For researchers
Is your paper here?
2,665 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
Gordon A.
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
Tcheandjieu C,
Zhu X,
Hilliard AT,
Clarke SL,
Napolioni V,
Ma S,
Lee KM,
Fang H,
Chen F,
Lu Y,
Tsao NL,
Raghavan S
and 70 more — show all
Koyama S,
Gorman BR,
Vujkovic M,
Klarin D,
Levin MG,
Sinnott-Armstrong N,
Wojcik GL,
Plomondon ME,
Maddox TM,
Waldo SW,
Bick AG,
Pyarajan S,
Huang J,
Song R,
Ho YL,
Buyske S,
Kooperberg C,
Haessler J,
Loos RJF,
Do R,
Verbanck M,
Chaudhary K,
North KE,
Avery CL,
Graff M,
Haiman CA,
Le Marchand L,
Wilkens LR,
Bis JC,
Leonard H,
Shen B,
Lange LA,
Giri A,
Dikilitas O,
Kullo IJ,
Stanaway IB,
Jarvik GP,
Gordon AS,
Hebbring S,
Namjou B,
Kaufman KM,
Ito K,
Ishigaki K,
Kamatani Y,
Verma SS,
Ritchie MD,
Kember RL,
Baras A,
Lotta LA,
Kathiresan S,
Hauser ER,
Miller DR,
Lee JS,
Saleheen D,
Reaven PD,
Cho K,
Gaziano JM,
Natarajan P,
Huffman JE,
Voight BF,
Rader DJ,
Chang KM,
Lynch JA,
Damrauer SM,
Wilson PWF,
Tang H,
Sun YV,
Tsao PS,
O'Donnell CJ,
Assimes TL
Regeneron Genetics Center · CARDIoGRAMplusC4D Consortium and 2 more consortia
Nature medicine · 2022 · PMID 35915156
6 pages
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
Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network
Palmer MR,
Kim DS,
Crosslin DR,
Stanaway IB,
Rosenthal EA,
Carrell DS,
Cronkite DJ,
Gordon A,
Du X,
Li YK,
Williams MS,
Weng C
and 12 more — show all
Feng Q,
Li R,
Pendergrass SA,
Hakonarson H,
Fasel D,
Sohn S,
Sleiman P,
Handelman SK,
Speliotes E,
Kullo IJ,
Larson EB,
Jarvik GP
eMERGE Consortium
Genetic epidemiology · 2021 · PMID 32964493 · open access
2 pages
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
Zeggini E,
Panoutsopoulou K,
Southam L,
Rayner NW,
Day-Williams AG,
Lopes MC,
Boraska V,
Esko T,
Evangelou E,
Hoffman A,
Houwing-Duistermaat JJ,
Ingvarsson T
and 64 more — show all
Jonsdottir I,
Jonnson H,
Kerkhof HJ,
Kloppenburg M,
Bos SD,
Mangino M,
Metrustry S,
Slagboom PE,
Thorleifsson G,
Raine EV,
Ratnayake M,
Ricketts M,
Beazley C,
Blackburn H,
Bumpstead S,
Elliott KS,
Hunt SE,
Potter SC,
Shin SY,
Yadav VK,
Zhai G,
Sherburn K,
Dixon K,
Arden E,
Aslam N,
Battley PK,
Carluke I,
Doherty S,
Gordon A,
Joseph J,
Keen R,
Koller NC,
Mitchell S,
O'Neill F,
Paling E,
Reed MR,
Rivadeneira F,
Swift D,
Walker K,
Watkins B,
Wheeler M,
Birrell F,
Ioannidis JP,
Meulenbelt I,
Metspalu A,
Rai A,
Salter D,
Stefansson K,
Stykarsdottir U,
Uitterlinden AG,
van Meurs JB,
Chapman K,
Deloukas P,
Ollier WE,
Wallis GA,
Arden N,
Carr A,
Doherty M,
McCaskie A,
Willkinson JM,
Ralston SH,
Valdes AM,
Spector TD,
Loughlin J
arcOGEN Consortium · arcOGEN Collaborators
Lancet (London, England) · 2012 · PMID 22763110 · 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.