John J Millichap

  • 1231 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

Keywords

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

Fingerprint Fingerprint is based on mining the text of the experts' scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

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

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Research Output 1996 2019

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

3 Citations (Scopus)

Comparative effectiveness of levetiracetam vs phenobarbital for infantile epilepsy

Grinspan, Z. M., Shellhaas, R. A., Coryell, J., Sullivan, J. E., Wirrell, E. C., Mytinger, J. R., Gaillard, W. D., Kossoff, E. H., Valencia, I., Knupp, K. G., Wusthoff, C., Keator, C., Ryan, N., Loddenkemper, T., Chu, C. J., Novotny, E. J., Millichap, J. J. & Berg, A. T., Apr 1 2018, In : JAMA Pediatrics. 172, 4, p. 352-360 9 p.

Research output: Contribution to journalArticle

etiracetam
Phenobarbital
Epilepsy
Seizures
Selection Bias
5 Citations (Scopus)

Defining the phenotypic spectrum of SLC6A1 mutations

Johannesen, K. M., Gardella, E., Linnankivi, T., Courage, C., de Saint Martin, A., Lehesjoki, A. E., Mignot, C., Afenjar, A., Lesca, G., Abi-Warde, M. T., Chelly, J., Piton, A., Merritt, J. L., Rodan, L. H., Tan, W. H., Bird, L. M., Nespeca, M., Gleeson, J. G., Yoo, Y., Choi, M. & 32 othersChae, J. H., Czapansky-Beilman, D., Reichert, S. C., Pendziwiat, M., Verhoeven, J. S., Schelhaas, H. J., Devinsky, O., Christensen, J., Specchio, N., Trivisano, M., Weber, Y. G., Nava, C., Keren, B., Doummar, D., Schaefer, E., Hopkins, S., Dubbs, H., Shaw, J. E., Pisani, L., Myers, C. T., Tang, S., Tang, S., Pal, D. K., Millichap, J. J., Carvill, G. L., Helbig, K. L., Mecarelli, O., Striano, P., Helbig, I., Rubboli, G., Mefford, H. C. & Møller, R. S., Feb 1 2018, In : Epilepsia. 59, 2, p. 389-402 14 p.

Research output: Contribution to journalArticle

Intellectual Disability
Generalized Epilepsy
Mutation
Myoclonic Epilepsy
Epilepsy
2 Citations (Scopus)

De novo variants in the alternative exon 5 of SCN8A cause epileptic encephalopathy

Epilepsy Genetics Initiative, Feb 1 2018, In : Genetics in Medicine. 20, 2, p. 275-281 7 p.

Research output: Contribution to journalArticle

Brain Diseases
Exome
Exons
Epilepsy
Molecular Sequence Annotation