Juvianee Ibrahim Estrada-Veras MD
Clinical Genetics, Medical Biochemical Genetics, Pediatric Medical Genetics
Clinical Geneticist at Walter Reed NMMC / Murtha Cancer Center Research Program/ HMJ Foundation / USU of the Health Sciences. Investigator at NHGRI-NIH.
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4954 N Palmer RdAmerica Bldg - 19, Room 3186Bethesda, MD 20889
Phone+1 301-295-4951
Fax+1 301-319-4757
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Summary
- Dr. Juvianee Estrada-Veras is a medical geneticist in Bethesda, MD. He received his medical degree from INTEC Santo Domingo School of Medicine and has been in practice 15 years. He also speaks multiple languages, including Spanish. He specializes in clinical biochemical genetics, clinical genetics, medical biochemical genetics, and pediatric medical genetics and is experienced in erdheim-chester disease, histiocytosis, inborn errors metabolism, inborn genetic diseases, and undiagnosed.
Education & Training
National Institutes of Health Clinical CenterFellowship, Medical Biochemical Genetics, 2011 - 2013- National Institutes of Health Clinical CenterResidency, Medical Genetics and Genomics, 2009 - 2012
SUNY Downstate Health Sciences UniversityResidency, Pediatrics, 2006 - 2009
INTEC Santo Domingo SOMClass of 2003
Certifications & Licensure
MD State Medical License 2016 - 2026
NY State Medical License 2009 - 2019
American Board of Medical Genetics and Genomics Medical Biochemical Genetics
American Board of Pediatrics Pediatrics- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Clinical Trials
- Clinical and Pathophysiological Investigations Into Erdheim Chester Disease Start of enrollment: 2011 Aug 01
- Dabrafenib and Trametinib in People With BRAF V600E Mutation Positive Lesions in Erdheim Chester Disease Start of enrollment: 2014 Nov 01
Publications & Presentations
PubMed
- Clinical, Laboratory, and Imaging Features Associated with Arginine Vasopressin Deficiency (Central Diabetes Insipidus) in Erdheim-Chester Disease (ECD).Sonal Vaid, Juvianee Estrada-Veras, William A Gahl, Nicholas Patronas, Rahul H Dave
Cancers. 2025-02-27 - 3 citationsTRIM71 mutations cause a neurodevelopmental syndrome featuring ventriculomegaly and hydrocephalus.Phan Q Duy, Bettina Jux, Shujuan Zhao, Kedous Y Mekbib, Evan Dennis
Brain. 2024-12-03 - Central nervous system involvement in Erdheim-Chester disease: a magnetic resonance imaging study.Aryan Zahergivar, Fatemeh Dehghani Firouzabadi, Fatemeh Homayounieh, Mahshid Golagha, Fahimul Huda
Clinical Imaging. 2024-11-01
Professional Memberships
- Member
- American Society for Human Genetics-ASHGMember
- Society for Inherited Metabolic Disorders-SIMDMember
Other Languages
- Spanish
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