Vincent JB - Search Results

1

Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families.

Egger G, Roetzer KM, Noor A, Lionel AC, Mahmood H, Schwarzbraun T, Boright O, Mikhailov A, Marshall CR, Windpassinger C, Petek E, Scherer SW, Kaschnitz W, Vincent JB. Egger G, et al. Among authors: vincent jb. Neurogenetics. 2014 May;15(2):117-27. doi: 10.1007/s10048-014-0394-0. Epub 2014 Mar 19. Neurogenetics. 2014. PMID: 24643514

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

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.

5

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

6

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

7

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

8

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

9

De novo translocation t(5;18)(q33.1;q12.1) associated with autistic disorder.

Kroisel PM, Windpassinger C, Wagner K, Petek E, Vincent JB, Scherer SW, Spiel G, Artner V, Valtiner E. Kroisel PM, et al. Among authors: vincent jb. Am J Med Genet A. 2004 Aug 15;129A(1):98-100. doi: 10.1002/ajmg.a.30150. Am J Med Genet A. 2004. PMID: 15266626 No abstract available.

10

Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands.

Vincent JB, Kolozsvari D, Roberts WS, Bolton PF, Gurling HM, Scherer SW. Vincent JB, et al. Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15;129B(1):82-4. doi: 10.1002/ajmg.b.30069. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15274046

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

321 results

Search Page

Filters