
Levy D,
Nakamura Y,
Parvez B,
Mahida S,
Furie KL,
Rosand J,
Muhammad R,
Psaty BM,
Meitinger T,
Perz S,
Wichmann HE,
Witteman JC,
Kao WH,
Kathiresan S,
Roden DM,
Uitterlinden AG,
Rivadeneira F,
McKnight B,
Sjögren M,
Newman AB,
Liu Y,
Gollob MH,
Melander O,
Tanaka T,
Stricker BH,
Felix SB,
Alonso A,
Darbar D,
Barnard J,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Gudnason V,
Kääb S
Nature genetics · 2012 · PMID 22544366
3 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
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.