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Bita Nehoray · SciRah

Researcher profile · Semantic Scholar

Bita Nehoray

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Bita Nehoray — researcher profile on SciRah

h-index: 14
Works: 49
Citations: 875

Most-cited papers

Baseline Surveillance in Li-Fraumeni Syndrome Using Whole-Body Magnetic Resonance Imaging: A Meta-analysis
M. Ballinger, Ana F. Best, Phuong L. Mai, Payal P. Khincha +32 more
2017JAMA Oncology188 citations Open access
Semantic Scholar
Clinical Application of Multigene Panels: Challenges of Next-Generation Counseling and Cancer Risk Management
T. Slavin, Mariana Niell-Swiller, Ilana Solomon, Bita Nehoray +3 more
2015Frontiers in Oncology113 citations Open access
Semantic Scholar
Somatic TP53 variants frequently confound germline testing results
J. Weitzel, Elizabeth C. Chao, Bita Nehoray, Lily R. Van Tongeren +14 more
2017Genetics in Medicine112 citations Open access
Semantic Scholar
Prospective Study of Cancer Genetic Variants: Variation in Rate of Reclassification by Ancestry
T. Slavin, Lily R. Van Tongeren, C. Behrendt, Ilana Solomon +13 more
2018Journal of the National Cancer Institute66 citations Open access
Semantic Scholar
Pathogenic and likely pathogenic variants in PALB2, CHEK2 and other known breast cancer susceptibility genes among 1054 BRCA-negative Hispanics with breast cancer
J. Weitzel, S. Neuhausen, Aaron W Adamson, Shu Tao +15 more
2019Cancer62 citations Open access
Semantic Scholar
Next-Generation Testing for Cancer Risk: Perceptions, Experiences, and Needs Among Early Adopters in Community Healthcare Settings
K. Blazer, Bita Nehoray, Ilana Solomon, Mariana Niell-Swiller +3 more
2015Genetic Testing and Molecular Biomarkers54 citations Open access
Semantic Scholar
Genetic Gastric Cancer Susceptibility in the International Clinical Cancer Genomics Community Research Network
T. Slavin, S. Neuhausen, Christina Rybak, Ilana Solomon +17 more
2017Cancer Genetics50 citations Open access
Semantic Scholar
Loss-of-function variants in CTNNA1 detected on multigene panel testing in individuals with gastric or breast cancer
D. Clark, Scott T. Michalski, R. Tondon, Bita Nehoray +8 more
2020Genetics in Medicine39 citations Open access
Semantic Scholar
Genetic epidemiology of BRCA1- and BRCA2-associated cancer across Latin America
J. Herzog, Y. Chávarri-Guerra, D. Castillo, J. Abugattas +23 more
2021npj Breast Cancer32 citations Open access
Semantic Scholar
The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genes
T. Slavin, S. Neuhausen, Bita Nehoray, Mariana Niell-Swiller +19 more
2017Familial Cancer30 citations Open access
Semantic Scholar
First estimates of diffuse gastric cancer risks for carriers of CTNNA1 germline pathogenic variants
Marie Coudert, Y. Drouet, Hélène Delhomelle, M. Svrcek +25 more
2022Journal of Medical Genetics21 citations Open access
Semantic Scholar
Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers
F. Qian, M. Rookus, Goska Leslie, H. Risch +134 more
2019British Journal of Cancer17 citations Open access
Semantic Scholar
The burden of breast cancer predisposition variants across the age spectrum among 10,000 patients
Y. Chávarri-Guerra, C. Hendricks, Sandra M. Brown, C. Marcum +11 more
2019Journal of The American Geriatrics Society16 citations Open access
Semantic Scholar
Development and Pilot Implementation of the Genomic Risk Assessment for Cancer Implementation and Sustainment (GRACIAS) Intervention in Mexico
K. Blazer, Y. Chávarri-Guerra, C. Villarreal Garza, Bita Nehoray +11 more
2021JCO Global Oncology14 citations Open access
Semantic Scholar
Clonal hematopoiesis and mosaicism revealed by a multi-tissue analysis of constitutional TP53 Status
D. Castillo, Tze-An Yuan, Bita Nehoray, Aleck E Cervantes +12 more
2022Cancer Epidemiology, Biomarkers and Prevention11 citations Open access
Semantic Scholar
Multigene assessment of genetic risk for women for two or more breast cancers
J. Weitzel, J. Kidd, R. Bernhisel, Susan Shehayeb +13 more
2021Breast Cancer Research and Treatment10 citations Open access
Semantic Scholar
