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Khedoudja Nafa

Formats
  1. Meeting Abstract (142)
  2. Journal Article (100)
  3. Research Letter (2)
Groups
  1. Department of Pathology and Laboratory Medicine (244)
  2. GSK Faculty (158)
  3. Human Oncology and Pathogenesis Program (121)
  4. Department of Medicine (116)
  5. Tow Center for Developmental Oncology (TCDO) (116)
  6. Solid Tumor Oncology Division (88)

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People
  1. Marc Ladanyi (110)
  2. Maria Arcila (108)
  3. Ahmet Zehir (53)
  4. Meera Hameed (49)
  5. Kenneth Offit (39)
  6. Michael Berger (35)

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Years
  1. 2025 (2)
  2. 2024 (8)
  3. 2023 (8)
  4. 2022 (6)
  5. 2021 (6)
  6. 2020 (9)

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Publications
  1. Journal of Molecular Diagnostics (69)
  2. Modern Pathology (25)
  3. Laboratory Investigation (24)
  4. Blood (19)
  5. Clinical Cancer Research (13)
  6. American Journal of Human Genetics (11)

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Publishers
  1. Elsevier Science, Inc. (73)
  2. Nature Publishing Group (31)
  3. Nature Research (25)
  4. American Society of Hematology (20)
  5. American Association for Cancer Research (19)
  6. Cell Press (11)

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Results (244)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Incidence of non-founder BRCA1 and BRCA2 mutations in high risk Ashkenazi breast and ovarian cancer families
    Journal Article

    Kauff, N. D.; Perez-Segura, P.; Robson, M. E.; Scheuer, L.; Siegel, B.; Schluger, A.; Rapaport, B.; Frank, T. S.; Nafa, K.; Ellis, N. A.; more...
    Journal of Medical Genetics (2002)

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  • The founder mutation MSH2*1906G→C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population
    Journal Article

    Foulkes, W. D.; Thiffault, I.; Gruber, S. B.; Horwitz, M.; Hamel, N.; Lee, C.; Shia, J.; Markowitz, A.; Figer, A.; Friedman, E.; more...
    American Journal of Human Genetics (2002)

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  • Mutations of the PML tumor suppressor gene in RA-resistant APL
    Meeting Abstract

    Gurrieri, C.; Nafa, K.; Merghoub, T.; Jain, V.; Douer, D.; Biondi, A.; Nimer, S.; Gallagher, R.; Pandolfi, P. P.
    Blood (2001)

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  • Loss of the tumor suppressor PML in tumors of multiple histological origins
    Meeting Abstract

    Gurrieri, C.; Capodieci, P.; Nafa, K.; Gerald, W. L.; Cordon-Cardo, C.; Pandolfi, P. P.
    Blood (2001)

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  • Analysis of MSH6 mutations by denaturing high performance liquid chromatography (DHPLC) in HNPCC families
    Meeting Abstract

    Peterlongo, P.; Nafa, K.; Lerman, G.; Pawar, S.; Guillem, J.; Markowitz, A.; Offit, K.; Ellis, N. A.
    American Journal of Human Genetics (2001)

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  • Replication error and mismatch repair gene analyses of families with strong histories of colorectal cancer
    Meeting Abstract

    Nafa, K.; Peterlongo, P.; Glogowski, E.; Guillem, J.; Markowitz, A.; Offit, K.; Ellis, N. A.
    American Journal of Human Genetics (2001)

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  • Association of clonal T-cell large granular lymphocyte disease and paroxysmal nocturnal haemoglobinuria (PNH): Further evidence for a pathogenetic link between T cells, aplastic anaemia and PNH
    Journal Article

    Karadimitris, A.; Li, K.; Notaro, R.; Araten, D. J.; Nafa, K.; Thertulien, R.; Ladanyi, M.; Stevens, A. E.; Rosenfeld, C. S.; Roberts, I. A. G.; more...
    British Journal of Haematology (2001)

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  • Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuria
    Journal Article

    Araten, D. J.; Swirsky, D.; Karadimitris, A.; Notaro, R.; Nafa, K.; Bessler, M.; Thaler, H. T.; Castro-Malaspina, H.; Childs, B. H.; Boulad, F.; more...
    British Journal of Haematology (2001)

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  • A novel association of T-LGL leukemia and PNH supports the central role of a T-cell-mediated immune response in the pathogenesis of PNH
    Meeting Abstract

    Karadimitris, A.; Li, K.; Araten, D. J.; Nafa, K.; Thertulien, R.; Stevens, A. E.; Ladanyi, M.; Roberts, I. A. G.; Luzzatto, L.
    Blood (2000)

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  • De novo BRCA2 mutation in a patient with early-onset breast cancer
    Meeting Abstract

    Robson, M.; Scheuer, L.; Baum, R.; Hull, J.; McDermott, D.; Pierce, H.; Nafa, K.; Ellis, N.; Offit, K.
    American Journal of Human Genetics (2000)

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