Hans C. Andersson, MD
Karen Gore Professor of Human Genetics, Tulane Cancer Center Member - Genes X Environment Research Program
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Biography
Hans C. Andersson, MD is the Karen Chair of Human Genetics, Professor of Pediatrics and Director of the Hayward Genetics Center at the Tulane University Medical School where he directs the Biochemical Genetics Lab. Following fellowship training in clinical genetics and cell biology at the National Institutes of Health (1987-91) and University of Gottingen, Germany (1992-93), Dr. Andersson achieved American Board of Medical Genetics certification in Clinical Genetics and Clinical Biochemical/Molecular Genetics and American Board of Pediatrics board certification in Pediatrics. His research has elucidated clinical features and pathophysiology of inherited metabolic genetic disorders, especially in lysosomal storage disorders. He leads the major regional referral center for such diseases in the Gulf South and is a member of the board for the International Collaborative Gaucher Group. He was Co-PI of the Region 3 Genetics and Newborn Screening Collaborative (HRSA; 2007-2017) where he directed the efforts in: 1) developing a regional emergency preparedness plan and 2) telemedicine core for genetic care. Dr. Andersson has been a Member of the ACGME Residency Review Committee, an Editorial Board Member of the Journal of Pediatrics, past and current President (2008-2010 and 2024-26) of the SouthEast Regional Genetics Group (SERGG), and holds membership of numerous national societies including the Society of Pediatric Research and Society of Inherited Metabolic Diseases. He is the past Chair of the National Coordinating Center Telegenetics Workgroup and a member of the Disaster Preparedness Workgroup. Dr. Andersson has been a life-long resident of New Orleans and played a critical role in reestablishment of clinical genetics in Louisiana following hurricanes Katrina and Rita. He has attended local and outreach genetics clinics in Louisiana for over 30 years.
Research
Tulane Cancer Center Contributing Member
Inherited metabolic disease; diagnosis and treatment of lysosomal storage disorders; novel therapies of PKU