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Rachel Monahan
Observed name:
Monahan, Rachel
Institutions:
NYU Langone Health,
NYU Langone’s Laura and Isaac Perlmutter Cancer Center,
New York University
Observed institutions:
Feinstein Institute for Medical Research,
NYU Langone Health,
NYU Langone’s Laura and Isaac Perlmutter Cancer Center,
New York University
ORCID:
0000-0003-1000-2790
Observed ORCID:
0000-0003-1000-2790
OpenAlex ID:
A5089394246
Uptake of Cancer Genetic Services for Chatbot vs Standard-of-Care Delivery Models
2024
·
Kimberly A. Kaphingst
, Wendy K. Kohlmann
, et al.
·
JAMA Network Open
·
53
PDF
Association of Disparities in Family History and Family Cancer History in the Electronic Health Record With Sex, Race, Hispanic or Latino Ethnicity, and Language Preference in 2 Large US Health Care Systems
2022
·
Daniel Chavez-Yenter
, Melody S. Goodman
, et al.
·
JAMA Network Open
·
45
PDF
Patient Interactions With an Automated Conversational Agent Delivering Pretest Genetics Education: Descriptive Study
2021
·
Daniel Chavez-Yenter
, Kadyn E Kimball
, et al.
·
Journal of Medical Internet Research
·
43
PDF
Comparing models of delivery for cancer genetics services among patients receiving primary care who meet criteria for genetic evaluation in two healthcare systems: BRIDGE randomized controlled trial
2021
·
Kimberly A. Kaphingst
, Wendy Kohlmann
, et al.
·
BMC Health Services Research
·
37
Circulating T cell subsets are altered in individuals with chronic spinal cord injury
2015
·
Rachel Monahan
, Adam Stein
, et al.
·
Immunologic Research
·
34
PDF
GARDE: a standards-based clinical decision support platform for identifying population health management cohorts
2022
·
Richard L Bradshaw
, Kensaku Kawamoto
, et al.
·
Journal of the American Medical Informatics Association
·
27
Barriers to family history collection among Spanish-speaking primary care patients: a BRIDGE qualitative study
2022
·
Erica Liebermann
, Peter Taber
, et al.
·
PEC Innovation
·
10
Bridging Technology and Pretest Genetic Services: Quantitative Study of Chatbot Interaction Patterns, User Characteristics, and Genetic Testing Decisions
2025
·
Yang Yi
, Lauren Kaiser-Jackson
, et al.
·
Journal of Medical Internet Research
·
8
PDF
Enhanced family history-based algorithms increase the identification of individuals meeting criteria for genetic testing of hereditary cancer syndromes but would not reduce disparities on their own
2023
·
Richard L. Bradshaw
, Kensaku Kawamoto
, et al.
·
Journal of Biomedical Informatics
·
7
Importance of Prior Patient Interactions With the Healthcare System to Engaging With Pretest Cancer Genetic Services via Digital Health Tools Among Unaffected Primary Care Patients: Findings From the BRIDGE Trial
2025
·
Lingzi Zhong
, Jemar R. Bather
, et al.
·
Health Services Research
·
5
PDF
Social vulnerability and genetic service utilization among unaffected BRIDGE trial patients with inherited cancer susceptibility
2025
·
Jemar R. Bather
, Melody S. Goodman
, et al.
·
BMC Cancer
·
5
PDF
Determinants of Breast Cancer Screening Adherence During the COVID-19 Pandemic in a Cohort at Increased Inherited Cancer Risk in the United States
2024
·
Adrian Harris
, Jemar R. Bather
, et al.
·
Cancer Control
·
4
Incomplete Family History and Meeting Algorithmic Criteria for Genetic Evaluation of Hereditary Cancer
2025
·
Adrian Harris
, Jemar R. Bather
, et al.
·
JAMA Network Open
·
3
PDF
Evaluation of the Stronger Together Peer Mentoring Model Among Patients With Breast and Gynecologic Cancer in Viet Nam
2024
·
PhuongThao D. Le
, Carolyn Taylor
, et al.
·
JCO Global Oncology
·
2
P377: Limitations of automated approaches to utilizing the EHR to identify high-risk patients for hereditary cancer genetic testing
2023
·
Rachelle Chambers
, Meenakshi Sigireddi
, et al.
·
Genetics in Medicine Open
·
1
PDF
Comparing patients’ perceptions and cognitive and emotional responses to pre-test cancer genetic services delivered via chatbot versus standard of care: findings from the BRIDGE trial
2026
·
Yang Yi
, Jemar R. Bather
, et al.
·
Genetics in Medicine Open
PDF
The efficacy of point of care (POC) hereditary cancer genetic testing among patients with prostate cancer.
2025
·
Matthew Siskin
, Jiyu Kim
, et al.
·
JCO Oncology Practice
PDF
Improved access to genetics for individuals with potential germline mutations identified on somatic testing.
2024
·
Elizabeth Manderski
, Rachel Monahan
, et al.
·
JCO Oncology Practice
PDF
Abstract A030: Identifying LGBTQ+-related barriers and gaps in patient and workplace environments: An LGBTQ+ environmental needs assessment at Perlmutter Cancer Center
2023
·
Alexandr Trifonov
, Rachel Monahan
, et al.
·
Cancer Epidemiology Biomarkers & Prevention
Abstract 52: Implementation of a Hospital-Based Peer Support Intervention Model for Cancer Patients: Results From a Pilot Study in Vietnam
2023
·
PhuongThao Le
, Carolyn Taylor
, et al.
·
Cancer Epidemiology Biomarkers & Prevention
Additional file 1 of Comparing models of delivery for cancer genetics services among patients receiving primary care who meet criteria for genetic evaluation in two healthcare systems: BRIDGE randomized controlled trial
2021
·
Kaphingst, Kimberly A.
, Kohlmann, Wendy
, et al.
·
Figshare
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Works count:
21
Citation count:
281
H-index:
7
I10-index:
7
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