For researchers
Is your paper here?
2,665 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.
38 matches for
Dunning A,
showing the first 18.
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Milne RL,
Kuchenbaecker KB,
Michailidou K,
Beesley J,
Kar S,
Lindström S,
Hui S,
Lemaçon A,
Soucy P,
Dennis J,
Jiang X,
Rostamianfar A
and 458 more — show all
Finucane H,
Bolla MK,
McGuffog L,
Wang Q,
Aalfs CM,
Adams M,
Adlard J,
Agata S,
Ahmed S,
Ahsan H,
Aittomäki K,
Al-Ejeh F,
Allen J,
Ambrosone CB,
Amos CI,
Andrulis IL,
Anton-Culver H,
Antonenkova NN,
Arndt V,
Arnold N,
Aronson KJ,
Auber B,
Auer PL,
Ausems MGEM,
Azzollini J,
Bacot F,
Balmaña J,
Barile M,
Barjhoux L,
Barkardottir RB,
Barrdahl M,
Barnes D,
Barrowdale D,
Baynes C,
Beckmann MW,
Benitez J,
Bermisheva M,
Bernstein L,
Bignon YJ,
Blazer KR,
Blok MJ,
Blomqvist C,
Blot W,
Bobolis K,
Boeckx B,
Bogdanova NV,
Bojesen A,
Bojesen SE,
Bonanni B,
Børresen-Dale AL,
Bozsik A,
Bradbury AR,
Brand JS,
Brauch H,
Brenner H,
Bressac-de Paillerets B,
Brewer C,
Brinton L,
Broberg P,
Brooks-Wilson A,
Brunet J,
Brüning T,
Burwinkel B,
Buys SS,
Byun J,
Cai Q,
Caldés T,
Caligo MA,
Campbell I,
Canzian F,
Caron O,
Carracedo A,
Carter BD,
Castelao JE,
Castera L,
Caux-Moncoutier V,
Chan SB,
Chang-Claude J,
Chanock SJ,
Chen X,
Cheng TD,
Chiquette J,
Christiansen H,
Claes KBM,
Clarke CL,
Conner T,
Conroy DM,
Cook J,
Cordina-Duverger E,
Cornelissen S,
Coupier I,
Cox A,
Cox DG,
Cross SS,
Cuk K,
Cunningham JM,
Czene K,
Daly MB,
Damiola F,
Darabi H,
Davidson R,
De Leeneer K,
Devilee P,
Dicks E,
Diez O,
Ding YC,
Ditsch N,
Doheny KF,
Domchek SM,
Dorfling CM,
Dörk T,
Dos-Santos-Silva I,
Dubois S,
Dugué PA,
Dumont M,
Dunning AM,
Durcan L,
Dwek M,
Dworniczak B,
Eccles D,
Eeles R,
Ehrencrona H,
Eilber U,
Ejlertsen B,
Ekici AB,
Eliassen AH,
Engel C,
Eriksson M,
Fachal L,
Faivre L,
Fasching PA,
Faust U,
Figueroa J,
Flesch-Janys D,
Fletcher O,
Flyger H,
Foulkes WD,
Friedman E,
Fritschi L,
Frost D,
Gabrielson M,
Gaddam P,
Gammon MD,
Ganz PA,
Gapstur SM,
Garber J,
Garcia-Barberan V,
García-Sáenz JA,
Gaudet MM,
Gauthier-Villars M,
Gehrig A,
Georgoulias V,
Gerdes AM,
Giles GG,
Glendon G,
Godwin AK,
Goldberg MS,
Goldgar DE,
González-Neira A,
Goodfellow P,
Greene MH,
Alnæs GIG,
Grip M,
Gronwald J,
Grundy A,
Gschwantler-Kaulich D,
Guénel P,
Guo Q,
Haeberle L,
Hahnen E,
Haiman CA,
Håkansson N,
Hallberg E,
Hamann U,
Hamel N,
Hankinson S,
Hansen TVO,
Harrington P,
Hart SN,
Hartikainen JM,
Healey CS,
Hein A,
Helbig S,
Henderson A,
Heyworth J,
Hicks B,
Hillemanns P,
Hodgson S,
Hogervorst FB,
Hollestelle A,
Hooning MJ,
Hoover B,
Hopper JL,
Hu C,
Huang G,
Hulick PJ,
Humphreys K,
Hunter DJ,
Imyanitov EN,
Isaacs C,
Iwasaki M,
Izatt L,
Jakubowska A,
James P,
Janavicius R,
Janni W,
Jensen UB,
John EM,
Johnson N,
Jones K,
Jones M,
Jukkola-Vuorinen A,
Kaaks R,
Kabisch M,
Kaczmarek K,
Kang D,
Kast K,
Keeman R,
Kerin MJ,
Kets CM,
Keupers M,
Khan S,
Khusnutdinova E,
Kiiski JI,
Kim SW,
Knight JA,
Konstantopoulou I,
