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Author Details

Dongliang Ge
Department of Pharmacy, Liyang People's Hospital
2003
91
43
PMIDPaper TitleJournal TitlePublished Year
34984027Development and Validation of Prognostic Survival Nomograms for Patients with Anal Canal Cancer: A SEER-Based Study.Int J Gen Med2021
28928388Differential Serum Cytokine Profiles in Patients with Chronic Hepatitis B, C, and Hepatocellular Carcinoma.Sci Rep2017
28212287Big Data Analytics for Genomic Medicine.Int J Mol Sci2017
28894136Soluble intercellular adhesion molecule-1 is associated with hepatocellular carcinoma risk: multiplex analysis of serum markers.Sci Rep2017
27218676Randomised clinical trial: a phase 1, dose-ranging study of the anti-matrix metalloproteinase-9 monoclonal antibody GS-5745 versus placebo for ulcerative colitis.Aliment Pharmacol Ther2016
25514556Baseline interpatient hepatitis B viral diversity differentiates HBsAg outcomes in patients treated with tenofovir disoproxil fumarate.J Hepatol2015
24503447Genome-wide association study to characterize serum bilirubin elevations in patients with HCV treated with GS-9256, an HCV NS3 serine protease inhibitor.Antivir Ther2014
21703177Genome-wide association study of interferon-related cytopenia in chronic hepatitis C patients.J Hepatol2012
23176824Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesis.Am J Hum Genet2012
22968431Limited contribution of common genetic variants to risk for liver injury due to a variety of drugs.Pharmacogenet Genomics2012
22939633Using ERDS to infer copy-number variants in high-coverage genomes.Am J Hum Genet2012
22939045Prioritizing genetic variants for causality on the basis of preferential linkage disequilibrium.Am J Hum Genet2012
22751097Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.Nat Genet2012
22786563Urinary norepinephrine and epinephrine excretion rates are heritable, but not associated with office and ambulatory blood pressure.Hypertens Res2012
22863191Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia.Am J Hum Genet2012
22863189Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.Am J Hum Genet2012
22908908Personal receptor repertoires: olfaction as a model.BMC Genomics2012
22877876Heritability of strabismus: genetic influence is specific to eso-deviation and independent of refractive error.Twin Res Hum Genet2012
22497812Interleukin 28B polymorphisms are the only common genetic variants associated with low-density lipoprotein cholesterol (LDL-C) in genotype-1 chronic hepatitis C and determine the association between LDL-C and treatment response.J Viral Hepat2012
22543885The association of genetic variants with hepatic steatosis in patients with genotype 1 chronic hepatitis C infection.Dig Dis Sci2012
21457907A genome-wide comparison of the functional properties of rare and common genetic variants in humans.Am J Hum Genet2011
22140359Copy number variation of KIR genes influences HIV-1 control.PLoS Biol2011
21799071The state of genome-wide association studies in pulmonary disease: a new perspective.Am J Respir Crit Care Med2011
21624899SVA: software for annotating and visualizing sequenced human genomes.Bioinformatics2011
20399780Interleukin-28B polymorphism improves viral kinetics and is the strongest pretreatment predictor of sustained virologic response in genotype 1 hepatitis C virus.Gastroenterology2010
20838461The characterization of twenty sequenced human genomes.PLoS Genet2010
20890887Hepatitis C trials that combine investigational agents with pegylated interferon should be stratified by interleukin-28B genotype.Hepatology2010
20547162Variants in the ITPA gene protect against ribavirin-induced hemolytic anemia and decrease the need for ribavirin dose reduction.Gastroenterology2010
20577567Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene.PLoS Genet2010
20598109Screening the human exome: a comparison of whole genome and whole transcriptome sequencing.Genome Biol2010
20125193Common genetic variation and performance on standardized cognitive tests.Eur J Hum Genet2010
20205591Host determinants of HIV-1 control in African Americans.J Infect Dis2010
20173735ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C.Nature2010
20195503Genome-wide mRNA expression correlates of viral control in CD4+ T-cells from HIV-1-infected individuals.PLoS Pathog2010
20398883Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.Am J Hum Genet2010
19197363A genome-wide investigation of SNPs and CNVs in schizophrenia.PLoS Genet2009
19935663HLA-C cell surface expression and control of HIV/AIDS correlate with a variant upstream of HLA-C.Nat Genet2009
20041166Common genetic variation and the control of HIV-1 in humans.PLoS Genet2009
19684573Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance.Nature2009
19734545A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.Hum Mol Genet2009
19759533Genetic variation in IL28B and spontaneous clearance of hepatitis C virus.Nature2009
19834617Genetic regulation of alpha-synuclein mRNA expression in various human brain tissues.PLoS One2009
19498036Expansion of the Parkinson disease-associated SNCA-Rep1 allele upregulates human alpha-synuclein in transgenic mouse brain.Hum Mol Genet2009
19454339The Duffy antigen receptor for chemokines null promoter variant does not influence HIV-1 acquisition or disease progression.Cell Host Microbe2009
19571808Common variants conferring risk of schizophrenia.Nature2009
19104006Stress-induced sodium excretion: a new intermediate phenotype to study the early genetic etiology of hypertension?Hypertension2009
19156168Pharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysis.Eur J Hum Genet2009
19300482A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci.PLoS Genet2009
18166564Relationships of cardiovascular phenotypes with healthy weight, at risk of overweight, and overweight in US youths.Pediatrics2008
19222302Tissue-specific genetic control of splicing: implications for the study of complex traits.PLoS Biol2008
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Vir Biotechnology Inc.
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Duke Clinical Research Institute and Duke University School of Medicine
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Genomics England Ltd.
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School of Pharmacy and Biomolecular Sciences, Ireland FutureNeuro SFI Research Centre
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