For researchers
Is your paper here?
2,660 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.
2 matches for
Rajkovic A.
Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer
Amundadottir L,
Kraft P,
Stolzenberg-Solomon RZ,
Fuchs CS,
Petersen GM,
Arslan AA,
Bueno-de-Mesquita HB,
Gross M,
Helzlsouer K,
Jacobs EJ,
LaCroix A,
Zheng W
and 60 more — show all
Zheng W,
Albanes D,
Bamlet W,
Berg CD,
Berrino F,
Bingham S,
Buring JE,
Bracci PM,
Canzian F,
Clavel-Chapelon F,
Clipp S,
Cotterchio M,
de Andrade M,
Duell EJ,
Fox JW Jr,
Gallinger S,
Gaziano JM,
Giovannucci EL,
Goggins M,
González CA,
Hallmans G,
Hankinson SE,
Hassan M,
Holly EA,
Hunter DJ,
Hutchinson A,
Jackson R,
Jacobs KB,
Jenab M,
Kaaks R,
Klein AP,
Kooperberg C,
Kurtz RC,
Li D,
Lynch SM,
Mandelson M,
McWilliams RR,
Mendelsohn JB,
Michaud DS,
Olson SH,
Overvad K,
Patel AV,
Peeters PH,
Rajkovic A,
Riboli E,
Risch HA,
Shu XO,
Thomas G,
Tobias GS,
Trichopoulos D,
Van Den Eeden SK,
Virtamo J,
Wactawski-Wende J,
Wolpin BM,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Chanock SJ,
Hartge P,
Hoover RN
Nature genetics · 2009 · PMID 19648918
3 pages
Genome-wide association study of age at menarche in African-American women
Demerath EW,
Liu CT,
Franceschini N,
Chen G,
Palmer JR,
Smith EN,
Chen CT,
Ambrosone CB,
Arnold AM,
Bandera EV,
Berenson GS,
Bernstein L
and 45 more — show all
Britton A,
Cappola AR,
Carlson CS,
Chanock SJ,
Chen W,
Chen Z,
Deming SL,
Elks CE,
Evans MK,
Gajdos Z,
Henderson BE,
Hu JJ,
Ingles S,
John EM,
Kerr KF,
Kolonel LN,
Le Marchand L,
Lu X,
Millikan RC,
Musani SK,
Nock NL,
North K,
Nyante S,
Press MF,
Rodriquez-Gil JL,
Ruiz-Narvaez EA,
Schork NJ,
Srinivasan SR,
Woods NF,
Zheng W,
Zheng W,
Ziegler RG,
Zonderman A,
Heiss G,
Gwen Windham B,
Wellons M,
Murray SS,
Nalls M,
Pastinen T,
Rajkovic A,
Hirschhorn J,
Adrienne Cupples L,
Kooperberg C,
Murabito JM,
Haiman CA
Human molecular genetics · 2013 · PMID 23599027
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.