Lindblad-Toh, Kerstin
Kerstin Lindblad-Toh svensk professor i komparativ genomik
VIAF ID: 64296098 (Personal)
Permalink: http://viaf.org/viaf/64296098
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Kerstin Lindblad-Toh
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svensk professor i komparativ genomik
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Lindblad-Toh
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Kerstin
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100 1 _ ‡a Lindblad-Toh, Kerstin
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100 1 _
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Lindblad-Toh, Kerstin
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100 1 _
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Lindblad-Toh, Kerstin
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100 1 _ ‡a Lindblad-Toh, Kerstin
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100 1 _
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Lindblad-Toh, Kerstin
4xx's: Alternate Name Forms (12)
Works
| Title | Sources |
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| The Antarctic Weddell seal genome reveals evidence of selection on cardiovascular phenotype and lipid handling |
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| Association of Protective HLA-A With HLA-B*27 Positive Ankylosing Spondylitis |
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| Bayesian mixed model analysis uncovered 21 risk loci for chronic kidney disease in boxer dogs |
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| Breed Distribution of SOD1 Alleles Previously Associated with Canine Degenerative Myelopathy |
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| Candidate genes and functional noncoding variants identified in a canine model of obsessive-compulsive disorder |
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| Canine Hereditary Ataxia in Old English Sheepdogs and Gordon Setters Is Associated with a Defect in the Autophagy Gene Encoding RAB24 |
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| Chiropterans Are a Hotspot for Horizontal Transfer of DNA Transposons in Mammalia |
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| A comparative genomics multitool for scientific discovery and conservation |
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| Comparison of cellular location and expression of Plakophilin-2 in epidermal cells from nonlesional atopic skin and healthy skin in German shepherd dogs |
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| Contribution of rare genetic variation to disease susceptibility in a large Scandinavian myositis cohort |
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| Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses |
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| Distinct HLA associations with autoantibody-defined subgroups in idiopathic inflammatory myopathies |
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| The dog and its genome, 2005: |
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| The ESR1 gene is associated with risk for canine mammary tumours |
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| Evolution of the ancestral mammalian karyotype and syntenic regions |
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| The genetic consequences of dog breed formation-Accumulation of deleterious genetic variation and fixation of mutations associated with myxomatous mitral valve disease in cavalier King Charles spaniels |
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| Genome sequencing of 2000 canids by the Dog10K consortium advances the understanding of demography, genome function and architecture |
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| Genome-wide analyses implicate 33 loci in heritable dog osteosarcoma, including regulatory variants near CDKN2A/B |
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| Genome wide association study in Swedish Labrador retrievers identifies genetic loci associated with hip dysplasia and body weight |
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| Genome-wide copy number variant discovery in dogs using the CanineHD genotyping array |
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| Hemangiosarcoma Cells Promote Conserved Host-derived Hematopoietic Expansion |
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| A high-resolution map of human evolutionary constraint using 29 mammals |
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| The HLA region in ANCA-associated vasculitis characterisation of genetic associations in a Scandinavian patient population. |
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| How to make a rodent giant Genomic basis and tradeoffs of gigantism in the capybara, the world's largest rodent. |
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| Human leukocyte antigen in sickness and in health Ankylosing spondylitis and <em>HLA</em> in Sweden. |
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| Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project |
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| Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping |
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| IgA deficiency in wolves |
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| An Improved Canine Genome and a Comprehensive Catalogue of Coding Genes and Non-Coding Transcripts |
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| In sickness and health - a questionnaire based study regarding immune mediated diseases and neoplasia in Swedish Nova Scotia Duck Tolling Retrievers |
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| Initial sequencing and comparative analysis of the mouse genome |
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| Integrated cytogenetic BAC map of the genome of the gray, short-tailed opossum, Monodelphis domestica |
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| Integrating evolutionary and regulatory information with multispecies approach implicates genes and pathways in obsessive-compulsive disorder |
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| Lack of evidence for a role of islet autoimmunity in the aetiology of canine diabetes mellitus |
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| Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse |
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| LGI2 truncation causes a remitting focal epilepsy in dogs |
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| Localization of canine brachycephaly using an across breed mapping approach |
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| LUPA: a European initiative taking advantage of the canine genome architecture for unravelling complex disorders in both human and dogs |
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| Mer-tyrosine kinase a novel susceptibility gene for SLE related end-stage renal disease. |
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| Microarray-based cytogenetic profiling reveals recurrent and subtype-associated genomic copy number aberrations in feline sarcomas |
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| Molecular pathways in patients with systemic lupus erythematosus revealed by gene-centred DNA sequencing |
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| Molecular profiling reveals prognostically significant subtypes of canine lymphoma |