Kosma VM,
Kristensen VN,
Kruse TA,
Kwong A,
Lænkholm AV,
Laitman Y,
Lalloo F,
Lambrechts D,
Landsman K,
Lasset C,
Lazaro C,
Le Marchand L,
Lecarpentier J,
Lee A,
Lee E,
Lee JW,
Lee MH,
Lejbkowicz F,
Lesueur F,
Li J,
Lilyquist J,
Lincoln A,
Lindblom A,
Lissowska J,
Lo WY,
Loibl S,
Long J,
Loud JT,
Lubinski J,
Luccarini C,
Lush M,
MacInnis RJ,
Maishman T,
Makalic E,
Kostovska IM,
Malone KE,
Manoukian S,
Manson JE,
Margolin S,
Martens JWM,
Martinez ME,
Matsuo K,
Mavroudis D,
Mazoyer S,
McLean C,
Meijers-Heijboer H,
Menéndez P,
Meyer J,
Miao H,
Miller A,
Miller N,
Mitchell G,
Montagna M,
Muir K,
Mulligan AM,
Mulot C,
Nadesan S,
Nathanson KL,
Neuhausen SL,
Nevanlinna H,
Nevelsteen I,
Niederacher D,
Nielsen SF,
Nordestgaard BG,
Norman A,
Nussbaum RL,
Olah E,
Olopade OI,
Olson JE,
Olswold C,
Ong KR,
Oosterwijk JC,
Orr N,
Osorio A,
Pankratz VS,
Papi L,
Park-Simon TW,
Paulsson-Karlsson Y,
Lloyd R,
Pedersen IS,
Peissel B,
Peixoto A,
Perez JIA,
Peterlongo P,
Peto J,
Pfeiler G,
Phelan CM,
Pinchev M,
Plaseska-Karanfilska D,
Poppe B,
Porteous ME,
Prentice R,
Presneau N,
Prokofieva D,
Pugh E,
Pujana MA,
Pylkäs K,
Rack B,
Radice P,
Rahman N,
Rantala J,
Rappaport-Fuerhauser C,
Rennert G,
Rennert HS,
Rhenius V,
Rhiem K,
Richardson A,
Rodriguez GC,
Romero A,
Romm J,
Rookus MA,
Rudolph A,
Ruediger T,
Saloustros E,
Sanders J,
Sandler DP,
Sangrajrang S,
Sawyer EJ,
Schmidt DF,
Schoemaker MJ,
Schumacher F,
Schürmann P,
Schwentner L,
Scott C,
Scott RJ,
Seal S,
Senter L,
Seynaeve C,
Shah M,
Sharma P,
Shen CY,
Sheng X,
Shimelis H,
Shrubsole MJ,
Shu XO,
Side LE,
Singer CF,
Sohn C,
Southey MC,
Spinelli JJ,
Spurdle AB,
Stegmaier C,
Stoppa-Lyonnet D,
Sukiennicki G,
Surowy H,
Sutter C,
Swerdlow A,
Szabo CI,
Tamimi RM,
Tan YY,
Taylor JA,
Tejada MI,
Tengström M,
Teo SH,
Terry MB,
Tessier DC,
Teulé A,
Thöne K,
Thull DL,
Tibiletti MG,
Tihomirova L,
Tischkowitz M,
Toland AE,
Tollenaar RAEM,
Tomlinson I,
Tong L,
Torres D,
Tranchant M,
Truong T,
Tucker K,
Tung N,
Tyrer J,
Ulmer HU,
Vachon C,
van Asperen CJ,
Van Den Berg D,
van den Ouweland AMW,
van Rensburg EJ,
Varesco L,
Varon-Mateeva R,
Vega A,
Viel A,
Vijai J,
Vincent D,
Vollenweider J,
Walker L,
Wang Z,
Wang-Gohrke S,
Wappenschmidt B,
Weinberg CR,
Weitzel JN,
Wendt C,
Wesseling J,
Whittemore AS,
Wijnen JT,
Willett W,
Winqvist R,
Wolk A,
Wu AH,
Xia L,
Yang XR,
Yannoukakos D,
Zaffaroni D,
Zheng W,
Zhu B,
Ziogas A,
Ziv E,
Zorn KK,
Gago-Dominguez M,
Mannermaa A,
Olsson H,
Teixeira MR,
Stone J,
Offit K,
Ottini L,
Park SK,
Thomassen M,
Hall P,
Meindl A,
Schmutzler RK,
Droit A,
Bader GD,
Pharoah PDP,
Couch FJ,
Easton DF,
Kraft P,
Chenevix-Trench G,
García-Closas M,
Schmidt MK,
Antoniou AC,
Simard J
ABCTB Investigators · EMBRACE and 4 more consortia
Nature genetics · 2017 · PMID 29058716
5 pages
Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma
Went M,
Sud A,
Försti A,
Halvarsson BM,
Weinhold N,
Kimber S,
van Duin M,
Thorleifsson G,
Holroyd A,
Johnson DC,
Johnson DC,
Li N
and 58 more — show all
