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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.
6 matches for
Clavel-Chapelon F.
Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma
Postel-Vinay S,
Véron AS,
Tirode F,
Pierron G,
Reynaud S,
Kovar H,
Oberlin O,
Lapouble E,
Ballet S,
Lucchesi C,
Kontny U,
González-Neira A
and 14 more — show all
Picci P,
Alonso J,
Patino-Garcia A,
de Paillerets BB,
Laud K,
Dina C,
Froguel P,
Clavel-Chapelon F,
Doz F,
Michon J,
Chanock SJ,
Thomas G,
Cox DG,
Delattre O
Nature genetics · 2012 · PMID 22327514
4 pages
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
A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25
Hung RJ,
McKay JD,
Gaborieau V,
Boffetta P,
Hashibe M,
Zaridze D,
Mukeria A,
Szeszenia-Dabrowska N,
Lissowska J,
Rudnai P,
Fabianova E,
Mates D
and 53 more — show all
Bencko V,
Foretova L,
Janout V,
Chen C,
Goodman G,
Field JK,
Liloglou T,
Xinarianos G,
Cassidy A,
McLaughlin J,
Liu G,
Narod S,
Krokan HE,
Skorpen F,
Elvestad MB,
Hveem K,
Vatten L,
Linseisen J,
Clavel-Chapelon F,
Vineis P,
Bueno-de-Mesquita HB,
Lund E,
Martinez C,
Bingham S,
Rasmuson T,
Hainaut P,
Riboli E,
Ahrens W,
Benhamou S,
Lagiou P,
Trichopoulos D,
Holcátová I,
Merletti F,
Kjaerheim K,
Agudo A,
Macfarlane G,
Talamini R,
Simonato L,
Lowry R,
Conway DI,
Znaor A,
Healy C,
Zelenika D,
Boland A,
Delepine M,
Foglio M,
Lechner D,
Matsuda F,
Blanche H,
Gut I,
Heath S,
Lathrop M,
Brennan P
Nature · 2008 · PMID 18385738
2 pages
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
Rothman N,
Garcia-Closas M,
Chatterjee N,
Malats N,
Wu X,
Figueroa JD,
Real FX,
Van Den Berg D,
Matullo G,
Baris D,
Thun M,
Kiemeney LA
and 98 more — show all
Vineis P,
De Vivo I,
Albanes D,
Purdue MP,
Rafnar T,
Hildebrandt MA,
Kiltie AE,
Cussenot O,
Golka K,
Kumar R,
Taylor JA,
Mayordomo JI,
Jacobs KB,
Kogevinas M,
Hutchinson A,
Wang Z,
Fu YP,
Prokunina-Olsson L,
Burdett L,
Yeager M,
Wheeler W,
Tardón A,
Serra C,
Carrato A,
García-Closas R,
Lloreta J,
Johnson A,
Schwenn M,
Karagas MR,
Schned A,
Andriole G Jr,
Grubb R 3rd,
Black A,
Jacobs EJ,
Diver WR,
Gapstur SM,
Weinstein SJ,
Virtamo J,
Cortessis VK,
Gago-Dominguez M,
Pike MC,
Stern MC,
Yuan JM,
Hunter DJ,
McGrath M,
Dinney CP,
Czerniak B,
Chen M,
Yang H,
Vermeulen SH,
Aben KK,
Witjes JA,
Makkinje RR,
Sulem P,
Besenbacher S,
Stefansson K,
Riboli E,
Brennan P,
Panico S,
Navarro C,
Allen NE,
Bueno-de-Mesquita HB,
Trichopoulos D,
Caporaso N,
Landi MT,
Canzian F,
Ljungberg B,
Tjonneland A,
Clavel-Chapelon F,
Bishop DT,
Teo MT,
Knowles MA,
Guarrera S,
Polidoro S,
Ricceri F,
Sacerdote C,
Allione A,
Cancel-Tassin G,
Selinski S,
Hengstler JG,
Dietrich H,
Fletcher T,
Rudnai P,
Gurzau E,
Koppova K,
Bolick SC,
Godfrey A,
Xu Z,
Sanz-Velez JI,
D García-Prats M,
Sanchez M,
Valdivia G,
Porru S,
Benhamou S,
Hoover RN,
Fraumeni JF Jr,
Silverman DT,
Chanock SJ
Nature genetics · 2010 · PMID 20972438 · open access
2 pages
