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Title	Author(s)	Issue Date	Views
Blood cell type-specific genome-wide DNA methylation analysis of Chinese patients with early-onset systemic lupus erythematosus identifies loss of DNA methylation in genes related to the Type I Interferon pathway Proceeding/Conference:American Society of Human Genetics Annual Meeting, ASHG2017	Chung, BHY Yeung, KS Mok, TKG Choufani, S Lau, YL Weksberg, R	2017	58
Causal somatic mutations in urine DNA from persons with the CLOVES subgroup of the PIK3CA Related Overgrowth Spectrum (PROS) Journal:Clinical Genetics	Michel, ME Konczyk, DJ Yeung, KS Murillo, R Vivero, MP Hall, AM Zurakowski, D Adams, D Gupta, A Huang, AY Chung, BHY Warman, ML	2018	65
Cell Lineage-specific Genome-wide DNA Methylation Analysis of Patients with Paediatric-onset Systemic Lupus Erythematosus Journal:Epigenetics	Yeung, KS Lee, TL Mok, MY Mak, CCY Yang, W Chong, PCY Lee, PPW Ho, MHK Choufani, S Lau, CS Lau, YL Weksberg, R Chung, BHY	2019	47
CFTR founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosis Journal:Molecular Genetics & Genomic Medicine	LEUNG, KC Ying, D MAK, CCY Chen, XY Xu, W YEUNG, KS Wong, WL Chu, WY Mok, TKG Chau, SKC McLuskey, J Ong, WPT Leong, HY Chan, YK Yang, W Chen, JH Li, AM Sham, PC Lau, YL Chung, BHY Lee, SL	2017	137
Coexistence of paternally-inherited ABCC8 mutation and mosaic paternal uniparental disomy 11p hyperinsulinism Journal:International Journal of Pediatric Endocrinology	Tung, JYL Lai, SHY Au, SLK Yeung, KS Kan, ASY Loong, F DeLeon, DD Kalish, JM Ganguly, A Chung, BHY Chan, KYK	2020	23
Comprehensive genetic evaluation in paediatric-onset mitochondrial diseases Proceeding/Conference:Joint Annual Scientific Meeting 2019 of The Hong Kong Paediatric Society, Hong Kong College of Paediatricians, Hong Kong Paediatric Nurses Association, & Hong Kong College of Paediatric Nursing	Tsang, MHY Kwong, AKY Fung, JLF Yu, MHC Yeung, KS Mak, CCY Rodenburg, R Smeitink, J Luk, HM Lo, FMI Chung, BHY Fung, CW	2019	38
De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients Journal:npj Genomic Medicine	MAK, CCY Chow, PC Liu, APY Chan, YK Chu, WY Mok, TKG LEUNG, KC YEUNG, KS Chau, AKT Lowther, C Scherer, SW Marshall, CR Bassett, AS Chung, BHY	2016	91
Delineation of molecular findings by whole-exome sequencing for suspected cases of paediatric-onset mitochondrial diseases in the Southern Chinese population Journal:Human Genomics	TSANG, MHY Kwong, AKY Chan, KLS Fung, JLF YU, MHC Mak, CCY Yeung, KS Rodenburg, RJT Smeitink, JAM Chan, R Tsoi, T Hui, J Wong, SSN Tai, SM Chan, VCM Ma, CK Fung, STH Wu, SP Chak, WK Chung, BHY Fung, CW	2020	16
Design and complexity optimization of a new digital IF for software radio receivers with prescribed output accuracy Journal:IEEE Transactions on Circuits and Systems I: Regular Papers	Chan, SC Tsui, KM Yeung, KS Yuk, TI	2007	198
Design and implementation of multiplier-less tunable 2-D FIR filters using McClellan transformation Proceeding/Conference:Proceedings - IEEE International Symposium on Circuits and Systems	Yeung, KS Chan, SC	2002	185
The design and multiplier-less realization of software radio receivers with reduced system delay Journal:IEEE Transactions on Circuits and Systems I: Regular Papers	Yeung, KS Chan, SC	2004	190
