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Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2.

Anna Marie Mulligan | Fergus J Couch | Daniel Barrowdale | Susan M Domchek | Diana Eccles | Heli Nevanlinna | Susan J Ramus | Mark Robson | Mark Sherman | Amanda B Spurdle | Barbara Wappenschmidt | Andrew Lee | Lesley McGuffog | Sue Healey | Olga M Sinilnikova | Ramunas Janavicius | Thomas vO Hansen | Finn C Nielsen | Bent Ejlertsen | Ana Osorio | Iván Muñoz-Repeto | Mercedes Durán | Javier Godino | Maroulio Pertesi | Javier Benítez | Paolo Peterlongo | Siranoush Manoukian | Bernard Peissel | Daniela Zaffaroni | Elisa Cattaneo | Bernardo Bonanni | Alessandra Viel | Barbara Pasini | Laura Papi | Laura Ottini | Antonella Savarese | Loris Bernard | Paolo Radice | Ute Hamann | Martijn Verheus | Hanne E J Meijers-Heijboer | Juul Wijnen | Encarna B Gómez García | Marcel R Nelen | C Marleen Kets | Caroline Seynaeve | Madeleine M A Tilanus-Linthorst | Rob B van der Luijt | Theo van Os | Matti Rookus | Debra Frost | J Louise Jones | D Gareth Evans | Fiona Lalloo | Ros Eeles | Louise Izatt | Julian Adlard | Rosemarie Davidson | Jackie Cook | Alan Donaldson | Huw Dorkins | Helen Gregory | Jacqueline Eason | Catherine Houghton | Julian Barwell | Lucy E Side | Emma McCann | Alex Murray | Susan Peock | Andrew K Godwin | Rita K Schmutzler | Kerstin Rhiem | Christoph Engel | Alfons Meindl | Ina Ruehl | Norbert Arnold | Dieter Niederacher | Christian Sutter | Helmut Deissler | Dorothea Gadzicki | Karin Kast | Sabine Preisler-Adams | Raymonda Varon-Mateeva | Ines Schoenbuchner | Britta Fiebig | Wolfram Heinritz | Dieter Schäfer | Heidrun Gevensleben | Virginie Caux-Moncoutier | Marion Fassy-Colcombet | François Cornelis | Sylvie Mazoyer | Mélanie Léoné | Nadia Boutry-Kryza | Agnès Hardouin | Pascaline Berthet | Danièle Muller | Jean-Pierre Fricker | Isabelle Mortemousque | Pascal Pujol | Isabelle Coupier | Marine Lebrun | Caroline Kientz | Michel Longy | Nicolas Sevenet | Dominique Stoppa-Lyonnet | Claudine Isaacs | Trinidad Caldes | Miguel de la Hoya | Tuomas Heikkinen | Kristiina Aittomäki | Ignacio Blanco | Conxi Lazaro | Rosa B Barkardottir | Penny Soucy | Martine Dumont | Jacques Simard | Marco Montagna | Silvia Tognazzo | Emma D'Andrea | Stephen Fox | Max Yan | Tim Rebbeck | Olufunmilayo Olopade | Jeffrey N Weitzel | Henry T Lynch | Patricia A Ganz | Gail E Tomlinson | Xianshu Wang | Zachary Fredericksen | Vernon S Pankratz | Noralane M Lindor | Csilla Szabo | Kenneth Offit | Rita Sakr | Mia Gaudet | Jasmine Bhatia | Noah Kauff | Christian F Singer | Muy-Kheng Tea | Daphne Gschwantler-Kaulich | Anneliese Fink-Retter | Phuong L Mai | Mark H Greene | Evgeny Imyanitov | Frances P O'Malley | Hilmi Ozcelik | Gordon Glendon | Amanda E Toland | Anne-Marie Gerdes | Mads Thomassen | Torben A Kruse | Uffe Birk Jensen | Anne-Bine Skytte | Maria A Caligo | Maria Soller | Karin Henriksson | von Anna Wachenfeldt | Brita Arver | Marie Stenmark-Askmalm | Per Karlsson | Yuan Chun Ding | Susan L Neuhausen | Mary Beattie | Paul D P Pharoah | Kirsten B Moysich | Katherine L Nathanson | Beth Y Karlan | Jenny Gross | Esther M John | Mary B Daly | Saundra M Buys | Melissa C Southey | John L Hopper | Mary Beth Terry | Wendy Chung | Alexander F Miron | David Goldgar | Georgia Chenevix-Trench | Douglas F Easton | Irene L Andrulis | Antonis C Antoniou | Breast Cancer Family Registry | EMBRACE | GEMO Study Collaborators | HEBON | kConFab Investigators | Ontario Cancer Genetics Network | SWE-BRCA | CIMBA
Breast cancer research : BCR | 2011

