Julian C. Knight

Wellcome Trust Centre for Human Genetics, University of Oxford

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 2	2010

Other Publications

Article	Year
Functional implications of genetic variation in non-coding DNA for disease susceptibility and gene regulation. Clinical science (London, England : 1979)\| PubMed ID: 12513691	2003
In vivo characterization of regulatory polymorphisms by allele-specific quantification of RNA polymerase loading. Nature genetics\| PubMed ID: 12627232	2003
Allele-specific repression of lymphotoxin-alpha by activated B cell factor-1. Nature genetics\| PubMed ID: 15052269	2004
Regulatory polymorphisms underlying complex disease traits. Journal of molecular medicine (Berlin, Germany)\| PubMed ID: 15592805	2005
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Human molecular genetics\| PubMed ID: 16600991	2006
Analysis of allele-specific gene expression. Methods in molecular biology (Clifton, N.J.)\| PubMed ID: 16888357	2006
Origins of magic: review of genetic and epigenetic effects. BMJ (Clinical research ed.)\| PubMed ID: 18156238	2007
Chromatin profiling across the human tumour necrosis factor gene locus reveals a complex, cell type-specific landscape with novel regulatory elements. Nucleic acids research\| PubMed ID: 18653526	2008
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\| PubMed ID: 18765817	2008
Expression of the multiple sclerosis-associated MHC class II Allele HLA-DRB1*1501 is regulated by vitamin D. PLoS genetics\| PubMed ID: 19197344	2009
A common variant associated with dyslexia reduces expression of the KIAA0319 gene. PLoS genetics\| PubMed ID: 19325871	2009
Multiple sclerosis and the major histocompatibility complex. Current opinion in neurology\| PubMed ID: 19387341	2009
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 hyperglyc... Diabetes\| PubMed ID: 19411616	2009
The human Major Histocompatibility Complex as a paradigm in genomics research. Briefings in functional genomics & proteomics\| PubMed ID: 19468039	2009
Insights into the nature and consequences of our variable genome. Briefings in functional genomics & proteomics\| PubMed ID: 19808931	2009
An integrated expression phenotype mapping approach defines common variants in LEP, ALOX15 and CAPNS1 associated with induction of IL-6. Human molecular genetics\| PubMed ID: 19942621	2010
Leprosy and the adaptation of human toll-like receptor 1. PLoS pathogens\| PubMed ID: 20617178	2010
Understanding human genetic variation in the era of high-throughput sequencing. EMBO reports\| PubMed ID: 20725090	2010
A ChIP-seq defined genome-wide map of vitamin D receptor binding: associations with disease and evolution. Genome research\| PubMed ID: 20736230	2010
Genetic determinants of HSP70 gene expression following heat shock. Human molecular genetics\| PubMed ID: 20876613	2010
Vitamin D receptor gene methylation is associated with ethnicity, tuberculosis, and TaqI polymorphism. Human immunology\| PubMed ID: 21168462	2011
A common haplotype of the TNF receptor 2 gene modulates endotoxin tolerance. Journal of immunology (Baltimore, Md. : 1950)\| PubMed ID: 21282507	2011
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\| PubMed ID: 21320718	2011
Pervasive haplotypic variation in the spliceo-transcriptome of the human major histocompatibility complex. Genome research\| PubMed ID: 21628452	2011