Dr. Heather Olson, MD

• Pediatric Neurology

*Healthgrades does not verify qualifications for medical specialties. Please verify your provider's specialty and qualifications directly with your provider and applicable medical board.

• Mayo Clinic Alix School Of Medicine

  Medical School, 2016

• Boston Children's Hospital, Neurogenetics & Epilepsy Genetics

  Fellowship Hospital, 2013

• Boston Children's Hospital, Epilepsy & Clinical Neurophysiology

  Fellowship Hospital, 2012

• Boston Children's Hospital, Epilepsy & Clinical Neurophysiology|boston Children's Hospital, Neurogenetics & Epilepsy Genetics

  Fellowship Hospital, 2012

• Boston Children's Hospital, Pediatric Neurology

  Residency Hospital, 2011

• Boston Children's Hospital/boston Medical Center, Pediatrics

  Internship Hospital, 2009

• Colby College

  Undergraduate School, 2001

• Characterization of a Novel Variant in Siblings with Asparagine Synthetase Deficiency, 2017-12-20

• Generation and characterization of human induced pluripotent stem cells (iPSCs) from three male and three female patients with CDKL5 Deficiency Disorder (CDD), 2021-03-05

• A Model Program for Translational Medicine in Epilepsy Genetics, 2017-01-06

• Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder: clinical review, 2019-02-23

• BRAT1Mutations Present with a Spectrum of Clinical Severity, 2016-06-09

• Genetic Forms of Epilepsies and other Paroxysmal Disorders, 2014-09-05

• Severity Assessment in CDKL5 Deficiency Disorder, 2019-03-27

• CDKL5 Deficiency Disorder: Relationship between genotype, epilepsy, cortical visual impairment and development., 2019-07-16

• Current neurologic treatment and emerging therapies in CDKL5 deficiency disorder, 2021-09-16

• A Randomized Controlled Trial of Levodopa in Patients with Angelman Syndrome, 2017-09-25

• Cerebral visual impairment in CDKL5 deficiency disorder: vision as an outcome measure, 2021-05-24

• Genetic diagnoses in epilepsy: the impact of dynamic exome analysis in a pediatric cohort, 2020-01-19

• Utility of Exome Sequencing for Diagnosis in Unexplained Pediatric-Onset Epilepsy Utility of Exome Sequencing for Diagnosis in Unexplained Pediatric-Onset Epilepsy, 2023-07-20

• Clinical and Functional Characterization of the Recurrent TUBA1A p.(Arg2His) Mutation, 2018-08-07

• CDKL5 Deficiency Disorder-Related Epilepsy: A Review of Current and Emerging Treatment, 2022-05-28

• Genetics and genotype-phenotype correlations in early onset epileptic encephalopathy with burst suppression, 2017-02-14

• Genetic Diagnosis Impacts Medical Management for Pediatric Epilepsies, 2022-10-26

• Characterization of theGABRB2associated neurodevelopmental disorders, 2020-12-24

• Content validation of clinician-reported items for a severity measure for CDKL5 Deficiency Disorder, 2021-08-11

• Mutations in Epilepsy and Intellectual Disability Genes in Patients with Features of Rett Syndrome, 2015-04-25

• Comparison of evoked potentials across four related developmental encephalopathies, 2023-03-04