Orlando G,
Law PJ,
Ali M,
Chen B,
Mitchell JS,
Gudbjartsson DF,
Kuiper R,
Stephens OW,
Bertsch U,
Broderick P,
Campo C,
Bandapalli OR,
Einsele H,
Gregory WA,
Gullberg U,
Hillengass J,
Hoffmann P,
Jackson GH,
Jöckel KH,
Johnsson E,
Kristinsson SY,
Mellqvist UH,
Nahi H,
Easton D,
Pharoah P,
Dunning A,
Peto J,
Canzian F,
Swerdlow A,
Eeles RA,
Kote-Jarai Z,
Muir K,
Pashayan N,
Nickel J,
Nöthen MM,
Rafnar T,
Ross FM,
da Silva Filho MI,
Thomsen H,
Turesson I,
Vangsted A,
Andersen NF,
Waage A,
Walker BA,
Wihlborg AK,
Broyl A,
Davies FE,
Thorsteinsdottir U,
Langer C,
Hansson M,
Goldschmidt H,
Kaiser M,
Sonneveld P,
Stefansson K,
Morgan GJ,
Hemminki K,
Nilsson B,
Houlston RS
PRACTICAL consortium
Nature communications · 2018 · PMID 30213928 · open access
5 pages
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Coignard J,
Lush M,
Beesley J,
O'Mara TA,
Dennis J,
Tyrer JP,
Barnes DR,
McGuffog L,
Leslie G,
Bolla MK,
Adank MA,
Agata S
and 207 more — show all
Ahearn T,
Aittomäki K,
Andrulis IL,
Anton-Culver H,
Arndt V,
Arnold N,
Aronson KJ,
Arun BK,
Augustinsson A,
Azzollini J,
Barrowdale D,
Baynes C,
Becher H,
Bermisheva M,
Bernstein L,
Białkowska K,
Blomqvist C,
Bojesen SE,
Bonanni B,
Borg A,
Brauch H,
Brenner H,
Burwinkel B,
Buys SS,
Caldés T,
Caligo MA,
Campa D,
Carter BD,
Castelao JE,
Chang-Claude J,
Chanock SJ,
Chung WK,
Claes KBM,
Clarke CL,
Collée JM,
Conroy DM,
Czene K,
Daly MB,
Devilee P,
Diez O,
Ding YC,
Domchek SM,
Dörk T,
Dos-Santos-Silva I,
Dunning AM,
Dwek M,
Eccles DM,
Eliassen AH,
Engel C,
Eriksson M,
Evans DG,
Fasching PA,
Flyger H,
Fostira F,
Friedman E,
Fritschi L,
Frost D,
Gago-Dominguez M,
Gapstur SM,
Garber J,
Garcia-Barberan V,
García-Closas M,
García-Sáenz JA,
Gaudet MM,
Gayther SA,
Gehrig A,
Georgoulias V,
Giles GG,
Godwin AK,
Goldberg MS,
Goldgar DE,
González-Neira A,
Greene MH,
Guénel P,
Haeberle L,
Hahnen E,
Haiman CA,
Håkansson N,
Hall P,
Hamann U,
Harrington PA,
Hart SN,
He W,
Hogervorst FBL,
Hollestelle A,
Hopper JL,
Horcasitas DJ,
Hulick PJ,
Hunter DJ,
Imyanitov EN,
Jager A,
Jakubowska A,
James PA,
Jensen UB,
John EM,
Jones ME,
Kaaks R,
Kapoor PM,
Karlan BY,
Keeman R,
Khusnutdinova E,
Kiiski JI,
Ko YD,
Kosma VM,
Kraft P,
Kurian AW,
Laitman Y,
Lambrechts D,
Le Marchand L,
Lester J,
Lesueur F,
Lindstrom T,
Lopez-Fernández A,
Loud JT,
Luccarini C,
Mannermaa A,
Manoukian S,
Margolin S,
Martens JWM,
Mebirouk N,
Meindl A,
Miller A,
Milne RL,
Montagna M,
Nathanson KL,
Neuhausen SL,
Nevanlinna H,
Nielsen FC,
O'Brien KM,
Olopade OI,
Olson JE,
Olsson H,
Osorio A,
Ottini L,
Park-Simon TW,
Parsons MT,
Pedersen IS,
Peshkin B,
Peterlongo P,
Peto J,
Pharoah PDP,
Phillips KA,
Polley EC,
Poppe B,
Presneau N,
Pujana MA,
Punie K,
Radice P,
Rantala J,
Rashid MU,
Rennert G,
Rennert HS,
Robson M,
Romero A,
Rossing M,
Saloustros E,
Sandler DP,
Santella R,
Scheuner MT,
Schmidt MK,
Schmidt G,
Scott C,
Sharma P,
Soucy P,
Southey MC,
Spinelli JJ,
Steinsnyder Z,
Stone J,
Stoppa-Lyonnet D,
Swerdlow A,
Tamimi RM,
