Sau W Cheung
Sau W Cheung
Professor of Molecular and Human Genetics, Baylor College of Medicine
Verified email at
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Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster
T Sahoo, D Del Gaudio, JR German, M Shinawi, SU Peters, RE Person, ...
Nature genetics 40 (6), 719-721, 2008
Recurrent reciprocal 1q21. 1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities
N Brunetti-Pierri, JS Berg, F Scaglia, J Belmont, CA Bacino, T Sahoo, ...
Nature genetics 40 (12), 1466-1471, 2008
High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping
DA Peiffer, JM Le, FJ Steemers, W Chang, T Jenniges, F Garcia, K Haden, ...
Genome research 16 (9), 1136-1148, 2006
Recurrent reciprocal 16p11. 2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size
M Shinawi, P Liu, SHL Kang, J Shen, JW Belmont, DA Scott, FJ Probst, ...
Journal of medical genetics 47 (5), 332-341, 2010
Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements
P Liu, A Erez, SCS Nagamani, SU Dhar, KE Kołodziejska, ...
Cell 146 (6), 889-903, 2011
Genomic and genic deletions of the FOX gene cluster on 16q24. 1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations
P Stankiewicz, P Sen, SS Bhatt, M Storer, Z Xia, BA Bejjani, Z Ou, ...
The American Journal of Human Genetics 84 (6), 780-791, 2009
SHANK3 overexpression causes manic-like behaviour with unique pharmacogenetic properties
K Han, JL Holder Jr, CP Schaaf, H Lu, H Chen, H Kang, J Tang, Z Wu, ...
Nature 503 (7474), 72-77, 2013
The array CGH and its clinical applications
M Shinawi, SW Cheung
Drug discovery today 13 (17-18), 760-770, 2008
Hep G2 is a hepatoblastoma-derived cell line
D López-Terrada, SW Cheung, MJ Finegold, BB Knowles
Human pathology 40 (10), 1512, 2009
Development and validation of a CGH microarray for clinical cytogenetic diagnosis
SW Cheung, CA Shaw, W Yu, J Li, Z Ou, A Patel, SA Yatsenko, ...
Genetics in Medicine 7 (6), 422-432, 2005
Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males
D Del Gaudio, P Fang, F Scaglia, PA Ward, WJ Craigen, DG Glaze, ...
Genetics in Medicine 8 (12), 784-792, 2006
The genetic basis of DOORS syndrome: an exome-sequencing study
PM Campeau, D Kasperaviciute, JT Lu, LC Burrage, C Kim, M Hori, ...
The Lancet Neurology 13 (1), 44-58, 2014
Detection of clinically relevant exonic copy‐number changes by array CGH
PM Boone, CA Bacino, CA Shaw, PA Eng, PM Hixson, AN Pursley, ...
Human mutation 31 (12), 1326-1342, 2010
Parental somatic mosaicism is underrecognized and influences recurrence risk of genomic disorders
IM Campbell, BO Yuan, C Robberecht, R Pfundt, P Szafranski, ...
The American Journal of Human Genetics 95 (2), 173-182, 2014
TBX6 null variants and a common hypomorphic allele in congenital scoliosis
N Wu, X Ming, J Xiao, Z Wu, X Chen, M Shinawi, Y Shen, G Yu, J Liu, ...
New England Journal of Medicine 372 (4), 341-350, 2015
Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11. 23 Williams-Beuren syndrome region
JS Berg, N Brunetti-Pierri, SU Peters, SHL Kang, CT Fong, J Salamone, ...
Genetics in Medicine 9 (7), 427-441, 2007
Methods of making fluorescent microspheres
SW Cheung
US Patent 5,194,300, 1993
Microdeletion 15q13. 3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders
S Ben-Shachar, B Lanpher, JR German, M Qasaymeh, L Potocki, ...
Journal of medical genetics 46 (6), 382-388, 2009
Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases
IB Van den Veyver, A Patel, CA Shaw, AN Pursley, SHL Kang, ...
Prenatal Diagnosis: Published in Affiliation With the International Society …, 2009
Microarray‐based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics
SW Cheung, CA Shaw, DA Scott, A Patel, T Sahoo, CA Bacino, A Pursley, ...
American journal of medical genetics Part A 143 (15), 1679-1686, 2007
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