Evica Rajcan‐Separovic
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Prenatal Screening and Diagnostics, Chromosomal and Genetic Variations, Genomics and Rare Diseases
Most-Cited Works
- → Oligonucleotide Microarray Analysis of Genomic Imbalance in Children with Mental Retardation(2006)326 cited
- → Expression and Genetic Analysis of XIAP-Associated Factor 1 (XAF1) in Cancer Cell Lines(2000)211 cited
- → Disruption at the PTCHD1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability(2010)194 cited
- → Non‐muscle myosin heavy chain (MYH9): A new partner fused to ALK in anaplastic large cell lymphoma(2003)132 cited
- → Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1(2006)127 cited
- → Genomic changes detected by array CGH in human embryos with developmental defects(2009)117 cited
- → Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss(2010)112 cited
- → Submicroscopic deletions and duplications in individuals with intellectual disability detected by array‐CGH(2005)107 cited
- → Autism‐associated familial microdeletion of Xp11.22(2008)106 cited
- → 15q Duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array‐CGH(2006)101 cited