Monica Hrynchak

Prenatal cytogenetic assessment and inv(2)(p11.2q13)

Meaghan Hysert, Hélène Bruyèrè, Gilbert B. Côté et al. · Prenatal Diagnosis · 2006 · 85 citations

Association of GTF2i in the Williams-Beuren Syndrome Critical Region with Autism Spectrum Disorders

Patrick Malenfant, Xudong Liu, Melissa L. Hudson et al. · Journal of Autism and Developmental Disorders · 2011 · 70 citations

Autism Spectrum Disorders, Syndromic Autism, Genetic Disorder +8

Understanding the impact of 1q21.1 copy number variant

Chansonette Harvard, Emma Strong, Eloi Mercier et al. · Orphanet Journal of Rare Diseases · 2011 · 55 citations · Full text

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

Ying Qiao, Christine Tyson, Monica Hrynchak et al. · Clinical Genetics · 2012 · 50 citations

Engineering, Genetics, Molecular Biology +18

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

Christine Tyson, Andrew J. Sharp, Monica Hrynchak et al. · European Journal of Human Genetics · 2013 · 44 citations · Full text

Biology, Visible Euchromatic Variant, 12-Kb Vntr +13