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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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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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PMCA4 (ATP2B4) mutation in familial spastic paraplegia

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

2014

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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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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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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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Polygenic scores via penalized regression on summary statistics

Genetic epidemiology, 2017-09, Vol.41 (6), p.469-480

2017

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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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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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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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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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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)

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

PMCA4 (ATP2B4) mutation in familial spastic paraplegia

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

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

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

Polygenic scores via penalized regression on summary statistics

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

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

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

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

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