Fellowship in Medical Biochemical Genetics

The Fellowship in Medical Biochemical Genetics at Johns Hopkins University School of Medicine provides specialized training in the diagnosis and management of inborn errors of metabolism and biochemical genetic disorders. The program emphasizes comprehensive clinical care through exposure to metabolic clinics, inpatient consultations, and newborn screening programs, allowing fellows to develop expertise in evaluating metabolic diseases across all age groups. Trainees gain hands-on experience in biochemical genetics laboratories, including metabolic testing, enzyme analysis, and interpretation of complex diagnostic results. The fellowship also includes training in dietary and medical management of metabolic conditions, emergency care of metabolic crises, and long-term patient follow-up. In addition, fellows participate in research activities, academic conferences, and interdisciplinary collaborations with specialists in pediatrics, neurology, and nutrition. Structured teaching and mentorship prepare trainees for certification by the American Board of Medical Genetics and Genomics.

1. Apply through ERAS

• Submit your application via ERAS when the application cycle opens (usually July).

1. Prepare Required Documents

• Completed application form
• Curriculum Vitae (CV)
• Personal Statement
• Recent photograph
• Academic transcripts
• USMLE scores
• Minimum three Letters of Recommendation (including one from Residency Program Director)

1. Application Review

• The program committee reviews all completed applications.

1. Interview Process

• Interviews are conducted by faculty to assess academic background, clinical skills, and interest in genetics.

1. Match Process (NRMP)

• Candidates are ranked and matched through the National Resident Matching Program (NRMP).