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.
5 matches for
Chute CG.
The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype
Stanaway IB,
Hall TO,
Rosenthal EA,
Palmer M,
Naranbhai V,
Knevel R,
Namjou-Khales B,
Carroll RJ,
Kiryluk K,
Gordon AS,
Linder J,
Howell KM
and 28 more — show all
Mapes BM,
Lin FTJ,
Joo YY,
Hayes MG,
Gharavi AG,
Pendergrass SA,
Ritchie MD,
de Andrade M,
Croteau-Chonka DC,
Raychaudhuri S,
Weiss ST,
Lebo M,
Amr SS,
Carrell D,
Larson EB,
Chute CG,
Rasmussen-Torvik LJ,
Roy-Puckelwartz MJ,
Sleiman P,
Hakonarson H,
Li R,
Karlson EW,
Peterson JF,
Kullo IJ,
Chisholm R,
Denny JC,
Jarvik GP,
Crosslin DR
eMERGE Network
Genetic epidemiology · 2019 · PMID 30298529 · open access
5 pages
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk
Ritchie MD,
Denny JC,
Zuvich RL,
Crawford DC,
Schildcrout JS,
Bastarache L,
Ramirez AH,
Mosley JD,
Pulley JM,
Basford MA,
Bradford Y,
Rasmussen LV
and 15 more — show all
Pathak J,
Chute CG,
Kullo IJ,
McCarty CA,
Chisholm RL,
Kho AN,
Carlson CS,
Larson EB,
Jarvik GP,
Sotoodehnia N,
Manolio TA,
Li R,
Masys DR,
Haines JL,
Roden DM
Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) QRS Group
Circulation · 2013 · PMID 23463857
3 pages
Identification of unique venous thromboembolism-susceptibility variants in African-Americans
Heit JA,
Armasu SM,
McCauley BM,
Kullo IJ,
Sicotte H,
Pathak J,
Chute CG,
Gottesman O,
Bottinger EP,
Denny JC,
Roden DM,
Li R
and 2 more — show all
Thrombosis and haemostasis · 2017 · PMID 28203683
3 pages
A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects
Shameer K,
Denny JC,
Ding K,
Jouni H,
Crosslin DR,
de Andrade M,
Chute CG,
Peissig P,
Pacheco JA,
Li R,
Bastarache L,
Kho AN
and 8 more — show all
Human genetics · 2014 · PMID 24026423
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.