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    Offit
  2. Robson
    Robson
  3. Nafa
    Nafa
  4. Joseph
    Joseph
  5. Markowitz
    Markowitz
  6. Norton
    Norton
  7. Shia
    Shia
  8. Mukherjee
    Mukherjee
  9. Stadler
    Stadler
  10. Begg
    Begg

Groups

  1. Clinical Genetics Service (41)
  2. Department of Medicine (41)
  3. Population Sciences Research Program (41)
  4. Solid Tumor Oncology Division (41)
  5. GSK Faculty (37)
  6. Survivorship Research (36)
  7. Breast Medicine Service (14)
  8. Department of Pathology and Laboratory Medicine (12)
  9. Surgery (8)
  10. Alan and Sandra Gerry Metastasis and Tumor Ecosystems Center (7)
Search Within
  1. "Clinical Genetics Service"
Formats
  1. Meeting Abstract (20)
  2. Journal Article (19)
  3. Correspondence (1)
  4. Editorial (1)
Groups
  1. Clinical Genetics Service (41)
  2. Department of Medicine (41)
  3. Population Sciences Research Program (41)
  4. Solid Tumor Oncology Division (41)
  5. GSK Faculty (37)
  6. Survivorship Research (36)

More Groups

People
  1. Kenneth Offit (35)
  2. Mark Robson (12)
  3. Nathan Ellis (9)
  4. Khedoudja Nafa (8)
  5. Arnold Markowitz (6)
  6. Deborah McDermott (6)

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Years
  1. 2025 (1)
  2. 2024 (1)
  3. 2022 (1)
  4. 2021 (4)
  5. 2020 (3)
  6. 2019 (1)

More Years

Publications
  1. American Journal of Human Genetics (32)
  2. Cancer Cell (3)
  3. Human Genetics and Genomics Advances (3)
  4. Cell (1)
  5. Cell Host & Microbe (1)
  6. Neuron (1)

Results (41)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Polygenic risk scores for prediction of breast cancer and breast cancer subtypes
    Journal Article

    Mavaddat, N.; Michailidou, K.; Dennis, J.; Lush, M.; Fachal, L.; Lee, A.; Tyrer, J. P.; Chen, T. H.; Wang, Q.; Bolla, M. K.; more...
    American Journal of Human Genetics (2019)

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  • Clinical sequencing defines the genomic landscape of metastatic colorectal cancer
    Journal Article

    Yaeger, R.; Chatila, W. K.; Lipsyc, M. D.; Hechtman, J. F.; Cercek, A.; Sanchez-Vega, F.; Jayakumaran, G.; Middha, S.; Zehir, A.; Donoghue, M. T. A.; more...
    Cancer Cell (2018)

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  • Evaluation of ACMG-guideline-based variant classification of cancer susceptibility and non-cancer-associated genes in families affected by breast cancer
    Journal Article

    Maxwell, K. N.; Hart, S. N.; Vijai, J.; Schrader, K. A.; Slavin, T. P.; Thomas, T.; Wubbenhorst, B.; Ravichandran, V.; Moore, R. M.; Hu, C.; more...
    American Journal of Human Genetics (2016)

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  • Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region
    Journal Article

    Skibola, C. F.; Berndt, S. I.; Vijai, J.; Conde, L.; Wang, Z.; Yeager, M.; de Bakker, P. I. W.; Birmann, B. M.; Vajdic, C. M.; Foo, J. N.; more...
    American Journal of Human Genetics (2014)

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  • Rare de novo germline copy-number variation in testicular cancer
    Journal Article

    Stadler, Z. K.; Esposito, D.; Shah, S.; Vijai, J.; Yamrom, B.; Levy, D.; Lee, Y. H.; Kendall, J.; Leotta, A.; Ronemus, M.; more...
    American Journal of Human Genetics (2012)

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  • Successes of Genome-wide association studies
    Journal Article

    Klein, R. J.; Xu, X.; Mukherjee, S.; Willis, J.; Hayes, J.
    Cell (2010)

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  • RAD51 135G→C modifies breast cancer risk among BRCA2 mutation carriers: Results from a combined analysis of 19 studies
    Journal Article

    Antoniou, A. C.; Sinilnikova, O. M.; Simard, J.; Léoné, M.; Dumont, M.; Neuhausen, S. L.; Struewing, J. P.; Stoppa-Lyonnet, D.; Barjhoux, L.; Hughes, D. J.; more...
    American Journal of Human Genetics (2007)

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  • Mutational analysis of the mismatch repair genes in HNPCC patients
    Meeting Abstract

    Nafa, K.; Peterlongo, P.; Shia, J.; Canale, L.; Lerman, G.; Glogowski, E.; Guillem, J.; Markowitz, A.; Offit, K.; Ellis, N. A.
    American Journal of Human Genetics (2003)

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  • BRCA mutations and the risk of prostate and colorectal cancer in Ashkenazi Jews
    Meeting Abstract

    Kirchhoff, T.; Kauff, N.; Kolachana, P.; Satagopan, J.; Mitra, N.; Huang, H.; Shia, J.; Palmer, C.; Nafa, K.; Ellis, N. A.; more...
    American Journal of Human Genetics (2003)

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  • Unique phenotype associated with biallelic BRCA2 mutations includes high risk of brain tumors, Wilms tumors and early onset acute leukemia in children with Fanconi anemia
    Meeting Abstract

    Auerbach, A. D.; Levran, O.; Mullaney, B.; Kutler, D. I.; Mah, K.; Deffenbaugh, A.; Scholl, T.; Berwick, M.; MacMillan, M. L.; Offit, K.; more...
    American Journal of Human Genetics (2003)

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