Use of single nucleotide polymorphism microarrays to distinguish between balanced and normal chromosomes in embryos from a translocation carrier

Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

C Shaw-Smith · Journal of Medical Genetics · 2004 · 510 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Array-Based Comparative Genomic Hybridization for the Genomewide Detection of Submicroscopic Chromosomal Abnormalities

Lisenka E.L.M. Vissers, Bert B.A. de Vries, Kazutoyo Osoegawa et al. · The American Journal of Human Genetics · 2003 · 473 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Karyomapping: a universal method for genome wide analysis of genetic disease based on mapping crossovers between parental haplotypes

Alan H. Handyside, G. Harton, Alan R. Thornhill et al. · Journal of Medical Genetics · 2009 · 409 citations

Medicine, Neurology, Oncology +16

Accurate single cell 24 chromosome aneuploidy screening using whole genome amplification and single nucleotide polymorphism microarrays

Nathan R. Treff, Jing Su, Xin Tao et al. · Fertility and Sterility · 2010 · 270 citations

Life Sciences, Genetics, Molecular Genetics +17

Development and validation of a CGH microarray for clinical cytogenetic diagnosis

Sau Wai Cheung, Chad A. Shaw, Wei Yu et al. · Genetics in Medicine · 2005 · 249 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16