American Journal of Human Genetics

Published by: Cell Press  

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    Markowitz
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Groups

  1. Clinical Genetics Service (4)
  2. Department of Medicine (4)
  3. GSK Faculty (4)
  4. Population Sciences Research Program (4)
  5. Solid Tumor Oncology Division (4)
  6. Survivorship Research (4)
  7. Biostatistics Service (1)
  8. Breast Medicine Service (1)
  9. Division of Subspecialty Medicine (1)
  10. Epidemiology and Biostatistics (1)
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  1. "Jeffrey Boyd"
Formats
  1. Journal Article (4)
  2. Meeting Abstract (3)
Groups
  1. Clinical Genetics Service (4)
  2. Department of Medicine (4)
  3. GSK Faculty (4)
  4. Population Sciences Research Program (4)
  5. Solid Tumor Oncology Division (4)
  6. Survivorship Research (4)

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  1. Jeffrey Boyd (7)
  2. Kenneth Offit (4)
  3. Arnold Markowitz (1)
  4. Catherine Lee (1)
  5. Cindy Yee (1)
  6. Deborah McDermott (1)

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  1. 2002 (1)
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  4. 1999 (1)
  5. 1998 (1)
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  1. Cell Press (7)

Results (7)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • 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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  • Comparison of methods for detection of mutations in the BRCA1 gene
    Meeting Abstract

    Bove, B. A.; Ozcelik, H.; Neuhausen, S.; Boyd, J.; Southey, M.; Santella, R.; Venter, D.; Beck, J.; Li, F.; Buys, S.; more...
    American Journal of Human Genetics (2001)

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  • Good response to chemotherapy (CT) and hormonotherapy (HT) in patients with BRCA1-related breast cancer (BRCA1-BC)
    Meeting Abstract

    Chappuis, P. O.; Goffin, J.; Hamel, N.; Wong, N.; Paradis, A. J.; Roberge, D.; Brunet, J. S.; Yee, C.; Tonin, P.; Boyd, J.; more...
    American Journal of Human Genetics (2001)

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  • The presence of a germ-line BRCA mutation is an independent poor prognostic marker in breast cancer: A two-center historical cohort study
    Meeting Abstract

    Foulkes, W. D.; Satagopan, J. M.; Chappuis, P. O.; Wong, N.; Begin, L. R.; Boyd, J.; Offit, K.; Robson, M. E.
    American Journal of Human Genetics (2000)

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  • The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographicaly diverse populations
    Journal Article

    Mazoyer, S.; Leary, J.; Kirk, J.; Fleischmann, E.; Wagner, T.; Claes, K.; Messiaen, L.; Foulkes, W.; Desrochers, M.; Simard, J.; more...
    American Journal of Human Genetics (2000)

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  • The APC I1307K allele and BRCA-associated ovarian cancer risk
    Journal Article

    Maresco, D. L.; Arnold, P. H.; Sonoda, Y.; Federici, M. G.; Bogomolniy, F.; Rhei, E.; Boyd, J.
    American Journal of Human Genetics (1999)

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  • Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: Results of an international study
    Journal Article

    Neuhausen, S. L.; Godwin, A. K.; Gershoni-Baruch, R.; Schubert, E.; Garber, J.; Stoppa-Lyonnet, D.; Olah, E.; Csokay, B.; Serova, O.; Lalloo, F.; more...
    American Journal of Human Genetics (1998)

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    • American Journal of Human Genetics – authorized name for:

    Name ISSN / ISBN Publisher
    American Journal of Human Genetics 0002-9297 Cell Press
    American Journal of Human Genetics 0002-9297 Cell Press
    American Journal of Human Genetics 00029297 The Author(s)
    American Journal of Human Genetics 00029297 The Authors
    American Journal of Human Genetics 0002-9297 Unknown
    American Journal of Human Genetics 0002-9297 Elsevier B.V.
    American Journal of Human Genetics 0002-9297 University of Chicago Press
    American Journal of Human Genetics 00029297 American Society of Human Genetics
    American Journal of Human Genetics 00029297 The American Society of Human Genetics
    American journal of human genetics 15376605 Elsevier Inc.
    American Journal of Human Genetics 0002-9297 The American Society of Human Genetics
    American Journal of Human Genetics 00029297 Unknown
    American Journal of Human Genetics 0002-9297 Cell Press
    American Journal of Human Genetics 00029297 2021
    American Journal of Human Genetics 00029297 2023
    American journal of human genetics 15376605 Elsevier Inc.