Bita Nehoray, M.S., L.C.G.C.
- Cancer Risk Counselor
- Pediatric Cancer Syndromes
- Li-Fraumeni Syndrome
- Clinical Cancer Genomics
- Hereditary Cancers
- Cancer Genetics
Bita Nehoray, M.S., L.C.G.C., is a licensed board-certified genetic counselor specializing in cancer genetics. She has a master’s degree in human genetics and genetic counseling from Stanford University and a bachelor’s degree in integrative biology from University of California Berkeley.
She is fluent in Spanish and Farsi, and is committed to advancing the provision of cancer genetics services to medically underserved and culturally diverse populations.
Nehoray joined the City of Hope Division of Clinical Cancer Genomics in 2012. Her clinical responsibilities include providing pro-bono cancer genetic counseling services to underserved Latino families through an outreach program established by the Division of Clinical Cancer Genomics, and supported through government and foundations grants and compassionate funding, as well as providing genetic counseling services for City of Hope’s pediatric population.
She is a member of the National Society of Genetic Counselors, the Collaborative Group of the Americas on Inherited Colorectal Cancer and the American Society of Human Genetics.
- July 2012-Present, Cancer Risk Counselor, Division of Clinical Cancer Genomics, City of Hope, Duarte, CA
- Stanford University, Stanford, CA, M.S., Human Genetics and Genetic Counseling
- University of California Berkeley, Berkeley, CA, B.S., Integrative Biology
Ballinger ML, Best A, Mai PL … Nehoray B, Robson M, Walsh M, Manelli L, Villani A, Thomas DM, Savage SA. Baseline Surveillance in Li-Fraumeni Syndrome Using Whole-Body Magnetic Resonance Imaging: A Meta-analysis. JAMA Oncol.(2017).
Blazer KR, Nehoray B, Solomon I, Niell-Swiller M, Culver JO, Uman GC, Weitzel JN. (2015). Next-Generation Testing for Cancer Risk: Perceptions, Experiences, and Needs Among Early Adopters in Community Healthcare Settings. Genetic Testing and Molecular Biomarkers, 19(12), 657-665. DOI: 10.1089/gtmb.2015.0061 10.1089/gtmb.2015.0061
Slavin T, Niell-Swiller M, Solomon I, Nehoray B, Rybak C, Blazer KR, Weitzel JN. (2015). Clinical application of multigene panels: challenges of next-generation counseling and cancer risk management. Frontiers in Oncology, 5. DOI: 10.3389/fonc.2015.00208
Slavin T, et al., Genetic Gastric Cancer Susceptibility in the International Clinical Cancer Genomics Community Research Network. Cancer Genet, 2017. 216-217: p. 111-119.
Slavin TP, et al., The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genes. Familial Cancer, 2017: p. 1-11.
Slavin TP, Van Tongeren LR…Nehoray B … Weitzel JN. Prospective Study of Cancer Genetic Variants: Variation in Rate of Reclassification by Ancestry. J Natl Cancer Inst, 2018.
Weitzel JN, Chao EC, Nehoray B…Jasperson K. Somatic TP53 variants frequently confound germ-line testing results. Genet Med, 2017.
Blazer KR, Nehoray B, Solomon I, Niell-Swiller M, Rybak C, Nunez G, ... Weitzel JN. (2015, October 21-23, 2015). Leveraging the Resources of an Innovative Clinical Cancer Genetics Training Program to Address Disparities in Cancer Prevention and Control in Latin America. Paper presented at the International Cancer Education Conference: Cancer Education in Diverse Populations: Disparities, Genomics & Innovations, Tucson, AZ, USA.
Chávarri-Guerra Y … Nehoray B … Weitzel JN. Factors associated with the uptake of risk-reducing surgeries among Hispanic women at high risk of breast and ovarian cancer. Abstract presented at the San Antonio Breast Cancer Symposium. 2017. San Antonio.
Chavez T, Nehoray B, Obregon-Tito A, Ricker C, Solomon I, Niell-Swiller M ... Weitzel JN. (2014, November 9-12). Exploring the Climate, Barriers, and Possible Approaches to Implementing Genetic Cancer Risk Assessment in Latin America: A Roundtable Discussion. Paper presented at the 7th AACR Conference on The Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved, San Antonio, TX.
Chavez T, Nehoray B, Obregon-Tito A, Ricker C, Solomon I, Niell-Swiller M ... Weitzel JN. (2015). Abstract A36: Exploring the climate, barriers, and possible approaches to implementing genetic cancer risk assessment in Latin America: A roundtable discussion. Cancer Epidemiology Biomarkers & Prevention, 24(10 Supplement), A36. DOI: 10.1158/1538-7755.disp14-a36
Chavez T, Yang K, Nehoray B, Ricker C, Nunez G, Arreola D ... Weitzel JN. (2015, January 28-30, 2016). Evaluating the effects of a pre-genetic cancer risk assessment telephone intervention on anxiety and cancer genetics knowledge. Paper presented at the 17th Annual Convention of the Society of Personality and Social Psychology, San Diego, CA, USA.