Corrigendum: Clinical Application of Multigene Panels: Challenges of Next-Generation Counseling and Cancer Risk Management
T. Slavin, Mariana Niell-Swiller, Ilana Solomon, Bita Nehoray +3 more
2015Frontiers in Oncology10 citations Open access
Semantic Scholar
A quantitative, Bayesian-informed approach to gene-specific variant classification: Updated Expert Panel recommendations improve classification of TP53 germline variants for Li-Fraumeni syndrome
Cristina Fortuno, Megan N. Frone, Jessica L. Mester, M. de la Hoya +33 more
2025Genome Medicine5 citations Open access
Semantic Scholar
Uptake of Risk-Reducing Surgeries in an International Real-World Cohort of Hispanic Women
Y. Chávarri-Guerra, A. Ferrigno Guajardo, C. Villarreal-Garza, B. Martinez-Cannon +18 more
2024JCO Global Oncology5 citations Open access
Semantic Scholar
Experience Gained from the Development and Execution of a Multidisciplinary Multi-Syndrome Hereditary Colon Cancer Family Conference
Ilana Solomon, Christina Rybak, Lily R. Van Tongeren, Lili Kuzmich +8 more
2018Journal of Cancer Education5 citations Open access
Semantic Scholar
Assessment of the clinical presentation of patients with at least two deleterious mutations on multi-gene panel testing.
J. Weitzel, K. Blazer, Bita Nehoray, J. Kidd +5 more
20154 citations
Semantic Scholar
Feasibility of a cancer screening program using multicancer early detection testing and whole‐body magnetic resonance imaging in a high‐risk population
Dan J Raz, Bita Nehoray, A. Ceniceros, P. Motarjem +3 more
2025Cancer3 citations
Semantic Scholar
Genetic counselors' and community clinicians' implementation and perceived barriers to informed consent during pre‐test counseling for hereditary cancer risk
Alex Capasso, Bita Nehoray, Nicholas Gorman, Emily A Quinn +2 more
2024Journal of Genetic Counseling3 citations Open access
Semantic Scholar
A prospective study of Annual Whole-Body MRI (WBMRI) as Part of a Multimodality Screening Program for Individuals with Li-Fraumeni Syndrome (LFS)
A. Maoz, N. Chen, P. Umaretiya, Sophie R Cahill +18 more
2025JCO Precision Oncology2 citations
Semantic Scholar
Questioning a Li-Fraumeni Syndrome diagnosis: Characterization of a commonly observed germline TP53 variant, p.Arg156His.
Bita Nehoray, Alison Schwartz, Sophie Hyman, Samantha M. Stokes +4 more
2022Journal of Clinical Oncology2 citations
Semantic Scholar
Abstract P051: The INSPIRE Study (Implementing Next-generation Sequencing for Precision Intervention and Risk Evaluation): scaling return of genomic results
Ilana Solomon, H. Hampel, K. McDonnell, K. Blazer +18 more
2023Cancer Prevention Research1 citations
Semantic Scholar
Clinical conundrums: Developing a strategy for discerning TP53-associated chip and coherent clinical care.
J. Weitzel, J. Garber, D. Castillo, S. Sand +10 more
20201 citations
Semantic Scholar
Hereditary Pancreatic Cancer Syndromes: Providing Care to At-Risk Families.
Elisabeth King, Bita Nehoray
2019Clinical Journal of Oncology Nursing1 citations
Semantic Scholar
Abstract PD7-02: Multiplex Identification of genetic etiologies among women with bilateral breast cancer using a 25-gene hereditary cancer panel
J. Weitzel, K. Blazer, Bita Nehoray, J. Kidd +6 more
20161 citations
Semantic Scholar
Abstract A36: Exploring the climate, barriers, and possible approaches to implementing genetic cancer risk assessment in Latin America: A roundtable discussion
T. Chavez, Bita Nehoray, A. Obregon-Tito, C. Ricker +21 more
20151 citations
Semantic Scholar
Abstract 2761: Evaluation of the BOADICEA model for predictingBRCA1andBRCA2mutation carrier probabilities in high-risk US Hispanic and Mexican families: A report from the Clinical Cancer Genetics Community Research Network
J. Clague, C. Villarreal-Garza, A. Navarro, A. Obregon-Tito +13 more
20151 citations
Semantic Scholar
P057: Incidence and phenotypic spectrum of SDHA pathogenic variants identified in an unselected precision medicine cohort*
Alex Capasso, A. Chitre, Katherine G. Roth, J. Bonner +8 more
2026Genetics in Medicine Open0 citations Open access
Semantic Scholar
Interpretable Active Learning for Pedigree Data Deduplication in Cancer Genetics.
M. S. Rosito, Aleck E Cervantes, C. Hong, J. Bonner +9 more
