R01 NS 35129/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1998	1
1999	2
2000	1
2001	1
2002	3
2010	1
2015	1
2016	1
2024	0

1

Novel loss-of-function variants in DIAPH1 associated with syndromic microcephaly, blindness, and early onset seizures.

Al-Maawali A, Barry BJ, Rajab A, El-Quessny M, Seman A, Coury SN, Barkovich AJ, Yang E, Walsh CA, Mochida GH, Stoler JM. Al-Maawali A, et al. Am J Med Genet A. 2016 Feb;170A(2):435-440. doi: 10.1002/ajmg.a.37422. Epub 2015 Oct 13. Am J Med Genet A. 2016. PMID: 26463574 Free PMC article.

2

Developmental and degenerative features in a complicated spastic paraplegia.

Manzini MC, Rajab A, Maynard TM, Mochida GH, Tan WH, Nasir R, Hill RS, Gleason D, Al Saffar M, Partlow JN, Barry BJ, Vernon M, LaMantia AS, Walsh CA. Manzini MC, et al. Ann Neurol. 2010 Apr;67(4):516-25. doi: 10.1002/ana.21923. Ann Neurol. 2010. PMID: 20437587 Free PMC article.

3

Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome.

Beltrán-Valero de Bernabé D, Currier S, Steinbrecher A, Celli J, van Beusekom E, van der Zwaag B, Kayserili H, Merlini L, Chitayat D, Dobyns WB, Cormand B, Lehesjoki AE, Cruces J, Voit T, Walsh CA, van Bokhoven H, Brunner HG. Beltrán-Valero de Bernabé D, et al. Am J Hum Genet. 2002 Nov;71(5):1033-43. doi: 10.1086/342975. Epub 2002 Oct 4. Am J Hum Genet. 2002. PMID: 12369018 Free PMC article.

4

Smooth, rough and upside-down neocortical development.

Olson EC, Walsh CA. Olson EC, et al. Curr Opin Genet Dev. 2002 Jun;12(3):320-7. doi: 10.1016/s0959-437x(02)00305-2. Curr Opin Genet Dev. 2002. PMID: 12076676 Review.

5

An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21.

Piao X, Basel-Vanagaite L, Straussberg R, Grant PE, Pugh EW, Doheny K, Doan B, Hong SE, Shugart YY, Walsh CA. Piao X, et al. Am J Hum Genet. 2002 Apr;70(4):1028-33. doi: 10.1086/339552. Epub 2002 Feb 13. Am J Hum Genet. 2002. PMID: 11845408 Free PMC article.

6

Molecular genetics of human microcephaly.

Mochida GH, Walsh CA. Mochida GH, et al. Curr Opin Neurol. 2001 Apr;14(2):151-6. doi: 10.1097/00019052-200104000-00003. Curr Opin Neurol. 2001. PMID: 11262728 Review.

7

Somatic and germline mosaic mutations in the doublecortin gene are associated with variable phenotypes.

Gleeson JG, Minnerath S, Kuzniecky RI, Dobyns WB, Young ID, Ross ME, Walsh CA. Gleeson JG, et al. Am J Hum Genet. 2000 Sep;67(3):574-81. doi: 10.1086/303043. Epub 2000 Jul 27. Am J Hum Genet. 2000. PMID: 10915612 Free PMC article.

8

Genes that regulate neuronal migration in the cerebral cortex.

Allen KM, Walsh CA. Allen KM, et al. Epilepsy Res. 1999 Sep;36(2-3):143-54. doi: 10.1016/s0920-1211(99)00048-0. Epilepsy Res. 1999. PMID: 10515162 Review.

9

Doublecortin is a microtubule-associated protein and is expressed widely by migrating neurons.

Gleeson JG, Lin PT, Flanagan LA, Walsh CA. Gleeson JG, et al. Neuron. 1999 Jun;23(2):257-71. doi: 10.1016/s0896-6273(00)80778-3. Neuron. 1999. PMID: 10399933 Free article.

10

PAK3 mutation in nonsyndromic X-linked mental retardation.

Allen KM, Gleeson JG, Bagrodia S, Partington MW, MacMillan JC, Cerione RA, Mulley JC, Walsh CA. Allen KM, et al. Nat Genet. 1998 Sep;20(1):25-30. doi: 10.1038/1675. Nat Genet. 1998. PMID: 9731525

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