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Office
300 Longwood Ave
Children's Hospital Boston
Boston, MA 02115Phone+1 617-355-7919
Summary
- Dr. Annapurna Poduri is a Child Neurologist and Epileptologist at Boston Children's Hospital, where she directs the Epilepsy Genetics Program and Program in Neurogenetics. She received her medical degree from the University of Pennsylvania School of Medicine, her MPH at the Harvard School of Public Health, and residency training at Boston Children's Hospital and the Children's Hospital of Philadelphia. Her research program in the Boston Children's Hospital Department of Neurology and the F.M. Kirby Neurobiology Center focuses on epilepsy genetics, from genetic causes of epilepsy in patients to translational models of neurodevelopmental conditions.
Education & Training
- Boston Children's HospitalPost-Doctoral Fellowship, Neurogenetics, 2005 - 2012
- Boston Children’s Hospital/Beth Israel Deaconess Medical Center/Harvard Medical SchoolFellowship, Epilepsy, 2003 - 2005
- Children's Hospital of PhiladelphiaFellowship, Child Neurology, 2000 - 2003
- Boston Children’s Hospital/Boston Medical CenterResidency, Pediatrics, 1998 - 2000
- Perelman School of Medicine at the University of PennsylvaniaClass of 1998
Certifications & Licensure
- MA State Medical License 2003 - 2026
- NH State Medical License 2024 - 2024
- LA State Medical License 2020 - 2022
- PA State Medical License 2001 - 2004
- American Board of Psychiatry and Neurology Neurology with Special Qualification in Child Neurology
- American Board of Psychiatry and Neurology Clinical Neurophysiology
Awards, Honors, & Recognition
- Boston's Most Influential Women Awardee Harvard Club of Boston, 2020
Clinical Trials
- Epilepsy Phenome/Genome Project Start of enrollment: 2007 Nov 01
- Genetics of Epilepsy and Related Disorders Start of enrollment: 2010 Nov 01
- Gene-STEPS: Shortening Time of Evaluation in Paediatric Epilepsy Services Start of enrollment: 2021 Sep 01
Roles: Contact
Publications & Presentations
PubMed
- 2 citationsCopy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age.Catherine A Brownstein, Elise Douard, Robin L Haynes, Hyun Yong Koh, Alireza Haghighi
Advanced Genetics. 2023-03-01 - 62 citationsGenotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications.Katrine M Johannesen, Yuanyuan Liu, Mahmoud Koko, Cathrine E Gjerulfsen, Lukas Sonnenberg
Brain. 2021-08-25 - 387 citationsSingle-neuron sequencing analysis of L1 retrotransposition and somatic mutation in the human brain.Gilad D. Evrony, Xuyu Cai, Eunjung Lee, L. Benjamin Hills, Princess C. Elhosary
Cell. 2012-10-26
Journal Articles
- Gain‐of‐Function Variants in the ODC1 Gene Cause a Syndromic Neurodevelopmental Disorder Associated with Macrocephaly, Alopecia, Dysmorphic Features, and Neuroimaging ...Sanjeev V Kothare, Farrah Rajabi, Annapurna Poduri, Lance H Rodan, Ralph J DeBerardinis, American Journal of Medical Genetics Part A
- The ClinGen Epilepsy Gene Curation Expert Panel—Bridging the Divide Between Clinical Domain Knowledge and Formal Gene Curation CriteriaGhayda Mirzaa, Kristen Park, Tristan T Sands, Erika Axeen, Tanya M Bardakjian, Annapurna Poduri, Katherine L Helbig, Heather C Mefford, Human Mutation
- Correction: The Landscape of Epilepsy-Related GATOR1 VariantsAnnapurna Poduri, Nature
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Authored Content
- Infantile Spasms of Unknown CauseMay 2018
- Infantile Spasms of Unknown Cause: Predictors of Outcome and Geneotype-Phenotype CorrelationMay 2018
Press Mentions
- Sudden, Unexplained Child Deaths Often Have a Genetic CauseMarch 8th, 2022
- Diving Deep on Epilepsy GeneticsNovember 3rd, 2021
- AT THE BENCH: Erik D. Roberson, MD, PhD: On Learning and Memory Formation, and the Role of Tau in Alzheimer's and FTDOctober 22nd, 2015
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Grant Support
- Genetics Of Familial Epilepsy SyndromesNational Institute Of Neurological Disorders And Stroke2010–2012
Professional Memberships
- Member
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