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Familial Cancer|June 11, 2017
Co-occurrence of Lynch syndrome and juvenile polyposis syndrome confirmed by multigene panel testingRachel Silva-Smith, Daniel A SussmanACG Case Reports Journal|February 10, 2025
A Family With Multiple Lynch Syndrome Mutations: Navigating Counseling ComplexitiesRachel Silva-Smith, Gretter Manso, Daniel Andrew SussmanCancer Prevention Research (Philadelphia, Pa.)|February 16, 2024
Triple Primary Cancers: An Analysis of Genetic and Environmental FactorsNicholas A Borja, Rachel Silva-Smith, Carmen Calfa, et al.Journal of Gastrointestinal Oncology|August 29, 2018
Exceptional response to FOLFIRINOX in a patient with pancreatic cancer and a germline RAD51C mutationSofia Palacio, Terri Pollack, Rachel Silva-Smith, et al.Gynecologic Oncology Reports|August 23, 2016
Primary Peritoneal Carcinoma in a BRCA1/2-negative, PALB2-positive patientRyan Kahn, Arlene Garcia-Soto, Rachel Silva-Smith, et al.Frontiers in Oncology|March 3, 2023
Atypical ATMs: Broadening the phenotypic spectrum of ATM-associated hereditary cancerNicholas A Borja, Rachel Silva-Smith, Marilyn Huang, et al.Journal of Gastrointestinal Oncology|January 18, 2020
DNA damage repair deficiency as a predictive biomarker for FOLFIRINOX efficacy in metastatic pancreatic cancerSofia Palacio, Hannah S McMurry, Robert Ali, et al.American Journal of Medical Genetics. Part A|June 21, 2021
Application of the ACMG/NSGC genetic referral guidelines for hereditary renal cell carcinoma at the University of Miami, from 2014 to 2017Jessica D Leuchter, Priyen M Patel, Kayla M Fourzali, et al.Hereditary Cancer in Clinical Practice|September 17, 2014
Mutation analysis of PALB2 in BRCA1 and BRCA2-negative breast and/or ovarian cancer families from Eastern Ontario, CanadaTaila Hartley, Luca Cavallone, Nelly Sabbaghian, et al.Nature Genetics|March 25, 2014
Germline and somatic SMARCA4 mutations characterize small cell carcinoma of the ovary, hypercalcemic typeLeora Witkowski, Jian Carrot-Zhang, Steffen Albrecht, et al.Pageof 2