Sau Wai Cheung
Chinese University of Hong Kong(HK)Baylor College of Medicine(US)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Prenatal Screening and Diagnostics, Genetics and Neurodevelopmental Disorders, Congenital heart defects research, Chromosomal and Genetic Variations
Most-Cited Works
- → Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster(2008)660 cited
- → Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities(2008)628 cited
- → High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping(2006)540 cited
- → Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations(2009)527 cited
- → Chromosome Catastrophes Involve Replication Mechanisms Generating Complex Genomic Rearrangements(2011)459 cited
- → SHANK3 overexpression causes manic-like behaviour with unique pharmacogenetic properties(2013)361 cited