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Office
2018 W Clinch Ave
Knoxville, TN 37916Phone+1 865-541-8000
Summary
- Dr. Joseph Peeden Jr., MD, is a pediatrician based in Knoxville, TN, with an extensive background in pediatrics and medical genetics. He completed his medical degree and residencies at the University of Tennessee and pursued additional specialization in medical genetics at the University of Tennessee Health Science Center. Dr. Peeden has several notable publications, including works in Clinical Pediatrics and the American Journal of Human Genetics. His research has contributed to understanding neurodevelopmental disorders and medical genetics. He has received recognition for his contributions to the field with honors such as the Emeritus Fellow from the American Academy of Medical Genetics and Genomics and the Etteldorf Outstanding Alumnus Award. He has also been recognized as an Outstanding Attending Physician in Pediatrics.
Education & Training
- University of Tennessee Health Science CenterMedical Genetics , 1982 - 1984
- University of TennesseeResidency, Pediatrics, 1977 - 1978
- University of TennesseeResidency, Pediatrics, 1977 - 1977
- University of TennesseeResidency, Pediatrics, 1976 - 1976
- University of Tennessee Health Science Center College of MedicineClass of 1975, MD
Certifications & Licensure
- TN State Medical License 1978 - 2026
- American Board of Medical Genetics and Genomics Clinical Genetics
- American Board of Pediatrics Pediatrics
Awards, Honors, & Recognition
- Emeritus Fellow American Academy of Medical Genetics and Genomics 2024
- Fellow (FAAP) American Academy of Pediatrics
- Outstanding Attending Physician University of Tennessee, College of Medicine, 2021
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Publications & Presentations
PubMed
- Streptococcal Mediastinitis Following Placement of a BravoCapsule.Joseph Peeden, Anna Conner, Dante Pappano
Clinical Pediatrics. 2024-11-17 - 14 citationsDe novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonusSerena Galosi, Ban H Edani, Simone Martinelli, Hana Hansikova, Erik A. Eklund
Brain. 2021-08-11 - 66 citationsA Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic EncephalopathyIngo Helbig, Tania López-Hernández, Oded Shor, Peter D. Galer, Shiva Ganesan
American Journal of Human Genetics. 2019-06-06
Professional Memberships
- Fellow
- American College of Medical GeneticsFellow
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