Tapper WJ,
Taylor JA,
Terry MB,
Teulé A,
Thull DL,
Tischkowitz M,
Toland AE,
Torres D,
Trainer AH,
Truong T,
Tung N,
Vachon CM,
Vega A,
Vijai J,
Wang Q,
Wappenschmidt B,
Weinberg CR,
Weitzel JN,
Wendt C,
Wolk A,
Yadav S,
Yang XR,
Yannoukakos D,
Zheng W,
Ziogas A,
Zorn KK,
Park SK,
Thomassen M,
Offit K,
Schmutzler RK,
Couch FJ,
Simard J,
Chenevix-Trench G,
Easton DF,
Andrieu N,
Antoniou AC
GEMO Study Collaborators · EMBRACE Collaborators and 3 more consortia
Nature communications · 2021 · PMID 33597508 · open access
5 pages
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility
Sud A,
Thomsen H,
Law PJ,
Försti A,
Filho MIDS,
Holroyd A,
Broderick P,
Orlando G,
Lenive O,
Wright L,
Cooke R,
Easton D
and 23 more — show all
Pharoah P,
Dunning A,
Peto J,
Canzian F,
Eeles R,
Kote-Jarai Z,
Muir K,
Pashayan N,
Hoffmann P,
Nöthen MM,
Jöckel KH,
Strandmann EPV,
Lightfoot T,
Kane E,
Roman E,
Lake A,
Montgomery D,
Jarrett RF,
Swerdlow AJ,
Engert A,
Orr N,
Hemminki K,
Houlston RS
PRACTICAL consortium
Nature communications · 2017 · PMID 29196614 · open access
4 pages
Genome-wide association study identifies five new breast cancer susceptibility loci
Turnbull C,
Ahmed S,
Morrison J,
Pernet D,
Renwick A,
Maranian M,
Seal S,
Ghoussaini M,
Hines S,
Healey CS,
Hughes D,
Warren-Perry M
and 14 more — show all
Tapper W,
Eccles D,
Evans DG,
Hooning M,
Schutte M,
van den Ouweland A,
Houlston R,
Ross G,
Langford C,
Pharoah PD,
Stratton MR,
Dunning AM,
Rahman N,
Easton DF
Breast Cancer Susceptibility Collaboration (UK)
Nature genetics · 2010 · PMID 20453838
3 pages
Five endometrial cancer risk loci identified through genome-wide association analysis
Cheng TH,
Thompson DJ,
O'Mara TA,
Painter JN,
Glubb DM,
Flach S,
Lewis A,
French JD,
Freeman-Mills L,
Church D,
Gorman M,
Martin L
and 76 more — show all
Hodgson S,
Webb PM,
Attia J,
Holliday EG,
McEvoy M,
Scott RJ,
Henders AK,
Martin NG,
Montgomery GW,
Nyholt DR,
Ahmed S,
Healey CS,
Shah M,
Dennis J,
Fasching PA,
Beckmann MW,
Hein A,
Ekici AB,
Hall P,
Czene K,
Darabi H,
Li J,
Dörk T,
Dürst M,
Hillemanns P,
Runnebaum I,
Amant F,
Schrauwen S,
Zhao H,
Lambrechts D,
Depreeuw J,
Dowdy SC,
Goode EL,
Fridley BL,
Winham SJ,
Njølstad TS,
Salvesen HB,
Trovik J,
Werner HM,
Ashton K,
Otton G,
Proietto T,
Liu T,
Mints M,
Tham E,
Consortium C,
Jun Li M,
Yip SH,
Wang J,
Bolla MK,
Michailidou K,
Wang Q,
Tyrer JP,
Dunlop M,
Houlston R,
Palles C,
Hopper JL,
Peto J,
Swerdlow AJ,
Burwinkel B,
Brenner H,
Meindl A,
Brauch H,
Lindblom A,
Chang-Claude J,
Couch FJ,
Giles GG,
Kristensen VN,
Cox A,
Cunningham JM,
Pharoah PDP,
Dunning AM,
Edwards SL,
Easton DF,
Tomlinson I,
Spurdle AB
National Study of Endometrial Cancer Genetics Group (NSECG) · Australian National Endometrial Cancer Study Group (ANECS) and 2 more consortia
Nature genetics · 2016 · PMID 27135401 · open access
3 pages
Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses
Painter JN,
O'Mara TA,
Morris AP,
Cheng THT,
Gorman M,
Martin L,
Hodson S,
