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Sohela Shah

Formats
  1. Journal Article (10)
  2. Meeting Abstract (4)
  3. Book Section (1)
Groups
  1. Clinical Genetics Service (15)
  2. Department of Medicine (15)
  3. GSK Faculty (15)
  4. Population Sciences Research Program (15)
  5. Solid Tumor Oncology Division (15)
  6. Survivorship Research (15)

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People
  1. Kenneth Offit (15)
  2. Vijai Joseph (12)
  3. Kasmintan Schrader (9)
  4. Rohini Rau Murthy (9)
  5. Mark Robson (6)
  6. Rajmohan Murali (6)

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Years
  1. 2017 (1)
  2. 2016 (1)
  3. 2014 (1)
  4. 2013 (9)
  5. 2012 (3)
Publications
  1. Journal of Clinical Oncology (3)
  2. Familial Cancer (2)
  3. PLoS Genetics (2)
  4. American Journal of Human Genetics (1)
  5. Cancer Research (1)
  6. International Journal of Clinical Pharmacology and Therapeutics (1)

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Publishers
  1. American Society of Clinical Oncology (3)
  2. Public Library of Science (3)
  3. Springer (2)
  4. American Association for Cancer Research (1)
  5. BMJ Publishing Group Ltd. (1)
  6. Cambridge University Press (1)

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Results (15)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Evaluating the association of multiple single nucleotide polymorphisms with response to gemcitabine and platinum combination chemotherapy in urothelial carcinoma of the bladder
    Journal Article

    Alanee, S. R.; Shah, S.; Zabor, E. C.; Vijai, J.; Ostrovnaya, I.; Garcia-Grossman, I. R.; Pendse, D. V.; Littman, J.; Regazzi, A. M.; Offit, K.; more...
    International Journal of Clinical Pharmacology and Therapeutics (2017)

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  • Genome sequencing of multiple primary tumors reveals a novel PALB2 variant
    Journal Article

    Schrader, K. A.; Stratton, K. L.; Murali, R.; Laitman, Y.; Cavallone, L.; Offit, L.; Wen, Y. H.; Thomas, T.; Shah, S.; Rau-Murthy, R.; more...
    Journal of Clinical Oncology (2016)

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  • Genome-wide association studies of cancer predisposition
    Book Section

    Stadler, Z. K.; Shah, S.; Offit, K.
    In Gelmann, E. P.; Sawyers, C. L.; Rauscher, F. J. 3rd (Eds.) Molecular Oncology: Causes of Cancer and Targets for Treatment (2014)

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  • Exome sequencing of extreme phenotypes to identify variants predictive of response to chemotherapy in bladder cancer
    Meeting Abstract

    Alanee, S.; Shah, S.; Stratton, K. L.; Garcia-Grossman, I. R.; Zabor, E.; Ostrovnaya, I.; Joseph, V.; Pendse, D.; Bajorin, D. F.; Offit, K.
    Journal of Clinical Oncology (2013)

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  • Genome sequencing of multiple primary tumors to reveal underlying germline cancer susceptibility
    Meeting Abstract

    Schrader, K. A.; Stratton, K. L.; Murali, R.; Laitman, Y.; Cavallone, L.; Offit, L.; Wen, Y. H.; Shah, S.; Rau-Murthy, R.; Manschreck, C.; more...
    Journal of Clinical Oncology (2013)

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  • Germline aberrations of PAX5 cause susceptibility to pre-B cell acute lymphoblastic leukemia
    Meeting Abstract

    Miething, C.; Shah, S.; Schrader, K.; Waanders, E.; Timms, A.; Joseph, V.; Sandlund, J.; Lowe, S.; Horwitz, M.; Mullighan, C.; more...
    Onkologie (2013)

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  • Prevalence of HOXB13 mutation in a population of Ashkenazi Jewish men treated for prostate cancer
    Journal Article

    Alanee, S.; Shah, S.; Vijai, J.; Schrader, K.; Hamilton, R.; Rau-Murthy, R.; Sarrel, K.; Manschreck, C.; Eastham, J.; Offit, K.
    Familial Cancer (2013)

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  • A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia
    Journal Article

    Shah, S.; Schrader, K. A.; Waanders, E.; Timms, A. E.; Vijai, J.; Miething, C.; Wechsler, J.; Yang, J.; Hayes, J.; Klein, R. J.; more...
    Nature Genetics (2013)

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  • Assessment of SLX4 Mutations in Hereditary Breast Cancers
    Journal Article

    Shah, S.; Kim, Y.; Ostrovnaya, I.; Murali, R.; Schrader, K. A.; Lach, F. P.; Sarrel, K.; Rau-Murthy, R.; Hansen, N.; Zhang, L.; more...
    PLoS ONE (2013)

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  • Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk
    Journal Article

    Gaudet, M. M.; Kuchenbaecker, K. B.; Vijai, J.; Klein, R. J.; Kirchhoff, T.; McGuffog, L.; Barrowdale, D.; Dunning, A. M.; Lee, A.; Dennis, J.; more...
    PLoS Genetics (2013)

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