For researchers
Is your paper here?
2,662 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.
3 matches for
Wilson AF.
Genome-wide meta-analyses of smoking behaviors in African Americans
David SP,
Hamidovic A,
Chen GK,
Bergen AW,
Wessel J,
Kasberger JL,
Brown WM,
Petruzella S,
Thacker EL,
Kim Y,
Nalls MA,
Tranah GJ
and 68 more — show all
Sung YJ,
Ambrosone CB,
Arnett D,
Bandera EV,
Becker DM,
Becker L,
Berndt SI,
Bernstein L,
Blot WJ,
Broeckel U,
Buxbaum SG,
Caporaso N,
Casey G,
Chanock SJ,
Deming SL,
Diver WR,
Eaton CB,
Evans DS,
Evans MK,
Fornage M,
Franceschini N,
Harris TB,
Henderson BE,
Hernandez DG,
Hitsman B,
Hu JJ,
Hunt SC,
Ingles SA,
John EM,
Kittles R,
Kolb S,
Kolonel LN,
Le Marchand L,
Liu Y,
Lohman KK,
McKnight B,
Millikan RC,
Murphy A,
Neslund-Dudas C,
Nyante S,
Press M,
Psaty BM,
Rao DC,
Redline S,
Rodriguez-Gil JL,
Rybicki BA,
Signorello LB,
Singleton AB,
Smoller J,
Snively B,
Spring B,
Stanford JL,
Strom SS,
Swan GE,
Taylor KD,
Thun MJ,
Wilson AF,
Witte JS,
Yamamura Y,
Yanek LR,
Yu K,
Zheng W,
Zheng W,
Ziegler RG,
Zonderman AB,
Jorgenson E,
Haiman CA,
Furberg H
Translational psychiatry · 2012 · PMID 22832964 · open access
1 page
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9
Justice CM,
Yagnik G,
Kim Y,
Peter I,
Jabs EW,
Erazo M,
Ye X,
Ainehsazan E,
Shi L,
Cunningham ML,
Kimonis V,
Roscioli T
and 21 more — show all
Wall SA,
Wilkie AO,
Stoler J,
Richtsmeier JT,
Heuzé Y,
Sanchez-Lara PA,
Buckley MF,
Druschel CM,
Mills JL,
Caggana M,
Romitti PA,
Kay DM,
Senders C,
Taub PJ,
Klein OD,
Boggan J,
Zwienenberg-Lee M,
Naydenov C,
Kim J,
Wilson AF,
Boyadjiev SA
Nature genetics · 2012 · PMID 23160099
1 page
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association
Desch KC,
Ozel AB,
Siemieniak D,
Kalish Y,
Shavit JA,
Thornburg CD,
Sharathkumar AA,
McHugh CP,
Laurie CC,
Crenshaw A,
Mirel DB,
Kim Y
and 10 more — show all
Proceedings of the National Academy of Sciences of the United States of America · 2013 · PMID 23267103
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.