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Author Details

Kevin V Shianna
Illumina Inc. 5200 Illumina Way
1998
77
53
PMIDPaper TitleJournal TitlePublished Year
26836631Genome assembly and geospatial phylogenomics of the bed bug Cimex lectularius.Nat Commun2016
24030663Tibetans living at sea level have a hyporesponsive hypoxia-inducible factor system and blunted physiological responses to hypoxia.J Appl Physiol (1985)2014
25210050Two further blood pressure loci identified in ion channel genes with a gene-centric approach.Circ Cardiovasc Genet2014
25187353Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles.Nat Commun2014
23020875Host genetics of HIV acquisition and viral control.Annu Rev Med2013
23372042A genome-wide association study of resistance to HIV infection in highly exposed uninfected individuals with hemophilia A.Hum Mol Genet2013
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
22958903Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome.Am J Hum Genet2012
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
22842232De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.Nat 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
22581936Clinical application of exome sequencing in undiagnosed genetic conditions.J Med Genet2012
22236196Cold urticaria, immunodeficiency, and autoimmunity related to PLCG2 deletions.N Engl J Med2012
22379998Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.Pharmacogenomics2012
22027585Single nucleotide polymorphism upstream of interleukin 28B associated with phase 1 and phase 2 of early viral kinetics in patients infected with HCV genotype 1.J Hepatol2012
22017462Alpha-nicotinic acetylcholine receptor and tobacco smoke exposure: effects on bronchial hyperresponsiveness in children.Pediatr Allergy Immunol2012
22158703Variants in the ITPA gene protect against ribavirin-induced hemolytic anemia in HIV/HCV-coinfected patients with all HCV genotypes.J Infect Dis2012
21274861Inosine triphosphatase genetic variants are protective against anemia during antiviral therapy for HCV2/3 but do not decrease dose reductions of RBV or increase SVR.Hepatology2011
22140359Copy number variation of KIR genes influences HIV-1 control.PLoS Biol2011
22174851Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure.PLoS One2011
21803148A whole-genome analysis of premature termination codons.Genomics2011
21920051Exome sequencing: the expert view.Genome Biol2011
21624899SVA: software for annotating and visualizing sequenced human genomes.Bioinformatics2011
21428769HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans.N Engl J Med2011
21457907A genome-wide comparison of the functional properties of rare and common genetic variants in humans.Am J Hum Genet2011
21199653Inosine triphosphate protects against ribavirin-induced adenosine triphosphate loss by adenylosuccinate synthase function.Gastroenterology2011
21160409Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population.AIDS2011
21254181Hepatitis C pharmacogenetics: state of the art in 2010.Hepatology2011
21254158Quantitation of pretreatment serum interferon-γ-inducible protein-10 improves the predictive value of an IL28B gene polymorphism for hepatitis C treatment response.Hepatology2011
21278214Host genetic determinants of T cell responses to the MRKAd5 HIV-1 gag/pol/nef vaccine in the step trial.J Infect Dis2011
19935381A polymorphism in the HCP5 gene associated with HLA-B*5701 does not restrict HIV-1 in vitro.AIDS2010
20693428Evidence of dysregulation of dendritic cells in primary HIV infection.Blood2010
20838461The characterization of twenty sequenced human genomes.PLoS Genet2010
20931559IL28B genotype is associated with differential expression of intrahepatic interferon-stimulated genes in patients with chronic hepatitis C.Hepatology2010
20976252Host genetics and HIV-1: the final phase?PLoS Pathog2010
20522523Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.Brain2010
20547162Variants in the ITPA gene protect against ribavirin-induced hemolytic anemia and decrease the need for ribavirin dose reduction.Gastroenterology2010
20534544Natural selection on EPAS1 (HIF2alpha) associated with low hemoglobin concentration in Tibetan highlanders.Proc Natl Acad Sci U S A2010
20577567Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene.PLoS Genet2010
20637200A polymorphism near IL28B is associated with spontaneous clearance of acute hepatitis C virus and jaundice.Gastroenterology2010
20598109Screening the human exome: a comparison of whole genome and whole transcriptome sequencing.Genome Biol2010
20621700An IL28B polymorphism determines treatment response of hepatitis C virus genotype 2 or 3 patients who do not achieve a rapid virologic response.Gastroenterology2010
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
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Collaborators

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Department of Pharmacy, Liyang People's Hospital
Co-authored papers 33
Ecole Polytechnique Federale de Lausanne
Co-authored papers 24
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School of Pharmacy and Biomolecular Sciences, Ireland FutureNeuro SFI Research Centre
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Foundation Medicine
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Duke University School of Medicine and Duke Health System
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FutureNeuro SFI Research Centre, The Royal College of Surgeons in Ireland
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UCL Institute of Neurology
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Frederick National Laboratory for Cancer Research, National Cancer Institute
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Hopital Universitaire de Bruxelles - Hopital Erasme
Co-authored papers 7
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Duke Clinical Research Institute and Duke University School of Medicine
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Vir Biotechnology Inc.
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Duke University Medical Center
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Johns Hopkins University School of Medicine
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Genomics England Ltd.
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Human Vaccine Institute, Duke University Medical Center Durham
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UCL Queen Square Institute of Neurology
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Universite Libre de Bruxelles (ULB)
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St James's Hospital
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Duke University School of Medicine
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West China Hospital of Sichuan University
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