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Complex Copy Number Variation of AMY1 does not Associate with Obesity in two East Asian Cohorts

Human mutation, 2016-07, Vol.37 (7), p.669-678

2016

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Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia

Human molecular genetics, 2013-12, Vol.22 (25), p.5288-5294

2013

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Toward Male Individualization with Rapidly Mutating Y-Chromosomal Short Tandem Repeats

Human mutation, 2014-08, Vol.35 (8), p.1021-1032

2014

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Association between an intronic apolipoprotein E polymorphism and bone mineral density in Singaporean Chinese females

Bone (New York, N.Y.), 2010-09, Vol.47 (3), p.503-510

2010

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Molecular characterization of a polymorphic 3-Mb deletion at chromosome Yp11.2 containing the AMELY locus in Singapore and Malaysia populations

Human genetics, 2007-11, Vol.122 (3-4), p.237-249

2007

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A distinct Y-STR haplotype for Amelogenin negative males characterized by a large Yp11.2 (DYS458-MSY1-AMEL-Y) deletion

Forensic science international, 2007-03, Vol.166 (2-3), p.115-120

2007

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Malignant Hyperthermia and Ryanodine Receptor Type 1 Gene (RyR1) Mutation in a Family in Singapore

Annals of the Academy of Medicine, Singapore, 2017-12, Vol.46 (12), p.455-460

2017

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A distinct Y-STR haplotype for Amelogenin negative males characterized by a large Y(p)11.2 (DYS458-MSY1-AMEL-Y) deletion

Forensic science international, 2007-03, Vol.166 (2-3), p.115-120

2007

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Young men driving dangerously: Development of the Motives for Dangerous Driving Scale (MDDS)

Australian journal of psychology, 2008-09, Vol.60 (2), p.91-100

2008

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Polymorphism studies of six miniSTR loci for three ethnic populations in Singapore

Legal medicine (Tokyo, Japan), 2009-07, Vol.11 (4), p.195-197

2009

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A Novel Susceptibility Locus On Chromosome 2 in the (New Zealand Black x New Zealand White)F1 Hybrid Mouse Model of Systemic Lupus Erythematosus

The Journal of immunology (1950), 2002-03, Vol.168 (6), p.3042-3049

2002

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Association of SNTB1 with High Myopia

Current eye research, 2021-01, Vol.46 (1), p.144-150

2021

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Polymorphism studies of four miniSTR loci for three ethnic populations in Singapore

Legal medicine (Tokyo, Japan), 2007-09, Vol.9 (5), p.278-281

2007

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Association of VIPR2 and ZMAT4 with high myopia

Ophthalmic genetics, 2020-01, Vol.41 (1), p.41-48

2020

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Identification of an INa-dependent and Ito-mediated proarrhythmic mechanism in cardiomyocytes derived from pluripotent stem cells of a Brugada syndrome patient

Scientific reports, 2018-07, Vol.8 (1), p.11246-11246, Article 11246

2018

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PE3-012 Brugada Syndrome and SCN5A-Encoded Cardiac Sodium Channel Mutations in Singapore

Journal of Arrhythmia, 2011-09, Vol.27 (suppl), p.377-377

2011

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Announcement of Population Data: Polymorphism studies of four miniSTR loci for three ethnic populations in Singapore

Legal medicine (Tokyo, Japan), 2007-09, Vol.9 (5), p.278-281

2007

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Brugada Syndrome and SCN5A-Encoded Cardiac Sodium Channel Mutations in Singapore

Journal of arrhythmia, 2011, Vol.27 (Supplement), p.PE3_012

2011

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Compound Heterozygosity in Brugada Syndrome: A Case Study

Journal of arrhythmia, 2011, Vol.27 (Supplement), p.PE3_011

2011

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Complex Copy Number Variation of AMY1 does not Associate with Obesity in two East Asian Cohorts: HUMAN MUTATION

Human mutation, 2016-07, Vol.37 (7), p.669-678

2016

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A Brugada syndrome proband with compound heterozygote SCN5A mutations identified from a Chinese family in Singapore

Europace (London, England), 2016-06, Vol.18 (6), p.897-904

2016

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A novel three base-pair deletion in domain two of the cardiac sodium channel causes Brugada syndrome

Journal of electrocardiology, 2018-07, Vol.51 (4), p.667-673

2018

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Heterozygosities and allelic frequencies of a set of microsatellite markers used for genome-wide scans in a Chinese population

Journal of human genetics, 2002-01, Vol.47 (11), p.623-631

2002

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Distortion in TGFβ1 peptide immunolocalization in biliary atresia: Comparison with the normal pattern in the developing human intrahepatic bile duct system

Pathology international, 1995-11, Vol.45 (11), p.815-824

1995

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Complex Copy Number Variation of AMY1 does not Associate with Obesity in two East Asian Cohorts

Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia

Toward Male Individualization with Rapidly Mutating Y-Chromosomal Short Tandem Repeats

Association between an intronic apolipoprotein E polymorphism and bone mineral density in Singaporean Chinese females

Molecular characterization of a polymorphic 3-Mb deletion at chromosome Yp11.2 containing the AMELY locus in Singapore and Malaysia populations

A distinct Y-STR haplotype for Amelogenin negative males characterized by a large Yp11.2 (DYS458-MSY1-AMEL-Y) deletion

Malignant Hyperthermia and Ryanodine Receptor Type 1 Gene (RyR1) Mutation in a Family in Singapore

A distinct Y-STR haplotype for Amelogenin negative males characterized by a large Y(p)11.2 (DYS458-MSY1-AMEL-Y) deletion

Identification of an I Na-dependent and I to-mediated proarrhythmic mechanism in cardiomyocytes derived from pluripotent stem cells of a Brugada syndrome patient

Young men driving dangerously: Development of the Motives for Dangerous Driving Scale (MDDS)

Polymorphism studies of six miniSTR loci for three ethnic populations in Singapore

A Novel Susceptibility Locus On Chromosome 2 in the (New Zealand Black x New Zealand White)F1 Hybrid Mouse Model of Systemic Lupus Erythematosus

Association of SNTB1 with High Myopia

Polymorphism studies of four miniSTR loci for three ethnic populations in Singapore

Association of VIPR2 and ZMAT4 with high myopia

Identification of an INa-dependent and Ito-mediated proarrhythmic mechanism in cardiomyocytes derived from pluripotent stem cells of a Brugada syndrome patient

PE3-012 Brugada Syndrome and SCN5A-Encoded Cardiac Sodium Channel Mutations in Singapore

Announcement of Population Data: Polymorphism studies of four miniSTR loci for three ethnic populations in Singapore

Brugada Syndrome and SCN5A-Encoded Cardiac Sodium Channel Mutations in Singapore

Compound Heterozygosity in Brugada Syndrome: A Case Study

Complex Copy Number Variation of AMY1 does not Associate with Obesity in two East Asian Cohorts: HUMAN MUTATION

A Brugada syndrome proband with compound heterozygote SCN5A mutations identified from a Chinese family in Singapore

A novel three base-pair deletion in domain two of the cardiac sodium channel causes Brugada syndrome

Heterozygosities and allelic frequencies of a set of microsatellite markers used for genome-wide scans in a Chinese population

Distortion in TGFβ1 peptide immunolocalization in biliary atresia: Comparison with the normal pattern in the developing human intrahepatic bile duct system

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