Dr. Lance Rodan, 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.

• Harvard Medical School

  Fellowship Hospital, 2016

• University Of Toronto

  Residency Hospital, 2013

• University Of Toronto

  Medical School, 2008

• University Of Toronto Faculty Of Medicine

  Medical School, 2008

• De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder, 2021-05-18

• The Spectrum of Movement Disorders in Childhood-Onset Lysosomal Storage Diseases, 2017-12-10

• Expansion of the clinical and neuroimaging spectrum associated with NDUFS8 -related disorder, 2022-08-23

• Systemic Manifestations in Pyridox(am)ine 5'-Phosphate Oxidase Deficiency, 2017-06-03

• O'Donnell-Luria-Rodan syndrome: description of a second multinational cohort and refinement of the phenotypic spectrum, 2021-07-28

• De novoand inherited variants inZNF292underlie a neurodevelopmental disorder with features of autism spectrum disorder, 2019-11-14

• Bi-allelic loss-of-function variants inTMEM147cause moderate to profound intellectual disability with facial dysmorphism and pseudo-Pelger-Huet anomaly, 2022-08-30

• Polymicrogyria is associated with pathogenic variants inPTEN, 2020-10-08

• Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior, 2021-03-03

• Loss-of-function mutations inUDP-Glucose 6-Dehydrogenasecause recessive developmental epileptic encephalopathy, 2020-01-30

• Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language, 2019-02-15

• RCL1copy number variants are associated with a range of neuropsychiatric phenotypes, 2021-02-17

• RecurrentSLC1A2variants cause epilepsy via a dominant negative mechanism, 2019-04-26

• Phenotypic expansion ofCACNA1C-associated disorders to include isolated neurological manifestations, 2021-06-23

• 5,10-methenyltetrahydrofolate synthetase deficiency causes a neurometabolic disorder associated with microcephaly, epilepsy, and cerebral hypomyelination, 2018-06-15

• Novel founder intronic variant inSLC39A14in two families causing Manganism and potential treatment strategies, 2018-04-06

• Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language, 2019-05-02

• CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language, 2018-11-05

• Defining the phenotypic spectrum ofSLC6A1mutations, 2018-01-08

• PathogenicMAST3variants in the STK domain are associated with epilepsy, 2021-07-13