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Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 28, 2020
Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survivalMichael E Coulter, Damir Musaev, Ellen M DeGennaro, et al.
Translational Psychiatry|April 12, 2018
CXCR4 involvement in neurodegenerative diseasesLuke W Bonham, Celeste M Karch, Chun C Fan, et al.
MMWR. Morbidity and Mortality Weekly Report|December 2, 2016
Description of 13 Infants Born During October 2015-January 2016 With Congenital Zika Virus Infection Without Microcephaly at Birth - BrazilVanessa van der Linden, André Pessoa, William Dobyns, et al.
Scientific Reports|September 8, 2018
Regionally specific TSC1 and TSC2 gene expression in tuberous sclerosis complexYi Li, Matthew J Barkovich, Celeste M Karch, et al.
Annals of Neurology|March 6, 2014
SLC25A22 is a novel gene for migrating partial seizures in infancyAnnapurna Poduri, Erin L Heinzen, Vida Chitsazzadeh, et al.
Brain : a Journal of Neurology|June 30, 2022
Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disordersNataliya Di Donato, Renzo Guerrini, Charles J Billington, et al.
Epilepsia|January 12, 2011
The clinicopathologic spectrum of focal cortical dysplasias: a consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods CommissionIngmar Blümcke, Maria Thom, Eleonora Aronica, et al.
Nature Genetics|March 3, 2017
Biallelic mutations in human DCC cause developmental split-brain syndromeSaumya S Jamuar, Klaus Schmitz-Abe, Alissa M D'Gama, et al.
American Journal of Human Genetics|April 19, 2016
De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 DeletionsBrieana Fregeau, Bum Jun Kim, Andrés Hernández-García, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 8, 2016
Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive featuresQing Ouyang, Tojo Nakayama, Ozan Baytas, et al.
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