Jones A,
Martin NG,
Gordon S,
Henders AK,
Attia J
and 65 more — show all
McEvoy M,
Holliday EG,
Scott RJ,
Webb PM,
Fasching PA,
Beckmann MW,
Ekici AB,
Hein A,
Rübner M,
Hall P,
Czene K,
Dörk T,
Dürst M,
Hillemanns P,
Runnebaum I,
Lambrechts D,
Lambrechts D,
Amant F,
Annibali D,
Depreeuw J,
Vanderstichele A,
Goode EL,
Cunningham JM,
Dowdy SC,
Winham SJ,
Trovik J,
Hoivik E,
Werner HMJ,
Krakstad C,
Ashton K,
Otton G,
Proietto T,
Tham E,
Mints M,
Ahmed S,
Healey CS,
Shah M,
Pharoah PDP,
Dunning AM,
Dennis J,
Bolla MK,
Michailidou K,
Wang Q,
Tyrer JP,
Hopper JL,
Peto J,
Swerdlow AJ,
Burwinkel B,
Brenner H,
Meindl A,
Brauch H,
Lindblom A,
Chang-Claude J,
Couch FJ,
Giles GG,
Kristensen VN,
Cox A,
Zondervan KT,
Nyholt DR,
MacGregor S,
Montgomery GW,
Tomlinson I,
Easton DF,
Thompson DJ,
Spurdle AB
Cancer medicine · 2018 · PMID 29608257 · open access
3 pages
Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma
Sud A,
Thomsen H,
Orlando G,
Försti A,
Law PJ,
Broderick P,
Cooke R,
Hariri F,
Pastinen T,
Easton DF,
Pharoah PDP,
Dunning AM
and 17 more — show all
Peto J,
Canzian F,
Eeles R,
Kote-Jarai Z,
Muir K,
Pashayan N,
Campa D,
Hoffmann P,
Nöthen MM,
Jöckel KH,
von Strandmann EP,
Swerdlow AJ,
Engert A,
Orr N,
Orr N,
Hemminki K,
Houlston RS
PRACTICAL Consortium
Blood · 2018 · PMID 30194254
3 pages
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma
Law MH,
Bishop DT,
Lee JE,
Brossard M,
Martin NG,
Moses EK,
Song F,
Barrett JH,
Kumar R,
Easton DF,
Pharoah PDP,
Swerdlow AJ
and 63 more — show all
Kypreou KP,
Taylor JC,
Harland M,
Randerson-Moor J,
Akslen LA,
Andresen PA,
Avril MF,
Azizi E,
Scarrà GB,
Brown KM,
Dębniak T,
Duffy DL,
Elder DE,
Fang S,
Friedman E,
Galan P,
Ghiorzo P,
Gillanders EM,
Goldstein AM,
Gruis NA,
Hansson J,
Helsing P,
Hočevar M,
Höiom V,
Ingvar C,
Kanetsky PA,
Chen WV,
Landi MT,
Lang J,
Lathrop GM,
Lubiński J,
Mackie RM,
Mann GJ,
Molven A,
Montgomery GW,
Novaković S,
Olsson H,
Puig S,
Puig-Butille JA,
Qureshi AA,
Radford-Smith GL,
van der Stoep N,
van Doorn R,
Whiteman DC,
Craig JE,
Schadendorf D,
Simms LA,
Burdon KP,
Nyholt DR,
Pooley KA,
Orr N,
Stratigos AJ,
Cust AE,
Ward SV,
Hayward NK,
Han J,
Schulze HJ,
Dunning AM,
Bishop JAN,
Demenais F,
Amos CI,
MacGregor S,
Iles MM
GenoMEL Consortium · Essen-Heidelberg Investigators and 4 more consortia
Nature genetics · 2015 · PMID 26237428 · open access
2 pages
Radiogenomics Consortium Genome-Wide Association Study Meta-Analysis of Late Toxicity After Prostate Cancer Radiotherapy
Kerns SL,
Fachal L,
Dorling L,
Barnett GC,
Baran A,
Peterson DR,
Hollenberg M,
Hao K,
Narzo AD,
Ahsen ME,
Pandey G,
Bentzen SM
and 28 more — show all
Janelsins M,
Elliott RM,
Pharoah PDP,
Burnet NG,
Dearnaley DP,
Gulliford SL,
Hall E,
Sydes MR,
Aguado-Barrera ME,
Gómez-Caamaño A,
Carballo AM,
Peleteiro P,
Lobato-Busto R,
Stock R,
Stone NN,
Ostrer H,
Usmani N,
Singhal S,
Tsuji H,
Imai T,
Saito S,
Eeles R,
DeRuyck K,
Parliament M,
Dunning AM,
Vega A,
Rosenstein BS,
West CML
