John J Millichap

  • 1430 Citations
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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

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 the Caribbean School of Medicine

… → 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.

  • 15 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

Loss of Heterozygosity
Brain Diseases
Synaptic Transmission
1 Citation (Scopus)

Biallelic variants in CTU2 cause DREAM-PL syndrome and impair thiolation of tRNA wobble U34

Shaheen, R., Mark, P., Prevost, C. T., AlKindi, A., Alhag, A., Estwani, F., Al-Sheddi, T., Alobeid, E., Alenazi, M. M., Ewida, N., Ibrahim, N., Hashem, M., Abdulwahab, F., Bryant, E. M., Spinelli, E., Millichap, J., Barnett, S. S., Kearney, H. M., Accogli, A., Scala, M. & 4 others, Capra, V., Nigro, V., Fu, D. & Alkuraya, F. S., Nov 1 2019, In : Human mutation. 40, 11, p. 2108-2120 13 p.

Research output: Contribution to journalArticle

Transfer RNA
Open Access
Brain Diseases
Movement Disorders

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 2019, In : Epilepsy and Behavior. 97, p. 44-50 7 p.

Research output: Contribution to journalArticle

Infantile Spasms
Quality Improvement

Message from the Editors to our Reviewers

Gross, R. A., Worrall, B. B., Amato, A. A., Cascino, G. D., Ciccarelli, O., Corboy, J. R., Dalmau, J. O., Gottesman, R. F., Grossman, M., Millichap, J. J., Mink, J. W., Pulst, S. M. & Uitti, R. J., Jul 2 2019, In : Neurology. 93, 1, p. 3-12 10 p.

Research output: Contribution to journalEditorial