Wiley Blackwell

SHERPA: Unknown

People

  1. Offit
    Offit
  2. Robson
    Robson
  3. Stadler
    Stadler
  4. Barnett
    Barnett
  5. Breen
    Breen
  6. Busam
    Busam
  7. Fleischut
    Fleischut
  8. Jhanwar
    Jhanwar
  9. Kennedy
    Kennedy
  10. Mao
    Mao

Groups

  1. Department of Medicine (4)
  2. Population Sciences Research Program (4)
  3. Solid Tumor Oncology Division (4)
  4. Clinical Genetics Service (3)
  5. Survivorship Research (3)
  6. Breast Medicine Service (2)
  7. Center for Pancreatic Cancer Research (2)
  8. GSK Faculty (2)
  9. Surgery (2)
  10. Department of Pathology and Laboratory Medicine (1)
Search Within
  1. "Clinical Genetics"
Formats
  1. Journal Article (12)
  2. Review (1)
Groups
  1. Department of Medicine (4)
  2. Population Sciences Research Program (4)
  3. Solid Tumor Oncology Division (4)
  4. Clinical Genetics Service (3)
  5. Survivorship Research (3)
  6. Breast Medicine Service (2)

More Groups

People
  1. Frank Traganos (2)
  2. Kenneth Offit (2)
  3. Liying Zhang (2)
  4. Mark Robson (2)
  5. Myron Melamed (2)
  6. Zsofia Stadler (2)

More People

Years
  1. 2022 (1)
  2. 2017 (1)
  3. 2015 (1)
  4. 2013 (1)
  5. 2012 (1)
  6. 2011 (2)

More Years

Publications
  1. Clinical Genetics (13)

Results (13)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Psychosocial interventions and needs among individuals and families with Li-Fraumeni syndrome: A scoping review
    Review

    Barnett, M.; Breen, K. E.; Kennedy, J. A.; Hernandez, M.; Matsoukas, K.; MacGregor, M.
    Clinical Genetics (2022)

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  • Effects of S906T polymorphism on the severity of a novel borderline mutation I692M in Na(ν)1.4 cause periodic paralysis
    Journal Article

    Fan, C.; Mao, N.; Lehmann-Horn, F.; Bürmann, J.; Jurkat-Rott, K.
    Clinical Genetics (2017)

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  • A recurrent germline BAP1 mutation and extension of the BAP1 tumor predisposition spectrum to include basal cell carcinoma
    Journal Article

    Wadt, K. A. W.; Aoude, L. G.; Johansson, P.; Solinas, A.; Pritchard, A.; Crainic, O.; Andersen, M. T.; Kiilgaard, J. F.; Heegaard, S.; Sunde, L.; more...
    Clinical Genetics (2015)

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  • Knowledge of the Genetic Information Nondiscrimination act among individuals affected by Huntington disease
    Journal Article

    Dorsey, E.; Darwin, K.; Nichols, P.; Kwok, J.; Bennet, C.; Rosenthal, L.; Bombard, Y.; Shoulson, I.; Oster, E.
    Clinical Genetics (2013)

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  • De novo CDH1 mutation in a family presenting with early-onset diffuse gastric cancer
    Journal Article

    Shah, M.; Salo-Mullen, E.; Stadler, Z.; Ruggeri, J.; Mirander, M.; Pristyazhnyuk, Y.; Zhang, L.
    Clinical Genetics (2012)

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  • Assessment of the prevalence of de novo mutations in the BRCA1 and BRCA2 genes
    Journal Article

    Zhang, L.; Fleischut, M.; Kohut, K.; Spencer, S.; Wong, K.; Stadler, Z.; Kauff, N.; Offit, K.; Robson, M.
    Clinical Genetics (2011)

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  • Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome
    Journal Article

    Raskin, L.; Schwenter, F.; Freytsis, M.; Tischkowitz, M.; Wong, N.; Chong, G.; Narod, S. A.; Levine, D. A.; Bogomolniy, F.; Aronson, M.; more...
    Clinical Genetics (2011)

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  • CHEK2, breast cancer, and the understanding of clinical utility
    Journal Article

    Robson, M.
    Clinical Genetics (2010)

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  • Advances in the genetics of sarcoidosis
    Journal Article

    Smith, G.; Brownell, I.; Sanchez, M.; Prystowsky, S.
    Clinical Genetics (2008)

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  • Will the new cytogenetics replace the old cytogenetics?
    Journal Article

    Salman, M.; Jhanwar, S. C.; Ostrer, H.
    Clinical Genetics (2004)

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