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Author Details

Kevin L Gunderson
Illumina Inc.
1991
55
40
PMIDPaper TitleJournal TitlePublished Year
28650462Haplotype phasing of whole human genomes using bead-based barcode partitioning in a single tube.Nat Biotechnol2017
28138849Contiguity-Preserving Transposition Sequencing (CPT-Seq) for Genome-Wide Haplotyping, Assembly, and Single-Cell ATAC-Seq.Methods Mol Biol2017
28360230Sequences of 95 human <i>MHC</i> haplotypes reveal extreme coding variation in genes other than highly polymorphic <i>HLA class I</i> and <i>II</i>.Genome Res2017
28135255Massively multiplex single-cell Hi-C.Nat Methods2017
25953818Multiplex single cell profiling of chromatin accessibility by combinatorial cellular indexing.Science2015
26414351Subangstrom single-molecule measurements of motor proteins using a nanopore.Nat Biotechnol2015
26198775Very long haplotype tracts characterized at high resolution from HLA homozygous cell lines.Immunogenetics2015
25860294Genetic and epigenetic profiling of CLL disease progression reveals limited somatic evolution and suggests a relationship to memory-cell development.Blood Cancer J2015
24399302Mutation in ST6GALNAC5 identified in family with coronary artery disease.Sci Rep2014
30117500Mobile genetic elements and genome evolution 2014.Mob DNA2014
25327137In vitro, long-range sequence information for de novo genome assembly via transposase contiguity.Genome Res2014
25326703Haplotype-resolved whole-genome sequencing by contiguity-preserving transposition and combinatorial indexing.Nat Genet2014
22039155Highly parallel oligonucleotide purification and functionalization using reversible chemistry.Nucleic Acids Res2012
21418647Genome-wide assessment of imprinted expression in human cells.Genome Biol2011
21839163High density DNA methylation array with single CpG site resolution.Genomics2011
20647332Deletion at fragile sites is a common and early event in Barrett's esophagus.Mol Cancer Res2010
20628616Computational analysis of whole-genome differential allelic expression data in human.PLoS Comput Biol2010
18997001Allele-specific gene expression patterns in primary leukemic cells reveal regulation of gene expression by CpG site methylation.Genome Res2009
22122642Genome-wide DNA methylation profiling using Infinium® assay.Epigenomics2009
19838192Global patterns of cis variation in human cells revealed by high-density allelic expression analysis.Nat Genet2009
19381978Whole-genome genotyping on bead arrays.Methods Mol Biol2009
19381970Design of tag SNP whole genome genotyping arrays.Methods Mol Biol2009
19558528Identification of critical regions for clinical features of distal 10q deletion syndrome.Clin Genet2009
19136950Increased LIS1 expression affects human and mouse brain development.Nat Genet2009
18691401Comparison of the Agilent, ROMA/NimbleGen and Illumina platforms for classification of copy number alterations in human breast tumors.BMC Genomics2008
19138988Single nucleotide polymorphism-based genome-wide chromosome copy change, loss of heterozygosity, and aneuploidy in Barrett's esophagus neoplastic progression.Cancer Prev Res (Phila)2008
18536049Delineation of the proximal 3q microdeletion syndrome.Am J Med Genet A2008
17225249Whole genome genotyping technologies on the BeadArray platform.Biotechnol J2007
17922574Power to detect risk alleles using genome-wide tag SNP panels.PLoS Genet2007
17916097Characterization of de novo microdeletions involving 17q11.2q12 identified through chromosomal comparative genomic hybridization.Clin Genet2007
17943131Genome-wide detection and characterization of positive selection in human populations.Nature2007
17943122A second generation human haplotype map of over 3.1 million SNPs.Nature2007
18000900Mosaic tetrasomy 12p with triplication of 12p detected by array-based comparative genomic hybridization of peripheral blood DNA.Am J Med Genet A2007
17651367Characterization of seed-specific benzoyloxyglucosinolate mutations in Arabidopsis thaliana.Plant J2007
17645438Indel arrays: an affordable alternative for genotyping.Plant J2007
17666889Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region.Genet Med2007
17330859Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review.Am J Med Genet A2007
16369550Whole-genome genotyping with the single-base extension assay.Nat Methods2006
16768648Whole-genome genotyping of haplotype tag single nucleotide polymorphisms.Pharmacogenomics2006
16847463Highly parallel genomic assays.Nat Rev Genet2006
16938560Whole-genome genotyping.Methods Enzymol2006
16938546Illumina universal bead arrays.Methods Enzymol2006
16899659High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping.Genome Res2006
15838508A genome-wide scalable SNP genotyping assay using microarray technology.Nat Genet2005
16207153Illumina, Inc.Pharmacogenomics2005
15829238High-throughput SNP genotyping on universal bead arrays.Mutat Res2005
15078854Decoding randomly ordered DNA arrays.Genome Res2004
15338605Highly parallel SNP genotyping.Cold Spring Harb Symp Quant Biol2003
10488089Redox reagents and divalent cations alter the kinetics of cystic fibrosis transmembrane conductance regulator channel gating.J Biol Chem1999
9847078Mutation detection by ligation to complete n-mer DNA arrays.Genome Res1998
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Collaborators

Richard Shen
Co-authored papers 10
Jian-Bing Fan
Nanfang Hospital and Basic Medical College, Southern Medical University
Co-authored papers 9
Mostafa Ronaghi
Co-authored papers 9
Mark S Chee
Medical Research Council Laboratory of Molecular Biology
Co-authored papers 7
Arnold Oliphant
University of Utah Medical Center
Co-authored papers 6
Marina Bibikova
Departments of Bioinformatics and Clinical Genomics, Illumina Inc.
Co-authored papers 5
Jay Shendure
University of Washington
Co-authored papers 5
Alexandre Montpetit
McGill University and Genome Quebec Innovation Centre
Co-authored papers 4
Sarah S Murray
University of California San Diego Health System
Co-authored papers 4
Luana Galver
Illumina Inc.
Co-authored papers 4
Panos Deloukas
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 3
Thomas J Hudson
Ontario Institute for Cancer Research
Co-authored papers 3
Andrew Adey
Knight Cancer Institute, Oregon Health and Science University
Co-authored papers 3
Sarah E Hunt
European Bioinformatics Institute
Co-authored papers 3
David R Bentley
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Co-authored papers 3
Kelly A Frazer
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Co-authored papers 3
John W Belmont
Baylor College of Medicine
Co-authored papers 3
Grace Lee
Bowdoin College
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Tomi Pastinen
Co-authored papers 3
Yangfan Liu
Co-authored papers 2
Li Jin
Fudan University
Co-authored papers 2
Thomas D Willis
Adaptive Biotechnologies
Co-authored papers 2
Suzanne M Leal
Center for Statistical Genetics, Columbia University Medical Center
Co-authored papers 2
David A Hinds
23andMe Inc.
Co-authored papers 2
Ludmila Pawlikowska
Center for Cerebrovascular Research
Co-authored papers 2
Albert V Smith
University of Michigan School of Public Health ann arbor
Co-authored papers 2
Jun Yu
Beijing Institute of Genomics, Chinese Academy of Sciences
Co-authored papers 2
Jessica Roy
Co-authored papers 2
Jean-Fran??ois Olivier
McGill University Health Center
Co-authored papers 2
Robert W Plumb
Co-authored papers 2
Release 1.2