John J Millichap

  • 1300 Citations
19962020
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Personal profile

Research Interests

My primary research focus is the study of EEG in early onset epileptic encephalopathies, primarily those with a genetic cause.

My clinical practice includes many patients with intractable epilepsies with genetic causes, infantile spasms, Lennox-Gastaut syndrome, and focal epilepsies.

Current clinical practice utilizes a multidisciplinary team approach to the diagnosis and treatment of pediatric epilepsy and comorbidities. Dr. Millichap has over 40 peer-reviewed medical publications and serves as the Section Editor of the Resident and Fellow Section of the journal Neurology and the Editor of Pediatric Neurology Briefs. As a member of the academic faculty of Northwestern University, he is involved in the education of trainees and grant-funded clinical research concerning epileptic encephalopathies and epilepsy genetics. ORCID | Web of Science | Google Scholar | MAS | Mendeley | ResearchGate | Google+ | Twitter

Certifications and Licenses

Epilepsy
Neurology with Special Qualification in Child Neurology

Training Experience

2010Residency, Northwestern University, McGaw Medical Center (Children’s Memorial Hospital)
2011Residency, Northwestern University, McGaw Medical Center (Children’s Memorial Hospital)

Education/Academic qualification

MD, American University of Caribbean

… → 2004

Research interests

  • EEG
  • Education
  • Epilepsy
  • Epilepsy Surgery
  • Genomic Medicine/Personalized Medicine
  • Ion Channels
  • Neurogenetics
  • Neuroinflammation
  • Pediatric Neurology

Fingerprint Dive into the research topics where John J Millichap is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 19 Similar Profiles
Epilepsy Medicine & Life Sciences
Seizures Medicine & Life Sciences
Brain Diseases Medicine & Life Sciences
Neurology Medicine & Life Sciences
Infantile Spasms Medicine & Life Sciences
Febrile Seizures Medicine & Life Sciences
Electroencephalography Medicine & Life Sciences
Mutation Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 1996 2019

Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

Deciphering Developmental Disorders Study, UK10K Consortium & NIHR BioResource, May 2 2019, In : American Journal of Human Genetics. 104, 5, p. 948-956 9 p.

Research output: Contribution to journalArticle

Hyperkinesis
Loss of Heterozygosity
Dyskinesias
Brain Diseases
Synaptic Transmission

Immediate outcomes in early life epilepsy: A contemporary account

Berg, A. T., Wusthoff, C., Shellhaas, R. A., Loddenkemper, T., Grinspan, Z. M., Saneto, R. P., Knupp, K. G., Patel, A., Sullivan, J. E., Kossoff, E. H., Chu, C. J., Massey, S., Valencia, I., Keator, C., Wirrell, E. C., Coryell, J., Millichap, J. J. & Gaillard, W. D., Aug 1 2019, In : Epilepsy and Behavior. 97, p. 44-50 7 p.

Research output: Contribution to journalArticle

Epilepsy
Infantile Spasms
Seizures
Benchmarking
Quality Improvement

Resident & Fellow Rounds

Millichap, J. J. & Strowd, R. E., Mar 26 2019, In : Neurology. 92, 13, p. 629-630 2 p.

Research output: Contribution to journalArticle

Open Access

Resident & Fellow Rounds

Millichap, J. J. & Strowd, R. E., Feb 26 2019, In : Neurology. 92, 9, p. 440-442 3 p.

Research output: Contribution to journalArticle

Resident & Fellow Rounds

Millichap, J. J. & Strowd, R. E., May 28 2019, In : Neurology. 92, 22, p. 1065-1067 3 p.

Research output: Contribution to journalArticle

Open Access