Christopher G. Mathew researcher
Mathew, Christopher G.
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
VIAF ID: 24677061 (Personal)
Permalink: http://viaf.org/viaf/24677061
Preferred Forms
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Christopher G. Mathew
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researcher
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Mathew
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Christopher G.
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Mathew, Christopher G.
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100 1 _ ‡a Mathew, Christopher G. (sparse)
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100 1 _
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Mathew, Christopher G.
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100 1 _ ‡a Mathew, Christopher G.
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100 1 _
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Mathew, Christopher G.
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100 1 _ ‡a Mathew, Christopher G.
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100 1 _
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Mathew, Christopher G.
4xx's: Alternate Name Forms (4)
Works
| Title | Sources |
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| Identification of missense and truncating mutations in the BRCA1 gene in sporadic and familial breast and ovarian cancer |
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| Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) gene |
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| Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease |
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| The Integrity and Yield of Genomic DNA Isolated from Whole Blood Following Long-Term Storage at -30°C. |
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| Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility |
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| Interaction of FANCD2 and NBS1 in the DNA damage response |
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| The interferon-gamma gene as a positional and functional candidate gene for inflammatory bowel disease |
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| Investigation of association of the DLG5 gene with phenotypes of inflammatory bowel disease in the British population |
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| Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship |
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| Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene |
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| Johannesburg Cancer Study (JCS): contribution to knowledge and opportunities arising from 20 years of data collection in an African setting |
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| Lamina propria macrophage phenotypes in relation to Escherichia coli in Crohn's disease. |
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| Linkage analysis of chromosome 17 markers in British and South African families with neurofibromatosis type I. |
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| Linkage of the gene for cystinosis to markers on the short arm of chromosome 17 |
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| Loss of heterozygosity mapping at chromosome arm 16q in 712 breast tumors reveals factors that influence delineation of candidate regions |
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| Loss of NF1 alleles in phaeochromocytomas from patients with type I neurofibromatosis |
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| Low prevalence of germline BRCA1 mutations in early onset breast cancer without a family history |
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| Mapping of a susceptibility locus for Crohn's disease on chromosome 16 |
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| Measurement methods and accuracy in copy number variation: failure to replicate associations of beta-defensin copy number with Crohn's disease. |
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| Meta-analysis and imputation refines the association of 15q25 with smoking quantity |
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| Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 |
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| Minisatellite DNA profiles: rapid sample identification in linkage analysis |
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| Molecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South Africa |
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| A Msel polymorphism in exon 48 of the dystrophin gene |
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| Multiple endocrine neoplasia type 2A (MEN 2A) syndrome in a South African family. Biochemistry and molecular genetics |
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| Muramyl dipeptide and toll-like receptor sensitivity in NOD2-associated Crohn's disease |
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| Mutation of the RAD51C gene in a Fanconi anemia-like disorder |
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| Mutation, selection, and evolution of the Crohn disease susceptibility gene CARD15. |
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| Mutational characterization of the bile acid receptor TGR5 in primary sclerosing cholangitis |
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| Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism |
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| Negligible impact of rare autoimmune-locus coding-region variants on missing heritability |
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| A new autosomal recessive anomaly mimicking Fanconi's anaemia phenotype |
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| New links to the pathogenesis of Crohn disease provided by genome-wide association scans |
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| Nijmegen breakage syndrome diagnosed as Fanconi anaemia. |
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| No association of the NFKB1 promoter polymorphism with ulcerative colitis in a British case control cohort. |
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| A Nonsynonymous SNP in ATG16L1 Predisposes to Ileal Crohn’s Disease and Is Independent of CARD15 and IBD5 |
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| Novel and Known Gene-Smoking Interactions With cIMT Identified as Potential Drivers for Atherosclerosis Risk in West-African Populations of the AWI-Gen Study |
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| Novel isoforms of the CARD8 (TUCAN) gene evade a nonsense mutation. |
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| A novel NcoI polymorphism creates a fifth haplotype in the 3' untranslated region of CKM |
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| Paternal origin of new mutations in von Recklinghausen neurofibromatosis. |
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| A patient-derived mutant form of the Fanconi anemia protein, FANCA, is defective in nuclear accumulation |
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| A pedigree-based linkage study of coeliac disease: failure to replicate previous positive findings |
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| The PISSLRE gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancer |
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| Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children |
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| Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes |
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| Population screening for cystic fibrosis |
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| Population-specific genetic associations with oesophageal squamous cell carcinoma in South Africa |
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| Positive diepoxybutane test in only one of two brothers found to be compound heterozygotes for Fanconi's anaemia complementation group C mutations. |
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| Presymptomatic screening for multiple endocrine neoplasia type 2A with linked DNA markers. The MEN 2A International Collaborative Group |
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| The protein composition of rat satellite chromatin |
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| A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis |
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| Protocols in human molecular genetics |
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| Psoriasis is associated with pleiotropic susceptibility loci identified in type II diabetes and Crohn disease. |
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| Quantitative analysis of non-histone chromosomal proteins HMG 14 and HMG 17 by polyacrylamide gel electrophoresis |
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| Quantitative PCR analysis reveals a high incidence of large intragenic deletions in the FANCA gene in Spanish Fanconi anemia patients. |
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| Rapid molecular method for prenatal detection of Down's syndrome |
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| A rapid, non-radioactive screening test for fragile X mutations at the FRAXA and FRAXE loci |
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| Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry |
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| Recruiting first-degree relatives for prevention research: a comparison of clinician and proband-led methods of contact in Crohn's disease |
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| Regional localization of polymorphic markers on chromosome 10 by physical and genetic mapping |
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| The Relationship Between Environmental Exposure and Genetic Architecture of the 2q33 Locus With Esophageal Cancer in South Africa |
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| Reply |
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| Risk factors for detecting germline BRCA1 and BRCA2 founder mutations in Ashkenazi Jewish women with breast or ovarian cancer |
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| Searching for genotype-phenotype structure: using hierarchical log-linear models in Crohn disease |
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| Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility |
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| Sequence variants of the estrogen receptor (ER) gene found in breast cancer patients with ER negative and progesterone receptor positive tumors |
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| Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31 |
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| Sex stratification of an inflammatory bowel disease genome search shows male-specific linkage to the HLA region of chromosome 6 |
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| Smokers with active Crohn's disease have a clinically relevant dysbiosis of the gastrointestinal microbiota. |
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| SNP subset selection for genetic association studies. |
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| Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance |
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| Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9 |
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| Spontaneous functional correction of homozygous Fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism |
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| Stratification by CARD15 variant genotype in a genome-wide search for inflammatory bowel disease susceptibility loci |
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| Studies on the association of the high mobility group non-histone chromatin proteins with isolated nucleosomes |
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| Styl RFLP recognised by a human IRBP cDNA localised to chromosome 10. |
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| Synergy between TLR9 and NOD2 innate immune responses is lost in genetic Crohn's disease |
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| Systematic association mapping identifies NELL1 as a novel IBD disease gene |
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| Tetratricopeptide-motif-mediated interaction of FANCG with recombination proteins XRCC3 and BRCA2. |
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| Trial Protocol: Communicating DNA-based risk assessments for Crohn's disease: a randomised controlled trial assessing impact upon stopping smoking |
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| Uptake of cystic fibrosis testing in primary care: supply push or demand pull? |
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| A variant of Wiskott-Aldrich syndrome with nephropathy is linked to DXS255. |
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| Yeast two-hybrid screens imply involvement of Fanconi anemia proteins in transcription regulation, cell signaling, oxidative metabolism, and cellular transport |
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| প্রত্যুত্তর |
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