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Epilepsy Research|December 15, 2015
Hlf is a genetic modifier of epilepsy caused by voltage-gated sodium channel mutationsNicole A Hawkins, Jennifer A Kearney
Expert Opinion on Drug Discovery|July 30, 2024
Innovative drug discovery strategies in epilepsy: integrating next-generation syndrome-specific mouse models to address pharmacoresistance and epileptogenesisMelissa Barker-Haliski, Nicole A Hawkins
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 11, 2024
Fine mapping and candidate gene analysis of Dravet syndrome modifier loci on mouse chromosomes 7 and 8Nicole A Hawkins, Nathan Speakes, Jennifer A Kearney
Biorxiv : the Preprint Server for Biology|April 25, 2024
Fine Mapping and Candidate Gene Analysis of Dravet Syndrome Modifier Loci on Mouse Chromosomes 7 and 8Nicole A Hawkins, Nathan Speakes, Jennifer A Kearney
Epilepsia Open|March 15, 2019
C57BL/6J and C57BL/6N substrains differentially influence phenotype severity in the <i>Scn1a</i> <sup>+/-</sup> mouse model of Dravet syndromeSeok K Kang, Nicole A Hawkins, Jennifer A Kearney
Biorxiv : the Preprint Server for Biology|June 19, 2023
Strain-dependent effects on neurobehavioral and seizure phenotypes in <i>Scn2a</i> miceDennis M Echevarria-Cooper, Nicole A Hawkins, Jennifer A Kearney
Epilepsia|May 31, 2017
Cacna1g is a genetic modifier of epilepsy in a mouse model of Dravet syndromeJeffrey D Calhoun, Nicole A Hawkins, Nicole J Zachwieja, et al.
Experimental Neurology|October 23, 2018
Gene expression profiling in a mouse model of Dravet syndromeNicole A Hawkins, Jeffrey D Calhoun, Alexandra M Huffman, et al.
Neurobiology of Disease|November 27, 2024
Novel mouse model of alternating hemiplegia of childhood exhibits prominent motor and seizure phenotypesNicole A Hawkins, Jean-Marc DeKeyser, Jennifer A Kearney, et al.
Epilepsia|April 27, 2016
Cacna1g is a genetic modifier of epilepsy caused by mutation of voltage-gated sodium channel Scn2aJeffrey D Calhoun, Nicole A Hawkins, Nicole J Zachwieja, et al.
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