Peter B. Crino

University of Maryland, Baltimore — United States

Medicine · Health Sciences

70h-index18.4kcitations229works3.32yr avg
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Research Topics

Tuberous Sclerosis Complex Research(80), Genetics and Neurodevelopmental Disorders(32), Neuroscience and Neuropharmacology Research(30), Epilepsy research and treatment(24), Genomics and Rare Diseases(21)

Publications228 total

Mechanistic Target of Rapamycin and Megalencephaly: Novel Research Strategies for Therapeutic Discovery
Epiliepsy currents/Epilepsy currents·2026Open Access
The Clinical Spectrum and Neurodevelopmental Pathogenesis of <scp> <i>KPTN</i> </scp> ‐Related Disorder in a Mouse Model
Annals of Neurology·2026Open Access
mTOR pathway gene knockout results in mTOR-dependent cellular aggregation
2025Open Access
Clinical Center for Adults With Neurodevelopmental Disorders
Neurology·2025
<i>SLC35A2</i> loss-of-function variants affect glycomic signatures, neuronal fate and network dynamics
Brain·2025· 6 citedOpen Access
Tuberous sclerosis complex
2025
SLC35A2 loss of function variants affect glycomic signatures, neuronal fate, and network dynamics
2024Open Access
Mouse models of <i>Slc35a2</i> brain mosaicism reveal mechanisms of mild malformations of cortical development with oligodendroglial hyperplasia in epilepsy
Epilepsia·2024· 10 citedOpen Access
Somatic variants in diverse genes leads to a spectrum of focal cortical malformations
UNC Libraries·2024Open Access
Loss of Slc35a2 alters development of the mouse cerebral cortex
Neuroscience Letters·2024· 17 citedOpen Access
Rapid modeling of an ultra-rare epilepsy variant in wild-type mice by in utero prime editing
2023· 4 citedOpen Access
Loss of <i>Slc35a2</i> alters development of the mouse cerebral cortex
2023· 3 citedOpen Access
PERSONALIZED PATIENT MODELS FOR RARE EPILEPSIES: IN VIVO PRIME EDITING OF GRIN2A
IBRO Neuroscience Reports·2023Open Access
SLC35A2 somatic variants in drug resistant epilepsy: FCD and MOGHE
Neurobiology of Disease·2023· 10 citedOpen Access
Models of <i>KPTN</i>-related disorder implicate mTOR signalling in cognitive and overgrowth phenotypes
Brain·2023· 10 citedOpen Access
Vascularization in mTOR Mouse Mutants: An Effort Not in Vein
eNeuro·2023Open Access
Mild TSC phenotype and non-penetrance associated with a frameshift variant in TSC2 prompts caution in evaluating pathogenicity of frameshift variants
Gene·2023· 7 cited
Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the <i>SLC35A2</i> Gene
Neurology·2022· 52 citedOpen Access
Author Correction: Coding and small non-coding transcriptional landscape of tuberous sclerosis complex cortical tubers: implications for pathophysiology and treatment
Scientific Reports·2022Open Access
Mouse and cellular models of <i>KPTN</i> -related disorder implicate mTOR signalling in cognitive and progressive overgrowth phenotypes
2022· 1 citedOpen Access
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Frequent Co-authors

Eleonora Aronica(10), Hope Northrup(8), Darcy A. Krueger(8), Mark Nellist(7), James Eberwine(7), Elizabeth P. Henske(6), Julian R. Sampson(6), Marianna Baybis(6), Steven L. Roberds(4), Kevin C. Ess(4), Anna Jansen(4), Elizabeth A. Thiele(4), E. Martina Bebin(4), Thomas N. Darling(4), Elizabeth S. Gosnell(4), John J. Bissler(4), Sergiusz Jóźwiak(4), Jonathan Roth(4), Howard L. Weiner(4), Francis X. McCormack(4)