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Office
841 Prudential Drive
Suite 900
Jacksonville, FL 32207Phone+1 904-427-8453Fax+1 904-633-0958
Summary
- Dr. Pamela Trapane is a medical geneticist in Jacksonville, FL and is affiliated with multiple hospitals in the area, including Baptist Medical Center Jacksonville and UF Health Jacksonville. She received her medical degree from University of Texas Health Science Center San Antonio Medical School and has been in practice 21 years. She specializes in clinical genetics and is experienced in medical education, connective tissue disorders, and neurofibromatoses. She serves on the Clinical Care Advisory Board for the Children's Tumor Foundation and is currently serving a second term as a member of the executive committee for the American Academy of Pediatrics Council on Genetics.
Education & Training
- Univeristy of IowaMME, Medical Education, 2010 - 2015
- University of Texas Health Science Center at HoustonResidency, Medical Genetics and Genomics, 1999 - 2001
- University of Texas Health Science Center at HoustonResidency, Pediatrics, 1996 - 1999
- The University of Texas Health Science Center at San AntonioClass of 1996
- University of Houston - Clear LakeMS, Biology, 1988 - 1989
- Univeristy of HoustonBS, Biology, cum laude, 1984 - 1988
Certifications & Licensure
- FL State Medical License 2018 - 2026
- IA State Medical License 2009 - 2020
- WI State Medical License 2005 - 2009
- TX State Medical License 1998 - 2005
- American Board of Pediatrics Pediatrics
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Awards, Honors, & Recognition
- Fellow (FACMGG) American College of Medical Genetics and Genomics
- Sahai Family Professor of Medical Education Carver College of Medicine, Univeristy of Iowa
- Fellow (FAAP) American Academy of Pediatrics
Publications & Presentations
PubMed
- 326 citationsChromosome catastrophes involve replication mechanisms generating complex genomic rearrangementsPengfei Liu, Ayelet Erez, Sandesh C.S. Nagamani, Shweta U. Dhar, Katarzyna E. Kolodziejska
Cell. 2011-09-16 - 90 citationsMolecular analysis expands the spectrum of phenotypes associated with GLI3 mutationsJennifer J. Johnston, Julie C. Sapp, Joyce T. Turner, David J. Amor, Salim Aftimos
Human Mutation. 2010-10-01 - 75 citationsClinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1Magdalena Koczkowska, Tom Callens, Yunjia Chen, Alicia Gomes, Alesha D. Hicks
Human Mutation. 2020-01-01
Journal Articles
- Dysmorphology: Why it is Important to Practicing PsychologistsOrme D, Trapane P, Professional Psychology: Research and Practice. 44(6): 398-404., 12/2013
Books/Book Chapters
Abstracts/Posters
- Case Report: Pilomyxoid Astrocytoma and Response to Chemotherapy in a Patient with NF1. (abstract 287).23. Panzer K, O’Dorisio MS, Trapane P., 2014 ACMG Annual Clinical Genetics Meeting, Nashville, Tennessee, 3/26/2014
- Two novel mutations in myosin heavy chain 11 (MYH11) reinforce the pathogenicity of mutations affecting IVS32 and suggest the peri-puerperium is a particularly vulnera...Gottlieb RL, Muilenburg A, Trapane P, Sheffield VC, 2011 American College of Cardiology Iowa Chapter Annual Meeting, Altoona, IA, 6/11/2011
- Attention and Inhibition in Young Children with NF-1: A Multimethod Study. (Abstract 50)Klein-Tasman BP, Kais LA, Trapane P, Hunter S, Tonsgard J, Janke K., 2011 NF Conference, Jackson Hole, WY, 6/1/2011
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Lectures
- Genetic Testing in the Genomic Era: What You Need to Know27th Annual Jauch Memorial Educational Symposium. Waterloo, IA. - 5/15/2015
- The Role of Genetics in Pediatric and Adult Medical CareNortheast Iowa Medical Education Foundation. Family Practice Residency Program, Waterloo, IA. - 3/11/2015
- Genetic Testing in the Genomic Era: What You Need to KnowGrand Rounds: University of Iowa, Carver College of Medicine, Department of Pediatrics. - 2/13/2015
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Professional Memberships
- Fellow
- American Society of Human GeneticsMember
- American College of Medical Genetics and GenomicsFellow
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