Christine Tyson

Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study

Human Genetics and Genomics Advances

Elliott, A.M. and Adam, S. and du Souich, C. and Lehman, A. and Nelson, T.N. and van Karnebeek, C. and Alderman, E. and Armstrong, L. and Aubertin, G. and Blood, K. and Boelman, C. and Boerkoel, C. and Bretherick, K. and Brown, L. and Chijiwa, C. and Clarke, L. and Couse, M. and Creighton, S. and Watts-Dickens, A. and Gibson, W.T. and Gill, H. and Tarailo-Graovac, M. and Hamilton, S. and Heran, H. and Horvath, G. and Huang, L. and Hulait, G.K. and Koehn, D. and Lee, H.K. and Lewis, S. and Lopez, E. and Louie, K. and Niederhoffer, K. and Matthews, A. and Meagher, K. and Peng, J.J. and Patel, M.S. and Race, S. and Richmond, P. and Rupps, R. and Salvarinova, R. and Seath, K. and Selby, K. and Steinraths, M. and Stockler, S. and Tang, K. and Tyson, C. and van Allen, M. and Wasserman, W. and Mwenifumbo, J. and Friedman, J.M.

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

Journal of Human Genetics

Yasin, H. and Gibson, W.T. and Langlois, S. and Stowe, R.M. and Tsang, E.S. and Lee, L. and Poon, J. and Tran, G. and Tyson, C. and Wong, C.K. and Marra, M.A. and Friedman, J.M. and Zahir, F.R.

Copy number variation of the REXO1L1 gene cluster; Euchromatic deletion variant or susceptibility factor?

European Journal of Human Genetics

Barber, J.C.K. and Sharp, A.J. and Hollox, E.J. and Tyson, C.

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

Clinical Genetics

Hitchcock, E. and Patankar, J.V. and Tyson, C. and Hrynchak, M. and Hayden, M.R. and Gibson, W.T.

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

European Journal of Human Genetics

Tyson, C. and Sharp, A.J. and Hrynchak, M. and Yong, S.L. and Hollox, E.J. and Warburton, P. and Barber, J.C.K.

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

Cancer Genetics

Gerrie, A.S. and Huang, S.J.T. and Bruyere, H. and Dalal, C. and Hrynchak, M. and Karsan, A. and Ramadan, K.M. and Smith, A.C. and Tyson, C. and Toze, C.L. and Gillan, T.L.

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

Clinical Genetics

Qiao, Y. and Tyson, C. and Hrynchak, M. and Lopez-Rangel, E. and Hildebrand, J. and Martell, S. and Fawcett, C. and Kasmara, L. and Calli, K. and Harvard, C. and Liu, X. and Holden, J.J.A. and Lewis, S.M.E. and Rajcan-Separovic, E.

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

European Journal of Medical Genetics

Wang, P. and Carrion, P. and Qiao, Y. and Tyson, C. and Hrynchak, M. and Calli, K. and Lopez-Rangel, E. and Andrieux, J. and Delobel, B. and Duban-Bedu, B. and Thuresson, A.-C. and Annern, G. and Liu, X. and Rajcan-Separovic, E. and Suzanne Lewis, M.E.

Understanding the impact of 1q21.1 copy number variant

Orphanet Journal of Rare Diseases

Harvard, C. and Strong, E. and Mercier, E. and Colnaghi, R. and Alcantara, D. and Chow, E. and Martell, S. and Tyson, C. and Hrynchak, M. and McGillivray, B. and Hamilton, S. and Marles, S. and Mhanni, A. and Dawson, A.J. and Pavlidis, P. and Qiao, Y. and Holden, J.J. and Lewis, S.M.E. and O'Driscoll, M. and Rajcan-Separovic, E.

Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics

Human Genetics

Qiao, Y. and Harvard, C. and Tyson, C. and Liu, X. and Fawcett, C. and Pavlidis, P. and Holden, J.J.A. and Lewis, M.E.S. and Rajcan-Separovic, E.

Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss

Human Reproduction

Rajcan-Separovic, E. and Diego-Alvarez, D. and Robinson, W.P. and Tyson, C. and Qiao, Y. and Harvard, C. and Fawcett, C. and Kalousek, D. and Philipp, T. and Somerville, M.J. and Stephenson, M.D.

Genomic changes detected by array CGH in human embryos with developmental defects

Molecular Human Reproduction

Rajcan-Separovic, E. and Qiao, Y. and Tyson, C. and Harvard, C. and Fawcett, C. and Kalousek, D. and Stephenson, M. and Philipp, T.

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

American Journal of Medical Genetics, Part A

Tyson, C. and Dawson, A.J. and Bal, S. and Tomiuk, M. and Anderson, T. and Tucker, D. and Riordan, D. and Chudoba, I. and Morash, B. and Mhanni, A. and Chudley, A.E. and McGillivray, B. and Parslow, M. and Rappold, G. and Roeth, R. and Fawcett, C. and Qiao, Y. and Harvard, C. and Rajcan-Separovic, E.

Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH

Molecular Cytogenetics

Christine Tyson and Ying Qiao and Chansonette Harvard and Xudong Liu and Francois P Bernier and Barbara McGillivray and Sandra A Farrell and Laura Arbour and Albert E Chudley and Lorne Clarke and William Gibson and Sarah Dyack and Ross McLeod and Teresa Costa and Margot I VanAllen and Siu-li Yong and Gail E Graham and Patrick MacLeod and Millan S Patel and Jane Hurlburt and Jeanette JA Holden and Suzanne ME Lewis and Evica Rajcan-Separovic

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

American Journal of Medical Genetics

Tyson, C. and Harvard, C. and Locker, R. and Friedman, J.M. and Langlois, S. and Lewis, M.E.S. and Van Allen, M. and Somerville, M. and Arbour, L. and Clarke, L. and McGilivray, B. and Yong, S.L. and Siegel-Bartel, J. and Rajcan-Separovic, E.

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

American Journal of Medical Genetics

Tyson, C. and McGillivray, B. and Chijiwa, C. and Rajcan-Separovic, E.

Analysis of proximal X chromosome pairing in early female mouse meiosis

Chromosoma

Christine O'Keeffe and Maj A. Hultn and Charles Tease

09 / 1997