Anne M. Comi
Experienced in Cortical Dysplasia

Dr. Anne M. Comi

Pediatric Neurology
Johns Hopkins Medicine
The Kennedy Krieger Institute
801 North Broadway, Room 553, Room 553, 
Baltimore, MD 

Experienced in Cortical Dysplasia
Johns Hopkins Medicine
The Kennedy Krieger Institute
801 North Broadway, Room 553, Room 553, 
Baltimore, MD 
OverviewInsuranceLocationsClinical ResearchSimilar Doctors

Overview

Dr. Comi graduated from SUNY Buffalo School of Medicine and received her training in pediatrics at the Children's Hospital of Buffalo and her child neurology training at Johns Hopkins Medicine. Her clinical specialization is in the treatment of the neurological aspects of Sturge-Weber syndrome and other disorders related to capillary malformation. Dr. Comi's clinical research interests focus on improving the early diagnosis and treatment of brain involvement in Sturge-Weber syndrome in order to prevent ischemic brain injury in affected infants and young children, and on studies to understand what causes Sturge-Weber syndrome. Her laboratory research work deals with the pathogenesis of Sturge-Weber syndrome, recently shown to be caused by a somatic mutation, and on developing new drug targets, screening assays, models and therapeutic strategies for Sturge-Weber syndrome. Her lab group also works on developing better neuroprotective and neuroregenerative responses to brain injury resulting from impaired blood flow to the brain.

Dr. Comi is rated as an Experienced provider by MediFind in the treatment of Cortical Dysplasia. Her top areas of expertise are Sturge-Weber Syndrome, Parkes Weber Syndrome, Stork Bite, Epilepsy in Children, and Endovascular Embolization.

Her clinical research consists of co-authoring 69 peer reviewed articles and participating in 5 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 4 articles in the study of Cortical Dysplasia.

Residency
Johns Hopkins University School of Medicine, Neurology, 1999
Specialties
Pediatric Neurology
Licenses
Neurology with Special Qualifications in Neurology in MD
Board Certifications
American Board Of Psychiatry And Neurology
Languages Spoken
English
Gender
Female

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Locations

The Kennedy Krieger Institute
801 North Broadway, Room 553, Room 553, Baltimore, MD 21205
Call: 443-923-9150

Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.


4 Clinical Trials

The Brain Vascular Malformations Clinical Research Network: Predictors of Clinical Course, Project 2: Innovative Approaches to Gauge Progression of Sturge-Weber Syndrome
The Brain Vascular Malformations Clinical Research Network: Predictors of Clinical Course, Project 2: Innovative Approaches to Gauge Progression of Sturge-Weber Syndrome
Enrollment Status: Active_not_recruiting
Publish Date: February 18, 2025
Novel Cognitive Treatment Targets for Epidiolex in Sturge- Weber Syndrome: A Phase II Trial
Novel Cognitive Treatment Targets for Epidiolex in Sturge- Weber Syndrome: A Phase II Trial
Enrollment Status: Completed
Publish Date: May 25, 2023
Intervention Type: Drug
Study Drug: Cannabidiol
Study Phase: Phase 2
Trial of Sirolimus for Cognitive Impairment in Sturge-Weber Syndrome
Trial of Sirolimus for Cognitive Impairment in Sturge-Weber Syndrome
Enrollment Status: Completed
Publish Date: November 01, 2021
Intervention Type: Drug
Study Drug: Sirolimus
Study Phase: Phase 2/Phase 3
Establishing Reliability for Quantitative EEG, Transcranial Doppler, Behavioral Outcomes and Optical Coherence Tomography in SWS: The Next Step Toward Biomarker Development
Establishing Reliability for Quantitative EEG, Transcranial Doppler, Behavioral Outcomes and Optical Coherence Tomography in SWS: The Next Step Toward Biomarker Development
Enrollment Status: Completed
Publish Date: April 16, 2020
View 3 Less Clinical Trials

69 Total Publications

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.
Journal: medRxiv : the preprint server for health sciences
Published: April 16, 2025
View All 69 Publications
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Areas of Expertise

MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.