Journal of the National Cancer Institute · 2020 · PMID 31095341 · open access
2 pages
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Zhang H,
Ahearn TU,
Lecarpentier J,
Barnes D,
Beesley J,
Qi G,
Jiang X,
O'Mara TA,
Zhao N,
Bolla MK,
Dunning AM,
Dennis J
and 261 more — show all
Wang Q,
Ful ZA,
Aittomäki K,
Andrulis IL,
Anton-Culver H,
Arndt V,
Aronson KJ,
Arun BK,
Auer PL,
Azzollini J,
Barrowdale D,
Becher H,
Beckmann MW,
Behrens S,
Benitez J,
Bermisheva M,
Bialkowska K,
Blanco A,
Blomqvist C,
Bogdanova NV,
Bojesen SE,
Bonanni B,
Bondavalli D,
Borg A,
Brauch H,
Brenner H,
Briceno I,
Broeks A,
Brucker SY,
Brüning T,
Burwinkel B,
Buys SS,
Byers H,
Caldés T,
Caligo MA,
Calvello M,
Campa D,
Castelao JE,
Chang-Claude J,
Chanock SJ,
Christiaens M,
Christiansen H,
Chung WK,
Claes KBM,
Clarke CL,
Cornelissen S,
Couch FJ,
Cox A,
Cross SS,
Czene K,
Daly MB,
Devilee P,
Diez O,
Domchek SM,
Dörk T,
Dwek M,
Eccles DM,
Ekici AB,
Evans DG,
Fasching PA,
Figueroa J,
Foretova L,
Fostira F,
Friedman E,
Frost D,
Gago-Dominguez M,
Gapstur SM,
Garber J,
García-Sáenz JA,
Gaudet MM,
Gayther SA,
Giles GG,
Godwin AK,
Goldberg MS,
Goldgar DE,
González-Neira A,
Greene MH,
Gronwald J,
Guénel P,
Häberle L,
Hahnen E,
Haiman CA,
Hake CR,
Hall P,
Hamann U,
Harkness EF,
Heemskerk-Gerritsen BAM,
Hillemanns P,
Hogervorst FBL,
Holleczek B,
Hollestelle A,
Hooning MJ,
Hoover RN,
Hopper JL,
Howell A,
Huebner H,
Hulick PJ,
Imyanitov EN,
Isaacs C,
Izatt L,
Jager A,
Jakimovska M,
Jakubowska A,
James P,
Janavicius R,
Janni W,
John EM,
Jones ME,
Jung A,
Kaaks R,
Kapoor PM,
Karlan BY,
Keeman R,
Khan S,
Khusnutdinova E,
Kitahara CM,
Ko YD,
Konstantopoulou I,
Koppert LB,
Koutros S,
Kristensen VN,
Laenkholm AV,
Lambrechts D,
Larsson SC,
Laurent-Puig P,
Lazaro C,
Lazarova E,
Lejbkowicz F,
Leslie G,
Lesueur F,
Lindblom A,
Lissowska J,
Lo WY,
Loud JT,
Lubinski J,
Lukomska A,
MacInnis RJ,
Mannermaa A,
Manoochehri M,
Manoukian S,
Margolin S,
Martinez ME,
Matricardi L,
McGuffog L,
McLean C,
Mebirouk N,
Meindl A,
Menon U,
Miller A,
Mingazheva E,
Montagna M,
Mulligan AM,
Mulot C,
Muranen TA,
Nathanson KL,
Neuhausen SL,
Nevanlinna H,
Neven P,
Newman WG,
Nielsen FC,
Nikitina-Zake L,
Nodora J,
Offit K,
Olah E,
Olopade OI,
Olsson H,
Orr N,
Papi L,
Papp J,
Park-Simon TW,
Parsons MT,
Peissel B,
Peixoto A,
Peshkin B,
Peterlongo P,
Peto J,
Phillips KA,
Piedmonte M,
Plaseska-Karanfilska D,
Prajzendanc K,
Prentice R,
Prokofyeva D,
Rack B,
Radice P,
Ramus SJ,
Rantala J,
Rashid MU,
Rennert G,
Rennert HS,
Risch HA,
Romero A,
Rookus MA,
Rübner M,
Rüdiger T,
Saloustros E,
Sampson S,
Sandler DP,
Sawyer EJ,
Scheuner MT,
Schmutzler RK,
Schneeweiss A,
Schoemaker MJ,
Schöttker B,
Schürmann P,
Senter L,
Sharma P,
Sherman ME,
Shu XO,
Singer CF,
Smichkoska S,
Soucy P,
Southey MC,
Spinelli JJ,
Stone J,
Stoppa-Lyonnet D,
Swerdlow AJ,
Szabo CI,
Tamimi RM,
Tapper WJ,
Taylor JA,
Teixeira MR,
Terry M,
Thomassen M,
Thull DL,
Tischkowitz M,
Toland AE,
Tollenaar RAEM,
Tomlinson I,
Torres D,
