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.
1 match for
Van Den Berg D.
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
Haiman CA,
Chen GK,
Vachon CM,
Canzian F,
Dunning A,
Millikan RC,
Wang X,
Ademuyiwa F,
Ahmed S,
Ambrosone CB,
Baglietto L,
Balleine R
and 119 more — show all
Bandera EV,
Beckmann MW,
Berg CD,
Bernstein L,
Blomqvist C,
Blot WJ,
Brauch H,
Buring JE,
Carey LA,
Carpenter JE,
Chang-Claude J,
Chanock SJ,
Chasman DI,
Clarke CL,
Cox A,
Cross SS,
Deming SL,
Diasio RB,
Dimopoulos AM,
Driver WR,
Dünnebier T,
Durcan L,
Eccles D,
Edlund CK,
Ekici AB,
Fasching PA,
Feigelson HS,
Flesch-Janys D,
Fostira F,
Försti A,
Fountzilas G,
Gerty SM,
Giles GG,
Godwin AK,
Goodfellow P,
Graham N,
Greco D,
Hamann U,
Hankinson SE,
Hartmann A,
Hein R,
Heinz J,
Holbrook A,
Hoover RN,
Hu JJ,
Hunter DJ,
Ingles SA,
Irwanto A,
Ivanovich J,
John EM,
Johnson N,
Jukkola-Vuorinen A,
Kaaks R,
Ko YD,
Kolonel LN,
Konstantopoulou I,
Kosma VM,
Kulkarni S,
Lambrechts D,
Lee AM,
Marchand LL,
Lesnick T,
Liu J,
Lindstrom S,
Mannermaa A,
Margolin S,
Martin NG,
Miron P,
Montgomery GW,
Nevanlinna H,
Nickels S,
Nyante S,
Olswold C,
Palmer J,
Pathak H,
Pectasides D,
Perou CM,
Peto J,
Pharoah PD,
Pooler LC,
Press MF,
Pylkäs K,
Rebbeck TR,
Rodriguez-Gil JL,
Rosenberg L,
Ross E,
Rüdiger T,
Silva Idos S,
Sawyer E,
Schmidt MK,
Schulz-Wendtland R,
Schumacher F,
Severi G,
Sheng X,
Signorello LB,
Sinn HP,
Stevens KN,
Southey MC,
Tapper WJ,
Tomlinson I,
Hogervorst FB,
Wauters E,
Weaver J,
Wildiers H,
Winqvist R,
Van Den Berg D,
Wan P,
Xia LY,
Yannoukakos D,
Zheng W,
Zheng W,
Ziegler RG,
Siddiq A,
Slager SL,
Stram DO,
Easton D,
Kraft P,
Henderson BE,
Couch FJ
Gene Environment Interaction and Breast Cancer in Germany (GENICA) Consortium
Nature genetics · 2011 · PMID 22037553
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.