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| Molecular subtypes of osteosarcoma identified by reducing tumor heterogeneity through an interspecies comparative approach |
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| The mosaic structure of variation in the laboratory mouse genome |
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| A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12. |
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| Multiple Changes of Gene Expression and Function Reveal Genomic and Phenotypic Complexity in SLE-like Disease |
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| Multiple Genetic Loci Associated with Pug Dog Thoracolumbar Myelopathy |
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| Multiple regulatory variants located in cell type-specific enhancers within the PKP2 locus form major risk and protective haplotypes for canine atopic dermatitis in German shepherd dogs |
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| A mutation in hairless dogs implicates FOXI3 in ectodermal development |
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| Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing |
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| The Naked Mole Rat Genome Resource: facilitating analyses of cancer and longevity-related adaptations |
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| Nordic OCD & Related Disorders Consortium: Rationale, design, and methods |
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| A novel canine reference genome resolves genomic architecture and uncovers transcript complexity |
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| Novel origins of copy number variation in the dog genome |
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| Patterns of molecular genetic variation among cat breeds. |
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| PIK3CA is recurrently mutated in canine mammary tumors, similarly to in human mammary neoplasia |
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| Progressive Cactus is a multiple-genome aligner for the thousand-genome era |
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| A quantitative framework for characterizing the evolutionary history of mammalian gene expression |
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| Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses |
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| Repeat expansion detection (RED) and the RED cloning strategy |
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| Rethinking dog domestication by integrating genetics, archeology, and biogeography |
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| SBE-TAGS: an array-based method for efficient single-nucleotide polymorphism genotyping |
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| The Shepherds' Tale: A Genome-Wide Study across 9 Dog Breeds Implicates Two Loci in the Regulation of Fructosamine Serum Concentration in Belgian Shepherds |
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| A Simple Repeat Polymorphism in the MITF-M Promoter Is a Key Regulator of White Spotting in Dogs |
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| Solenodon genome reveals convergent evolution of venom in eulipotyphlan mammals |
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| The spotted gar genome illuminates vertebrate evolution and facilitates human-teleost comparisons |
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| Standards recommendations for the Earth BioGenome Project |
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| Stratified genetic analysis reveals sex differences in MPO-ANCA-associated vasculitis |
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| Strong Association of Combined Genetic Deficiencies in the Classical Complement Pathway With Risk of Systemic Lupus Erythematosus and Primary Sjögren's Syndrome |
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| A survey of ficolin-3 activity in Systemic lupus erythematosus reveals a link to hematological disease manifestations and autoantibody profile |
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| SweHLA the high confidence HLA typing bio-resource drawn from 1000 Swedish genomes. |
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| A synonymous germline variant in a gene encoding a cell adhesion molecule is associated with cutaneous mast cell tumour development in Labrador and Golden Retrievers |
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| Systematic discovery of regulatory motifs in conserved regions of the human genome, including thousands of CTCF insulator sites |
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| Systematic discovery of regulatory motifs in human promoters and 3' UTRs by comparison of several mammals |
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| Thoracolumbar meningeal fibrosis in pugs |
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| Thorough investigation of a canine autoinflammatory disease (AID) syndrome confirms one main risk factor and suggests a modifier locus for amyloidosis |
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| Three's company |
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| Toll-like receptors revisited; a possible role for TLR1 in lupus nephritis |
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| Transcriptomes from German shepherd dogs reveal differences in immune activity between atopic dermatitis affected and control skin |
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| Two Loci on Chromosome 5 Are Associated with Serum IgE Levels in Labrador Retrievers |
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| A unique T cell receptor discovered in marsupials |
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| Unsupervised genome-wide recognition of local relationship patterns |
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| Using evolutionary constraint to define novel candidate driver genes in medulloblastoma |
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| Utilizing the Dog Genome in the Search for Novel Candidate Genes Involved in Glioma Development-Genome Wide Association Mapping followed by Targeted Massive Parallel Sequencing Identifies a Strongly Associated Locus |
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| Variants within the SP110 nuclear body protein modify risk of canine degenerative myelopathy |
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| What animals can teach us about evolution, the human genome, and human disease |
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| Whole-genome genotyping and resequencing reveal the association of a deletion in the complex interferon alpha gene cluster with hypothyroidism in dogs |
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| Whole-genome resequencing reveals loci under selection during chicken domestication |
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| Whole-genome sequencing of glioblastoma reveals enrichment of non-coding constraint mutations in known and novel genes |
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| Why sequence all eukaryotes? |
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| ZBED6, a novel transcription factor derived from a domesticated DNA transposon regulates IGF2 expression and muscle growth |
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| ZBED6: The birth of a new transcription factor in the common ancestor of placental mammals |
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