John Schreiber

11PUBLICATIONS
25CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Clinical social work practiceDisease surveillance
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Publications (11)

|Feb 16, 2026
The Clinical Spectrum and Neurodevelopmental Pathogenesis of KPTN-Related Disorder in a Mouse Model.

Lettie E Rawlins, Philip H Iffland, John Page

|Jun 19, 2025
Evaluation, Diagnosis, and Treatment of Concomitant Movement Disorders in Genetic Epilepsies.

Jordan Garris, Megan Abbott, Erika Axeen

|Apr 10, 2025
Investigating Quality of Life and Adaptive Functioning in Patients With SCN8A-Related Epilepsy.

Vivien X Xie, Madison M Berl, Zachary Kramer

|Nov 18, 2024
Patients carrying pathogenic SCN8A variants with loss- and gain-of-function effects can be classified into five subgroups exhibiting varying developmental and epileptic components of encephalopathy.

Joshua B Hack, Joseph C Watkins, John M Schreiber

|May 28, 2024
Global modified Delphi consensus on diagnosis, phenotypes, and treatment of SCN8A-related epilepsy and/or neurodevelopmental disorders.

Gabrielle Conecker, Maya Y Xia, JayEtta Hecker

|May 28, 2024
Global modified-Delphi consensus on comorbidities and prognosis of SCN8A-related epilepsy and/or neurodevelopmental disorders.

Gabrielle Conecker, Maya Y Xia, JayEtta Hecker

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Frequent Collaborators

4 joint publications

Michael Hammer

2 joint publications

Lowell H Frank

2 joint publications

William D Gaillard

2 joint publications

Mitsuhiro Kato