Learn more about MediFind’s expert tiers

Find Dr. Comi's expertise for a condition
ConditionClose
  • Elite
  • Parkes Weber Syndrome
    Dr. Comi is
    Elite
    . Learn about Parkes Weber Syndrome.
    See more Parkes Weber Syndrome experts
  • Stork Bite
    Dr. Comi is
    Elite
    . Learn about Stork Bite.
    See more Stork Bite experts
  • Sturge-Weber Syndrome
    Dr. Comi is
    Elite
    . Learn about Sturge-Weber Syndrome.
    See more Sturge-Weber Syndrome experts
  • Distinguished
  • Cowden Syndrome
    Dr. Comi is
    Distinguished
    . Learn about Cowden Syndrome.
    See more Cowden Syndrome experts
  • Epilepsy in Children
    Dr. Comi is
    Distinguished
    . Learn about Epilepsy in Children.
    See more Epilepsy in Children experts
  • Hypothalamic Hamartomas
    Dr. Comi is
    Distinguished
    . Learn about Hypothalamic Hamartomas.
    See more Hypothalamic Hamartomas experts
  • Linear Nevus Sebaceous Syndrome
    Dr. Comi is
    Distinguished
    . Learn about Linear Nevus Sebaceous Syndrome.
    See more Linear Nevus Sebaceous Syndrome experts
  • Peutz-Jeghers Syndrome
    Dr. Comi is
    Distinguished
    . Learn about Peutz-Jeghers Syndrome.
    See more Peutz-Jeghers Syndrome experts
  • Phacomatosis Pigmentokeratotica
    Dr. Comi is
    Distinguished
    . Learn about Phacomatosis Pigmentokeratotica.
    See more Phacomatosis Pigmentokeratotica experts
View All 10 Distinguished Conditions
  • Advanced
  • Aplasia Cutis Congenita
    Dr. Comi is
    Advanced
    . Learn about Aplasia Cutis Congenita.
    See more Aplasia Cutis Congenita experts
  • Autosomal Dominant Partial Epilepsy with Auditory Features
    Dr. Comi is
    Advanced
    . Learn about Autosomal Dominant Partial Epilepsy with Auditory Features.
    See more Autosomal Dominant Partial Epilepsy with Auditory Features experts
  • Benign Rolandic Epilepsy
    Dr. Comi is
    Advanced
    . Learn about Benign Rolandic Epilepsy.
    See more Benign Rolandic Epilepsy experts
  • Clouston Syndrome
    Dr. Comi is
    Advanced
    . Learn about Clouston Syndrome.
    See more Clouston Syndrome experts
  • Ectodermal Dysplasias
    Dr. Comi is
    Advanced
    . Learn about Ectodermal Dysplasias.
    See more Ectodermal Dysplasias experts
  • Epilepsy
    Dr. Comi is
    Advanced
    . Learn about Epilepsy.
    See more Epilepsy experts
View All 9 Advanced Conditions
  • Experienced
  • 2q37 Deletion Syndrome
    Dr. Comi is
    Experienced
    . Learn about 2q37 Deletion Syndrome.
    See more 2q37 Deletion Syndrome experts
  • 47 XYY Syndrome
    Dr. Comi is
    Experienced
    . Learn about 47 XYY Syndrome.
    See more 47 XYY Syndrome experts
  • Aase Syndrome
    Dr. Comi is
    Experienced
    . Learn about Aase Syndrome.
    See more Aase Syndrome experts
  • Abruzzo-Erickson Syndrome
    Dr. Comi is
    Experienced
    . Learn about Abruzzo-Erickson Syndrome.
    See more Abruzzo-Erickson Syndrome experts
  • Absence Seizure
    Dr. Comi is
    Experienced
    . Learn about Absence Seizure.
    See more Absence Seizure experts
  • Achalasia Microcephaly Syndrome
    Dr. Comi is
    Experienced
    . Learn about Achalasia Microcephaly Syndrome.
    See more Achalasia Microcephaly Syndrome experts
View All 112 Experienced Conditions
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