Publications by authors named "Barbara Beyer"

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Multidimensional Genetic Analysis of Repeated Seizures in the Hybrid Mouse Diversity Panel Reveals a Novel Epileptogenesis Susceptibility Locus.
Russell J Ferland, Jason Smith, Dominick Papandrea, Jessica Gracias, Leah Hains, Barbara S Beyer

G3 (Bethesda)· August 2017

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Dynamin 1 isoform roles in a mouse model of severe childhood epileptic encephalopathy.
Samuel Asinof, Connie Mahaffey, Barbara Beyer, Wayne N Frankel, Rebecca Boumil

Neurobiol Dis· November 2016

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Eight Flurothyl-Induced Generalized Seizures Lead to the Rapid Evolution of Spontaneous Seizures in Mice: A Model of Epileptogenesis with Seizure Remission.
Sridhar B Kadiyala, Joshua Q Yannix, Julia W Nalwalk, Dominick Papandrea, Barbara S Beyer

J Neurosci· July 2016

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Angiogenesis QTL on Mouse Chromosome 8 Colocalizes with Differential β-Defensin Expression.
Jason Smith, Fang Liu, Barbara Beyer, Krista Morales, Andrew Reilly

J Biomol Tech· July 2015

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Independent Neuronal Origin of Seizures and Behavioral Comorbidities in an Animal Model of a Severe Childhood Genetic Epileptic Encephalopathy.
Samuel K Asinof, Stacey J Sukoff Rizzo, Alexandra R Buckley, Barbara J Beyer, Verity A Letts

PLoS Genet· June 2015

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Unraveling genetic modifiers in the gria4 mouse model of absence epilepsy.
Wayne N Frankel, Connie L Mahaffey, Tracy C McGarr, Barbara J Beyer, Verity A Letts

PLoS Genet· July 2014

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Loss of MeCP2 from forebrain excitatory neurons leads to cortical hyperexcitation and seizures.
Wen Zhang, Matthew Peterson, Barbara Beyer, Wayne N Frankel, Zhong-wei Zhang

J Neurosci· February 2014

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Overexpression of RCAN1 isoform 4 in mouse neurons leads to a moderate behavioral impairment.
Devang L Bhoiwala, Issam Koleilat, Jiang Qian, Barbara Beyer, Shazaan F Hushmendy

Neurol Res· January 2013

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Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice.
Ligia A Papale, Barbara Beyer, Julie M Jones, Lisa M Sharkey, Sergio Tufik

Hum Mol Genet· May 2009

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Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4.
Barbara Beyer, Charlotte Deleuze, Verity A Letts, Connie L Mahaffey, Rebecca M Boumil

Hum Mol Genet· June 2008

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Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2.
Jennifer A Kearney, Yan Yang, Barbara Beyer, Sarah K Bergren, Lieve Claes

Hum Mol Genet· March 2006

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Development of a new genetic model for absence epilepsy: spike-wave seizures in C3H/He and backcross mice.
Wayne N Frankel, Barbara Beyer, Christina R Maxwell, Stephanie Pretel, Verity A Letts

J Neurosci· March 2005

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A targeted mutation in Cacng4 exacerbates spike-wave seizures in stargazer (Cacng2) mice.
Verity A Letts, Connie L Mahaffey, Barbara Beyer, Wayne N Frankel

Proc Natl Acad Sci U S A· February 2005

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Phenotypic heterogeneity in the stargazin allelic series.
Verity A Letts, Myoung-Goo Kang, Connie L Mahaffey, Barbara Beyer, Heather Tenbrink

Mamm Genome· August 2003

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Spontaneous deletion of epilepsy gene orthologs in a mutant mouse with a low electroconvulsive threshold.
Yan Yang, Barbara J Beyer, James F Otto, Timothy P O'Brien, Verity A Letts

Hum Mol Genet· May 2003

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