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Single-cell RNA sequencing shows the immunosuppressive landscape and tumor heterogeneity of HBV-associated hepatocellular carcinoma

Nature communications, 2021-06, Vol.12 (1), p.3684-3684, Article 3684

2021

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Single-cell transcriptomics reveals the landscape of intra-tumoral heterogeneity and stemness-related subpopulations in liver cancer

Cancer letters, 2019-09, Vol.459, p.176-185

2019

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SumVg: Total Heritability Explained by All Variants in Genome-Wide Association Studies Based on Summary Statistics with Standard Error Estimates

International journal of molecular sciences, 2024-01, Vol.25 (2), p.1347

2024

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Diabetes Prevalence and Therapeutic Target Achievement in the United States, 1999 to 2006

The American journal of medicine, 2009-05, Vol.122 (5), p.443-453

2009

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Prevalence, psychosocial correlates and service utilization of depressive and anxiety disorders in Hong Kong: the Hong Kong Mental Morbidity Survey (HKMMS)

Social Psychiatry and Psychiatric Epidemiology, 2015-09, Vol.50 (9), p.1379-1388

2015

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The role of dopamine dysregulation and evidence for the transdiagnostic nature of elevated dopamine synthesis in psychosis: a positron emission tomography (PET) study comparing schizophrenia, delusional disorder, and other psychotic disorders

Neuropsychopharmacology (New York, N.Y.), 2020-10, Vol.45 (11), p.1870-1876

2020

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Computational Retinal Microvascular Biomarkers from an OCTA Image in Clinical Investigation

Biomedicines, 2024-04, Vol.12 (4), p.868

2024

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Identification and characterization of a novel incompatibility group X3 plasmid carrying blaNDM-1 in Enterobacteriaceae isolates with epidemiological links to multiple geographical areas in China

Emerging microbes & infections, 2012-11, Vol.1 (1), p.e39-6

2012

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High-sensitivity troponin I and B-type natriuretic peptide biomarkers for prediction of cardiovascular events in patients with coronary artery disease with and without diabetes mellitus

Cardiovascular diabetology, 2019-12, Vol.18 (1), p.171-171, Article 171

2019

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

Scientific reports, 2018-07, Vol.8 (1), p.10846-7, Article 10846

2018

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PMCA4 (ATP2B4) mutation in familial spastic paraplegia

PloS one, 2014-08, Vol.9 (8), p.e104790-e104790

2014

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Gabrb2-knockout mice displayed schizophrenia-like and comorbid phenotypes with interneuron-astrocyte-microglia dysregulation

Translational psychiatry, 2018-07, Vol.8 (1), p.128-14, Article 128

2018

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Prenatal immune activation alters the adult neural epigenome but can be partly stabilised by a n-3 polyunsaturated fatty acid diet

Translational psychiatry, 2018-07, Vol.8 (1), p.125-12, Article 125

2018

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Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanism

EBioMedicine, 2021-09, Vol.71, p.103530-103530, Article 103530

2021

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Genetic Overlap Between Attention Deficit/Hyperactivity Disorder and Autism Spectrum Disorder in SHANK2 Gene

Frontiers in neuroscience, 2021-04, Vol.15, p.649588-649588

2021

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The role of gene variants in the pathogenesis of neurodegenerative disorders as revealed by next generation sequencing studies: a review

Translational neurodegeneration, 2017-10, Vol.6 (1), p.27-27, Article 27

2017

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

Proceedings of the National Academy of Sciences - PNAS, 2009-02, Vol.106 (8), p.2694-2699

2009

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Genetic variant in vitamin D binding protein is associated with serum 25-hydroxyvitamin D and vitamin D insufficiency in southern Chinese

Journal of human genetics, 2013-11, Vol.58 (11), p.749-751

2013

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A fast and accurate SNP detection algorithm for next-generation sequencing data

Nature communications, 2012, Vol.3 (1), p.1258-1258, Article 1258

2012

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Coagulation factors and the incidence of COVID-19 severity: Mendelian randomization analyses and supporting evidence

Signal transduction and targeted therapy, 2021-06, Vol.6 (1), p.222-222, Article 222

2021

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The support of human genetic evidence for approved drug indications

Nature genetics, 2015-08, Vol.47 (8), p.856-860

2015

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Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease

Scientific reports, 2015-11, Vol.5 (1), p.16473-16473, Article 16473

2015

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LINE1 and Mecp2 methylation of the adult striatum and prefrontal cortex exposed to prenatal immune activation

Data in brief, 2019-08, Vol.25, p.104003-104003, Article 104003

2019

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Gene network analysis of candidate loci for human anorectal malformations

PloS one, 2013-08, Vol.8 (8), p.e69142-e69142

2013

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Patient complexity and genotype-phenotype correlations in biliary atresia: a cross-sectional analysis

BMC medical genomics, 2017-04, Vol.10 (1), p.22-22, Article 22

2017

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Single-cell RNA sequencing shows the immunosuppressive landscape and tumor heterogeneity of HBV-associated hepatocellular carcinoma

Single-cell transcriptomics reveals the landscape of intra-tumoral heterogeneity and stemness-related subpopulations in liver cancer

SumVg: Total Heritability Explained by All Variants in Genome-Wide Association Studies Based on Summary Statistics with Standard Error Estimates

Diabetes Prevalence and Therapeutic Target Achievement in the United States, 1999 to 2006

Prevalence, psychosocial correlates and service utilization of depressive and anxiety disorders in Hong Kong: the Hong Kong Mental Morbidity Survey (HKMMS)

The role of dopamine dysregulation and evidence for the transdiagnostic nature of elevated dopamine synthesis in psychosis: a positron emission tomography (PET) study comparing schizophrenia, delusional disorder, and other psychotic disorders

Computational Retinal Microvascular Biomarkers from an OCTA Image in Clinical Investigation

Identification and characterization of a novel incompatibility group X3 plasmid carrying blaNDM-1 in Enterobacteriaceae isolates with epidemiological links to multiple geographical areas in China

High-sensitivity troponin I and B-type natriuretic peptide biomarkers for prediction of cardiovascular events in patients with coronary artery disease with and without diabetes mellitus

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

PMCA4 (ATP2B4) mutation in familial spastic paraplegia

Gabrb2-knockout mice displayed schizophrenia-like and comorbid phenotypes with interneuron-astrocyte-microglia dysregulation

Prenatal immune activation alters the adult neural epigenome but can be partly stabilised by a n-3 polyunsaturated fatty acid diet

Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanism

Genetic Overlap Between Attention Deficit/Hyperactivity Disorder and Autism Spectrum Disorder in SHANK2 Gene

The role of gene variants in the pathogenesis of neurodegenerative disorders as revealed by next generation sequencing studies: a review

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

Genetic variant in vitamin D binding protein is associated with serum 25-hydroxyvitamin D and vitamin D insufficiency in southern Chinese

A fast and accurate SNP detection algorithm for next-generation sequencing data

Coagulation factors and the incidence of COVID-19 severity: Mendelian randomization analyses and supporting evidence

The support of human genetic evidence for approved drug indications

Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease

LINE1 and Mecp2 methylation of the adult striatum and prefrontal cortex exposed to prenatal immune activation

Gene network analysis of candidate loci for human anorectal malformations

Patient complexity and genotype-phenotype correlations in biliary atresia: a cross-sectional analysis

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