C G Mathew
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Explore the profile of C G Mathew including associated specialties, affiliations and a list of published articles.
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128
Citations
2696
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Recent Articles
11.
Lewis C, Whitwell S, Forbes A, Sanderson J, Mathew C, Marteau T
J Med Genet
. 2007 Jul;
44(11):689-94.
PMID: 17660460
Background: Progress has been made in identifying mutations that confer susceptibility to complex diseases, with the prospect that these genetic risks might be used in determining individual disease risk. Aim:...
12.
Mathew C
Oncogene
. 2006 Sep;
25(43):5875-84.
PMID: 16998502
Fanconi anaemia (FA) is a rare recessive disorder associated with chromosomal fragility, aplastic anaemia, congenital abnormalities and a high risk of cancer, including acute myeloid leukaemia and squamous cell carcinomas....
13.
Onnie C, Fisher S, King K, Mirza M, Roberts R, Forbes A, et al.
Genes Immun
. 2006 May;
7(5):359-65.
PMID: 16724073
Chromosome 5q31 contains a cluster of genes involved in immune response, including a 250 kb risk haplotype associated with Crohn's disease (CD) susceptibility. Recently, two functional variants in SLC22A4 and...
14.
Prescott N, Fisher S, Onnie C, Pattni R, Steer S, Sanderson J, et al.
Tissue Antigens
. 2005 Sep;
66(4):318-20.
PMID: 16185328
A single-nucleotide polymorphism (C1858T) causing an amino acid substitution (R620W) in the lymphoid protein tyrosine phosphatase gene PTPN22 has been implicated in type 1 diabetes, rheumatoid arthritis, systemic lupus erythematosus,...
15.
Mirza M, Fisher S, Onnie C, Lewis C, Mathew C, Sanderson J, et al.
Gut
. 2005 Jul;
54(8):1205-6.
PMID: 16009698
No abstract available.
16.
van Heel D, Ghosh S, Hunt K, Mathew C, Forbes A, Jewell D, et al.
Gut
. 2005 Jun;
54(11):1553-7.
PMID: 15928043
Background: Nucleotide binding oligomerisation domain 2 (NOD2; also known as CARD15) mutations are associated with Crohn's disease but how mutations cause disease is poorly understood. Innate immune responses are reportedly...
17.
New H, Cale C, Tischkowitz M, Jones A, Telfer P, Veys P, et al.
Pediatr Blood Cancer
. 2004 Dec;
44(5):494-9.
PMID: 15593232
Background: Fanconi anaemia (FA) and Nijmegen breakage syndrome (NBS) are rare chromosomal instability disorders with overlapping clinical features. It has recently been shown that, like FA, NBS is also associated...
18.
Cuthbert A, Fisher S, Lewis C, Mathew C, Sanderson J, Forbes A
Gut
. 2004 Aug;
53(9):1386.
PMID: 15306604
No abstract available.
19.
Callen E, Tischkowitz M, Creus A, Marcos R, Bueren J, Casado J, et al.
Cytogenet Genome Res
. 2004 May;
104(1-4):341-5.
PMID: 15162062
Fanconi anaemia is an autosomal recessive disease characterized by chromosome fragility, multiple congenital abnormalities, progressive bone marrow failure and a high predisposition to develop malignancies. Most of the Fanconi anaemia...
20.
Tischkowitz M, Morgan N, Grimwade D, Eddy C, Ball S, Vorechovsky I, et al.
Leukemia
. 2004 Jan;
18(3):420-5.
PMID: 14749703
Fanconi anemia (FA) is an autosomal recessive chromosomal instability disorder caused by mutations in one of seven known genes (FANCA,C,D2,E,F,G and BRCA2). Mutations in the FANCA gene are the most...