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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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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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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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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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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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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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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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GWASdb v2: an update database for human genetic variants identified by genome-wide association studies

Nucleic acids research, 2016-01, Vol.44 (D1), p.D869-D876

2016

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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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Reciprocal causation mixture model for robust Mendelian randomization analysis using genome-scale summary data

Nature communications, 2023-02, Vol.14 (1), p.1131-1131, Article 1131

2023

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Transcriptomics of Hirschsprung disease patient-derived enteric neural crest cells reveals a role for oxidative phosphorylation

Nature communications, 2023-04, Vol.14 (1), p.2157-2157, Article 2157

2023

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Are psychiatric comorbidities and associated cognitive functions related to treatment response to methylphenidate in boys with attention-deficit/hyperactivity disorder?

Neuropsychiatric disease and treatment, 2017, Vol.13, p.1071-1080

2017

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An autoimmune pleiotropic SNP modulates IRF5 alternative promoter usage through ZBTB3-mediated chromatin looping

Nature communications, 2023-03, Vol.14 (1), p.1208-1208, Article 1208

2023

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Whole-exome sequencing identifies MST1R as a genetic susceptibility gene in nasopharyngeal carcinoma

Proceedings of the National Academy of Sciences - PNAS, 2016-03, Vol.113 (12), p.3317-3322

2016

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

Oncogene, 2021-09, Vol.40 (35), p.5451-5453

2021

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Discovering the structure and organization of a free Cantonese emotion-label word association graph to understand mental lexicons of emotions

Scientific reports, 2022-11, Vol.12 (1), p.19581-19581, Article 19581

2022

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Whole genome sequencing reveals epistasis effects within RET for Hirschsprung disease

Scientific reports, 2022-11, Vol.12 (1), p.20423-20423, Article 20423

2022

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Genome-wide association study of hepatocellular carcinoma in Southern Chinese patients with chronic hepatitis B virus infection

PloS one, 2011-12, Vol.6 (12), p.e28798-e28798

2011

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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

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

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

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

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

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

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

GWASdb v2: an update database for human genetic variants identified by genome-wide association studies

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

Reciprocal causation mixture model for robust Mendelian randomization analysis using genome-scale summary data

Transcriptomics of Hirschsprung disease patient-derived enteric neural crest cells reveals a role for oxidative phosphorylation

Are psychiatric comorbidities and associated cognitive functions related to treatment response to methylphenidate in boys with attention-deficit/hyperactivity disorder?

An autoimmune pleiotropic SNP modulates IRF5 alternative promoter usage through ZBTB3-mediated chromatin looping

Whole-exome sequencing identifies MST1R as a genetic susceptibility gene in nasopharyngeal carcinoma

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

Discovering the structure and organization of a free Cantonese emotion-label word association graph to understand mental lexicons of emotions

Whole genome sequencing reveals epistasis effects within RET for Hirschsprung disease

Genome-wide association study of hepatocellular carcinoma in Southern Chinese patients with chronic hepatitis B virus infection

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