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List of works by Clara Sze-Man Tang

A complementary study approach unravels novel players in the pathoetiology of Hirschsprung disease

scientific article published on 05 November 2020

A gene-based test of association using canonical correlation analysis

scientific article published on 31 January 2012

A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits.

scientific article

A structural split in the human genome

scientific article

Actionable pharmacogenetic variants in Hong Kong Chinese exome sequencing data and projected prescription impact in the Hong Kong population

scientific article published in 2021

Actionable secondary findings from whole-genome sequencing of 954 East Asians

scientific article published on 11 November 2017

Adaptive Evolution Hotspots at the GC-Extremes of the Human Genome: Evidence for Two Functionally Distinct Pathways of Positive Selection

scientific article published on 3 May 2010

Age-Biomarkers-Clinical Risk Factors for Prediction of Cardiovascular Events in Patients With Coronary Artery Disease

scientific article published on 01 October 2018

An Exome-Chip Association Analysis in Chinese Subjects Reveals a Functional Missense Variant of GCKR That Regulates FGF21 Levels.

scientific article published on 6 April 2017

Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study ⬇️

scientific article published on 23 February 2017

Cancer gene mutations in congenital pulmonary airway malformation patients

article

Chinese family with diffuse oesophageal leiomyomatosis: a new COL4A5/COL4A6 deletion and a case of gonosomal mosaicism

scientific article published on 16 July 2015

Common genetic variants regulating ADD3 gene expression alter biliary atresia risk.

scientific article published on 19 July 2013

Coverage and diagnostic yield of Whole Exome Sequencing for the Evaluation of Cases with Dilated and Hypertrophic Cardiomyopathy

scientific article published in Scientific Reports

De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloaca

scientific article published on 21 November 2017

Depletion of the IKBKAP ortholog in zebrafish leads to hirschsprung disease-like phenotype

scientific article

Epidemiological characteristics of Hirschsprung's disease (HSCR): Results of a case series of fifty patients from Bangladesh

scientific article published on 31 January 2018

Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease.

scientific article published on 30 October 2017

Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease

scientific article

Exome-chip association analysis reveals an Asian-specific missense variant in PAX4 associated with type 2 diabetes in Chinese individuals.

scientific article published on 15 October 2016

Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese

scientific article

Fine mapping of the 9q31 Hirschsprung's disease locus.

scientific article

Fine mapping of the NRG1 Hirschsprung's disease locus

scientific article

Genetic Regulation of Pigment Epithelium-Derived Factor (PEDF): An Exome-Chip Association Analysis in Chinese Subjects with Type 2 Diabetes

article

Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes

scientific article

Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype

scientific article

Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease

scientific journal article

Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2

Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2.

scientific article

Genome-wide copy number analysis uncovers a new HSCR gene: NRG3

scientific article

Genome-wide copy number variation study in anorectal malformations.

scientific article published on 29 October 2012

Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population.

scientific article

Intron length and accelerated 3′ gene evolution

article

Mapping of a Hirschsprung's disease locus in 3p21

scientific article published on 20 February 2008

Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization

scientific article

Mutations in the NRG1 gene are associated with Hirschsprung disease

article

No NRG1 V266L in Chinese patients with schizophrenia

article

RET mutational spectrum in Hirschsprung disease: evaluation of 601 Chinese patients.

scientific article

Roles of Enteric Neural Stem Cell Niche and Enteric Nervous System Development in Hirschsprung Disease

scientific article published on 07 September 2021

Seventy-five genetic loci influencing the human red blood cell

scientific article published on 5 December 2012

Targeted Next-Generation Sequencing on Hirschsprung Disease: A Pilot Study Exploits DNA Pooling

scientific article published on 20 June 2014

Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.

scientific article published on 3 October 2016

Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese

article

Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing

scientific article published on 26 February 2018

Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes

scientific article

Whole-exome sequencing identifies MST1R as a genetic susceptibility gene in nasopharyngeal carcinoma

scientific article published on 7 March 2016

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