Synapse - Megan Fleischut

Results (36)

Determining the prevalence of germline BAP1 mutations in malignant mesothelioma (MM)

Meeting Abstract

Zauderer, M. G.; DuBoff, M. A.; Siegel, B.; Robson, M. E.; Arnold, A. G.; Berliner, J.; Fleischut, M. H.; Mandelker, D.; Ladanyi, M.
Journal of Clinical Oncology (2017)

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Germline BRCA2 mutations detected in pediatric sequencing studies impact parents' evaluation and care

Journal Article

Walsh, M. F.; Kennedy, J.; Harlan, M.; Kentsis, A.; Shukla, N.; Musinsky, J.; Roberts, S.; Kung, A. L.; Robson, M.; Kushner, B. H.; more...
Cold Spring Harbor Molecular Case Studies (2017)

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Mutation detection in patients with advanced cancer by universal sequencing of cancer-related genes in tumor and normal DNA vs guideline-based germline testing

Journal Article

Mandelker, D.; Zhang, L.; Kemel, Y.; Stadler, Z. K.; Joseph, V.; Zehir, A.; Pradhan, N.; Arnold, A.; Walsh, M. F.; Li, Y.; more...
JAMA - Journal of the American Medical Association (2017)

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Educational and psychosocial support needs in lynch syndrome: Implementation and assessment of an educational workshop and support group

Journal Article

Corines, M. J.; Hamilton, J. G.; Glogowski, E.; Anrig, C. A.; Goldberg, R.; Niehaus, K.; Salo-Mullen, E.; Harlan, M.; Sheehan, M. R.; Trottier, M.; more...
Journal of Genetic Counseling (2017)

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Psychosocial factors associated with the uptake of contralateral prophylactic mastectomy among BRCA1/2 mutation noncarriers with newly diagnosed breast cancer

Journal Article

Hamilton, J. G.; Genoff, M. C.; Salerno, M.; Amoroso, K.; Boyar, S. R.; Sheehan, M.; Fleischut, M. H.; Siegel, B.; Arnold, A. G.; Salo-Mullen, E. E.; more...
Breast Cancer Research and Treatment (2017)

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The heritability of retinoblastoma: An institutional review

Meeting Abstract

Walsh, M. F.; Musinsky, J.; Fleischut, M. H.; Kennedy, J.; Lincoln, A.; Stadler, Z. K.; Robson, M. E.; Dunkel, I. J.; Abramson, D. H.; Offit, K.
Journal of Clinical Oncology (2016)

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Feasibility and long-term utility of a psychosocial support group for patients with Lynch syndrome

Meeting Abstract

Tran, C.; Hamilton, J. G.; Lincoln, A.; Corines, M.; Musinsky, J.; Gaddam, P.; Jacobs, L. M.; Glogowski, E.; Anrig, C.; Goldberg, R.; more...
Journal of Clinical Oncology (2016)

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Information preferences and short-term psychological responses to multiplex genetic testing among individuals at risk for hereditary breast cancer

Meeting Abstract

Robson, M. E.; Gaissert, P.; Salo-Mullen, E. E.; Amoroso, K.; Sheehan, M.; Berliner, J. L.; Trottier, M.; Arnold, A. G.; Sekhri, N.; Marcell, V.; more...
Cancer Research (2016)

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Germline mutations in cancer predisposition genes in a subset of pediatric oncology patients undergoing targeted solid tumor sequencing using matched normal DNA