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Publications 2001

Alpha-catulin maps to the familial dysautonomia region on 9q31.
Demacio PC, Ray PN. Genome. 2001 Dec;44(6):990-4. PMID: 11768226 PubMed

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. Genomics. 2001 Nov;78(1-2):7-11. PMID: 11707066 PubMed

A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.
Osborne LR, Li M, Pober B, Chitayat D, Bodurtha J, Mandel A, Costa T, Grebe T, Cox S, Tsui LC, Scherer SW. Nat Genet. 2001 Nov;29(3):321-5. PMID: 11685205 PubMed

Potential mapping of corneal dermoids to Xq24-qter.
Dar P, Javed AA, Ben-Yishay M, Ferreira JC, Paterson AD, Gross SJ, Chitayat D, Morrow BE, Nitowsky HM. J Med Genet. 2001 Oct;38(10):719-23. PMID: 11594343 PubMed

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.
Hadano S, Hand CK, Osuga H, Yanagisawa Y, Otomo A, Devon RS, Miyamoto N, Showguchi-Miyata J, Okada Y, Singaraja R, Figlewicz DA, Kwiatkowski T, Hosler BA, Sagie T, Skaug J, Nasir J, Brown RH Jr, Scherer SW, Rouleau GA, Hayden MR, Ikeda JE. Nat Genet. 2001 Oct;29(2):166-73. PMID: 11586298 PubMed

Murine phosphatidylserine-specific phospholipase A1 (Ps-pla1) maps to chromosome 16 but is distinct from the lpd (lipid defect) locus. Wen XY, Stewart AK, Skaug J, Wei E, Tsui LC. Mamm Genome. 2001 Feb;12(2):129-32.
PMID: 11210182 PubMed