K. King

Mutation, selection, and evolution of the Crohn disease susceptibility gene CARD15

S. Fisher, A. Forbes, Clive M. Onnie, 2006, Human mutation.

Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

S. Fisher, C. Lewis, C. Mathew, 2001, The Lancet.

A two‐tier approach to mutation detection in the COL4A5 gene for Alport syndrome

F. Flinter, K. King, Peter M. Green, 2006, Human mutation.

Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease.

S. Fisher, A. Forbes, C. Lewis, 2003, American journal of human genetics.

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease.

Alastair Forbes, Christopher G Mathew, Jochen Hampe, 2002, Gastroenterology.

Unusual deep intronic mutations in the COL4A5 gene cause X linked Alport syndrome

P. Green, F. Flinter, K. King, 2002, Human Genetics.

Hair roots as the ideal source of mRNA for genetic testing

P. Green, F. Flinter, K. King, 2001, Journal of medical genetics.

Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31

S. Fisher, A. Forbes, C. Lewis, 2006, Genes and Immunity.

Detection of muramyl dipeptide‐sensing pathway defects in patients with Crohn's disease

A. Forbes, C. Mathew, K. Hunt, 2006, Inflammatory bowel diseases.

Sequence variation in the CARD15 (NOD2) gene and susceptibity to Crohn's disease

S. Fisher, A. Forbes, J. Sanderson, 2003 .

Genetic variation in the IGSF6 gene and lack of association with inflammatory bowel disease.

S. Fisher, A. Forbes, C. Lewis, 2003, European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics.

Identification, evolution, and association study of a novel promoter and first exon of the human NOD2 (CARD15) gene.

S. Fisher, C. Mathew, P. Rosenstiel, 2007, Genomics.