C. Tyson

发表

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

P. Pavlidis, J. Holden, E. Rajcan-Separovic, 2010, Human Genetics.

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

Phillip A. Richmond, W. Wasserman, C. Boerkoel, 2022, HGG advances.

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

M. Hayden, W. Gibson, J. Patankar, 2016, Clinical genetics.

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

D. Kalousek, E. Rajcan-Separovic, C. Harvard, 2010, Molecular human reproduction.

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

G. Annéren, J. Andrieux, B. Delobel, 2013, European journal of medical genetics.

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

M. Somerville, W. Robinson, M. Stephenson, 2010, Human reproduction.

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

M. Somerville, W. Robinson, M. Stephenson, 2010 .

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

E. Rajcan-Separovic, Y Qiao, C Tyson, 2013, Clinical genetics.

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

M. Marra, F. Zahir, S. Langlois, 2019, Journal of Human Genetics.

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

M Somerville, M. Somerville, S. Langlois, 2005, American journal of medical genetics. Part A.

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

Andrew J Sharp, Edward J Hollox, A. Sharp, 2013, European Journal of Human Genetics.

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

M. Marra, F. Zahir, S. Langlois, 2019, Journal of Human Genetics.

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

B. McGillivray, E. Rajcan-Separovic, C. Tyson, 2004, American journal of medical genetics. Part A.

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.

A. Karsan, H. Bruyèrè, Adam C. Smith, 2014, Cancer genetics.

Understanding the impact of 1q21.1 copy number variant

P. Pavlidis, E. Strong, M. O’Driscoll, 2011, Orphanet journal of rare diseases.

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

A. Sharp, J. Barber, E. Hollox, 2016, European Journal of Human Genetics.

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

F. Bernier, P. Macleod, A. Chudley, 2008, Molecular Cytogenetics.