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2,675 papers hold this site up. Every variant and condition page names
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26 matches for
Canzian F,
showing the first 6.
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21
Tenesa A,
Farrington SM,
Prendergast JG,
Porteous ME,
Walker M,
Haq N,
Barnetson RA,
Theodoratou E,
Cetnarskyj R,
Cartwright N,
Semple C,
Clark AJ
and 45 more — show all
Reid FJ,
Smith LA,
Kavoussanakis K,
Koessler T,
Pharoah PD,
Buch S,
Schafmayer C,
Tepel J,
Schreiber S,
Völzke H,
Schmidt CO,
Hampe J,
Chang-Claude J,
Hoffmeister M,
Brenner H,
Wilkening S,
Canzian F,
Capella G,
Moreno V,
Deary IJ,
Starr JM,
Tomlinson IP,
Kemp Z,
Howarth K,
Carvajal-Carmona L,
Webb E,
Broderick P,
Vijayakrishnan J,
Houlston RS,
Rennert G,
Ballinger D,
Rozek L,
Gruber SB,
Matsuda K,
Kidokoro T,
Nakamura Y,
Zanke BW,
Greenwood CM,
Rangrej J,
Kustra R,
Montpetit A,
Hudson TJ,
Gallinger S,
Campbell H,
Dunlop MG
Nature genetics · 2008 · PMID 18372901
1 page
Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study
Kote-Jarai Z,
Olama AA,
Giles GG,
Severi G,
Schleutker J,
Weischer M,
Campa D,
Riboli E,
Key T,
Gronberg H,
Hunter DJ,
Kraft P
and 119 more — show all
Thun MJ,
Ingles S,
Chanock S,
Albanes D,
Hayes RB,
Neal DE,
Hamdy FC,
Donovan JL,
Pharoah P,
Schumacher F,
Henderson BE,
Stanford JL,
Ostrander EA,
Sorensen KD,
Dörk T,
Andriole G,
Dickinson JL,
Cybulski C,
Lubinski J,
Spurdle A,
Clements JA,
Chambers S,
Aitken J,
Gardiner RA,
Thibodeau SN,
Schaid D,
John EM,
Maier C,
Vogel W,
Cooney KA,
Park JY,
Cannon-Albright L,
Brenner H,
Habuchi T,
Zhang HW,
Lu YJ,
Kaneva R,
Muir K,
Benlloch S,
Leongamornlert DA,
Saunders EJ,
Tymrakiewicz M,
Mahmud N,
Guy M,
O'Brien LT,
Wilkinson RA,
Hall AL,
Sawyer EJ,
Dadaev T,
Morrison J,
Dearnaley DP,
Horwich A,
Huddart RA,
Khoo VS,
Parker CC,
Van As N,
Woodhouse CJ,
Thompson A,
Christmas T,
Ogden C,
Cooper CS,
Lophatonanon A,
Southey MC,
Hopper JL,
English DR,
Wahlfors T,
Tammela TL,
Klarskov P,
Nordestgaard BG,
Røder MA,
Tybjærg-Hansen A,
Bojesen SE,
Travis R,
Canzian F,
Kaaks R,
Wiklund F,
Aly M,
Lindstrom S,
Diver WR,
Gapstur S,
Stern MC,
Corral R,
Virtamo J,
Cox A,
Haiman CA,
Le Marchand L,
Fitzgerald L,
Kolb S,
Kwon EM,
Karyadi DM,
Orntoft TF,
Borre M,
Meyer A,
Serth J,
Yeager M,
Berndt SI,
Marthick JR,
Patterson B,
Wokolorczyk D,
Batra J,
Lose F,
McDonnell SK,
Joshi AD,
Shahabi A,
Rinckleb AE,
Ray A,
Sellers TA,
Lin HY,
Stephenson RA,
Farnham J,
Muller H,
Rothenbacher D,
Tsuchiya N,
Narita S,
Cao GW,
Slavov C,
Mitev V,
Easton DF,
Eeles RA
UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons' Section of Oncology · UK ProtecT Study Collaborators, The Australian Prostate Cancer BioResource and 1 more consortia
Nature genetics · 2011 · PMID 21743467
1 page
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
A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease
Amin Al Olama A,
Kote-Jarai Z,
Schumacher FR,
Wiklund F,
Berndt SI,
Benlloch S,
Giles GG,
Severi G,
Neal DE,
Hamdy FC,
Donovan JL,
Hunter DJ
and 135 more — show all
Henderson BE,
Thun MJ,
Gaziano M,
Giovannucci EL,
Siddiq A,
Travis RC,
Cox DG,
Canzian F,
Riboli E,
Key TJ,
Andriole G,
Albanes D,
Hayes RB,
Schleutker J,
Auvinen A,
Tammela TL,
Weischer M,
Stanford JL,
