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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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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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Attention‐deficit/hyperactivity disorder and dopamine receptor D4 (DRD4) exon 3 variable number of tandem repeats (VNTR) 2‐repeat allele

Annals of human genetics, 2024-09, Vol.88 (5), p.382-391

2024

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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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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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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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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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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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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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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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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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Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia

PloS one, 2013-06, Vol.8 (6), p.e66631-e66631

2013

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Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3

Nature genetics, 2012-09, Vol.44 (9), p.1026-1029

2012

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Brain transcriptome-wide association study implicates novel risk genes underlying schizophrenia risk

Psychological medicine, 2023-10, Vol.53 (14), p.6867-6877

2023

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Alterations in Gastric Microbiota After H. Pylori Eradication and in Different Histological Stages of Gastric Carcinogenesis

Scientific reports, 2017-03, Vol.7 (1), p.44935-44935, Article 44935

2017

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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

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

Attention‐deficit/hyperactivity disorder and dopamine receptor D4 (DRD4) exon 3 variable number of tandem repeats (VNTR) 2‐repeat allele

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

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

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

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

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

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

Gene network analysis of candidate loci for human anorectal malformations

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

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

Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia

Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3

Brain transcriptome-wide association study implicates novel risk genes underlying schizophrenia risk

Alterations in Gastric Microbiota After H. Pylori Eradication and in Different Histological Stages of Gastric Carcinogenesis

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