Frances Paola Velez-Bartolomei MD
Clinical Biochemical Genetics, Clinical Genetics, Medical Biochemical Genetics
Physician
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Edif Medico San Jorge Suite 408Calle San Jorge 252San Juan, PR 00912
Phone+1 787-728-8316
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Summary
- Frances Velez-Bartolomei, MD, is a Medical Genetics specialist located in San Juan, PR, with subspecialties in Clinical Biochemical Genetics, Clinical Genetics, and Medical Biochemical Genetics. She completed her fellowship in Medical Biochemical Genetics and a residency in Medical Genetics and Genomics at Stanford Health Care, following a Pediatrics residency at San Juan City Hospital and earning her medical degree from Universidad Central del Caribe School of Medicine. Her experience focuses on inborn errors of metabolism. She has contributed to several publications, including topics such as Spondylothoracic Dysostosis and Kabuki syndrome, and her work has been published in reputable journals like The Journal of Bone and Joint Surgery and the American Journal of Medical Genetics.
Education & Training
Stanford Health Care-Sponsored Stanford UniversityFellowship, Medical Biochemical Genetics, 2020 - 2021- Stanford Health Care-Sponsored Stanford UniversityResidency, Medical Genetics and Genomics, 2018 - 2020
San Juan City HospitalResidency, Pediatrics, 2015 - 2018
Universidad Central del Caribe School of MedicineClass of 2015
Certifications & Licensure
PR State Medical License 2021 - 2026
VI State Medical License Active through 2026
CA State Medical License 2018 - 2025
American Board of Medical Genetics and Genomics Medical Biochemical Genetics- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Publications & Presentations
PubMed
- 2 citationsLong-Term Follow-up of Untreated Adult Patients with Spondylothoracic Dysostosis (Jarcho-Levin Syndrome).Norman Ramírez, Carlos Monroig-Rivera, Wilfredo De Jesús-Rojas, Edwin Rosado, Norma J Arciniegas Medina
The Journal of Bone and Joint Surgery. American Volume. 2024-03-20 - 6 citationsCharacterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletions.Courtney P Verscaj, Frances Velez-Bartolomei, Ethan Bodle, Katie Chan, Michael J Lyons
Prenatal Diagnosis. 2024-02-01 - 1 citationsInsights into the perinatal phenotype of Kabuki syndrome in infants identified by genome-wide sequencing.Kristen Wigby, Monia Hammer, Mari Tokita, Priyanka Patel, Marilyn C Jones
American Journal of Medical Genetics. Part A. 2023-04-01
Authored Content
- MERFFJanuary 2021
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