JohnMichaelSchreiberMD

Child Neurology • Fairfax, VA

Physician

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Office
3023 Hamaker Ct
300
Fairfax, VA 22031
Phone+1 703-876-2788

Fax+1 703-839-8798
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Education & Training

Children's National Medical Center/George Washington UniversityFellowship, Child Neurology, 2008
National Capital ConsortiumFellowship, Clinical Neurophysiology, 2012 - 2013
Children's National Medical Center/George Washington UniversityResidency, Child Neurology, 2008 - 2011
Children's National Medical CenterResidency, Pediatrics, 2006 - 2008
University of Maryland School of MedicineClass of 2006

Certifications & Licensure

MD State Medical License 2011 - 2025
DC State Medical License 2006 - 2024
VA State Medical License 2013 - 2024
FL State Medical License 2017 - 2019
American Board of Psychiatry and Neurology Neurology with Special Qualification in Child Neurology
American Board of Psychiatry and Neurology Clinical Neurophysiology
American Board of Psychiatry and Neurology Epilepsy

Clinical Trials

A Study of Soticlestat as an Add-on Therapy in Children, Teenagers, and Adults With Lennox-Gastaut Syndrome Start of enrollment: 2021 Nov 08
Completed
Phase 3
Roles: Principal Investigator
A Study of Soticlestat as an Add-on Therapy in Children and Young Adults With Dravet Syndrome Start of enrollment: 2021 Oct 28
Active, not recruiting
Phase 3
Roles: Principal Investigator

