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
Palmer M.
Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease
Liu H,
Doke T,
Guo D,
Sheng X,
Ma Z,
Park J,
Vy HMT,
Nadkarni GN,
Abedini A,
Miao Z,
Palmer M,
Voight BF
and 5 more — show all
Nature genetics · 2022 · PMID 35710981
12 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
Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain
Suri P,
Palmer MR,
Tsepilov YA,
Freidin MB,
Boer CG,
Yau MS,
Evans DS,
Gelemanovic A,
Bartz TM,
Nethander M,
Arbeeva L,
Karssen L
and 25 more — show all
Neogi T,
Campbell A,
Mellstrom D,
Ohlsson C,
Marshall LM,
Orwoll E,
Uitterlinden A,
Rotter JI,
Lauc G,
Psaty BM,
Karlsson MK,
Lane NE,
Jarvik GP,
Polasek O,
Hochberg M,
Jordan JM,
Van Meurs JBJ,
Jackson R,
Nielson CM,
Mitchell BD,
Smith BH,
Hayward C,
Smith NL,
Aulchenko YS,
Williams FMK
PLoS genetics · 2018 · PMID 30261039 · 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.