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Author Details
Full Name
Dongliang Ge
Affiliation
Department of Pharmacy, Liyang People's Hospital
ORCID
Career Start Year
2003
Papers
91
H Index
43
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34984027
Development and Validation of Prognostic Survival Nomograms for Patients with Anal Canal Cancer: A SEER-Based Study.
Int J Gen Med
2021
28928388
Differential Serum Cytokine Profiles in Patients with Chronic Hepatitis B, C, and Hepatocellular Carcinoma.
Sci Rep
2017
28212287
Big Data Analytics for Genomic Medicine.
Int J Mol Sci
2017
28894136
Soluble intercellular adhesion molecule-1 is associated with hepatocellular carcinoma risk: multiplex analysis of serum markers.
Sci Rep
2017
27218676
Randomised 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 Ther
2016
25514556
Baseline interpatient hepatitis B viral diversity differentiates HBsAg outcomes in patients treated with tenofovir disoproxil fumarate.
J Hepatol
2015
24503447
Genome-wide association study to characterize serum bilirubin elevations in patients with HCV treated with GS-9256, an HCV NS3 serine protease inhibitor.
Antivir Ther
2014
21703177
Genome-wide association study of interferon-related cytopenia in chronic hepatitis C patients.
J Hepatol
2012
23176824
Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesis.
Am J Hum Genet
2012
22968431
Limited contribution of common genetic variants to risk for liver injury due to a variety of drugs.
Pharmacogenet Genomics
2012
22939633
Using ERDS to infer copy-number variants in high-coverage genomes.
Am J Hum Genet
2012
22939045
Prioritizing genetic variants for causality on the basis of preferential linkage disequilibrium.
Am J Hum Genet
2012
22751097
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.
Nat Genet
2012
22786563
Urinary norepinephrine and epinephrine excretion rates are heritable, but not associated with office and ambulatory blood pressure.
Hypertens Res
2012
22863191
Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia.
Am J Hum Genet
2012
22863189
Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.
Am J Hum Genet
2012
22908908
Personal receptor repertoires: olfaction as a model.
BMC Genomics
2012
22877876
Heritability of strabismus: genetic influence is specific to eso-deviation and independent of refractive error.
Twin Res Hum Genet
2012
22497812
Interleukin 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 Hepat
2012
22543885
The association of genetic variants with hepatic steatosis in patients with genotype 1 chronic hepatitis C infection.
Dig Dis Sci
2012
21457907
A genome-wide comparison of the functional properties of rare and common genetic variants in humans.
Am J Hum Genet
2011
22140359
Copy number variation of KIR genes influences HIV-1 control.
PLoS Biol
2011
21799071
The state of genome-wide association studies in pulmonary disease: a new perspective.
Am J Respir Crit Care Med
2011
21624899
SVA: software for annotating and visualizing sequenced human genomes.
Bioinformatics
2011
20399780
Interleukin-28B polymorphism improves viral kinetics and is the strongest pretreatment predictor of sustained virologic response in genotype 1 hepatitis C virus.
Gastroenterology
2010
20838461
The characterization of twenty sequenced human genomes.
PLoS Genet
2010
20890887
Hepatitis C trials that combine investigational agents with pegylated interferon should be stratified by interleukin-28B genotype.
Hepatology
2010
20547162
Variants in the ITPA gene protect against ribavirin-induced hemolytic anemia and decrease the need for ribavirin dose reduction.
Gastroenterology
2010
20577567
Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene.
PLoS Genet
2010
20598109
Screening the human exome: a comparison of whole genome and whole transcriptome sequencing.
Genome Biol
2010
20125193
Common genetic variation and performance on standardized cognitive tests.
Eur J Hum Genet
2010
20205591
Host determinants of HIV-1 control in African Americans.
J Infect Dis
2010
20173735
ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C.
Nature
2010
20195503
Genome-wide mRNA expression correlates of viral control in CD4+ T-cells from HIV-1-infected individuals.
PLoS Pathog
2010
20398883
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
Am J Hum Genet
2010
19197363
A genome-wide investigation of SNPs and CNVs in schizophrenia.
PLoS Genet
2009
19935663
HLA-C cell surface expression and control of HIV/AIDS correlate with a variant upstream of HLA-C.
Nat Genet
2009
20041166
Common genetic variation and the control of HIV-1 in humans.
PLoS Genet
2009
19684573
Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance.
Nature
2009
19734545
A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.
Hum Mol Genet
2009
19759533
Genetic variation in IL28B and spontaneous clearance of hepatitis C virus.
Nature
2009
19834617
Genetic regulation of alpha-synuclein mRNA expression in various human brain tissues.
PLoS One
2009
19498036
Expansion of the Parkinson disease-associated SNCA-Rep1 allele upregulates human alpha-synuclein in transgenic mouse brain.
Hum Mol Genet
2009
19454339
The Duffy antigen receptor for chemokines null promoter variant does not influence HIV-1 acquisition or disease progression.
Cell Host Microbe
2009
19571808
Common variants conferring risk of schizophrenia.
Nature
2009
19104006
Stress-induced sodium excretion: a new intermediate phenotype to study the early genetic etiology of hypertension?
Hypertension
2009
19156168
Pharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysis.
Eur J Hum Genet
2009
19300482
A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci.
PLoS Genet
2009
18166564
Relationships of cardiovascular phenotypes with healthy weight, at risk of overweight, and overweight in US youths.
Pediatrics
2008
19222302
Tissue-specific genetic control of splicing: implications for the study of complex traits.
PLoS Biol
2008
1 - 50 of 91
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