Publications & Presentations

PubMed

Seizure Control Outcomes following Resection of Cortical Dysplasia in Patients with DEPDC5 Variants: A Systematic Review and Individual Patient Data Analysis.
Christopher McGinley, Saige Teti, Katherine Hofmann, John M Schreiber, Nathan T Cohen, William D Gaillard, Chima O Oluigbo> ;Neuropediatrics. 2024 Feb 1
1 citations
Clinical severity is correlated with age at seizure onset and biophysical properties of recurrent gain of function variants associated with SCN8A-related epilepsy.
Kyung Mi Chung, Joshua Hack, Jennifer Andrews, Maureen Galindo-Kelly, John Schreiber, Joseph Watkins, Michael F Hammer> ;Epilepsia. 2023 Dec 1
1 citations
Models of KPTN-related disorder implicate mTOR signalling in cognitive and overgrowth phenotypes.
Maria O Levitin, Lettie E Rawlins, Gabriela Sanchez-Andrade, Osama A Arshad, Stephan C Collins, Stephen J Sawiak, Phillip H Iffland 2nd, Malin H L Andersson, Caleb Bup...> ;Brain. 2023 Nov 2
2 citations
Distinguishing Loss-of-Function and Gain-of-FunctionVariants Using a Random Forest Classification Model Trained on Clinical Features.
Joshua B Hack, Kyle Horning, Denise M Juroske Short, John M Schreiber, Joseph C Watkins, Michael F Hammer> ;Neurology. Genetics. 2023 Jun 1
2 citations
Wide range of phenotypic severity in individuals with late truncations unique to the predominant CDKL5 transcript in the brain.
Laura Keehan, Isabel Haviland, Yoel Gofin, Lindsay C Swanson, Christelle Moufawad El Achkar, John Schreiber, Grace E VanNoy, Emily O'Heir, Anne O'Donnell-Luria, Richar...> ;American Journal of Medical Genetics. Part A. 2022 Dec 1
Clinical characteristics and treatment experience of individuals with SCN8A developmental and epileptic encephalopathy (SCN8A-DEE): Findings from an online caregiver s...
Alison Cutts, Hillary Savoie, Michael F Hammer, John Schreiber, Celene Grayson, Constanza Luzon, Noam Butterfield, Simon N Pimstone, Ernesto Aycardi, Cynthia Harden, C...> ;Seizure. 2022 Apr 1
Telehealth for patients with rare epilepsies.
Zachary J Kramer, Carrin Brandt, Kathryn Havens, Archana Pasupuleti, William D Gaillard, John M Schreiber> ;Therapeutic Advances in Rare Disease. 2022 Mar 8
10 citations
Results of the First GNAO1-Related Neurodevelopmental Disorders Caregiver Survey
Erika Axeen, Emily Bell, Amy Robichaux Viehoever, John M. Schreiber, Christos Sidiropoulos, Howard P. Goodkin> ;Pediatric Neurology. 2021 Aug 1
3 citations
A Randomized Controlled Trial of SGS-742, a γ-aminobutyric acid B (GABA-B) Receptor Antagonist, for Succinic Semialdehyde Dehydrogenase Deficiency.
John M. Schreiber, Edythe Wiggs, Rose Cuento, Gina Norato, Irene H. Dustin, Rachel Rolinski, Alison Austermuehle, Xiangping Zhou, Sara K. Inati, K. Michael Gibson, Phi...> ;Journal of Child Neurology. 2021 May 20
10 citations
Responsive neurostimulation for the treatment of medically refractory epilepsy in pediatric patients: strategies, outcomes, and technical considerations
Armin Mortazavi, Ross-Jordon S. Elliott, Tiffany N Phan, John M. Schreiber, William D. Gaillard, Chima O. Oluigbo> ;Journal of Neurosurgery. Pediatrics. 2021 Apr 30
Response: Let us not miss the forest for the trees. Reply to ''Echocardiography in epilepsy: A tool to be explored''.
Lowell H. Frank, John M. Schreiber, Barbara Kroner, Adrian Bumbut, Moussa O. Ismail, William D. Gaillard> ;Epilepsia. 2021 Mar 23
11 citations
Spatiotemporal distribution and age of seizure onset in a pediatric epilepsy surgery cohort with cortical dysplasia
Natrujee Wiwattanadittakul, Sirorat Suwannachote, Xiaozhen You, Nathan T. Cohen, Tan Tran, Rochana Phuackchantuck, Tammy N. Tsuchida, Dewi F. Depositario-Cabacar, Tesf...> ;Epilepsy Research. 2021 Mar 2
8 citations
Children with refractory epilepsy demonstrate alterations in myocardial strain
John M. Schreiber, Lowell H. Frank, Barbara Kroner, Adrian Bumbut, Moussa O. Ismail, William D. Gaillard> ;Epilepsia. 2020 Oct 1
6 citations
Measure thrice, cut twice: On the benefit of reoperation for failed pediatric epilepsy surgery.
Nathan T. Cohen, Julie Ziobro, Dewi F. Depositario-Cabacar, Kathryn Havens, Amy Kao, John M. Schreiber, Tammy N. Tsuchida, Tesfaye Zelleke, Chima O. Oluigbo, William D...> ;Epilepsy Research. 2020 Feb 11
Intermittent Atrioventricular Heart Block Resembling Seizures.
Nathan T. Cohen, John M. Schreiber> ;Pediatric Neurology. 2020 Jan 1
15 citations
A multi-disciplinary clinic for SCN8A-related epilepsy.
John M. Schreiber, Laura Tochen, Mackenzie Brown, Sarah Evans, Laura J Ball, Adrian Bumbut, Rapeepat Thewamit, Matthew T. Whitehead, Chelsea L. Black, Emanuel M. Boutz...> ;Epilepsy Research. 2020 Jan 1
15 citations
Novel variants and phenotypes widen the phenotypic spectrum of GABRG2-related disorders
Jonna Komulainen-Ebrahim, John M. Schreiber, Salla M. Kangas, Katri Pylkäs, Maria Suo-Palosaari, Elisa Rahikkala, Johanna Liinamaa, Esa-Ville Immonen, Ilmo E. Hassinen...> ;Seizure. 2019 Mar 19
Spatially clustering de novo variants in CYFIP2, encoding the cytoplasmic FMRP interacting protein 2, cause intellectual disability and seizures.
Zweier, M.,Begemann, A.,McWalter, K.,Cho, M. T.,Abela, L.,Banka, S.,Behring, B.,Berger, A.,Brown, C. W.,Carneiro, M.,Chen, J.,Cooper, G. M.,Finnila, C. R.,Guillen Saco...> ;Eur. J. Hum. Genet.. 2019 Jan 22
38 citations
Is the use of Stereotactic Electroencephalography Safe and Effective in Children? A Meta-Analysis of the use of Stereotactic Electroencephalography in Comparison to Su...
Matthew F. Sacino, Sean Shenghsiu Huang, John M. Schreiber, William D. Gaillard, Chima O. Oluigbo> ;Neurosurgery. 2019 Jun 1
38 citations
Early ictal and interictal patterns in FIRES: The sparks before the blaze.
Raquel Farias-Moeller, Luca Bartolini, Katelyn Staso, John M. Schreiber, Jessica L. Carpenter> ;Epilepsia. 2017 May 26
93 citations
Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylation
Christina Lam, Carlos Ferreira, Donna M. Krasnewich, Camilo Toro, Lea Latham, Wadih M. Zein, Tanya J. Lehky, Carmen C. Brewer, Eva H. Baker, Audrey Thurm, Cristan Farm...> ;Genetics in Medicine. 2017 Feb 1
24 citations
Temporal lobe epilepsy and focal cortical dysplasia in children: A tip to find the abnormality.
Luca Bartolini, Matthew T. Whitehead, Cheng-Ying Ho, Leigh N. Sepeta, Chima O. Oluigbo, Kathryn Havens, Emily R. Freilich, John M. Schreiber, William D. Gaillard> ;Epilepsia. 2017 Jan 1
94 citations
SCN8A encephalopathy: Research progress and prospects
Miriam H. Meisler, Guy Helman, Michael F. Hammer, Brandy E. Fureman, William D. Gaillard, Alan L. Goldin, Shinichi Hirose, Atsushi Ishii, Barbara Kroner, Christoph Los...> ;Epilepsia. 2016 Jul 1
35 citations
Inherited disorders of gamma-aminobutyric acid metabolism and advances in ALDH5A1 mutation identification.
Phillip L. Pearl, Mahsa Parviz, Kara R. Vogel, John M. Schreiber, William H. Theodore, K. Michael Gibson> ;Developmental Medicine and Child Neurology. 2015 Jul 1
79 citations
Loss-of-Function Alanyl-tRNA Synthetase Mutations Cause an Autosomal-Recessive Early-Onset Epileptic Encephalopathy with Persistent Myelination Defect
Cas Simons, Laurie B. Griffin, Guy Helman, Gretchen Golas, Amy Pizzino, Miriam Bloom, Jennifer L. Murphy, Joanna Crawford, Sarah H. Evans, Scott Topper, Matthew T. Whi...> ;American Journal of Human Genetics. 2015 Apr 2
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