Robert C. Green
Biochemistry, Genetics and Molecular Biology · Indiana University
Publications
725
Citations
66,192
Est. group size
—
Recurring co-author estimate
Active years
60
Publishing since 1967
Robert C. Green studies how genome sequencing and genetic testing can be used in medical care, examining what happens when genetic information is shared with patients, families, and even newborns. His work spans how genetic risk information affects health decisions, the accuracy and fairness of genetic tests across different population groups, and conditions ranging from Alzheimer's disease to hereditary cancers and rare inherited disorders. A recurring focus is on real-world clinical use of genomics, including secondary findings, screening practices, and disparities in access to testing.
Publication activity has been fairly steady over the past decade, generally in the range of roughly 30-40 papers per year with some year-to-year fluctuation.
Generated by claude-opus-4-8 from public bibliographic data · Jul 11, 2026
- Elective genomic sequencing for adults in research, clinical and commercial contexts
medRxiv · 2026
- A Lack of Information About Family Health History Motivates Adopted Individuals to Pursue Elective Genomic Testing
American Journal of Medical Genetics Part A · 2025
- Awareness and utilization of genetic testing among Hispanic and Latino adults living in the US: The Hispanic Community Health Study/Study of Latinos
UNC Libraries · 2025
- Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
UNC Libraries · 2025
- Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
UNC Libraries · 2025
- P675: Opportunities for precision medicine in hereditary disease inferred from large-scale, real-world diagnostic genetic testing results
Genetics in Medicine Open · 2025
- P805: Advancing precision care in pregnancy through a treatable fetal findings list
Genetics in Medicine Open · 2025
- Returning Individual-Level Urgent or Emergent Research Results to Participants: The Project Baseline Health Study Experience
American Journal of Medicine Open · 2025
- Advancing precision care in pregnancy through a treatable fetal findings list
The American Journal of Human Genetics · 2025
- Genetics and context for precision health in Greater Boston
Nature Communications · 2025
- Nonadherence to guidelines for genetic testing in families with ovarian cancer shows racial bias
Genetics in Medicine · 2025
- Accelerating eSource scale-up in oncology clinical trials: The i~HD Task Force initiative
Cambridge Prisms Precision Medicine · 2025
- O35: A genotype-first approach among adults at risk for treatable monogenic disorders reveals underdiagnosis and incomplete penetrance
Genetics in Medicine Open · 2025
- Addressing Small and Imbalanced Medical Image Datasets Using Generative Models
Artificial Intelligence and Applications · 2025
- Addressing Small and Imbalanced Medical Image Datasets Using Generative Models: A Comparative Study of DDPM and PGGANs with Random and Greedy K Sampling
arXiv (Cornell University) · 2024
- Genetics in Medicine×34
- Scientific Reports×28
- Nature Communications×18
- The American Journal of Human Genetics×15
- Alzheimer s & Dementia×15
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 11, 2026.
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