Cynthia L. Neben

Color (United States) — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

18h-index2.0kcitations36works123.42yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Genetic Associations and Epidemiology(10), BRCA gene mutations in cancer(9), Connective tissue disorders research(7), Genomics and Rare Diseases(7), Hedgehog Signaling Pathway Studies(5)

Publications36 total

HSD72 Virtual Cancer Screening and Support Program: A Model for Improving Cancer Care Continuity Through Screening, Diagnosis, Treatment, and Survivorship
Value in Health·2025
CO134 Pathways to Precision Cancer Care: Integrating Genetic Services into a Nationwide, Virtual Cancer Screening and Support Program
Value in Health·2025
Improving access to cancer screening through national telehealth-based lung and colorectal cancer screening programs.
Journal of Clinical Oncology·2025
P584: Pathways to precision cancer care: Integrating genetic services into a nationwide, risk-adjusted cancer program
Genetics in Medicine Open·2025Open Access
Genomic data in the All of Us Research Program
Nature·2024· 617 citedOpen Access
Clinical Implementation of Combined Monogenic and Polygenic Risk Disclosure for Coronary Artery Disease
JACC Advances·2022· 34 citedOpen Access
CNPY4 inhibits the Hedgehog pathway by modulating membrane sterol lipids
Nature Communications·2022· 8 citedOpen Access
Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program
Genome Medicine·2022· 61 citedOpen Access
Additional file 2 of Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program
Figshare·2022Open Access
PPM4 Closing the knowledge gap in genomics research: A patient-centered approach to report development in the All of Us Research Program
Value in Health·2021
Association of Genetic Variation With Cirrhosis: A Multi-Trait Genome-Wide Association and Gene–Environment Interaction Study
Gastroenterology·2020· 124 citedOpen Access
Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions
Nature Communications·2020· 456 citedOpen Access
Burden of hereditary cancer susceptibility in unselected patients with pancreatic ductal adenocarcinoma referred for germline screening
Cancer Medicine·2020· 42 citedOpen Access
Patient acceptance of genetic testing for familial hypercholesterolemia in the CASCADE FH Registry
Journal of clinical lipidology·2020· 35 cited
Color Data v2: a user-friendly, open-access database with hereditary cancer and hereditary cardiovascular conditions datasets
2020· 1 citedOpen Access
Color Data v2: a user-friendly, open-access database with hereditary cancer and hereditary cardiovascular conditions datasets
Database·2020· 5 citedOpen Access
Polygenic background modifies penetrance of monogenic variants conferring risk for coronary artery disease, breast cancer, or colorectal cancer
2019· 19 citedOpen Access
Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores
Genome Medicine·2019· 113 citedOpen Access
Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores
2019· 14 citedOpen Access
Multi-Gene Panel Testing of 23,179 Individuals for Hereditary Cancer Risk Identifies Pathogenic Variant Carriers Missed by Current Genetic Testing Guidelines
Journal of Molecular Diagnostics·2019· 105 citedOpen Access
page 1 of 2Next →

Frequent Co-authors

Alicia Y. Zhou(16), Amy E. Merrill(11), Scott Topper(7), Anjali D. Zimmer(7), Amit V. Khera(6), Julian R. Homburger(5), Deanna Brockman(5), Ophir D. Klein(5), J Salvá(5), Creighton T. Tuzon(5), Anthony Philippakis(4), Brian Idoni(4), Deborah Krakow(4), Alexander G. Bick(3), Ginger Metcalf(3), Anjene Musick(3), Kimberly F. Doheny(3), Stacey Gabriel(3), Richard A. Gibbs(3), Heidi L. Rehm(3)