Scherer SW - Search Results

1

Dynamic variation in allele-specific gene expression of Paraoxonase-1 in murine and human tissues.

Parker-Katiraee L, Bousiaki E, Monk D, Moore GE, Nakabayashi K, Scherer SW. Parker-Katiraee L, et al. Among authors: scherer sw. Hum Mol Genet. 2008 Nov 1;17(21):3263-70. doi: 10.1093/hmg/ddn222. Epub 2008 Aug 4. Hum Mol Genet. 2008. PMID: 18678600 Free PMC article.

2

Refined localization and yeast artificial chromosome (YAC) contig--mapping of genes and DNA segments in the 7q21-q32 region.

Scherer SW, Rommens JM, Soder S, Wong E, Plavsic N, Tompkins BJ, Beattie A, Kim J, Tsui LC. Scherer SW, et al. Hum Mol Genet. 1993 Jun;2(6):751-60. doi: 10.1093/hmg/2.6.751. Hum Mol Genet. 1993. PMID: 8353494

3

Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development.

Crackower MA, Scherer SW, Rommens JM, Hui CC, Poorkaj P, Soder S, Cobben JM, Hudgins L, Evans JP, Tsui LC. Crackower MA, et al. Among authors: scherer sw. Hum Mol Genet. 1996 May;5(5):571-9. doi: 10.1093/hmg/5.5.571. Hum Mol Genet. 1996. PMID: 8733122

4

Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephaly.

Roessler E, Belloni E, Gaudenz K, Vargas F, Scherer SW, Tsui LC, Muenke M. Roessler E, et al. Among authors: scherer sw. Hum Mol Genet. 1997 Oct;6(11):1847-53. doi: 10.1093/hmg/6.11.1847. Hum Mol Genet. 1997. PMID: 9302262

5

Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactyly.

Vargas FR, Roessler E, Gaudenz K, Belloni E, Whitehead AS, Kirke PN, Mills JL, Hooper G, Stevenson RE, Cordeiro I, Correia P, Felix T, Gereige R, Cunningham ML, Canún S, Antonarakis SE, Strachan T, Tsui LC, Scherer SW, Muenke M. Vargas FR, et al. Among authors: scherer sw. Hum Genet. 1998 Apr;102(4):387-92. doi: 10.1007/s004390050709. Hum Genet. 1998. PMID: 9600232 Review.

6

Genetic variation in paraoxonase-1 and paraoxonase-2 is associated with variation in plasma lipoproteins in Alberta Hutterites.

Boright AP, Connelly PW, Brunt JH, Scherer SW, Tsui LC, Hegele RA. Boright AP, et al. Among authors: scherer sw. Atherosclerosis. 1998 Jul;139(1):131-6. doi: 10.1016/s0021-9150(98)00071-9. Atherosclerosis. 1998. PMID: 9699900

7

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.

8

The human contactin-associated protein-like 2 gene (CNTNAP2) spans over 2 Mb of DNA at chromosome 7q35.

Nakabayashi K, Scherer SW. Nakabayashi K, et al. Among authors: scherer sw. Genomics. 2001 Apr 1;73(1):108-12. doi: 10.1006/geno.2001.6517. Genomics. 2001. PMID: 11352571

9

Mutation analysis of the origin recognition complex subunit 5 (ORC5L) gene in adult patients with myeloid leukemias exhibiting deletions of chromosome band 7q22.

Fröhling S, Nakabayashi K, Scherer SW, Döhner H, Döhner K. Fröhling S, et al. Among authors: scherer sw. Hum Genet. 2001 Apr;108(4):304-9. doi: 10.1007/s004390100498. Hum Genet. 2001. PMID: 11379876

10

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

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