The MS in Human Genetics at the University of Michigan trains students in advanced genetic principles, molecular biology, and clinical applications. With access to cutting-edge labs and interdisciplinary faculty, students explore how genes influence health, disease, and development while preparing for careers in research, diagnostics, and biomedical innovation.
Investigating BRCA1 and BRCA2 Mutations in Hereditary Breast Cancer
Genomic Characterization of Rare Mendelian Diseases
Role of Non-Coding RNA in Gene Expression Regulation in Human Cells
Prenatal Genetic Screening: Ethical Considerations and Emerging Technologies
Genome Editing Applications for Sickle Cell Disease Therapy
Population-Based Study of Genetic Risk Factors for Alzheimer's Disease
Analysis of X-Chromosome Inactivation Patterns in Female Patients
Molecular Diagnosis of Lysosomal Storage Disorders Using NGS
Whole Exome Sequencing for Undiagnosed Genetic Syndromes
Exploring Pharmacogenomics for Personalized Drug Dosing
Genotype-Phenotype Correlation in Neurodevelopmental Disorders
CRISPR-Cas9 Gene Disruption in Human iPSC Models
Mitochondrial Genome Variability in Inherited Metabolic Disorders
Heritability of Autism Spectrum Disorders Across Sibling Populations
Translational Research in Genetic Counseling Practices
Epigenetic Modifications in Human Placental Development
Investigating Gene-Environment Interactions in Asthma Susceptibility
Machine Learning for Variant Classification in Clinical Genomics
Carrier Screening Program Evaluation in Diverse Populations
Comparative Study of Germline vs Somatic Mutations in Cancer Risk
This program equips students to contribute to discoveries in genetic diagnostics, personalized medicine, and translational genomics in both academic and clinical settings.
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