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Multicenter study on the genetics of glomerular diseases among southeast and south Asians: Deciphering Diversities ‐ Renal Asian Genetics Network (DRAGoN)

Clinical genetics, 2022-05, Vol.101 (5-6), p.541-551

2022

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A novel de novo androgen receptor nonsense mutation in a sex-reversed 46,XY infant

Human genome variation, 2021-09, Vol.8 (1), p.35-3, Article 35

2021

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Variability in newborn telomere length is explained by inheritance and intrauterine environment

BMC medicine, 2022-01, Vol.20 (1), p.20-20, Article 20

2022

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The socioeconomic landscape of the exposome during pregnancy

Environment international, 2022-05, Vol.163, p.107205-107205, Article 107205

2022

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Plasma lipidomic profiling reveals metabolic adaptations to pregnancy and signatures of cardiometabolic risk: a preconception and longitudinal cohort study

BMC medicine, 2023-02, Vol.21 (1), p.53-53, Article 53

2023

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Paper-Based MicroRNA Expression Profiling from Plasma and Circulating Tumor Cells

Clinical chemistry (Baltimore, Md.), 2017-03, Vol.63 (3), p.731-741

2017

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A direct sequencing assay for pharmacogenetic testing of thiopurine-intolerant NUDT15 alleles in an Asian population

BMC research notes, 2022-04, Vol.15 (1), p.148-148, Article 148

2022

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Spectrum of pathogenic alterations identified after two decades of HBB gene sequencing for molecular diagnosis of beta-thalassaemias and haemoglobinopathies

Pathology, 2021-06, Vol.53 (4), p.536-538

2021

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Association of plasma kynurenine pathway metabolite concentrations with metabolic health risk in prepubertal Asian children

International Journal of Obesity, 2022-06, Vol.46 (6), p.1128-1137

2022

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A Novel Indel in the Alpha Globin 2 (HBA2) Gene Resulting in False Positive -α3.7 on Multiplex gap-PCR Assay

Clinical chemistry (Baltimore, Md.), 2021-09, Vol.67 (9), p.1284-1287

2021

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The Kynurenine Pathway Metabolites in Cord Blood Positively Correlate With Early Childhood Adiposity

The journal of clinical endocrinology and metabolism, 2022-05, Vol.107 (6), p.e2464-e2473

2022

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Pitfalls of PCR-RFLP in Detecting SARS-CoV-2 D614G Mutation

Global medical genetics, 2022-06, Vol.9 (2), p.189-190

2022

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Variant Curation is Crucial to Claim Digenic Inheritance in Juvenile Open Angle Glaucoma

Global medical genetics, 2022-03, Vol.9 (1), p.054-055

2022

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Reclassification of Whole Exome Sequencing-derived Genetic Variants in Pendred Syndrome with ACMG/AMP Standards

Global medical genetics, 2021-09, Vol.8 (3), p.129-131

2021

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Role of maternal tryptophan metabolism in allergic diseases in the offspring

Clinical and experimental allergy, 2021-10, Vol.51 (10), p.1346-1360

2021

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Targeted next-generation sequencing of the ATP7B gene for molecular diagnosis of Wilson disease

Clinical biochemistry, 2016-01, Vol.49 (1-2), p.166-171

2016

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Laboratory Verification of a BRCA1 and BRCA2 Massively Parallel Sequencing Assay from Wet Bench to Bioinformatics for Germline DNA Analysis

Global medical genetics, 2021-06, Vol.8 (2), p.062-068

2021

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Dietary Supplement Intake and Fecundability in a Singapore Preconception Cohort Study

Nutrients, 2022-12, Vol.14 (23), p.5110

2022

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Improved Discrimination of Patients with Breast Cancer from Healthy Controls Using Paper-Based microRNA Expression Profiling of Plasma, Following Precipitation

Clinical chemistry (Baltimore, Md.), 2017-12, Vol.63 (12), p.1899-1901

2017

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Genetic testing of GCK-MODY identifies a novel pathogenic variant in a Chinese boy with early onset hyperglycemia

Human genome variation, 2020, Vol.7 (1), p.7-7, Article 7

2020

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One-step molecular detection of the MYD88 L265P mutation by unlabeled probe genotyping analysis

Molecular and cellular probes, 2015-02, Vol.29 (1), p.74-77

2015

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Associations Between Eczema and Attention Deficit Hyperactivity Disorder Symptoms in Children

Frontiers in pediatrics, 2022-03, Vol.10, p.837741-837741

2022

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Functional Characterization of Variants in MC4R Gene Promoter Region Found in Obese Children

The journal of clinical endocrinology and metabolism, 2014-05, Vol.99 (5), p.E931-E935

2014

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Multicenter study on the genetics of glomerular diseases among southeast and south Asians: Deciphering Diversities ‐ Renal Asian Genetics Network (DRAGoN)

A novel de novo androgen receptor nonsense mutation in a sex-reversed 46,XY infant

Variability in newborn telomere length is explained by inheritance and intrauterine environment

Population-based plasma lipidomics reveals developmental changes in metabolism and signatures of obesity risk: a mother-offspring cohort study

The socioeconomic landscape of the exposome during pregnancy

Plasma lipidomic profiling reveals metabolic adaptations to pregnancy and signatures of cardiometabolic risk: a preconception and longitudinal cohort study

Dynamic altruistic cooperation within breast tumors

Paper-Based MicroRNA Expression Profiling from Plasma and Circulating Tumor Cells

A direct sequencing assay for pharmacogenetic testing of thiopurine-intolerant NUDT15 alleles in an Asian population

Spectrum of pathogenic alterations identified after two decades of HBB gene sequencing for molecular diagnosis of beta-thalassaemias and haemoglobinopathies

Association of plasma kynurenine pathway metabolite concentrations with metabolic health risk in prepubertal Asian children

A Novel Indel in the Alpha Globin 2 (HBA2) Gene Resulting in False Positive -α3.7 on Multiplex gap-PCR Assay

The Kynurenine Pathway Metabolites in Cord Blood Positively Correlate With Early Childhood Adiposity

Pitfalls of PCR-RFLP in Detecting SARS-CoV-2 D614G Mutation

Variant Curation is Crucial to Claim Digenic Inheritance in Juvenile Open Angle Glaucoma

Reclassification of Whole Exome Sequencing-derived Genetic Variants in Pendred Syndrome with ACMG/AMP Standards

Role of maternal tryptophan metabolism in allergic diseases in the offspring

Targeted next-generation sequencing of the ATP7B gene for molecular diagnosis of Wilson disease

Laboratory Verification of a BRCA1 and BRCA2 Massively Parallel Sequencing Assay from Wet Bench to Bioinformatics for Germline DNA Analysis

Dietary Supplement Intake and Fecundability in a Singapore Preconception Cohort Study

Improved Discrimination of Patients with Breast Cancer from Healthy Controls Using Paper-Based microRNA Expression Profiling of Plasma, Following Precipitation

Genetic testing of GCK-MODY identifies a novel pathogenic variant in a Chinese boy with early onset hyperglycemia

One-step molecular detection of the MYD88 L265P mutation by unlabeled probe genotyping analysis

Associations Between Eczema and Attention Deficit Hyperactivity Disorder Symptoms in Children

Functional Characterization of Variants in MC4R Gene Promoter Region Found in Obese Children

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