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.
4 matches for
Smith CE.
Genome-wide association study of breakfast skipping links clock regulation with food timing
Dashti HS,
Merino J,
Lane JM,
Song Y,
Smith CE,
Tanaka T,
McKeown NM,
Tucker C,
Sun D,
Bartz TM,
Li-Gao R,
Nisa H
and 15 more — show all
Reutrakul S,
Lemaitre RN,
Alshehri TM,
de Mutsert R,
Bazzano L,
Qi L,
Knutson KL,
Psaty BM,
Mook-Kanamori DO,
Perica VB,
Neuhouser ML,
Scheer FAJL,
Rutter MK,
Garaulet M,
Saxena R
The American journal of clinical nutrition · 2019 · PMID 31190057
2 pages
Genome-wide association studies and fine-mapping identify genomic loci for n-3 and n-6 polyunsaturated fatty acids in Hispanic American and African American cohorts
Yang C,
Veenstra J,
Bartz TM,
Pahl MC,
Hallmark B,
Chen YI,
Westra J,
Steffen LM,
Brown CD,
Siscovick D,
Tsai MY,
Wood AC
and 9 more — show all
Communications biology · 2023 · PMID 37587153 · open access
2 pages
Genome-wide contribution of genotype by environment interaction to variation of diabetes-related traits
Zheng JS,
Arnett DK,
Lee YC,
Shen J,
Parnell LD,
Smith CE,
Richardson K,
Li D,
Borecki IB,
Ordovás JM,
Lai CQ
PloS one · 2013 · PMID 24204828 · open access
1 page
A Genome-Wide Association Study Identifies Blood Disorder-Related Variants Influencing Hemoglobin A<sub>1c</sub> With Implications for Glycemic Status in U.S. Hispanics/Latinos
Moon JY,
Louie TL,
Jain D,
Sofer T,
Schurmann C,
Below JE,
Lai CQ,
Aviles-Santa ML,
Talavera GA,
Smith CE,
Petty LE,
Bottinger EP
and 13 more — show all
Chen YI,
Taylor KD,
Daviglus ML,
Cai J,
Wang T,
Tucker KL,
Ordovás JM,
Hanis CL,
Loos RJF,
Schneiderman N,
Rotter JI,
Kaplan RC,
Qi Q
Diabetes care · 2019 · PMID 31213470
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.