For researchers
Is your paper here?
2,663 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
DeWan A.
Rare-variant association analysis reveals known and new age-related hearing loss genes
Cornejo-Sanchez DM,
Li G,
Fabiha T,
Wang R,
Acharya A,
Everard JL,
Kadlubowska MK,
Huang Y,
Schrauwen I,
Wang GT,
DeWan AT,
Leal SM
European journal of human genetics : EJHG · 2023 · PMID 36788145
7 pages
GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21
Wiemels JL,
Walsh KM,
de Smith AJ,
Metayer C,
Gonseth S,
Hansen HM,
Francis SS,
Ojha J,
Smirnov I,
Barcellos L,
Xiao X,
Morimoto L
and 6 more — show all
Nature communications · 2018 · PMID 29348612 · open access
2 pages
Genome-wide association study of childhood B-cell acute lymphoblastic leukemia reveals novel African ancestry-specific susceptibility loci
Im C,
Raduski AR,
Mills LJ,
Bhattarai KR,
Mobley RJ,
Barnett KR,
Lu Z,
Liao K,
Anderson N,
Johnson RA,
Langer E,
Hooten AJ
and 31 more — show all
Seif AE,
Bernt KM,
Tsang M,
Mamou BA,
Gil-de-Gómez L,
Wolfson JA,
Friedman DN,
Shukla N,
Klesse LJ,
Marcotte EL,
Ji L,
Dang A,
Luo M,
Zhong Y,
Langie J,
Chiang CWK,
de Smith A,
Wiemels JL,
DeWan A,
Ma X,
Metayer C,
Wang Z,
Nelson HH,
Pankratz N,
Yang T,
Basu S,
Turcotte LM,
Yang JJ,
Savic D,
Scheurer ME,
Spector LG
Nature communications · 2025 · PMID 41125582 · open access
2 pages
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
Thorleifsson G,
Walters GB,
Hewitt AW,
Masson G,
Helgason A,
DeWan A,
Sigurdsson A,
Jonasdottir A,
Gudjonsson SA,
Magnusson KP,
Stefansson H,
Lam DS
and 35 more — show all
Tam PO,
Gudmundsdottir GJ,
Southgate L,
Burdon KP,
Gottfredsdottir MS,
Aldred MA,
Mitchell P,
St Clair D,
Collier DA,
Tang N,
Sveinsson O,
Macgregor S,
Martin NG,
Cree AJ,
Gibson J,
Macleod A,
Jacob A,
Ennis S,
Young TL,
Chan JC,
Karwatowski WS,
Hammond CJ,
Thordarson K,
Zhang M,
Wadelius C,
Lotery AJ,
Trembath RC,
Pang CP,
Hoh J,
Craig JE,
Kong A,
Mackey DA,
Jonasson F,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2010 · PMID 20835238
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.