Tyson C - Search Results

1

Population-based characterization of the genetic landscape of chronic lymphocytic leukemia patients referred for cytogenetic testing in British Columbia, Canada: the role of provincial laboratory standardization.

Gerrie AS, Huang SJ, Bruyere H, Dalal C, Hrynchak M, Karsan A, Ramadan KM, Smith AC, Tyson C, Toze CL, Gillan TL. Gerrie AS, et al. Among authors: tyson c. Cancer Genet. 2014 Jul-Aug;207(7-8):316-25. doi: 10.1016/j.cancergen.2014.08.006. Epub 2014 Aug 29. Cancer Genet. 2014. PMID: 25441686

2

Expansion of a 12-kb VNTR containing the REXO1L1 gene cluster underlies the microscopically visible euchromatic variant of 8q21.2.

Tyson C, Sharp AJ, Hrynchak M, Yong SL, Hollox EJ, Warburton P, Barber JC. Tyson C, et al. Eur J Hum Genet. 2014 Apr;22(4):458-63. doi: 10.1038/ejhg.2013.185. Epub 2013 Sep 18. Eur J Hum Genet. 2014. PMID: 24045839 Free PMC article.

3

Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability.

Qiao Y, Tyson C, Hrynchak M, Lopez-Rangel E, Hildebrand J, Martell S, Fawcett C, Kasmara L, Calli K, Harvard C, Liu X, Holden JJ, Lewis SM, Rajcan-Separovic E. Qiao Y, et al. Among authors: tyson c. Clin Genet. 2013 Feb;83(2):145-54. doi: 10.1111/j.1399-0004.2012.01860.x. Epub 2012 Apr 9. Clin Genet. 2013. PMID: 22369279

4

A novel microdeletion affecting the CETP gene raises HDL-associated cholesterol levels.

Hitchcock E, Patankar JV, Tyson C, Hrynchak M, Hayden MR, Gibson WT. Hitchcock E, et al. Among authors: tyson c. Clin Genet. 2016 Apr;89(4):495-500. doi: 10.1111/cge.12633. Epub 2015 Jul 23. Clin Genet. 2016. PMID: 26126777

5

Genotype-phenotype analysis of 18q12.1-q12.2 copy number variation in autism.

Wang P, Carrion P, Qiao Y, Tyson C, Hrynchak M, Calli K, Lopez-Rangel E, Andrieux J, Delobel B, Duban-Bedu B, Thuresson AC, Annerén G, Liu X, Rajcan-Separovic E, Suzanne Lewis ME. Wang P, et al. Among authors: tyson c. Eur J Med Genet. 2013 Aug;56(8):420-5. doi: 10.1016/j.ejmg.2013.05.006. Epub 2013 May 29. Eur J Med Genet. 2013. PMID: 23727450 Review.

6

Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGH.

Tyson C, Harvard C, Locker R, Friedman JM, Langlois S, Lewis ME, Van Allen M, Somerville M, Arbour L, Clarke L, McGilivray B, Yong SL, Siegel-Bartel J, Rajcan-Separovic E. Tyson C, et al. Am J Med Genet A. 2005 Dec 15;139(3):173-85. doi: 10.1002/ajmg.a.31015. Am J Med Genet A. 2005. PMID: 16283669

7

Elucidation of a cryptic interstitial 7q31.3 deletion in a patient with a language disorder and mild mental retardation by array-CGH.

Tyson C, McGillivray B, Chijiwa C, Rajcan-Separovic E. Tyson C, et al. Am J Med Genet A. 2004 Sep 1;129A(3):254-60. doi: 10.1002/ajmg.a.30245. Am J Med Genet A. 2004. PMID: 15326624

8

Understanding the impact of 1q21.1 copy number variant.

Harvard C, Strong E, Mercier E, Colnaghi R, Alcantara D, Chow E, Martell S, Tyson C, Hrynchak M, McGillivray B, Hamilton S, Marles S, Mhanni A, Dawson AJ, Pavlidis P, Qiao Y, Holden JJ, Lewis SM, O'Driscoll M, Rajcan-Separovic E. Harvard C, et al. Among authors: tyson c. Orphanet J Rare Dis. 2011 Aug 8;6:54. doi: 10.1186/1750-1172-6-54. Orphanet J Rare Dis. 2011. PMID: 21824431 Free PMC article.

9

Molecular cytogenetic investigation of two patients with Y chromosome rearrangements and intellectual disability.

Tyson C, Dawson AJ, Bal S, Tomiuk M, Anderson T, Tucker D, Riordan D, Chudoba I, Morash B, Mhanni A, Chudley AE, McGillivray B, Parslow M, Rappold G, Roeth R, Fawcett C, Qiao Y, Harvard C, Rajcan-Separovic E. Tyson C, et al. Am J Med Genet A. 2009 Mar;149A(3):490-5. doi: 10.1002/ajmg.a.32535. Am J Med Genet A. 2009. PMID: 19213034

10

A distinct neurodevelopmental syndrome with intellectual disability, autism spectrum disorder, characteristic facies, and macrocephaly is caused by defects in CHD8.

Yasin H, Gibson WT, Langlois S, Stowe RM, Tsang ES, Lee L, Poon J, Tran G, Tyson C, Wong CK, Marra MA, Friedman JM, Zahir FR. Yasin H, et al. Among authors: tyson c. J Hum Genet. 2019 Apr;64(4):271-280. doi: 10.1038/s10038-019-0561-0. Epub 2019 Jan 22. J Hum Genet. 2019. PMID: 30670789

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