Suzanne DeBrosse

Suzanne DeBrosse, MD, is a Clinical Assistant Professor in the Department of Neurology at Case Western Reserve University School of Medicine, with board certifications in Clinical Genetics and Genomics, Pediatrics, and Neurology (with special qualifications in Child Neurology). She practices at University Hospitals Case Medical Center and is affiliated with UH Hospitals.

Education and Training

• Doctor of Medicine (2004), Case Western Reserve University School of Medicine
• Undergraduate (2000), Case Western Reserve University
• Residency in Medical Genetics (2011), Child Neurology (2009), and Pediatrics (2006) at University Hospitals of Cleveland.

Research Interests
Suzanne DeBrosse focuses on Medical Genetics and Neurology, particularly Genetic Disorders and Mitochondrial Diseases. Her work explores the intersection of Pediatric Neurology and Metabolic Disorders, with an emphasis on Neurogenetics and Genotype-Phenotype Correlations.

Publication Trends
Her research spans 2012–2023, featuring collaborations on Neurodevelopmental Disorders (e.g., Kleefstra syndrome), Genetic Epilepsies (e.g., SCN3A mutations), Mitochondrial Encephalopathies, and Ciliopathies (e.g., OFD1-related disorders). She contributes to Clinical Reviews and Case Studies in pediatric neurogenetics.

Advising and Collaborations
While no direct student advisement is listed, Suzanne collaborates with multidisciplinary teams in Neurology, Genetics, and Pediatrics. She participates in international consortia like the DDD Study Group and CENet Study Group, advancing rare disease research.