Chavez T, Nehoray B, Ricker C, Blazer KR, Sand S, Ashing KT . Weitzel JN. (2015, November 13-16, 2015). Differences in perceived personal control among Latina women undergoing genetic cancer risk assessment for hereditary breast and ovarian cancer. Paper presented at the 8th Annual American Association for Cancer Research Conference on The Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved, Sheraton Atlanta Hotel, Atlanta, Georgia, USA.
Clague J, Villarreal-Garza C, Navarro, AD, Obregon-Tito AJ, Sand S, Chavez TA . . . Weitzel, Jeffrey N. (2015). Abstract 2761: Evaluation of the BOADICEA model for predicting BRCA1 and BRCA2 mutation carrier probabilities in high-risk US Hispanic and Mexican families: A report from the Clinical Cancer Genetics Community Research Network. Cancer Research, 75(15 Supplement), 2761. doi: 10.1158/1538-7445.am2015-2761
Cordova J, Chavez T, Yang K, Blazer K, Nehoray B, Sand S, Weitzel J. (2015). Genetic Cancer Risk Assessment and Cancer Genetics Knowledge: Serving to Decrease Patient Anxiety? Paper presented at the Eugene and Ruth Roberts Summer Student Academy City of Hope, Duarte, CA.
Nehoray B, Ricker C, Yang K, Weitzel J, Blazer, KR. (2015, October 6-10, 2015). Examining Preparedness Among Hispanic Women Undergoing Genetic Cancer Risk Assessment.(Poster #2199F). Paper presented at the 65th American Society of Human Genetics (ASHG) Annual Meeting, Baltimore, MD, USA.
Nehoray B. (October 2015) Physicians & GINA: Awareness & Knowledge of Anti-Genetic Discrimination Laws Amongst Obstetrician-Gynecologists & Oncologists. Poster presented at the National Society of Genetic Counselors Annual Education Conference, Boston, MA.
Nehoray B, et al. Cancer susceptibility mutations in very young Israeli women with breast cancer. Abstract presented at The American Society of Human Genetics. 2017. Orlando Fl.
Rybak C, Solomon I, Niell-Swiller M, Nehoray B, Yang K, Blazer KR, Weitzel J. (October 11-12, 2015 ). Bridging the void: Gaps in follow-up care of individuals at increased gastrointestinal cancer risk. Paper presented at the The 2015 The Collaborative Group of the Americas on Inherited Colorectal Cancer (CGA) Annual Meeting Sheraton Inner Harbor in Baltimore, MD, USA.
Neuhausen S, Weitzel JN, Adamson A, Tao S, Slavin TP, Ricker C ... Ziv E. (2016, October 18-22, 2016). Latinas and breast cancer: discovery of mutations in non BRCA1/2 high and moderate penetrance breast cancer susceptibility genes. Paper presented at the ASHG 2016, Vancouver, Canada.
Slavin T, Neuhausen S, Nehoray B, Niell-Swiller M, Rybak C, Solomon Iana ... Clinical Cancer Genomics Community Research Network. (2016, October 18-22, 2016). Fanconi anemia gene variants predispose to hereditary pancreatic cancer. Paper presented at the ASHG 2016, Vancouver, Canada.
Slavin T, et al. The Spectrum of Germline Variants in Early-Onset Colorectal Cancer. Abstract presented at the Collaborative Group of the Americas in Inherited Colorectal Cancer. 2017. Orlando, FL.
Solomon I, Nehoray B, Niell-Swiller M, Rybak C, Yang K, Weitzel J, Blazer K. (2015, October 6-10, 2015). Best Practices in Genetic Cancer Risk Assessment: Delivery models and barriers in community settings (Poster #:2217F). Paper presented at the 65th American Society of Human Genetics (ASHG) Annual Meeting, Baltimore, MD, USA.
Weitzel J, Blazer K, Nehoray B, Kidd JM, Slavin T, Solomon I ... Saam J. (2015). Assessment of the clinical presentation of patients with at least two deleterious mutations on multi-gene panel testing. Paper presented at the American Society Clinical Oncology Annual Meeting, Chicago, IL.
May 2014, “A Review of Hereditary Cancer Syndromes, With a Focus on Gynecologic Malignancy” Gynecology Department Grand Rounds, Olive View Medical Center
June 2012, “Physicians & GINA: Awareness & Knowledge of Anti-Genetic Discrimination Laws Amongst Obstetrician-Gynecologists & Oncologists” Human Genetics & Genetic Counseling Research Colloquium, Stanford University
April 2012, “CFTR potentiators in patients with cystic fibrosis with gating mutations.” Human Genetics Journal Club, Stanford University
February 2012, “Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial.” Helen Diller Family Comprehensive Cancer Center Journal Club, University of California San Francisco
November 2011, “Overview of Hereditary Periodic Fever Syndromes” Medical Genetics Grand Rounds, Stanford University Medical Center
September 2011, “Entender lo Genético: La Genética de los trastornos hemorrágicos” Hemophilia Education Workshop, Hemophilia Foundation of Northern California
- National Society of Genetic Counselors
- Cancer SIG and Pediatric Cancer Subcommittee
- American Society of Human Genetics