Monica Hrynchak
Royal Columbian Hospital(CA)
Publications by Year
Research Areas
Lymphoma Diagnosis and Treatment, Chronic Lymphocytic Leukemia Research, Genomic variations and chromosomal abnormalities, Autism Spectrum Disorder Research, Congenital heart defects research
Most-Cited Works
- → Isodicentric Yp: prenatal diagnosis and outcome in 12 cases(2006)94 cited
- → Prenatal cytogenetic assessment and inv(2)(p11.2q13)(2006)85 cited
- → Association of GTF2i in the Williams-Beuren Syndrome Critical Region with Autism Spectrum Disorders(2011)73 cited
- → Understanding the impact of 1q21.1 copy number variant(2011)55 cited
- → Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability(2012)50 cited
- → Expansion of a 12-kb VNTR containing the REXO1L1 gene cluster underlies the microscopically visible euchromatic variant of 8q21.2(2013)44 cited
- → Cytogenetic findings in seven lacrimal gland neoplasms(1994)43 cited
- → Genotype–phenotype analysis of 18q12.1-q12.2 copy number variation in autism(2013)43 cited
- → Complex karyotypic alterations in an endometrial stromal sarcoma(1994)25 cited
- → Partial duplication of 3q (q25.1→q26.1) without the Brachmann‐de Lange phenotype(1993)18 cited