A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11
Siddiq A,
Couch FJ,
Chen GK,
Lindström S,
Eccles D,
Millikan RC,
Michailidou K,
Stram DO,
Beckmann L,
Rhie SK,
Ambrosone CB,
Aittomäki K
and 129 more — show all
Amiano P,
Apicella C,
Baglietto L,
Bandera EV,
Beckmann MW,
Berg CD,
Bernstein L,
Blomqvist C,
Brauch H,
Brinton L,
Bui QM,
Buring JE,
Buys SS,
Campa D,
Carpenter JE,
Chasman DI,
Chang-Claude J,
Chen C,
Clavel-Chapelon F,
Cox A,
Cross SS,
Czene K,
Deming SL,
Diasio RB,
Diver WR,
Dunning AM,
Durcan L,
Ekici AB,
Fasching PA,
Feigelson HS,
Fejerman L,
Figueroa JD,
Fletcher O,
Flesch-Janys D,
Gaudet MM,
Gerty SM,
Rodriguez-Gil JL,
Giles GG,
van Gils CH,
Godwin AK,
Graham N,
Greco D,
Hall P,
Hankinson SE,
Hartmann A,
Hein R,
Heinz J,
Hoover RN,
Hopper JL,
Hu JJ,
Huntsman S,
Ingles SA,
Irwanto A,
Isaacs C,
Jacobs KB,
John EM,
Justenhoven C,
Kaaks R,
Kolonel LN,
Coetzee GA,
Lathrop M,
Le Marchand L,
Lee AM,
Lee IM,
Lesnick T,
Lichtner P,
Liu J,
Lund E,
Makalic E,
Martin NG,
McLean CA,
Meijers-Heijboer H,
Meindl A,
Miron P,
Monroe KR,
Montgomery GW,
Müller-Myhsok B,
Nickels S,
Nyante SJ,
Olswold C,
Overvad K,
Palli D,
Park DJ,
Palmer JR,
Pathak H,
Peto J,
Pharoah P,
Rahman N,
Rivadeneira F,
Schmidt DF,
Schmutzler RK,
Slager S,
Southey MC,
Stevens KN,
Sinn HP,
Press MF,
Ross E,
Riboli E,
Ridker PM,
Schumacher FR,
Severi G,
Dos Santos Silva I,
Stone J,
Sund M,
Tapper WJ,
Thun MJ,
Travis RC,
Turnbull C,
Uitterlinden AG,
Waisfisz Q,
Wang X,
Wang Z,
Weaver J,
Schulz-Wendtland R,
Wilkens LR,
Van Den Berg D,
Zheng W,
Zheng W,
Ziegler RG,
Ziv E,
Nevanlinna H,
Easton DF,
Hunter DJ,
Henderson BE,
Chanock SJ,
Garcia-Closas M,
Kraft P,
Haiman CA,
Vachon CM
Australian Breast Cancer Tissue Bank Investigators · Familial Breast Cancer Study and 1 more consortia
Human molecular genetics · 2012 · PMID 22976474
1 page
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer
Wang Y,
McKay JD,
Rafnar T,
Wang Z,
Timofeeva MN,
Broderick P,
Zong X,
Laplana M,
Wei Y,
Han Y,
Lloyd A,
Delahaye-Sourdeix M
and 71 more — show all
Chubb D,
Gaborieau V,
Wheeler W,
Chatterjee N,
Thorleifsson G,
Sulem P,
Liu G,
Kaaks R,
Henrion M,
Kinnersley B,
Vallée M,
LeCalvez-Kelm F,
Stevens VL,
Gapstur SM,
Chen WV,
Zaridze D,
Szeszenia-Dabrowska N,
Lissowska J,
Rudnai P,
Fabianova E,
Mates D,
Bencko V,
Foretova L,
Janout V,
Krokan HE,
Gabrielsen ME,
Skorpen F,
Vatten L,
Njølstad I,
Chen C,
Goodman G,
Benhamou S,
Vooder T,
Välk K,
Nelis M,
Metspalu A,
Lener M,
Lubiński J,
Johansson M,
Vineis P,
Agudo A,
Clavel-Chapelon F,
Bueno-de-Mesquita HB,
Trichopoulos D,
Khaw KT,
Johansson M,
Weiderpass E,
Tjønneland A,
Riboli E,
Lathrop M,
Scelo G,
Albanes D,
Caporaso NE,
Ye Y,
Gu J,
Wu X,
Spitz MR,
Dienemann H,
Rosenberger A,
Su L,
Matakidou A,
Eisen T,
Stefansson K,
Risch A,
Chanock SJ,
Christiani DC,
Hung RJ,
Brennan P,
Landi MT,
Houlston RS,
Amos CI
Nature genetics · 2014 · PMID 24880342 · open access
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.