Julian C. Knight Wellcome Trust Centre for Human Genetics University of Oxford Biography Publications Institution JoVE Articles Julian C. Knight has not added a biography. If you are Julian C. Knight and would like to personalize this page please email our Author Liaison for assistance. Publications Pervasive Haplotypic Variation in the Spliceo-transcriptome of the Human Major Histocompatibility Complex Genome Research. Jul, 2011 | Pubmed ID: 21628452 Allele-specific Transcription of the Asthma-associated PHD Finger Protein 11 Gene (PHF11) Modulated by Octamer-binding Transcription Factor 1 (Oct-1) The Journal of Allergy and Clinical Immunology. Apr, 2011 | Pubmed ID: 21320718 A Common Haplotype of the TNF Receptor 2 Gene Modulates Endotoxin Tolerance Journal of Immunology (Baltimore, Md. : 1950). Mar, 2011 | Pubmed ID: 21282507 Vitamin D Receptor Gene Methylation is Associated with Ethnicity, Tuberculosis, and TaqI Polymorphism Human Immunology. Mar, 2011 | Pubmed ID: 21168462 Genetic Determinants of HSP70 Gene Expression Following Heat Shock Human Molecular Genetics. Dec, 2010 | Pubmed ID: 20876613 A ChIP-seq Defined Genome-wide Map of Vitamin D Receptor Binding: Associations with Disease and Evolution Genome Research. Oct, 2010 | Pubmed ID: 20736230 Understanding Human Genetic Variation in the Era of High-throughput Sequencing EMBO Reports. Sep, 2010 | Pubmed ID: 20725090 Leprosy and the Adaptation of Human Toll-like Receptor 1 PLoS Pathogens. 2010 | Pubmed ID: 20617178 An Integrated Expression Phenotype Mapping Approach Defines Common Variants in LEP, ALOX15 and CAPNS1 Associated with Induction of IL-6 Human Molecular Genetics. Feb, 2010 | Pubmed ID: 19942621 Insights into the Nature and Consequences of Our Variable Genome Briefings in Functional Genomics & Proteomics. Sep, 2009 | Pubmed ID: 19808931 The Human Major Histocompatibility Complex As a Paradigm in Genomics Research Briefings in Functional Genomics & Proteomics. Sep, 2009 | Pubmed ID: 19468039 Identification of a Novel Beta-cell Glucokinase (GCK) Promoter Mutation (-71G>C) That Modulates GCK Gene Expression Through Loss of Allele-specific Sp1 Binding Causing Mild Fasting Hyperglycemia in Humans Diabetes. Aug, 2009 | Pubmed ID: 19411616 Multiple Sclerosis and the Major Histocompatibility Complex Current Opinion in Neurology. Jun, 2009 | Pubmed ID: 19387341 A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene PLoS Genetics. Mar, 2009 | Pubmed ID: 19325871 Expression of the Multiple Sclerosis-associated MHC Class II Allele HLA-DRB1*1501 is Regulated by Vitamin D PLoS Genetics. Feb, 2009 | Pubmed ID: 19197344 HLA Class I Alleles Tag HLA-DRB1*1501 Haplotypes for Differential Risk in Multiple Sclerosis Susceptibility Proceedings of the National Academy of Sciences of the United States of America. Sep, 2008 | Pubmed ID: 18765817 Chromatin Profiling Across the Human Tumour Necrosis Factor Gene Locus Reveals a Complex, Cell Type-specific Landscape with Novel Regulatory Elements Nucleic Acids Research. Sep, 2008 | Pubmed ID: 18653526 Origins of Magic: Review of Genetic and Epigenetic Effects BMJ (Clinical Research Ed.). Dec, 2007 | Pubmed ID: 18156238 Analysis of Allele-specific Gene Expression Methods in Molecular Biology (Clifton, N.J.). 2006 | Pubmed ID: 16888357 The Chromosome 6p22 Haplotype Associated with Dyslexia Reduces the Expression of KIAA0319, a Novel Gene Involved in Neuronal Migration Human Molecular Genetics. May, 2006 | Pubmed ID: 16600991 Regulatory Polymorphisms Underlying Complex Disease Traits Journal of Molecular Medicine (Berlin, Germany). Feb, 2005 | Pubmed ID: 15592805 Allele-specific Repression of Lymphotoxin-alpha by Activated B Cell Factor-1 Nature Genetics. Apr, 2004 | Pubmed ID: 15052269 In Vivo Characterization of Regulatory Polymorphisms by Allele-specific Quantification of RNA Polymerase Loading Nature Genetics. Apr, 2003 | Pubmed ID: 12627232 Functional Implications of Genetic Variation in Non-coding DNA for Disease Susceptibility and Gene Regulation Clinical Science (London, England : 1979). May, 2003 | Pubmed ID: 12513691 Um alelo-específico do ensaio Expressão Gênica para testar as bases funcionais das Associações de Genética Silvia Paracchini1, Anthony P. Monaco1, Julian C. Knight1 1Wellcome Trust Centre for Human Genetics, University of Oxford JoVE 2279 Biology
Um alelo-específico do ensaio Expressão Gênica para testar as bases funcionais das Associações de Genética Silvia Paracchini1, Anthony P. Monaco1, Julian C. Knight1 1Wellcome Trust Centre for Human Genetics, University of Oxford JoVE 2279 Biology