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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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Integrative omics of schizophrenia: from genetic determinants to clinical classification and risk prediction

Molecular psychiatry, 2022-01, Vol.27 (1), p.113-126

2022

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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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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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Evaluation of tools for highly variable gene discovery from single-cell RNA-seq data

Briefings in bioinformatics, 2019-07, Vol.20 (4), p.1583-1589

2019

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

Nature communications, 2012-12, Vol.3 (1), p.1258-1258, Article 1258

2012

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Novel pre-mRNA splicing of intronically integrated HBV generates oncogenic chimera in hepatocellular carcinoma

Journal of hepatology, 2016-06, Vol.64 (6), p.1256-1264

2016

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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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On the Transformation of Genetic Effect Size from Logit to Liability Scale

Behavior genetics, 2021-05, Vol.51 (3), p.215-222

2021

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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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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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Correction to: On the Transformation of Genetic Effect Size from Logit to Liability Scale

Behavior genetics, 2021-11, Vol.51 (6), p.773-773

2021

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Genome-wide DNA methylation data from adult brain following prenatal immune activation and dietary intervention

Data in brief, 2019-10, Vol.26, p.104561-104561, Article 104561

2019

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Diversity spectrum analysis identifies mutation-specific effects of cancer driver genes

Communications biology, 2020-01, Vol.3 (1), p.6-6, Article 6

2020

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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

Integrative omics of schizophrenia: from genetic determinants to clinical classification and risk prediction

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

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

Evaluation of tools for highly variable gene discovery from single-cell RNA-seq data

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

Novel pre-mRNA splicing of intronically integrated HBV generates oncogenic chimera in hepatocellular carcinoma

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

On the Transformation of Genetic Effect Size from Logit to Liability Scale

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

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

Correction to: On the Transformation of Genetic Effect Size from Logit to Liability Scale

Genome-wide DNA methylation data from adult brain following prenatal immune activation and dietary intervention

Diversity spectrum analysis identifies mutation-specific effects of cancer driver genes

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