List of works - Kevin V Shianna

A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci.

scientific article

A genome-wide association study of resistance to HIV infection in highly exposed uninfected individuals with hemophilia A.

scientific article published on 30 January 2013

A genome-wide comparison of the functional properties of rare and common genetic variants in humans

scientific article

A genome-wide investigation of SNPs and CNVs in schizophrenia

scientific article

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

scientific article

A polymorphism in the HCP5 gene associated with HLA-B*5701 does not restrict HIV-1 in vitro

scientific article published on January 2010

A whole-genome analysis of premature termination codons

scientific article published on 22 July 2011

CCL3L1 and HIV/AIDS susceptibility

scientific article published on October 2009

Clinical application of exome sequencing in undiagnosed genetic conditions

scientific article

Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles

scientific article

Cold urticaria, immunodeficiency, and autoimmunity related to PLCG2 deletions

scientific article published on 11 January 2012

Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study

scientific journal article

Common genetic variation and the control of HIV-1 in humans

scientific article published in December 2009

Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population

scientific article

Common variants conferring risk of schizophrenia

scientific article

Copy number variation of KIR genes influences HIV-1 control

scientific article

Correction: A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia

Correction: Genomewide Association Study for Determinants of HIV-1 Acquisition and Viral Set Point in HIV-1 Serodiscordant Couples with Quantified Virus Exposure.

scientific article published on 17 January 2012

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

scientific article

Evidence of dysregulation of dendritic cells in primary HIV infection

scientific article published on 6 August 2010

Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome

scientific article

Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy

scientific article

Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia

scientific article

Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance

scientific article

Genome assembly and geospatial phylogenomics of the bed bug Cimex lectularius

scientific article published on 2 February 2016

Genome-wide association study of interferon-related cytopenia in chronic hepatitis C patients

scientific article

Genome-wide mRNA expression correlates of viral control in CD4+ T-cells from HIV-1-infected individuals

scientific article

Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions

scientific article

Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure

scientific article

Geographical genomics of human leukocyte gene expression variation in southern Morocco

scientific article

HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans

scientific article

High-throughput isolation and mapping of C. elegans mutants susceptible to pathogen infection

scientific article

Host determinants of HIV-1 control in African Americans

scientific article

Host genetic determinants of T cell responses to the MRKAd5 HIV-1 gag/pol/nef vaccine in the step trial

scientific article

Host genetics and HIV-1: the final phase?

scientific article

IL28B genotype is associated with differential expression of intrahepatic interferon-stimulated genes in patients with chronic hepatitis C.

scientific article

Interleukin-28B polymorphism improves viral kinetics and is the strongest pretreatment predictor of sustained virologic response in genotype 1 hepatitis C virus

scientific article

Large recurrent microdeletions associated with schizophrenia

scientific article

Natural selection on EPAS1 (HIF2alpha) associated with low hemoglobin concentration in Tibetan highlanders

scientific article

Nucleolar proteins suppress Caenorhabditis elegans innate immunity by inhibiting p53/CEP-1

scientific article (publication date: September 2009)

Prioritizing genetic variants for causality on the basis of preferential linkage disequilibrium

scientific article

Quantitation of pretreatment serum interferon-γ-inducible protein-10 improves the predictive value of an IL28B gene polymorphism for hepatitis C treatment response

scientific article

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes

scientific article

SVA: software for annotating and visualizing sequenced human genomes

scientific article

Screening the human exome: a comparison of whole genome and whole transcriptome sequencing

scientific article

The Duffy antigen receptor for chemokines null promoter variant does not influence HIV-1 acquisition or disease progression

scientific article

The characterization of twenty sequenced human genomes

scientific article

Tissue-specific genetic control of splicing: implications for the study of complex traits

scientific article

Using ERDS to infer copy-number variants in high-coverage genomes

scientific article

Variants in the ITPA gene protect against ribavirin-induced hemolytic anemia and decrease the need for ribavirin dose reduction

scientific article

Variants in the ITPA gene protect against ribavirin-induced hemolytic anemia in HIV/HCV-coinfected patients with all HCV genotypes

scientific article published on 9 December 2011

Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene

scientific article published in June 2010

List of works by Kevin V Shianna

A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci.

A genome-wide association study of resistance to HIV infection in highly exposed uninfected individuals with hemophilia A.

A genome-wide comparison of the functional properties of rare and common genetic variants in humans

A genome-wide investigation of SNPs and CNVs in schizophrenia

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

A polymorphism in the HCP5 gene associated with HLA-B*5701 does not restrict HIV-1 in vitro

A whole-genome analysis of premature termination codons

CCL3L1 and HIV/AIDS susceptibility

Clinical application of exome sequencing in undiagnosed genetic conditions

Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles

Cold urticaria, immunodeficiency, and autoimmunity related to PLCG2 deletions

Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study

Common genetic variation and the control of HIV-1 in humans

Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population

Common variants conferring risk of schizophrenia

Copy number variation of KIR genes influences HIV-1 control

Correction: A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia

Correction: Genomewide Association Study for Determinants of HIV-1 Acquisition and Viral Set Point in HIV-1 Serodiscordant Couples with Quantified Virus Exposure.

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

Evidence of dysregulation of dendritic cells in primary HIV infection

Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome

Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy

Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia

Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance

Genome assembly and geospatial phylogenomics of the bed bug Cimex lectularius

Genome-wide association study of interferon-related cytopenia in chronic hepatitis C patients

Genome-wide mRNA expression correlates of viral control in CD4+ T-cells from HIV-1-infected individuals

Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions

Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure

Geographical genomics of human leukocyte gene expression variation in southern Morocco

HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans

High-throughput isolation and mapping of C. elegans mutants susceptible to pathogen infection

Host determinants of HIV-1 control in African Americans

Host genetic determinants of T cell responses to the MRKAd5 HIV-1 gag/pol/nef vaccine in the step trial

Host genetics and HIV-1: the final phase?

IL28B genotype is associated with differential expression of intrahepatic interferon-stimulated genes in patients with chronic hepatitis C.

Interleukin-28B polymorphism improves viral kinetics and is the strongest pretreatment predictor of sustained virologic response in genotype 1 hepatitis C virus

Large recurrent microdeletions associated with schizophrenia

Natural selection on EPAS1 (HIF2alpha) associated with low hemoglobin concentration in Tibetan highlanders

Nucleolar proteins suppress Caenorhabditis elegans innate immunity by inhibiting p53/CEP-1

Prioritizing genetic variants for causality on the basis of preferential linkage disequilibrium

Quantitation of pretreatment serum interferon-γ-inducible protein-10 improves the predictive value of an IL28B gene polymorphism for hepatitis C treatment response

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes

SVA: software for annotating and visualizing sequenced human genomes

Screening the human exome: a comparison of whole genome and whole transcriptome sequencing

The Duffy antigen receptor for chemokines null promoter variant does not influence HIV-1 acquisition or disease progression

The characterization of twenty sequenced human genomes

Tissue-specific genetic control of splicing: implications for the study of complex traits

Using ERDS to infer copy-number variants in high-coverage genomes

Variants in the ITPA gene protect against ribavirin-induced hemolytic anemia and decrease the need for ribavirin dose reduction

Variants in the ITPA gene protect against ribavirin-induced hemolytic anemia in HIV/HCV-coinfected patients with all HCV genotypes

Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene