M. Mirza

发表

Multiple common variants for celiac disease influencing immune gene expression

P. Deloukas, R. Ophoff, L. Peltonen, 2010, Nature Genetics.

Association of NOD2 (CARD 15) genotype with clinical course of Crohn's disease: a cohort study

M. Vatn, J. Hampe, S. Schreiber, 2002, The Lancet.

Prognostic Value of Serum Hyaluronic Acid and Type I and III Procollagen Propeptides in Extrahepatic Biliary Atresia

P. Cheeseman, M. Mirza, J. Risteli, 1995, Pediatric Research.

Genetic Variation at the Chromosome 16 Chemokine Gene Cluster: Development of a Strategy for Association Studies in Complex Disease

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

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

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

Combined evidence from three large British Association studies rejects TUCAN/CARD8 as an IBD susceptibility gene.

S. Fisher, A. Forbes, C. Lewis, 2007, Gastroenterology.

Association of NOD 2 ( CARD 15 ) genotype with clinical course of Crohn ’ s disease : a cohort study

M. Vatn, J. Hampe, M. Krawczak, 2022 .

Corrigendum: Multiple common variants for celiac disease influencing immune gene expression

P. Deloukas, R. Ophoff, L. Peltonen, 2010, Nature Genetics.

Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

D. MacArthur, J. Todd, J. Barrett, 2013, Nature.

Ulcerative colitis is not associated with differences inMUC2 mucin allele length

J. Rotter, L. Vinall, D. Swallow, 1999, Journal of medical genetics.

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.

Linkage of inflammatory bowel disease to human chromosome 6p.

N J Lynch, A. Forbes, C. Mathew, 1999, American journal of human genetics.

A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort.

L. Cardon, C. Mathew, J. Hampe, 1999, American journal of human genetics.

A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5.

S. Fisher, A. Forbes, C. Lewis, 2007, Gastroenterology.

Exome Sequencing of 75 Individuals from Multiply Affected Coeliac Families and Large Scale Resequencing Follow Up

M. Simpson, S. Neuhausen, V. Plagnol, 2015, PloS one.

Pooled Sequencing of 531 Genes in Inflammatory Bowel Disease Identifies an Associated Rare Variant in BTNL2 and Implicates Other Immune Related Genes

J. Barrett, M. Parkes, J. Satsangi, 2015, PLoS Genetics.

Integrative Biology Approach Identifies Cytokine Targeting Strategies for Psoriasis

S. Tsoka, W. Ouyang, M. Mirza, 2014, Science Translational Medicine.

Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p

K. Huse, C. Mathew, J. Hampe, 2001, Proceedings of the National Academy of Sciences of the United States of America.

A whole genome screen for linkage in Turkish multiple sclerosis

S. Sawcer, A. Compston, M. Mirza, 2003, Journal of Neuroimmunology.

Genetic analysis of inflammatory bowel disease in a large European cohort supports linkage to chromosomes 12 and 16.

L. Cardon, C. Mathew, J. Hampe, 1998, Gastroenterology.

Evidence of linkage of the inflammatory bowel disease susceptibility locus on chromosome 16 (IBD1) to ulcerative colitis.

C. Mathew, D. Easton, J. Hugot, 1998, Journal of medical genetics.

Diverse effects of the CARD15 and IBD5 loci on clinical phenotype in 630 patients with Crohn's disease

S. Fisher, A. Forbes, C. Lewis, 2008, European journal of gastroenterology & hepatology.

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.

Stratified gene expression analysis identifies major amyotrophic lateral sclerosis genes

Ashley R. Jones, J. D. Macklis, J. Powell, 2015, Neurobiology of Aging.

Novel isoforms of the CARD8 (TUCAN) gene evade a nonsense mutation

N. Prescott, C. Mathew, M. Mirza, 2008, European Journal of Human Genetics.

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

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

Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory bowel disease

S. Schreiber, D. F. Easton, D. Teare, 2000, Immunogenetics.

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

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

No association of the NFKB1 promoter polymorphism with ulcerative colitis in a British case control cohort

S. Fisher, A. Forbes, C. Lewis, 2005, Gut.

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.

Multiple SNPs at the IBD5 locus contribute to the risk of Crohn's disease.

S. Fisher, A. Forbes, Clive M. Onnie, 2005 .