For researchers
Is your paper here?
2,662 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
Schwienbacher C.
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
Sotoodehnia N,
Isaacs A,
de Bakker PI,
Dörr M,
Newton-Cheh C,
Nolte IM,
van der Harst P,
Müller M,
Eijgelsheim M,
Alonso A,
Hicks AA,
Padmanabhan S
and 91 more — show all
Hayward C,
Smith AV,
Polasek O,
Giovannone S,
Fu J,
Magnani JW,
Marciante KD,
Pfeufer A,
Gharib SA,
Teumer A,
Li M,
Bis JC,
Rivadeneira F,
Aspelund T,
Köttgen A,
Johnson T,
Rice K,
Sie MP,
Wang YA,
Klopp N,
Fuchsberger C,
Wild SH,
Mateo Leach I,
Estrada K,
Völker U,
Wright AF,
Asselbergs FW,
Qu J,
Chakravarti A,
Sinner MF,
Kors JA,
Petersmann A,
Harris TB,
Soliman EZ,
Munroe PB,
Psaty BM,
Oostra BA,
Cupples LA,
Perz S,
de Boer RA,
Uitterlinden AG,
Völzke H,
Spector TD,
Liu FY,
Boerwinkle E,
Dominiczak AF,
Rotter JI,
van Herpen G,
Levy D,
Wichmann HE,
van Gilst WH,
Witteman JC,
Kroemer HK,
Kao WH,
Heckbert SR,
Meitinger T,
Hofman A,
Campbell H,
Folsom AR,
van Veldhuisen DJ,
Schwienbacher C,
O'Donnell CJ,
Volpato CB,
Caulfield MJ,
Connell JM,
Launer L,
Lu X,
Franke L,
Fehrmann RS,
te Meerman G,
Groen HJ,
Weersma RK,
van den Berg LH,
Wijmenga C,
Ophoff RA,
Navis G,
Rudan I,
Snieder H,
Wilson JF,
Pramstaller PP,
Siscovick DS,
Wang TJ,
Gudnason V,
van Duijn CM,
Felix SB,
Fishman GI,
Jamshidi Y,
Stricker BH,
Samani NJ,
Kääb S,
Arking DE
Nature genetics · 2010 · PMID 21076409 · open access
5 pages
Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease
Tang W,
Schwienbacher C,
Lopez LM,
Ben-Shlomo Y,
Oudot-Mellakh T,
Johnson AD,
Samani NJ,
Basu S,
Gögele M,
Davies G,
Lowe GD,
Tregouet DA
and 23 more — show all
Tan A,
Pankow JS,
Tenesa A,
Levy D,
Volpato CB,
Rumley A,
Gow AJ,
Minelli C,
Yarnell JW,
Porteous DJ,
Starr JM,
Gallacher J,
Boerwinkle E,
Visscher PM,
Pramstaller PP,
Cushman M,
Emilsson V,
Plump AS,
Matijevic N,
Morange PE,
Deary IJ,
Hicks AA,
Folsom AR
American journal of human genetics · 2012 · PMID 22703881
3 pages
Discovery and fine mapping of serum protein loci through transethnic meta-analysis
Franceschini N,
van Rooij FJ,
Prins BP,
Feitosa MF,
Karakas M,
Eckfeldt JH,
Folsom AR,
Kopp J,
Vaez A,
Andrews JS,
Baumert J,
Boraska V
and 89 more — show all
Broer L,
Hayward C,
Ngwa JS,
Okada Y,
Polasek O,
Westra HJ,
Wang YA,
Del Greco M F,
Glazer NL,
Kapur K,
Kema IP,
Lopez LM,
Schillert A,
Smith AV,
Winkler CA,
Zgaga L,
Bandinelli S,
Bergmann S,
Boban M,
Bochud M,
Chen YD,
Davies G,
Dehghan A,
Ding J,
Doering A,
Durda JP,
Ferrucci L,
Franco OH,
Franke L,
Gunjaca G,
Hofman A,
Hsu FC,
Kolcic I,
Kraja A,
Kubo M,
Lackner KJ,
Launer L,
Loehr LR,
Li G,
Meisinger C,
Nakamura Y,
Schwienbacher C,
Starr JM,
Takahashi A,
Torlak V,
Uitterlinden AG,
Vitart V,
Waldenberger M,
Wild PS,
Kirin M,
Zeller T,
Zemunik T,
Zhang Q,
Ziegler A,
Blankenberg S,
Boerwinkle E,
Borecki IB,
Campbell H,
Deary IJ,
Frayling TM,
Gieger C,
Harris TB,
Hicks AA,
Koenig W,
O' Donnell CJ,
Fox CS,
Pramstaller PP,
Psaty BM,
Reiner AP,
Rotter JI,
Rudan I,
Snieder H,
Tanaka T,
van Duijn CM,
Vollenweider P,
Waeber G,
Wilson JF,
Witteman JC,
Wolffenbuttel BH,
Wright AF,
Wu Q,
Liu Y,
Jenny NS,
North KE,
Felix JF,
Alizadeh BZ,
Cupples LA,
Perry JR,
Morris AP
LifeLines Cohort Study
American journal of human genetics · 2012 · PMID 23022100
3 pages
Genetic determinants of circulating sphingolipid concentrations in European populations
Hicks AA,
Pramstaller PP,
Johansson A,
Vitart V,
Rudan I,
Ugocsai P,
Aulchenko Y,
Franklin CS,
Liebisch G,
Erdmann J,
Jonasson I,
Zorkoltseva IV
and 34 more — show all
Pattaro C,
Hayward C,
Isaacs A,
Hengstenberg C,
Campbell S,
Gnewuch C,
Janssens AC,
Kirichenko AV,
König IR,
Marroni F,
Polasek O,
Demirkan A,
Kolcic I,
Schwienbacher C,
Igl W,
Biloglav Z,
Witteman JC,
Pichler I,
Zaboli G,
Axenovich TI,
Peters A,
Schreiber S,
Wichmann HE,
Schunkert H,
Hastie N,
Oostra BA,
Wild SH,
Meitinger T,
Gyllensten U,
van Duijn CM,
Wilson JF,
Wright A,
Schmitz G,
Campbell H
PLoS genetics · 2009 · PMID 19798445 · open access
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.