JenniferAnn RegoKearneyMD

PubMed

• HASH(0x3326660)
  Nomura, T.,Hawkins, N. A.,Kearney, J. A.,George, A. L.,Contractor, A.> ;J. Physiol. (Lond.). 2019 May 03
• HASH(0x3953100)
  Kang, S. K.,Hawkins, N. A.,Kearney, J. A.> ;Epilepsia Open. 2019 Mar 15
• Gene expression profiling in a mouse model of Dravet syndrome.
  Hawkins, N. A.,Calhoun, J. D.,Huffman, A. M.,Kearney, J. A.> ;Exp. Neurol.. 2018 Oct 23
• Fine Mapping of a Dravet Syndrome Modifier Locus on Mouse Chromosome 5 and Candidate Gene Analysis by RNA-Seq.
  Hawkins NA, Zachwieja NJ, Miller AR, Anderson LL, Kearney JA> ;PLoS Genet.. 2016-10-01
• CaMKII Modulates Sodium Current in Neurons from Epileptic Scn2a Mutant Mice
  Jennifer Kearney, MD> ;Proceedings of the National Academy of Sciences. 2017 Feb 01
• Cacna1g is a genetic modifier of epilepsy caused by mutation of voltage-gated sodium channel Scn2a.
  Calhoun JD, Hawkins NA, Zachwieja NJ, Kearney JA> ;Epilepsia. 2016-06-01
• Hlf is a genetic modifier of epilepsy caused by voltage-gated sodium channel mutations.
  Hawkins NA, Kearney JA> ;Epilepsy Res.. 2016-01-01
• De novo KCNB1 mutations in epileptic encephalopathy.
  Torkamani A, Bersell K, Jorge BS, Bjork RL, Friedman JR, Bloss CS, Cohen J, Gupta S, Naidu S, Vanoye CG, George AL, Kearney JA> ;Ann. Neurol.. 2014-10-01
• Antiepileptic activity of preferential inhibitors of persistent sodium current.
  Anderson LL, Thompson CH, Hawkins NA, Nath RD, Petersohn AA, Rajamani S, Bush WS, Frankel WN, Vanoye CG, Kearney JA, George AL> ;Epilepsia. 2014-08-01
• Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome mice.
  Mistry AM, Thompson CH, Miller AR, Vanoye CG, George AL, Kearney JA> ;Neurobiol. Dis.. 2014-05-01
• Mapping genetic modifiers of survival in a mouse model of Dravet syndrome.
  Miller AR, Hawkins NA, McCollom CE, Kearney JA> ;Genes Brain Behav.. 2014-02-01
• Novel SCN3A variants associated with focal epilepsy in children.
  Vanoye CG, Gurnett CA, Holland KD, George AL, Kearney JA> ;Neurobiol. Dis.. 2014-02-01
• Confirmation of an epilepsy modifier locus on mouse chromosome 11 and candidate gene analysis by RNA-Seq.
  Hawkins NA, Kearney JA> ;Genes Brain Behav.. 2012-06-01
• 53 citations
  Voltage-gated potassium channel KCNV2 (Kv8.2) contributes to epilepsy susceptibility
  Benjamin S. Jorge, Courtney M. Campbell, Alison R. Miller, Elizabeth D. Rutter, Christina A. Gurnett, Carlos G. Vanoye, Alfred L. George, Jennifer A. Kearney> ;Proceedings of the National Academy of Sciences of the United States of America. 2011 Mar 29
• Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus.
  Hawkins, N.A., Martin, M.S., Frankel, W.N., Kearney, J.A., Escayg, A.> ;Neurobiol Dis. 2011 Mar
• Genetic modifiers of neurological disease.
  Kearney, J.A.> ;Curr Opin Genet Dev. 2011 Jun
• Fine mapping of an epilepsy modifier gene on mouse Chromosome 19.
  Bergren, S.K., Rutter, E.D., Kearney, J.A.> ;Mamm Genome. 2009-06-01
• Impaired motor function in mice with cell-specific knockout of sodium channel Scn8a (NaV1.6) in cerebellar purkinje neurons and granule cells.
  Levin, S.I., Khaliq, Z.M., Aman, T.K., Grieco, T.M., Kearney, J.A., Raman, I.M., Meisler, M.H.> ;J Neurophysiol. 2006 Aug
• Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy.
  Kearney, J.A., Wiste, A.K., Stephani, U., Trudeau, M.M., Siegel, A., RamachandranNair, R., Elterman, R.D., Muhle, H., Reinsdorf, J., Shields, W.D., Meisler, M.H., Esca...> ;Pediatr Neurol. 2006 Feb
• Genetic modifiers affecting severity of epilepsy caused by mutation of sodium channel Scn2a.
  Bergren, S.K., Chen, S., Galecki, A., Kearney, J.A.> ;Mamm Genome. 2005 Sep
• Sodium channel mutations in epilepsy and other neurological disorders.
  Meisler, M.H., Kearney, J.A.> ;J Clin Invest. 2005 Aug
• Sodium channels and neurological disease: insights from Scn8a mutations in the mouse.
  Meisler MH, Kearney J, Escayg A, MacDonald BT, Sprunger LK> ;Neuroscientist. 2001-04-01
• Identification of epilepsy genes in human and mouse.
  Meisler MH, Kearney J, Ottman R, Escayg A> ;Annu. Rev. Genet.. 2001-01-01
• Restoration of all dystrophin protein interactions by functional domains in trans does not rescue dystrophy.
  Gardner, K. L., Kearney, J. A., Edwards, J. D., Rafael-Fortney, J. A.> ;Gene Ther. 2006 May
• Alessandro Agnoli Lecture. Models of basal ganglia dysfunction: predictions and pitfalls.
  Albin, R. L., Kearney, J. A.> ;Funct Neurol. 2000 Nov 04
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