2026JCO Clinical Cancer Informatics0 citations
Semantic Scholar
Age-specific risks of leukemia in Li Fraumeni syndrome in children, adolescents, young adults, and adults.
R. Lee, J. Bonner, Danielle Braun, S. Lindsey +7 more
2026Journal of Clinical Oncology0 citations
Semantic Scholar
A prospective study of whole-body MRI (WBMRI) as part of a multimodality screening program for individuals with Li-Fraumeni syndrome (LFS).
A. Maoz, Nan Chen, P. Umaretiya, Sophie R Cahill +16 more
2025Journal of Clinical Oncology0 citations
Semantic Scholar
Effect of cancer screening with multi-cancer early detection testing and whole body MRI on cancer worry in a high-risk population.
Dan J Raz, Bita Nehoray, A. Ceniceros, P. Motarjem +3 more
2024Journal of Clinical Oncology0 citations
Semantic Scholar
P471: Uptake of a chatbot for disclosure of germline genetic test results through a universal genetic testing program*
Elyssa Zukin, Bita Nehoray, Michael García, Heather Hampel +8 more
2024Genetics in Medicine Open0 citations Open access
Semantic Scholar
Universal germline testing for cancer susceptibility and actionable noncancer disorders among 19,842 patients: Initial findings from the City of Hope INSPIRE study.
S. Gray, Ilana Solomon, Heather Hampel, Michael García +16 more
2024Journal of Clinical Oncology0 citations Open access
Semantic Scholar
Abstract P039: Framework for genomic cancer risk assessment dissemination and implementation in Latin America: The GRACIAS (genetic risk assessment for cancer implementation and sustainment) study
J. Weitzel, J. Abugattas, C. Villarreal-Garza, A. Navarro +14 more
2023Cancer Prevention Research0 citations
Semantic Scholar
Abstract 2214: Disparity in the uptake of risk-reducing surgery after GCRA in Hispanic patients in Latin America and in the United States
J. Weitzel, Y. Chávarri-Guerra, A. Ferrigno, Pamela Mora-Alferez +13 more
2022Cancer Research0 citations
Semantic Scholar
Cross-sectional Clinical Cancer Genomics Community of Practice survey analysis of provider attitudes and beliefs regarding the use of deceased family member tissue to guide living family member genetic cancer risk assessment.
Bita Nehoray, T. Slavin, Can-Lan Sun, Karen E. Hurley +11 more
2022Journal of Genetic Counseling0 citations Open access
Semantic Scholar
Abstract P3-13-07: A comprehensive germline genetic landscape in young Jewish & Arab women with breast cancer
G. Rennert, Bita Nehoray, F. Lejbkowicz, S. Dishon +8 more
2022Cancer Research0 citations
Semantic Scholar
Abstract PO-049: Genetic cancer risk assessment (GCRA) increases perceived personal control in Latinas at risk for hereditary breast and ovarian cancer
C. Ricker, Bita Nehoray, Guadalupe Carvajal, K. Blazer +6 more
20200 citations
Semantic Scholar
The effect of Genetic Cancer Risk Assessment (GCRA) on the uptake of risk-reducing surgeries (RRS) in Hispanic women with breast cancer (BC).
Y. Guerra, Kai Yang, J. Abugattas, Sandra M. Brown +16 more
20180 citations
Semantic Scholar
Abstract P6-09-05: Factors associated with the uptake of risk-reducing surgeries among Hispanic women at high risk of breast and ovarian cancer
Y. Chávarri-Guerra, Kai Yang, I. Komenaka, Sandra M. Brown +16 more
20180 citations
Semantic Scholar
Abstract 4273: Variant reclassifications in hereditary cancer genetics and their implications for clinical care
T. Slavin, S. Gray, Lily R. Van Tongeren, Ilana Solomon +11 more
20170 citations
Semantic Scholar
Germline cancer susceptibility mutations in older women with breast cancer (BC).
Y. Guerra, S. Sand, Sandra M. Brown, C. Hendricks +15 more
20170 citations
Semantic Scholar
Abstract 2551: Identifying hereditary gastric cancer predisposition in the clinical cancer genomics community research network
T. Slavin, Kai Yang, S. Sand, T. Chavez +10 more
20160 citations
Semantic Scholar
Abstract A50: Differences in perceived personal control among Latina women undergoing genetic cancer risk assessment for hereditary breast and ovarian cancer
T. Chavez, Bita Nehoray, C. Ricker, K. Blazer +7 more
20160 citations
Semantic Scholar

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