Ostrander EA,
Cybulski C,
Lubinski J,
Thibodeau SN,
Schaid DJ,
Sorensen KD,
Batra J,
Clements JA,
Chambers S,
Aitken J,
Gardiner RA,
Maier C,
Vogel W,
Dörk T,
Brenner H,
Habuchi T,
Ingles S,
John EM,
Dickinson JL,
Cannon-Albright L,
Teixeira MR,
Kaneva R,
Zhang HW,
Lu YJ,
Park JY,
Cooney KA,
Muir KR,
Leongamornlert DA,
Saunders E,
Tymrakiewicz M,
Mahmud N,
Guy M,
Govindasami K,
O'Brien LT,
Wilkinson RA,
Hall AL,
Sawyer EJ,
Dadaev T,
Morrison J,
Dearnaley DP,
Horwich A,
Huddart RA,
Khoo VS,
Parker CC,
Van As N,
Woodhouse CJ,
Thompson A,
Dudderidge T,
Ogden C,
Cooper CS,
Lophatonanon A,
Southey MC,
Hopper JL,
English D,
Virtamo J,
Le Marchand L,
Campa D,
Kaaks R,
Lindstrom S,
Diver WR,
Gapstur S,
Yeager M,
Cox A,
Stern MC,
Corral R,
Aly M,
Isaacs W,
Adolfsson J,
Xu J,
Zheng SL,
Wahlfors T,
Taari K,
Kujala P,
Klarskov P,
Nordestgaard BG,
Røder MA,
Frikke-Schmidt R,
Bojesen SE,
FitzGerald LM,
Kolb S,
Kwon EM,
Karyadi DM,
Orntoft TF,
Borre M,
Rinckleb A,
Luedeke M,
Herkommer K,
Meyer A,
Serth J,
Marthick JR,
Patterson B,
Wokolorczyk D,
Spurdle A,
Lose F,
McDonnell SK,
Joshi AD,
Shahabi A,
Pinto P,
Santos J,
Ray A,
Sellers TA,
Lin HY,
Stephenson RA,
Teerlink C,
Muller H,
Rothenbacher D,
Tsuchiya N,
Narita S,
Cao GW,
Slavov C,
Mitev V,
Chanock S,
Gronberg H,
Haiman CA,
Kraft P,
Easton DF,
Eeles RA
UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons' Section of Oncology · UK ProtecT Study Collaborators and 2 more consortia
Human molecular genetics · 2013 · PMID 23065704
1 page
Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients
Ziv E,
Dean E,
Hu D,
Martino A,
Serie D,
Curtin K,
Campa D,
Aftab B,
Bracci P,
Buda G,
Zhao Y,
Caswell-Jin J
and 27 more — show all
Diasio R,
Dumontet C,
Dudziński M,
Fejerman L,
Greenberg A,
Huntsman S,
Jamroziak K,
Jurczyszyn A,
Kumar S,
Atanackovic D,
Glenn M,
Cannon-Albright LA,
Jones B,
Lee A,
Marques H,
Martin T,
Martinez-Lopez J,
Martinez-Lopez J,
Rajkumar V,
Sainz J,
Vangsted AJ,
Wątek M,
Wolf J,
Slager S,
Camp NJ,
Canzian F,
Vachon C
Nature communications · 2015 · PMID 26198393
1 page
Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia
McMaster ML,
Berndt SI,
Zhang J,
Slager SL,
Li SA,
Vajdic CM,
Smedby KE,
Yan H,
Birmann BM,
Brown EE,
Smith A,
Kleinstern G
and 69 more — show all
Fansler MM,
Mayr C,
Zhu B,
Chung CC,
Park JH,
Burdette L,
Hicks BD,
Hutchinson A,
Teras LR,
Adami HO,
Bracci PM,
McKay J,
Monnereau A,
Link BK,
Vermeulen RCH,
Ansell SM,
Maria A,
Diver WR,
Melbye M,
Ojesina AI,
Kraft P,
Boffetta P,
Clavel J,
Giovannucci E,
Besson CM,
Canzian F,
Travis RC,
Vineis P,
Weiderpass E,
Montalvan R,
Wang Z,
Yeager M,
Becker N,
Benavente Y,
Brennan P,
Foretova L,
Maynadie M,
Nieters A,
de Sanjose S,
Staines A,
Conde L,
Riby J,
Glimelius B,
Hjalgrim H,
Pradhan N,
Feldman AL,
Novak AJ,
Lawrence C,
Bassig BA,
Lan Q,
Zheng T,
North KE,
Tinker LF,
Cozen W,
Severson RK,
Hofmann JN,
Zhang Y,
Jackson RD,
Morton LM,
Purdue MP,
Chatterjee N,
Offit K,
Cerhan JR,
Chanock SJ,
Rothman N,
Vijai J,
Goldin LR,
Skibola CF,
Caporaso NE
Nature communications · 2018 · PMID 30305637 · open access
1 page
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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
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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.