John J Millichap

  • 1533 Citations
19962020

Research output per year

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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 the Caribbean

… → 2004

Research interests

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

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Grants

Research Output

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., Jan 7 2020, In : Neurology. 94, 1, p. 3-11 9 p.

Research output: Contribution to journalEditorial

Oligosaccharyltransferase complex-congenital disorders of glycosylation: A novel congenital disorder of glycosylation

Bryant, E. M., Millichap, J. J., Spinelli, E., Calhoun, J. D., Miller, C., Giannelli, J., Wolak, J., Sanders, V., Carvill, G. L. & Charrow, J., Jun 1 2020, In : American Journal of Medical Genetics, Part A. 182, 6, p. 1460-1465 6 p.

Research output: Contribution to journalArticle

  • 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

  • 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

  • 2 Scopus citations
    Open Access