GerardThomasBerrySr.MD
Medical Genetics • Boston, MAClinical Biochemical Genetics
Professor, Pediatrics, Children's Hospital, Harvard Medical School
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Office
300 Longwood Ave
Boston Children's Hospital
Boston, MA 02115Phone+1 617-857-4636Fax+1 617-730-4874
Summary
- Dr. Gerard Berry is a medical geneticist in Boston, MA and is affiliated with multiple hospitals in the area, including Brigham and Women's Hospital and Boston Children's Hospital. He received his medical degree from Sidney Kimmel Medical College at Thomas Jefferson University and has been in practice 45 years. He specializes in clinical biochemical genetics and is experienced in inborn errors of metabolism. He has more than 250 publications and over 500 citings.
Education & Training
Children's Hospital of PhiladelphiaFellowship, Clinical Biochemical Genetics, 1979 - 1981
Sidney Kimmel Medical College at Thomas Jefferson University/Nemours Children's Health, WilmingtonResidency, Pediatrics, 1976 - 1978
Mercy Catholic Medical CenterInternship, Internal Medicine, 1975 - 1976- Sidney Kimmel Medical College at Thomas Jefferson UniversityClass of 1975
Certifications & Licensure
MA State Medical License 2006 - 2026
PA State Medical License 1976 - 2024
DC State Medical License 2002 - 2004
MD State Medical License 2003 - 2004
NJ State Medical License 1982 - 1987- American Board of Medical Genetics and Genomics Clinical Biochemical Genetics
- American Board of Pediatrics Pediatrics
- American Board of Pediatrics Pediatric Endocrinology
Awards, Honors, & Recognition
- Sidney Kimmel Medical College at Thomas Jefferson University Alumni Achievement Award Sidney Kimmel Medical College at Thomas Jefferson University, 2016
Clinical Trials
- Long-term Outcome of N-Carbamylglutamate Treatment in Propionic Acidemia and Methylmalonic Acidemia Start of enrollment: 2012 Sep 01
- Short-Term Outcome of N-Carbamylglutamate in the Treatment of Acute Hyperammonemia Start of enrollment: 2012 Sep 01
- A Study of UX007 (Triheptanoin) in Participants With Long-Chain Fatty Acid Oxidation Disorders (LC-FAOD) Start of enrollment: 2014 Feb 06
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Publications & Presentations
PubMed
- 121 citationsCopy number variation plays an important role in clinical epilepsyHeather E. Olson, Yiping Shen, Jennifer Avallone, Beth Rosen Sheidley, Rebecca Pinsky
Annals of Neurology. 2014-06-01 - 10 citationsUridine-responsive epileptic encephalopathy due to inherited variants in CAD: A Tale of Two Siblings.Christopher M. McGraw, Sonal Mahida, Parul Jayakar, Hyun Yong Koh, Alan Taylor
Annals of Clinical and Translational Neurology. 2021-01-26 - 211 citationsDeletions of NRXN1 (Neurexin-1) Predispose to a Wide Spectrum of Developmental DisordersMichael S L Ching, Yiping Shen, Wen-Hann Tan, Shafali S. Jeste, Eric M. Morrow
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics. 2010-06-01
Journal Articles
- KCTD7 Deficiency Defines a Distinct Neurodegenerative Disorder with a Conserved Autophagy‐Lysosome DefectMarsha Pratt, Katrina Peariso, Adam L Hartman, Adolfo Garnica, Satish Agadi, Gerard T Berry, Tobias Loddenkemper, Thomas A Burrow, Pankaj B Agrawal, Annals of Neurology
Press Mentions
Pediatrician and Geneticist Dr. Harvey Levy Receives 2020 David L. Rimoin Lifetime Achievement Award in Medical Genetics from the ACMG Foundation for Genetic and Genomic MedicineMarch 18th, 2020
Professional Memberships
- SIMDPresident
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