Browsing "Paediatrics & Adolescent Medicine: Conference papers" by Author yang, j

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Showing results 1 to 12 of 12
TitleAuthor(s)Issue DateViews
 
Molecular Diagnosis for Paediatric Genetic Disorders Using Whole Exome Sequencing of the Next Generation Sequencing Technology
Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)
Yang, JLee, PPWYing, DHo, MHKLee, TLYang, WLau, YL
2014
36
 
Meta-analysis followed by replication identifies novel genetic variants in X chromosome associated with systemic lupus erythematosus in Asians and analysis of genetic differences between male and female cases
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2013
Yang, JZhang, YYang, WLau, YL
2013
23
 
Identifying causal mutations for Primary Immunodeficiencies in Southeast Asian region using whole exome sequencing
Proceeding/Conference:ICHG / ASHG 2011
Yang, JYang, WLee, PPWZeng, SZhang, LSham, PCLau, YL
2011
122
 
Haplotype-based Association Analysis Reveals a Novel Risk Locus for Systemic Lupus Erythematosus in Chinese Han Populations
Proceeding/Conference:American College of Medical Genetics and Genomics (ACMG) Annual Clinical Genetics Meeting
Wang, YZhang, YYang, JLau, YLYang, W
2015
27
 
Genome-wide association studies in Hong Kong identified novel susceptibility genes for systemic lupus erythematosus
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2010
Yang, WLi, RYang, JYe, DQLau, YL
2010
101
 
Gene-Gene Interaction in disease association for systemic lupus erythematosus in Asian populations
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012
Yang, JZhang, YZhang, XLau, YLYang, W
2012
32
 
Functional Properties of Genomic Region Associated with Multiple Traits in Genome-Wide Association Studies
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2016
Wang, YFGuo, MWang, TYZhang, YYang, JLau, YLYang, W
2016
49
 
From Sanger sequencing to NGS approaches for molecular diagnosis for primary immunodeficiency diseases (PID)
Proceeding/Conference:International Congress of Human Genetics, ICHG 2016
Yang, JYang, WLee, PPWLau, YL
2016
52
 
Exome sequencing identifies novel compound heterozygous mutations of interleukin-10 receptor A in Crohn’s disease of neonatal onset
Proceeding/Conference:Annual Scientific Meeting of The Hong Kong Society for Paediatric Immunology and Infectious Diseases, HKSPIID 2011
Mao, HYang, WHo, MHKYang, JZeng, SChong, CYLee, TLTu, WLau, YL
2011
115
 
Exome Sequencing Identifies Novel Compound Heterozygous Mutations in Interleukin-10 Receptor A in Neonatal-Onset Crohn’s Disease
Proceeding/Conference:Congress of Asian Society for Pediatric Research, ASPR 2012
Mao, HYang, WLee, PWHo, HKYang, JZeng, SChong, CYLee, TLTu, WLau, YL
2012
81
 
ELF1 is associated with systemic lupus erythematosus in Asian populations
Proceeding/Conference:Annual Meeting of American Society of Human Genetics, ASHG 2010
Yang, JYang, WLau, YL
2010
102
 
Actionable pharmacogenetic variants in Hong Kong Chinese exome sequencing data and projected prescription impact in the Hong Kong population (e-poster)
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)
YU, MHCChan, MCYCHUNG, CCYLi, AWTYip, CYWMak, CCYCHAU, FTJLEE, MFung, LFTSANG, HYChan, JCKWong, WHSYang, JChui, WCMChung, PHYYang, WLee, SLChan, GCFTam, PKHLau, YLTang, SMYeung, KSChung, BHY
2020
47
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