Troester MA,
Truong T,
Tung N,
Untch M,
Vachon CM,
van den Ouweland AMW,
van der Kolk LE,
van Veen EM,
vanRensburg EJ,
Vega A,
Wappenschmidt B,
Weinberg CR,
Weitzel JN,
Wildiers H,
Winqvist R,
Wolk A,
Yang XR,
Yannoukakos D,
Zheng W,
Zheng W,
Zorn KK,
Milne RL,
Kraft P,
Simard J,
Pharoah PDP,
Michailidou K,
Antoniou AC,
Schmidt MK,
Chenevix-Trench G,
Easton DF,
Chatterjee N,
García-Closas M
kConFab Investigators · ABCTB Investigators and 2 more consortia
Nature genetics · 2020 · PMID 32424353 · open access
2 pages
Genome-wide association study identifies novel breast cancer susceptibility loci
Easton DF,
Pooley KA,
Dunning AM,
Pharoah PD,
Thompson D,
Ballinger DG,
Struewing JP,
Morrison J,
Field H,
Luben R,
Wareham N,
Ahmed S
and 90 more — show all
Healey CS,
Bowman R,
Meyer KB,
Haiman CA,
Kolonel LK,
Henderson BE,
Le Marchand L,
Brennan P,
Sangrajrang S,
Gaborieau V,
Odefrey F,
Shen CY,
Wu PE,
Wang HC,
Eccles D,
Evans DG,
Peto J,
Fletcher O,
Johnson N,
Seal S,
Stratton MR,
Rahman N,
Chenevix-Trench G,
Bojesen SE,
Nordestgaard BG,
Axelsson CK,
Garcia-Closas M,
Brinton L,
Chanock S,
Lissowska J,
Peplonska B,
Nevanlinna H,
Fagerholm R,
Eerola H,
Kang D,
Yoo KY,
Noh DY,
Ahn SH,
Hunter DJ,
Hankinson SE,
Cox DG,
Hall P,
Wedren S,
Liu J,
Low YL,
Bogdanova N,
Schürmann P,
Dörk T,
Tollenaar RA,
Jacobi CE,
Devilee P,
Klijn JG,
Sigurdson AJ,
Doody MM,
Alexander BH,
Zhang J,
Cox A,
Brock IW,
MacPherson G,
Reed MW,
Couch FJ,
Goode EL,
Olson JE,
Meijers-Heijboer H,
van den Ouweland A,
Uitterlinden A,
Rivadeneira F,
Milne RL,
Ribas G,
Gonzalez-Neira A,
Benitez J,
Hopper JL,
McCredie M,
Southey M,
Giles GG,
Schroen C,
Justenhoven C,
Brauch H,
Hamann U,
Ko YD,
Spurdle AB,
Beesley J,
Chen X,
Mannermaa A,
Kosma VM,
Kataja V,
Hartikainen J,
Day NE,
Cox DR,
Ponder BA
SEARCH collaborators · kConFab and 1 more consortia
Nature · 2007 · PMID 17529967
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 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
A three-stage genome-wide association study identifies a susceptibility locus for late radiotherapy toxicity at 2q24.1
Fachal L,
Gómez-Caamaño A,
Barnett GC,
Peleteiro P,
Carballo AM,
Calvo-Crespo P,
Kerns SL,
Sánchez-García M,
Lobato-Busto R,
Dorling L,
Elliott RM,
Dearnaley DP
and 8 more — show all
Nature genetics · 2014 · PMID 24974847
1 page
Meta-analysis of Genome Wide Association Studies Identifies Genetic Markers of Late Toxicity Following Radiotherapy for Prostate Cancer
Kerns SL,
Dorling L,
Fachal L,
Bentzen S,
Pharoah PD,
Barnes DR,
Gómez-Caamaño A,
Carballo AM,
Dearnaley DP,
Peleteiro P,
Gulliford SL,
Hall E
and 16 more — show all
Michailidou K,
Carracedo Á,
Sia M,
Stock R,
Stone NN,
Sydes MR,
Tyrer JP,
Ahmed S,
Parliament M,
Ostrer H,
Rosenstein BS,
Vega A,
Burnet NG,
Dunning AM,
Barnett GC,
West CM
Radiogenomics Consortium
EBioMedicine · 2016 · PMID 27515689 · open access
1 page
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Day FR,
Thompson DJ,
Helgason H,
Chasman DI,
