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Author Details
Full Name
Kevin V Shianna
Affiliation
Illumina Inc. 5200 Illumina Way
ORCID
Career Start Year
1998
Papers
77
H Index
53
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
26836631
Genome assembly and geospatial phylogenomics of the bed bug Cimex lectularius.
Nat Commun
2016
24030663
Tibetans living at sea level have a hyporesponsive hypoxia-inducible factor system and blunted physiological responses to hypoxia.
J Appl Physiol (1985)
2014
25210050
Two further blood pressure loci identified in ion channel genes with a gene-centric approach.
Circ Cardiovasc Genet
2014
25187353
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles.
Nat Commun
2014
23020875
Host genetics of HIV acquisition and viral control.
Annu Rev Med
2013
23372042
A genome-wide association study of resistance to HIV infection in highly exposed uninfected individuals with hemophilia A.
Hum Mol Genet
2013
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
22958903
Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome.
Am J Hum Genet
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
22842232
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
Nat 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
22581936
Clinical application of exome sequencing in undiagnosed genetic conditions.
J Med Genet
2012
22236196
Cold urticaria, immunodeficiency, and autoimmunity related to PLCG2 deletions.
N Engl J Med
2012
22379998
Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.
Pharmacogenomics
2012
22027585
Single 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 Hepatol
2012
22017462
Alpha-nicotinic acetylcholine receptor and tobacco smoke exposure: effects on bronchial hyperresponsiveness in children.
Pediatr Allergy Immunol
2012
22158703
Variants in the ITPA gene protect against ribavirin-induced hemolytic anemia in HIV/HCV-coinfected patients with all HCV genotypes.
J Infect Dis
2012
21274861
Inosine triphosphatase genetic variants are protective against anemia during antiviral therapy for HCV2/3 but do not decrease dose reductions of RBV or increase SVR.
Hepatology
2011
22140359
Copy number variation of KIR genes influences HIV-1 control.
PLoS Biol
2011
22174851
Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure.
PLoS One
2011
21803148
A whole-genome analysis of premature termination codons.
Genomics
2011
21920051
Exome sequencing: the expert view.
Genome Biol
2011
21624899
SVA: software for annotating and visualizing sequenced human genomes.
Bioinformatics
2011
21428769
HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans.
N Engl J Med
2011
21457907
A genome-wide comparison of the functional properties of rare and common genetic variants in humans.
Am J Hum Genet
2011
21199653
Inosine triphosphate protects against ribavirin-induced adenosine triphosphate loss by adenylosuccinate synthase function.
Gastroenterology
2011
21160409
Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population.
AIDS
2011
21254181
Hepatitis C pharmacogenetics: state of the art in 2010.
Hepatology
2011
21254158
Quantitation of pretreatment serum interferon-γ-inducible protein-10 improves the predictive value of an IL28B gene polymorphism for hepatitis C treatment response.
Hepatology
2011
21278214
Host genetic determinants of T cell responses to the MRKAd5 HIV-1 gag/pol/nef vaccine in the step trial.
J Infect Dis
2011
19935381
A polymorphism in the HCP5 gene associated with HLA-B*5701 does not restrict HIV-1 in vitro.
AIDS
2010
20693428
Evidence of dysregulation of dendritic cells in primary HIV infection.
Blood
2010
20838461
The characterization of twenty sequenced human genomes.
PLoS Genet
2010
20931559
IL28B genotype is associated with differential expression of intrahepatic interferon-stimulated genes in patients with chronic hepatitis C.
Hepatology
2010
20976252
Host genetics and HIV-1: the final phase?
PLoS Pathog
2010
20522523
Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.
Brain
2010
20547162
Variants in the ITPA gene protect against ribavirin-induced hemolytic anemia and decrease the need for ribavirin dose reduction.
Gastroenterology
2010
20534544
Natural selection on EPAS1 (HIF2alpha) associated with low hemoglobin concentration in Tibetan highlanders.
Proc Natl Acad Sci U S A
2010
20577567
Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene.
PLoS Genet
2010
20637200
A polymorphism near IL28B is associated with spontaneous clearance of acute hepatitis C virus and jaundice.
Gastroenterology
2010
20598109
Screening the human exome: a comparison of whole genome and whole transcriptome sequencing.
Genome Biol
2010
20621700
An IL28B polymorphism determines treatment response of hepatitis C virus genotype 2 or 3 patients who do not achieve a rapid virologic response.
Gastroenterology
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
1 - 50 of 77
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