Design of FIR digital filters with prescribed flatness and peak error constraints using second-order cone programming Journal:IEEE Transactions on Circuits and Systems II: Express Briefs	Tsui, KM Chan, SC Yeung, KS	2005	270
The design of two-channel prefect reconstruction FIR triplet wavelet filter banks using semidefinite programming Proceeding/Conference:Proceedings - IEEE International Symposium on Circuits and Systems	Yeung, KS Chan, SC	2003	99
Detecting expansion of short tandem repeat in whole exome sequencing data of movement disorder cohort with bioinformatics tool expansion hunter Proceeding/Conference:Joint Annual Scientific Meeting 2020 of The Hong Kong Paediatric Society (HKPS), Hong Kong College of Paediatricians (HKCPaed), Hong Kong Paediatric Nurses Association (HKPNA) and Hong Kong College of Paediatric Nursing (HKCPN)	Chui, MCM CHAU, FTJ YU, MHC Fung, JLF LEE, M Mak, CCY Tsang, MHY Chan, JCK CHUNG, CCY Yeung, KS Chung, BHY	2020	30
Diagnostic outcome of whole exome sequencing in Hong Kong familes with autism spectrum disorder Proceeding/Conference:Joint Annual Scientific Meeting 2019 of The Hong Kong Paediatric Society, Hong Kong College of Paediatricians, Hong Kong Paediatric Nurses Association, & Hong Kong College of Paediatric Nursing	Chan, MCY Mak, CCY Tsang, HY Yeung, KS Fung, JLF Yu, MHC Lee, MMY Chung, CCY Lee, SL Chung, BHY	2019	61
EHMT1 pathogenic variants and 9q34.3 microdeletions share altered DNA methylation patterns in patients with Kleefstra syndrome Journal:Journal of Translational Genetics and Genomics	Goodman, SJ Cytrynbaum, C Chung, BHY Chater-Diehl, E Aziz, C Turinsky, AL Kellam, B Keller, M Ko, JM Caluseriu, O Grafodatskaya, D McCready, E Perrier, R Yeung, KS Luk, HM Machado, J Brudno, M Stavropoulos, DJ Scherer, SW Innes, AM Cheung, SW Choufani, S Weksberg, R	2020	35
Evaluating the Clinical Utility of Genome Sequencing for Cytogenetically Balanced Chromosomal Abnormalities in Prenatal Diagnosis Journal:Frontiers in Genetics	YU, MHC CHAU, JFT Au, SLK Lo, HM Yeung, KS Fung, JLF Mak, CCY CHUNG, CCY Chan, KYK Chung, BHY Kan, ASY	2021	37
Evaluating the clinical utility of genome sequencing for cytogenetically balanced chromosomal abnormalities in prenatal diagnosis Proceeding/Conference:Health Research Symposium 2021	Yu, MHC Chau, FTJ Au, SLK Lo, HM Yeung, KS Fung, JLF Mak, CCY Chung, CCY Chan, KYK Chung, BHY Kan, ASY	2021	7
Evaluating the diagnostgic impact and cost of rapid whole-exome sequencing for rare genetic diseases in Hong Kong Proceeding/Conference:Joint Annual Scientific Meeting 2019 of The Hong Kong Paediatric Society, Hong Kong College of Paediatricians, Hong Kong Paediatric Nurses Association, & Hong Kong College of Paediatric Nursing	Chung, CY Yeung, KS Yu, HC Mak, CCY Fung, LF Leung, GKC Chan, GCF Lee, SL Chung, BHY	2019	33
Evidence of spread of X Chromosome inactivation on Chromosome 15 in a girl with an Unbalanced t(X;15) Translocation Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)	Yeung, KS Chee, WYY Luk, HM Tang, MHY Lau, ETK Shuen, YA Lo, IFM Chan, YK Chung, BHY	2013	74

Showing results 13 to 32 of 76 < previous next >