For researchers
Is your paper here?
2,675 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.
7 matches for
McCarty CA.
Genome-wide association of lipid-lowering response to statins in combined study populations
Barber MJ,
Mangravite LM,
Hyde CL,
Chasman DI,
Smith JD,
McCarty CA,
Li X,
Wilke RA,
Rieder MJ,
Williams PT,
Ridker PM,
Chatterjee A
and 4 more — show all
PloS one · 2010 · PMID 20339536 · open access
3 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
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci
Jones GT,
Tromp G,
Kuivaniemi H,
Gretarsdottir S,
Baas AF,
Giusti B,
Strauss E,
Van't Hof FN,
Webb TR,
Erdman R,
Ritchie MD,
Elmore JR
and 105 more — show all
Verma A,
Pendergrass S,
Kullo IJ,
Ye Z,
Peissig PL,
Gottesman O,
Verma SS,
Malinowski J,
Rasmussen-Torvik LJ,
Borthwick KM,
Smelser DT,
Crosslin DR,
de Andrade M,
Ryer EJ,
McCarty CA,
Böttinger EP,
Pacheco JA,
Crawford DC,
Carrell DS,
Gerhard GS,
Franklin DP,
Carey DJ,
Phillips VL,
Williams MJ,
Wei W,
Blair R,
Hill AA,
Vasudevan TM,
Lewis DR,
Thomson IA,
Krysa J,
Hill GB,
Roake J,
Merriman TR,
Oszkinis G,
Galora S,
Saracini C,
Abbate R,
Pulli R,
Pratesi C,
Saratzis A,
Verissimo AR,
Bumpstead S,
Badger SA,
Clough RE,
Cockerill G,
Hafez H,
Scott DJ,
Futers TS,
Romaine SP,
Bridge K,
Griffin KJ,
Bailey MA,
Smith A,
Thompson MM,
van Bockxmeer FM,
Matthiasson SE,
Thorleifsson G,
Thorsteinsdottir U,
Blankensteijn JD,
Teijink JA,
Wijmenga C,
de Graaf J,
Kiemeney LA,
Lindholt JS,
Hughes A,
Bradley DT,
Stirrups K,
Golledge J,
Norman PE,
Powell JT,
Humphries SE,
Hamby SE,
Goodall AH,
Nelson CP,
Sakalihasan N,
Courtois A,
Ferrell RE,
Eriksson P,
Folkersen L,
Franco-Cereceda A,
Eicher JD,
Johnson AD,
Betsholtz C,
Ruusalepp A,
Franzén O,
Schadt EE,
Björkegren JL,
Lipovich L,
Drolet AM,
Verhoeven EL,
Zeebregts CJ,
Geelkerken RH,
van Sambeek MR,
van Sterkenburg SM,
de Vries JP,
Stefansson K,
Thompson JR,
de Bakker PI,
Deloukas P,
Sayers RD,
Harrison SC,
van Rij AM,
Samani NJ,
Bown MJ
Circulation research · 2017 · PMID 27899403 · open access
3 pages
Genetic variation associated with circulating monocyte count in the eMERGE Network
Crosslin DR,
McDavid A,
Weston N,
Zheng X,
Hart E,
de Andrade M,
Kullo IJ,
McCarty CA,
Doheny KF,
Pugh E,
Kho A,
Hayes MG
and 52 more — show all
Ritchie MD,
Saip A,
Crawford DC,
Crane PK,
Newton K,
Carrell DS,
Gallego CJ,
Nalls MA,
Li R,
Mirel DB,
Crenshaw A,
Couper DJ,
Tanaka T,
van Rooij FJ,
Chen MH,
Smith AV,
Zakai NA,
Yango Q,
Garcia M,
Liu Y,
Lumley T,
Folsom AR,
Reiner AP,
Felix JF,
Dehghan A,
Wilson JG,
Bis JC,
Fox CS,
Glazer NL,
Cupples LA,
Coresh J,
Eiriksdottir G,
Gudnason V,
Bandinelli S,
Frayling TM,
Chakravarti A,
van Duijn CM,
Melzer D,
Levy D,
Boerwinkle E,
Singleton AB,
Hernandez DG,
Longo DL,
Witteman JC,
Psaty BM,
Ferrucci L,
Harris TB,
O'Donnell CJ,
Ganesh SK,
Larson EB,
Carlson CS,
Jarvik GP
CHARGE Hematology Working Group · electronic Medical Records and Genomics (eMERGE) Network
Human molecular genetics · 2013 · PMID 23314186
2 pages
Genome-wide association study identifies common variants associated with circulating vitamin E levels
Major JM,
Yu K,
Wheeler W,
Zhang H,
Cornelis MC,
Wright ME,
Yeager M,
Snyder K,
Weinstein SJ,
Mondul A,
Eliassen H,
Purdue M
and 8 more — show all
Human molecular genetics · 2011 · PMID 21729881 · open access
1 page
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
Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms
van 't Hof FN,
Ruigrok YM,
Lee CH,
Ripke S,
Anderson G,
de Andrade M,
Baas AF,
Blankensteijn JD,
Böttinger EP,
Bown MJ,
Broderick J,
Bijlenga P
and 59 more — show all
Carrell DS,
Crawford DC,
Crosslin DR,
Ebeling C,
Eriksson JG,
Eriksson JG,
Fornage M,
Foroud T,
von Und Zu Fraunberg M,
Friedrich CM,
Gaál EI,
Gottesman O,
Guo DC,
Harrison SC,
Hernesniemi J,
Hofman A,
Inoue I,
Jääskeläinen JE,
Jones GT,
Kiemeney LA,
Kivisaari R,
Ko N,
Koskinen S,
Kubo M,
Kullo IJ,
Kuivaniemi H,
Kurki MI,
Laakso A,
Lai D,
Leal SM,
Lehto H,
LeMaire SA,
Low SK,
Malinowski J,
McCarty CA,
Milewicz DM,
Mosley TH,
Nakamura Y,
Nakaoka H,
Niemelä M,
Pacheco J,
Peissig PL,
Pera J,
Rasmussen-Torvik L,
Ritchie MD,
Rivadeneira F,
van Rij AM,
Santos-Cortez RL,
Saratzis A,
Slowik A,
Takahashi A,
Tromp G,
Uitterlinden AG,
Verma SS,
Vermeulen SH,
Wang GT,
Han B,
Rinkel GJ,
de Bakker PI
Aneurysm Consortium; Vascular Research Consortium of New Zealand
Journal of the American Heart Association · 2016 · PMID 27418160 · 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.