Finucane H,
Sulem P,
Ruth KS,
Whalen S,
Sarkar AK,
Albrecht E,
Altmaier E,
Amini M
and 204 more — show all
Barbieri CM,
Boutin T,
Campbell A,
Demerath E,
Giri A,
He C,
Hottenga JJ,
Karlsson R,
Kolcic I,
Loh PR,
Lunetta KL,
Mangino M,
Marco B,
McMahon G,
Medland SE,
Nolte IM,
Noordam R,
Nutile T,
Paternoster L,
Perjakova N,
Porcu E,
Rose LM,
Schraut KE,
Segrè AV,
Smith AV,
Stolk L,
Teumer A,
Andrulis IL,
Bandinelli S,
Beckmann MW,
Benitez J,
Bergmann S,
Bochud M,
Boerwinkle E,
Bojesen SE,
Bolla MK,
Brand JS,
Brauch H,
Brenner H,
Broer L,
Brüning T,
Buring JE,
Campbell H,
Catamo E,
Chanock S,
Chenevix-Trench G,
Corre T,
Couch FJ,
Cousminer DL,
Cox A,
Crisponi L,
Czene K,
Davey Smith G,
de Geus EJCN,
de Mutsert R,
De Vivo I,
Dennis J,
Devilee P,
Dos-Santos-Silva I,
Dunning AM,
Eriksson JG,
Fasching PA,
Fernández-Rhodes L,
Ferrucci L,
Flesch-Janys D,
Franke L,
Gabrielson M,
Gandin I,
Giles GG,
Grallert H,
Gudbjartsson DF,
Guénel P,
Hall P,
Hallberg E,
Hamann U,
Harris TB,
Hartman CA,
Heiss G,
Hooning MJ,
Hopper JL,
Hu F,
Hunter DJ,
Ikram MA,
Im HK,
Järvelin MR,
Joshi PK,
Karasik D,
Kellis M,
Kutalik Z,
LaChance G,
Lambrechts D,
Langenberg C,
Launer LJ,
Laven JSE,
Lenarduzzi S,
Li J,
Lind PA,
Lindstrom S,
Liu Y,
Luan J,
Mägi R,
Mannermaa A,
Mbarek H,
McCarthy MI,
Meisinger C,
Meitinger T,
Menni C,
Metspalu A,
Michailidou K,
Milani L,
Milne RL,
Montgomery GW,
Mulligan AM,
Nalls MA,
Navarro P,
Nevanlinna H,
Nyholt DR,
Oldehinkel AJ,
O'Mara TA,
Padmanabhan S,
Palotie A,
Pedersen N,
Peters A,
Peto J,
Pharoah PDP,
Pouta A,
Radice P,
Rahman I,
Ring SM,
Robino A,
Rosendaal FR,
Rudan I,
Rueedi R,
Ruggiero D,
Sala CF,
Schmidt MK,
Scott RA,
Shah M,
Sorice R,
Southey MC,
Sovio U,
Stampfer M,
Steri M,
Strauch K,
Tanaka T,
Tikkanen E,
Timpson NJ,
Traglia M,
Truong T,
Tyrer JP,
Uitterlinden AG,
Edwards DRV,
Vitart V,
Völker U,
Vollenweider P,
Wang Q,
Widen E,
van Dijk KW,
Willemsen G,
Winqvist R,
Wolffenbuttel BHR,
Zhao JH,
Zoledziewska M,
Zygmunt M,
Alizadeh BZ,
Boomsma DI,
Ciullo M,
Cucca F,
Esko T,
Franceschini N,
Gieger C,
Gudnason V,
Hayward C,
Kraft P,
Lawlor DA,
Magnusson PKE,
Martin NG,
Mook-Kanamori DO,
Nohr EA,
Polasek O,
Porteous D,
Price AL,
Ridker PM,
Snieder H,
Spector TD,
Stöckl D,
Toniolo D,
Ulivi S,
Visser JA,
Völzke H,
Wareham NJ,
Wilson JF,
Spurdle AB,
Thorsteindottir U,
Pollard KS,
Easton DF,
Tung JY,
Chang-Claude J,
Hinds D,
Murray A,
Murabito JM,
Stefansson K,
Ong KK,
Perry JRB
LifeLines Cohort Study · InterAct Consortium and 4 more consortia
Nature genetics · 2017 · PMID 28436984
1 page
A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis
Schack LMH,
Naderi E,
Fachal L,
Dorling L,
Luccarini C,
Dunning AM,
Ong EHW,
Chua MLK,
Langendijk JA,
Alizadeh BZ,
Overgaard J,
Eriksen JG
and 2 more — show all
Head and Neck Group of the Radiogenomics Consortium · Danish Head and Neck Cancer Group (DAHANCA)
British journal of cancer · 2022 · PMID 35039627 · 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.