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S.W. Cheung | Researchclopedia

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S.W. Cheung

13

Works

1,433

Citations

10

h-index

10

i10-index

Research Topics

Genomic variations and chromosomal abnormalities Congenital heart defects research Chromosomal and Genetic Variations

Affiliations

Tri-Service General Hospital2005–2005

Baylor College of Medicine2005–2014

Baylor School2005–2005

Top Works

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

Marwan Shinawi,P. Liu,et al.

2009595 citations

CRISPR and Genetic Engineering

Prenatal Screening and Diagnostics

Parental Somatic Mosaicism Is Underrecognized and Influences Recurrence Risk of Genomic Disorders

Ian M. Campbell,Bo Yuan,et al.

2014279 citations

Microdeletions including <i>YWHAE</i> in the Miller–Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairment

Sandesh C. Sreenath Nagamani,Feng Zhang,et al.

2009169 citations

Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testing

Joanna Wiszniewska,Weimin Bi,et al.

2013128 citations

Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia

Margaret Wat,Danielle Veenma,et al.

201192 citations

Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes

Claudia M.B. Carvalho,Shivakumar Vasanth,et al.

201477 citations

Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond–Blackfan anaemia

Margaret Wat,Victoria B. Enciso,et al.

201044 citations

Application of metaphase HR‐CGH and targeted chromosomal microarray analyses to genomic characterization of 116 patients with mental retardation and dysmorphic features

Beata Nowakowska,Paweł Stankiewicz,et al.

200823 citations

The donor chromosome breakpoint for a jumping translocation is associated with large low-copy repeats in 21q21.3

Paweł Stankiewicz,S.W. Cheung,et al.

200314 citations