Vincent JB - Search Results

1

CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa.

Noor A, Windpassinger C, Patel M, Stachowiak B, Mikhailov A, Azam M, Irfan M, Siddiqui ZK, Naeem F, Paterson AD, Lutfullah M, Vincent JB, Ayub M. Noor A, et al. Among authors: vincent jb. Am J Hum Genet. 2008 Apr;82(4):1011-8. doi: 10.1016/j.ajhg.2008.01.021. Am J Hum Genet. 2008. PMID: 18387594 Free PMC article.

2

Search for unstable DNA in schizophrenia families with evidence for genetic anticipation.

Petronis A, Bassett AS, Honer WG, Vincent JB, Tatuch Y, Sasaki T, Ying DJ, Klempan TA, Kennedy JL. Petronis A, et al. Among authors: vincent jb. Am J Hum Genet. 1996 Oct;59(4):905-11. Am J Hum Genet. 1996. PMID: 8808607 Free PMC article.

3

No evidence of expansion of CAG or GAA repeats in schizophrenia families and monozygotic twins.

Vincent JB, Kalsi G, Klempan T, Tatuch Y, Sherrington RP, Breschel T, McInnis MG, Brynjolfsson J, Petursson H, Gurling HM, Gottesman II, Torrey EF, Petronis A, Kennedy JL. Vincent JB, et al. Hum Genet. 1998 Jul;103(1):41-7. doi: 10.1007/s004390050780. Hum Genet. 1998. PMID: 9737774

4

An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: a common expansion locus.

Vincent JB, Neves-Pereira ML, Paterson AD, Yamamoto E, Parikh SV, Macciardi F, Gurling HM, Potkin SG, Pato CN, Macedo A, Kovacs M, Davies M, Lieberman JA, Meltzer HY, Petronis A, Kennedy JL. Vincent JB, et al. Am J Hum Genet. 2000 Mar;66(3):819-29. doi: 10.1086/302803. Am J Hum Genet. 2000. PMID: 10712198 Free PMC article.

5

The unstable trinucleotide repeat story of major psychosis.

Vincent JB, Paterson AD, Strong E, Petronis A, Kennedy JL. Vincent JB, et al. Am J Med Genet. 2000 Spring;97(1):77-97. doi: 10.1002/(sici)1096-8628(200021)97:1<77::aid-ajmg11>3.0.co;2-3. Am J Med Genet. 2000. PMID: 10813808 Review.

6

Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual.

Vincent JB, Herbrick JA, Gurling HM, Bolton PF, Roberts W, Scherer SW. Vincent JB, et al. Am J Hum Genet. 2000 Aug;67(2):510-4. doi: 10.1086/303005. Epub 2000 Jul 7. Am J Hum Genet. 2000. PMID: 10889047 Free PMC article.

7

Long repeat tracts at SCA8 in major psychosis.

Vincent JB, Yuan QP, Schalling M, Adolfsson R, Azevedo MH, Macedo A, Bauer A, DallaTorre C, Medeiros HM, Pato MT, Pato CN, Bowen T, Guy CA, Owen MJ, O'Donovan MC, Paterson AD, Petronis A, Kennedy JL. Vincent JB, et al. Am J Med Genet. 2000 Dec 4;96(6):873-6. doi: 10.1002/1096-8628(20001204)96:6<873::aid-ajmg37>3.0.co;2-9. Am J Med Genet. 2000. PMID: 11121201

8

Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome.

Petek E, Windpassinger C, Vincent JB, Cheung J, Boright AP, Scherer SW, Kroisel PM, Wagner K. Petek E, et al. Among authors: vincent jb. Am J Hum Genet. 2001 Apr;68(4):848-58. doi: 10.1086/319523. Epub 2001 Mar 9. Am J Hum Genet. 2001. PMID: 11254443 Free PMC article.

9

The RAY1/ST7 tumor-suppressor locus on chromosome 7q31 represents a complex multi-transcript system.

Vincent JB, Petek E, Thevarkunnel S, Kolozsvari D, Cheung J, Patel M, Scherer SW. Vincent JB, et al. Genomics. 2002 Sep;80(3):283-94. doi: 10.1006/geno.2002.6835. Genomics. 2002. PMID: 12213198

10

Association and transmission analysis of the FMR1 IVS10 + 14C-T variant in autism.

Vincent JB, Thevarkunnel S, Kolozsvari D, Paterson AD, Roberts W, Scherer SW. Vincent JB, et al. Am J Med Genet B Neuropsychiatr Genet. 2004 Feb 15;125B(1):54-6. doi: 10.1002/ajmg.b.20088. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 14755444

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