Julian C Knight

发表

Pervasive haplotypic variation in the spliceo-transcriptome of the human major histocompatibility complex.

Martin S. Taylor, John Broxholme, Katharine Plant, 2011, Genome research.

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.

Richard Wade-Martins, Yu Wang, C. Francks, 2006, Human molecular genetics.

Genomic landscape of the individual host response and outcomes in sepsis: a prospective cohort study

Anna Rautanen, Peter Humburg, J. Knight, 2016, The Lancet. Respiratory medicine.

Genome-wide analysis identifies a role for common copy number variants in specific language impairment

William W. Cohen, Gillian Baird, A Pickles, 2015, European Journal of Human Genetics.

Shared and Distinct Aspects of the Sepsis Transcriptomic Response to Fecal Peritonitis and Pneumonia

Peter Humburg, J. Knight, P. Humburg, 2017, American journal of respiratory and critical care medicine.

Functional implications of genetic variation in non-coding DNA for disease susceptibility and gene regulation.

J. Knight, Julian C Knight, 2003, Clinical science.

“Not pathogenic until proven otherwise”: perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and the 100,000 Genomes Project

Edward Blair, J. Knight, H. Watkins, 2017, Genetics in Medicine.

The human Major Histocompatibility Complex as a paradigm in genomics research.

J. Knight, Claire Vandiedonck, Julian C Knight, 2009, Briefings in functional genomics & proteomics.

A ChIP-seq defined genome-wide map of vitamin D receptor binding: associations with disease and evolution.

Gavin Giovannoni, Andreas Heger, Sreeram V Ramagopalan, 2010, Genome research.

Classification of patients with sepsis according to blood genomic endotype: a prospective cohort study.

Peter Nürnberg, Marcus J Schultz, Janneke Horn, 2017, The Lancet. Respiratory medicine.

Allele-specific transcription of the asthma-associated PHD finger protein 11 gene (PHF11) modulated by octamer-binding transcription factor 1 (Oct-1).

R. Holt, J. Knight, A. Dixon, 2011, The Journal of allergy and clinical immunology.

A community approach to mortality prediction in sepsis via gene expression analysis

Purvesh Khatri, Larsson Omberg, Marshall Nichols, 2018, Nature Communications.

Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization

Kari Stefansson, Melanie Waldenberger, Dirkje S Postma, 2013, Nature Genetics.

Fine mapping genetic determinants of the highly variably expressed MHC gene ZFP57

Katharine Plant, J. Knight, B. Fairfax, 2013, European Journal of Human Genetics.