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Results (1110)

Germline variants identified in patients with early-onset renal cell carcinoma referred for germline genetic testing

Journal Article

Truong, H.; Sheikh, R.; Kotecha, R.; Kemel, Y.; Reisz, P. A.; Lenis, A. T.; Mehta, N. N.; Khurram, A.; Joseph, V.; Mandelker, D.; more...
European Urology Oncology (2021)

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Clinical and molecular features of a prospectively-sequenced cohort of glioblastoma patients with inherited disorders in mismatch repair

Meeting Abstract

Elmore, K.; Stadler, Z.; Piotrowski, A.; Schaff, L.; Gavrilovic, I.; Stone, J.; Dunkel, I.; Tabar, V.; Mellinghoff, I.; Bale, T.; more...
Neurology (2021)

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Paired tumor-normal sequencing provides insights into the TP53-related cancer spectrum in patients with Li-Fraumeni syndrome

Journal Article

Ceyhan-Birsoy, O.; Selenica, P.; Chui, M. H.; Jayakumaran, G.; Ptashkin, R.; Misyura, M.; Aypar, U.; Jairam, S.; Yang, C.; Li, Y.; more...
JNCI: Journal of the National Cancer Institute (2021)

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Molecular and phenotypic profiling of colorectal cancer patients in West Africa reveals biological insights

Journal Article

Alatise, O. I.; Knapp, G. C.; Sharma, A.; Chatila, W. K.; Arowolo, O. A.; Olasehinde, O.; Famurewa, O. C.; Omisore, A. D.; Komolafe, A. O.; Olaofe, O. O.; more...
Nature Communications (2021)

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Tumor-infiltrating lymphocytes, tumor mutational burden, and genetic alterations in microsatellite unstable, microsatellite stable, or mutant POLE/POLD1 colon cancer

Journal Article

Keshinro, A.; Vanderbilt, C.; Kim, J. K.; Firat, C.; Chen, C. T.; Yaeger, R.; Ganesh, K.; Segal, N. H.; Gonen, M.; Shia, J.; more...
JCO Precision Oncology (2021)

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Frequency of minimal residual disease as measured by ctDNA in mismatch repair deficient tumors following curative resection

Meeting Abstract

Lumish, M. A.; Jayakumaran, G.; Fox, M.; Sabwa, S.; Cercek, A.; Stadler, Z. K.; Ku, G. Y.; Segal, N. H.; Won, E.; Maron, S. B.; more...
Journal of Clinical Oncology (2021)

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Characterization of findings on prostate cancer tumor sequencing that should prompt consideration for germline testing

Meeting Abstract

Truong, H.; Breen, K.; Kemel, Y.; Lenis, A. T.; Reisz, P.; Benfante, N.; Ehdaie, B.; Touijer, K. A.; Laudone, V. P.; Scardino, P. T.; more...
Journal of Clinical Oncology (2021)

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Disparities in pan-cancer patients undergoing germline cancer risk assessment by self-reported race/ethnicity and ancestry

Meeting Abstract

Liu, Y. L.; Maio, A.; Kemel, Y.; Salo-Mullen, E. E.; Sheehan, M.; Tejada, P. R.; Trottier, M.; Fleischut, M. H.; Latham, A.; Carlo, M. I.; more...
Journal of Clinical Oncology (2021)

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Feasibility and clinical utility of cancer whole genome and transcriptome sequencing for pediatric and young adult solid tumors

Meeting Abstract

Shukla, N.; Levine, M.; Gundem, G.; Spitzer, B.; Gutierrez-Abril, J.; Bouvier, N.; Arango Ossa, J. E.; Medina-Martinez, J.; Stockfisch, E.; O'Donohue, T.; more...
Journal of Clinical Oncology (2021)

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Uptake and acceptability of a mainstreaming model of hereditary cancer multigene panel testing among patients with ovarian, pancreatic, and prostate cancer

Journal Article

Hamilton, J. G.; Symecko, H.; Spielman, K.; Breen, K.; Mueller, R.; Catchings, A.; Trottier, M.; Salo-Mullen, E. E.; Shah, I.; Arutyunova, A.; more...
Genetics in Medicine (2021)

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