R01 NS053792/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2008	1
2009	1
2010	2
2011	3
2012	2
2013	2
2014	5
2015	1
2016	3
2017	4
2019	1
2020	1
2021	1
2023	1
2025	0

1

Rescue of neuropsychiatric phenotypes in a mouse model of 16p11.2 duplication syndrome by genetic correction of an epilepsy network hub.

Forrest MP, Dos Santos M, Piguel NH, Wang YZ, Hawkins NA, Bagchi VA, Dionisio LE, Yoon S, Simkin D, Martin-de-Saavedra MD, Gao R, Horan KE, George AL Jr, LeDoux MS, Kearney JA, Savas JN, Penzes P. Forrest MP, et al. Nat Commun. 2023 Feb 17;14(1):825. doi: 10.1038/s41467-023-36087-x. Nat Commun. 2023. PMID: 36808153 Free PMC article.

2

Genetic modifiers of neurological disease.

Kearney JA. Kearney JA. Curr Opin Genet Dev. 2011 Jun;21(3):349-53. doi: 10.1016/j.gde.2010.12.007. Epub 2011 Jan 19. Curr Opin Genet Dev. 2011. PMID: 21251811 Free PMC article. Review.

3

Epilepsy and neurobehavioral abnormalities in mice with a dominant-negative KCNB1 pathogenic variant.

Hawkins NA, Misra SN, Jurado M, Kang SK, Vierra NC, Nguyen K, Wren L, George AL Jr, Trimmer JS, Kearney JA. Hawkins NA, et al. Neurobiol Dis. 2021 Jan;147:105141. doi: 10.1016/j.nbd.2020.105141. Epub 2020 Oct 22. Neurobiol Dis. 2021. PMID: 33132203 Free PMC article.

4

Advances in epilepsy genetics and genomics.

Kearney JA. Kearney JA. Epilepsy Curr. 2012 Jul;12(4):143-6. doi: 10.5698/1535-7511-12.4.143. Epilepsy Curr. 2012. PMID: 22936886 Free PMC article.

5

CaMKII modulates sodium current in neurons from epileptic Scn2a mutant mice.

Thompson CH, Hawkins NA, Kearney JA, George AL Jr. Thompson CH, et al. Proc Natl Acad Sci U S A. 2017 Feb 14;114(7):1696-1701. doi: 10.1073/pnas.1615774114. Epub 2017 Jan 30. Proc Natl Acad Sci U S A. 2017. PMID: 28137877 Free PMC article.

6

De novo KCNB1 mutations in epileptic encephalopathy.

Torkamani A, Bersell K, Jorge BS, Bjork RL Jr, Friedman JR, Bloss CS, Cohen J, Gupta S, Naidu S, Vanoye CG, George AL Jr, Kearney JA. Torkamani A, et al. Ann Neurol. 2014 Oct;76(4):529-540. doi: 10.1002/ana.24263. Epub 2014 Sep 19. Ann Neurol. 2014. PMID: 25164438 Free PMC article.

7

Mapping genetic modifiers of survival in a mouse model of Dravet syndrome.

Miller AR, Hawkins NA, McCollom CE, Kearney JA. Miller AR, et al. Genes Brain Behav. 2014 Feb;13(2):163-72. doi: 10.1111/gbb.12099. Epub 2013 Nov 14. Genes Brain Behav. 2014. PMID: 24152123 Free PMC article.

8

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 Jr. Anderson LL, et al. Epilepsia. 2014 Aug;55(8):1274-83. doi: 10.1111/epi.12657. Epub 2014 May 23. Epilepsia. 2014. PMID: 24862204 Free PMC article.

9

Confirmation of an epilepsy modifier locus on mouse chromosome 11 and candidate gene analysis by RNA-Seq.

Hawkins NA, Kearney JA. Hawkins NA, et al. Genes Brain Behav. 2012 Jun;11(4):452-60. doi: 10.1111/j.1601-183X.2012.00790.x. Epub 2012 Apr 27. Genes Brain Behav. 2012. PMID: 22471526 Free PMC article.

10

Characterization of a KCNB1 variant associated with autism, intellectual disability, and epilepsy.

Calhoun JD, Vanoye CG, Kok F, George AL Jr, Kearney JA. Calhoun JD, et al. Neurol Genet. 2017 Dec 11;3(6):e198. doi: 10.1212/NXG.0000000000000198. eCollection 2017 Dec. Neurol Genet. 2017. PMID: 29264390 Free PMC article.

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