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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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Evaluation of bi-directional causal association between depression and cardiovascular diseases: a Mendelian randomization study

Psychological medicine, 2022-07, Vol.52 (9), p.1765-1776

2022

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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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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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C-terminal truncated HBx initiates hepatocarcinogenesis by downregulating TXNIP and reprogramming glucose metabolism

Oncogene, 2021-02, Vol.40 (6), p.1147-1161

2021

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Exploring shared genetic bases and causal relationships of schizophrenia and bipolar disorder with 28 cardiovascular and metabolic traits

Psychological medicine, 2019-06, Vol.49 (8), p.1286-1298

2019

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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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PMCA4 (ATP2B4) mutation in familial spastic paraplegia

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

2014

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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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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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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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HLA-DP and IL28B Polymorphisms: Influence of Host Genome on Hepatitis B Surface Antigen Seroclearance in Chronic Hepatitis B

Clinical infectious diseases, 2013-06, Vol.56 (12), p.1695-1703

2013

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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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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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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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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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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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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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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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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

Evaluation of bi-directional causal association between depression and cardiovascular diseases: a Mendelian randomization study

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

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

C-terminal truncated HBx initiates hepatocarcinogenesis by downregulating TXNIP and reprogramming glucose metabolism

Exploring shared genetic bases and causal relationships of schizophrenia and bipolar disorder with 28 cardiovascular and metabolic traits

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

PMCA4 (ATP2B4) mutation in familial spastic paraplegia

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

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

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

HLA-DP and IL28B Polymorphisms: Influence of Host Genome on Hepatitis B Surface Antigen Seroclearance in Chronic Hepatitis B

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

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

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

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

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

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

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

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