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Kasmintan Alexandra Schrader

Formats
  1. Journal Article (19)
  2. Meeting Abstract (13)
Groups
  1. Clinical Genetics Service (32)
  2. Department of Medicine (32)
  3. GSK Faculty (32)
  4. Population Sciences Research Program (32)
  5. Solid Tumor Oncology Division (32)
  6. Survivorship Research (32)

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People
  1. Kenneth Offit (32)
  2. Vijai Joseph (25)
  3. Mark Robson (12)
  4. Robert Klein (11)
  5. Rohini Rau Murthy (11)
  6. Tinu Thomas (11)

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Years
  1. 2019 (1)
  2. 2017 (1)
  3. 2016 (5)
  4. 2015 (5)
  5. 2014 (6)
  6. 2013 (12)

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Publications
  1. Journal of Clinical Oncology (8)
  2. Cancer Research (5)
  3. Familial Cancer (2)
  4. PLoS Genetics (2)
  5. American Journal of Human Genetics (1)
  6. Breast Cancer Research (1)

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Publishers
  1. American Society of Clinical Oncology (8)
  2. American Association for Cancer Research (5)
  3. Nature Publishing Group (4)
  4. Public Library of Science (3)
  5. Springer (2)
  6. American Medical Association (1)

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Results (32)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Variable penetrance of CDH1 mutation diffuse gastric cancer: A genomic analysis
    Meeting Abstract

    Kelsen, D. P.; Schrader, K. A.; Khanin, R.; Tang, L. H.; Salo-Mullen, E. E.; Offit, K.; Joseph, V.; Viale, A.; Mirander, M.; Coit, D. G.; 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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  • Description and pilot results from a novel method for evaluating return of incidental findings from next-generation sequencing technologies
    Journal Article

    Goddard, K. A. B.; Whitlock, E. P.; Berg, J. S.; Williams, M. S.; Webber, E. M.; Webster, J. A.; Lin, J. S.; Schrader, K. A.; Campos-Outcalt, D.; Offit, K.; more...
    Genetics in Medicine (2013)

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  • A Recessive Founder Mutation in Regulator of Telomere Elongation Helicase 1, RTEL1, Underlies Severe Immunodeficiency and Features of Hoyeraal Hreidarsson Syndrome
    Journal Article

    Ballew, B. J.; Joseph, V.; De, S.; Sarek, G.; Vannier, J. B.; Stracker, T.; Schrader, K. A.; Small, T. N.; O'reilly, R.; Manschreck, C.; more...
    PLoS Genetics (2013)

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  • COMPLEXO: Identifying the missing heritability of breast cancer via next generation collaboration
    Journal Article

    Southey, M. C.; Park, D. J.; Nguyen-Dumont, T.; Campbell, I.; Thompson, E.; Trainer, A. H.; Chenevix-Trench, G.; Simard, J.; Dumont, M.; Soucy, P.; more...
    Breast Cancer Research (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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  • Susceptibility Loci Associated with Specific and Shared Subtypes of Lymphoid Malignancies
    Journal Article

    Vijai, J.; Kirchhoff, T.; Schrader, K. A.; Brown, J.; Dutra Clarke, A. V.; Manschreck, C.; Hansen, N.; Rau-Murthy, R.; Sarrel, K.; Przybylo, J.; more...
    PLoS Genetics (2013)

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  • Absence of loss of heterozygosity of BRCA1 in a renal tumor from a BRCA1 germline mutation carrier
    Journal Article

    Alanee, S.; Shah, S.; Murali, R.; Rau-Murthy, R.; Schrader, K. A.; Offit, K.
    Familial Cancer (2013)

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