Bennett CL - Search Results

1

A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4) localizes to a 500-kb interval on chromosome 9q34.

Blair IP, Bennett CL, Abel A, Rabin BA, Griffin JW, Fischbeck KH, Cornblath DR, Chance PF. Blair IP, et al. Among authors: bennett cl. Neurogenetics. 2000 Sep;3(1):1-6. doi: 10.1007/pl00022976. Neurogenetics. 2000. PMID: 11085590

2

DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4).

Chen YZ, Bennett CL, Huynh HM, Blair IP, Puls I, Irobi J, Dierick I, Abel A, Kennerson ML, Rabin BA, Nicholson GA, Auer-Grumbach M, Wagner K, De Jonghe P, Griffin JW, Fischbeck KH, Timmerman V, Cornblath DR, Chance PF. Chen YZ, et al. Among authors: bennett cl. Am J Hum Genet. 2004 Jun;74(6):1128-35. doi: 10.1086/421054. Epub 2004 Apr 21. Am J Hum Genet. 2004. PMID: 15106121 Free PMC article.

3

Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizures.

Bennett CL, Huynh HM, Chance PF, Glass IA, Gospe SM Jr. Bennett CL, et al. Neurogenetics. 2005 Sep;6(3):143-9. doi: 10.1007/s10048-005-0221-8. Epub 2005 Aug 2. Neurogenetics. 2005. PMID: 16075246

4

Search for genes involved in Joubert syndrome: evidence that one or more major loci are yet to be identified and exclusion of candidate genes EN1, EN2, FGF8, and BARHL1.

Blair IP, Gibson RR, Bennett CL, Chance PF. Blair IP, et al. Among authors: bennett cl. Am J Med Genet. 2002 Jan 22;107(3):190-6. Am J Med Genet. 2002. PMID: 11807898

5

X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3.

Bennett CL, Yoshioka R, Kiyosawa H, Barker DF, Fain PR, Shigeoka AO, Chance PF. Bennett CL, et al. Am J Hum Genet. 2000 Feb;66(2):461-8. doi: 10.1086/302761. Am J Hum Genet. 2000. PMID: 10677306 Free PMC article.

6

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3.

Bennett CL, Christie J, Ramsdell F, Brunkow ME, Ferguson PJ, Whitesell L, Kelly TE, Saulsbury FT, Chance PF, Ochs HD. Bennett CL, et al. Nat Genet. 2001 Jan;27(1):20-1. doi: 10.1038/83713. Nat Genet. 2001. PMID: 11137993

7

Molecular pathogenesis of hereditary motor, sensory and autonomic neuropathies.

Bennett CL, Chance PF. Bennett CL, et al. Curr Opin Neurol. 2001 Oct;14(5):621-7. doi: 10.1097/00019052-200110000-00011. Curr Opin Neurol. 2001. PMID: 11562574 Review.

8

In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndrome.

Bassuk AG, Chen YZ, Batish SD, Nagan N, Opal P, Chance PF, Bennett CL. Bassuk AG, et al. Among authors: bennett cl. Neurogenetics. 2007 Jan;8(1):45-9. doi: 10.1007/s10048-006-0067-8. Epub 2006 Nov 10. Neurogenetics. 2007. PMID: 17096168

9

Late-onset hereditary axonal neuropathies.

Bennett CL, Lawson VH, Brickell KL, Isaacs K, Seltzer W, Lipe HP, Weiss MD, Carter GT, Flanigan KM, Chance PF, Bird TD. Bennett CL, et al. Neurology. 2008 Jul 1;71(1):14-20. doi: 10.1212/01.wnl.0000304048.94023.73. Epub 2008 May 21. Neurology. 2008. PMID: 18495953

10

Joubert syndrome: a haplotype segregation strategy and exclusion of the zinc finger protein of cerebellum 1 (ZIC1) gene.

Bennett CL, Parisi MA, Eckert ML, Huynh HM, Chance PF, Glass IA. Bennett CL, et al. Am J Med Genet A. 2004 Mar 1;125A(2):117-24; discussion 117. doi: 10.1002/ajmg.a.20438. Am J Med Genet A. 2004. PMID: 14981711

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