Previous studies have demonstrated that common breast cancer susceptibility alleles are differentially associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers. It is currently unknown how these alleles are associated with different breast cancer subtypes in BRCA1 and BRCA2 mutation carriers defined by estrogen (ER) or progesterone receptor (PR) status of the tumour.

Pubmed ID: 22053997 RIS Download

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Associated grants

  • Agency: NCI NIH HHS, United States
    Id: CA116201
  • Agency: NCI NIH HHS, United States
    Id: CA128978
  • Agency: NCI NIH HHS, United States
    Id: U01 CA69417
  • Agency: Cancer Research UK, United Kingdom
    Id: C12292/A11174
  • Agency: NCI NIH HHS, United States
    Id: R01 CA128978
  • Agency: NCI NIH HHS, United States
    Id: CA116167
  • Agency: NCI NIH HHS, United States
    Id: U01 CA69398
  • Agency: NCI NIH HHS, United States
    Id: N02-CP-65504
  • Agency: Cancer Research UK, United Kingdom
    Id: 11174
  • Agency: NCI NIH HHS, United States
    Id: P30-CA051008
  • Agency: Cancer Research UK, United Kingdom
    Id: C1287/A11990.
  • Agency: NCI NIH HHS, United States
    Id: P50 CA 058207
  • Agency: Cancer Research UK, United Kingdom
    Id: C5047/A8385
  • Agency: NCI NIH HHS, United States
    Id: RFA-CA-06-503
  • Agency: Cancer Research UK, United Kingdom
    Id: 11022
  • Agency: NCI NIH HHS, United States
    Id: N02-CP-11019-50
  • Agency: CIHR, Canada
  • Agency: Intramural NIH HHS, United States
  • Agency: NCI NIH HHS, United States
    Id: 5U01CA113916
  • Agency: NCI NIH HHS, United States
    Id: U01 CA69638
  • Agency: NCI NIH HHS, United States
    Id: U01 CA69446
  • Agency: PHS HHS, United States
    Id: HHSN261200744000C
  • Agency: NCI NIH HHS, United States
    Id: U01 CA69631
  • Agency: NCI NIH HHS, United States
    Id: U01CA69631
  • Agency: Cancer Research UK, United Kingdom
    Id: 10118
  • Agency: Cancer Research UK, United Kingdom
    Id: C1287/A10118
  • Agency: NCI NIH HHS, United States
    Id: U01 CA69467

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RRID:SCR_002846

THIS RESOURCE IS NO LONGER IN SERVICE, documented August 22, 2016. A multi-country collaboration among scientists and funding agencies to develop a public resource where genetic similarities and differences in human beings are identified and catalogued. Using this information, researchers will be able to find genes that affect health, disease, and individual responses to medications and environmental factors. All of the information generated by the Project will be released into the public domain. Their goal is to compare the genetic sequences of different individuals to identify chromosomal regions where genetic variants are shared. Public and private organizations in six countries are participating in the International HapMap Project. Data generated by the Project can be downloaded with minimal constraints. HapMap project related data, software, and documentation include: bulk data on genotypes, frequencies, LD data, phasing data, allocated SNPs, recombination rates and hotspots, SNP assays, Perlegen amplicons, raw data, inferred genotypes, and mitochondrial and chrY haplogroups; Generic Genome Browser software; protocols and information on assay design, genotyping and other protocols used in the project; and documentation of samples/individuals and the XML format used in the project.

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RRID:SCR_009288

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