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  1. Clinical Genetics Service (24)
  2. Department of Medicine (24)
  3. GSK Faculty (24)
  4. Population Sciences Research Program (24)
  5. Solid Tumor Oncology Division (24)
  6. Survivorship Research (23)
  7. Breast Medicine Service (9)
  8. Department of Pathology and Laboratory Medicine (4)
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  10. Epidemiology and Biostatistics (3)
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  1. "Clinical Genetics Service"
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  1. Journal Article (24)
Groups
  1. Clinical Genetics Service (24)
  2. Department of Medicine (24)
  3. GSK Faculty (24)
  4. Population Sciences Research Program (24)
  5. Solid Tumor Oncology Division (24)
  6. Survivorship Research (23)

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People
  1. Kenneth Offit (23)
  2. Mark Robson (8)
  3. Vijai Joseph (6)
  4. Jaya Satagopan (3)
  5. Ahmet Zehir (2)
  6. Aijazuddin Syed (2)

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Years
  1. 2024 (1)
  2. 2023 (1)
  3. 2022 (2)
  4. 2020 (3)
  5. 2018 (1)
  6. 2017 (2)

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Publications
  1. Breast Cancer Research (12)
  2. BMC Genetics (3)
  3. BMC Medicine (2)
  4. Genome Medicine (2)
  5. BMC Medical Genetics (1)
  6. BMC Medical Genomics (1)

More Publications

Results (24)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women
    Journal Article

    Rebbeck, T. R.; Friebel, T. M.; Mitra, N.; Wan, F.; Chen, S.; Andrulis, I. L.; Apostolou, P.; Arnold, N.; Arun, B. K.; Barrowdale, D.; more...
    Breast Cancer Research (2016)

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  • Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus
    Journal Article

    Zeng, C.; Guo, X.; Long, J.; Kuchenbaecker, K. B.; Droit, A.; Michailidou, K.; Ghoussaini, M.; Kar, S.; Freeman, A.; Hopper, J. L.; more...
    Breast Cancer Research (2016)

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  • Male breast cancer in BRCA1 and BRCA2 mutation carriers: Pathology data from the Consortium of Investigators of Modifiers of BRCA1/2
    Journal Article

    Silvestri, V.; Barrowdale, D.; Mulligan, A. M.; Neuhausen, S. L.; Fox, S.; Karlan, B. Y.; Mitchell, G.; James, P.; Thull, D. L.; Zorn, K. K.; more...
    Breast Cancer Research (2016)

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  • An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers
    Journal Article

    Blein, S.; Bardel, C.; Danjean, V.; McGuffog, L.; Healey, S.; Barrowdale, D.; Lee, A.; Dennis, J.; Kuchenbaecker, K. B.; Soucy, P.; more...
    Breast Cancer Research (2015)

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  • Refined histopathological predictors of BRCA1 and BRCA2 mutation status: A large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia
    Journal Article

    Spurdle, A. B.; Couch, F. J.; Parsons, M. T.; McGuffog, L.; Barrowdale, D.; Bolla, M. K.; Wang, Q.; Healey, S.; Schmutzler, R. K.; Wappenschmidt, B.; more...
    Breast Cancer Research (2014)

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  • COMPLEXO: Identifying the missing heritability of breast cancer via next generation collaboration
    Journal Article

    Southey, M. C.; Park, D. J.; Nguyen-Dumont, T.; Campbell, I.; Thompson, E.; Trainer, A. H.; Chenevix-Trench, G.; Simard, J.; Dumont, M.; Soucy, P.; more...
    Breast Cancer Research (2013)

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  • Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers
    Journal Article

    Antoniou, A. C.; Kuchenbaecker, K. B.; Soucy, P.; Beesley, J.; Chen, X.; McGuffog, L.; Lee, A.; Barrowdale, D.; Healey, S.; Sinilnikova, O. M.; more...
    Breast Cancer Research (2012)

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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
    Journal Article

    Mulligan, A. M.; Couch, F. J.; Barrowdale, D.; Domchek, S. M.; Eccles, D.; Nevanlinna, H.; Ramus, S. J.; Robson, M.; Sherman, M.; Spurdle, A. B.; more...
    Breast Cancer Research (2011)

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  • Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping
    Journal Article

    Olshen, A. B.; Gold, B.; Lohmueller, K. E.; Struewing, J. P.; Satagopan, J.; Stefanov, S. A.; Eskin, E.; Kirchhoff, T.; Lautenberger, J. A.; Klein, R. J.; more...
    BMC Genetics (2008)

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  • The BRCA1 Ashkenazi founder mutations occur on common haplotypes and are not highly correlated with anonymous single nucleotide polymorphisms likely to be used in genome-wide case-control association studies
    Journal Article

    Pereira, L. H. M.; Pineda, M. A.; Rowe, W. H.; Fonseca, L. R.; Greene, M. H.; Offit, K.; Ellis, N. A.; Zhang, J.; Collins, A.; Struewing, J. P.
    BMC Genetics (2007)

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