Vincent JB - Search Results

1

Mapping of three novel loci for non-syndromic autosomal recessive mental retardation (NS-ARMR) in consanguineous families from Pakistan.

Rafiq MA, Ansar M, Marshall CR, Noor A, Shaheen N, Mowjoodi A, Khan MA, Ali G, Amin-ud-Din M, Feuk L, Vincent JB, Scherer SW. Rafiq MA, et al. Among authors: vincent jb. Clin Genet. 2010 Nov;78(5):478-83. doi: 10.1111/j.1399-0004.2010.01405.x. Clin Genet. 2010. PMID: 20345473

2

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.

3

The human homologue of flamingo, EGFL2, encodes a brain-expressed large cadherin-like protein with epidermal growth factor-like domains, and maps to chromosome 1p13.3-p21.1.

Vincent JB, Skaug J, Scherer SW. Vincent JB, et al. DNA Res. 2000 Jun 30;7(3):233-5. doi: 10.1093/dnares/7.3.233. DNA Res. 2000. PMID: 10907856 Free article. No abstract available.

4

Human secretin (SCT): gene structure, chromosome location, and distribution of mRNA.

Whitmore TE, Holloway JL, Lofton-Day CE, Maurer MF, Chen L, Quinton TJ, Vincent JB, Scherer SW, Lok S. Whitmore TE, et al. Among authors: vincent jb. Cytogenet Cell Genet. 2000;90(1-2):47-52. doi: 10.1159/000015658. Cytogenet Cell Genet. 2000. PMID: 11060443

5

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.

6

Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31.

Cheung J, Petek E, Nakabayashi K, Tsui LC, Vincent JB, Scherer SW. Cheung J, et al. Among authors: vincent jb. Genomics. 2001 Nov;78(1-2):7-11. doi: 10.1006/geno.2001.6651. Genomics. 2001. PMID: 11707066

7

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

8

Cloning and characterization of human CADPS and CADPS2, new members of the Ca2+-dependent activator for secretion protein family.

Cisternas FA, Vincent JB, Scherer SW, Ray PN. Cisternas FA, et al. Among authors: vincent jb. Genomics. 2003 Mar;81(3):279-91. doi: 10.1016/s0888-7543(02)00040-x. Genomics. 2003. PMID: 12659812

9

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

10

A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome.

Mnatzakanian GN, Lohi H, Munteanu I, Alfred SE, Yamada T, MacLeod PJ, Jones JR, Scherer SW, Schanen NC, Friez MJ, Vincent JB, Minassian BA. Mnatzakanian GN, et al. Among authors: vincent jb. Nat Genet. 2004 Apr;36(4):339-41. doi: 10.1038/ng1327. Epub 2004 Mar 21. Nat Genet. 2004. PMID: 15034579

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