Scherer SW - 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: scherer sw. 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. Among authors: scherer sw. 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. Among authors: scherer sw. 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: scherer sw. 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: scherer sw. Genomics. 2001 Nov;78(1-2):7-11. doi: 10.1006/geno.2001.6651. Genomics. 2001. PMID: 11707066

6

Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome.

Estivill X, Cheung J, Pujana MA, Nakabayashi K, Scherer SW, Tsui LC. Estivill X, et al. Among authors: scherer sw. Hum Mol Genet. 2002 Aug 15;11(17):1987-95. doi: 10.1093/hmg/11.17.1987. Hum Mol Genet. 2002. PMID: 12165560

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. Among authors: scherer sw. 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: scherer sw. Genomics. 2003 Mar;81(3):279-91. doi: 10.1016/s0888-7543(02)00040-x. Genomics. 2003. PMID: 12659812

9

Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22.

Chan EM, Bulman DE, Paterson AD, Turnbull J, Andermann E, Andermann F, Rouleau GA, Delgado-Escueta AV, Scherer SW, Minassian BA. Chan EM, et al. Among authors: scherer sw. J Med Genet. 2003 Sep;40(9):671-5. doi: 10.1136/jmg.40.9.671. J Med Genet. 2003. PMID: 12960212 Free PMC article.

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. Among authors: scherer sw. 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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