Sau W Cheung
Sau W Cheung
Professor of Molecular and Human Genetics, Baylor College of Medicine
Verified email at bcm.edu
Title
Cited by
Cited by
Year
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
5752008
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
5652006
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
5612008
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
4802010
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
3732011
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
3442009
The array CGH and its clinical applications
M Shinawi, SW Cheung
Drug discovery today 13 (17-18), 760-770, 2008
3092008
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
2742013
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
2742005
Methods of making fluorescent microspheres
SW Cheung
US Patent 5,194,300, 1993
2661993
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
2652006
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
2462007
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
2442010
Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases
X Lu, CA Shaw, A Patel, J Li, ML Cooper, WR Wells, CM Sullivan, ...
PloS one 2 (3), e327, 2007
2362007
Hep G2 is a hepatoblastoma-derived cell line
D López-Terrada, SW Cheung, MJ Finegold, BB Knowles
Human pathology 40 (10), 1512, 2009
2302009
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
2302009
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
2272009
Increased LIS1 expression affects human and mouse brain development
W Bi, T Sapir, OA Shchelochkov, F Zhang, MA Withers, JV Hunter, T Levy, ...
Nature genetics 41 (2), 168-177, 2009
2172009
22q11. 2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome
S Ben-Shachar, Z Ou, CA Shaw, JW Belmont, MS Patel, M Hummel, ...
The American Journal of Human Genetics 82 (1), 214-221, 2008
2122008
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
2092007
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