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CHRISTINE MATHEW, MD
MD
Pediatrics Physician
NPI: 1760619894Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
BP10035442(TX)
Research & Publications (20)
Searching for genotype-phenotype structure: using hierarchical log-linear models in Crohn disease.
PMID 19185283·Am J Hum Genet·2009
8-other
Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship.
PMID 19068216·Gastroenterology·2009
8-other
FANCG promotes formation of a newly identified protein complex containing BRCA2, FANCD2 and XRCC3.
PMID 18212739·Oncogene·2008
7-preclinical
Diverse effects of the CARD15 and IBD5 loci on clinical phenotype in 630 patients with Crohn's disease.
PMID 18090989·Eur J Gastroenterol Hepatol·2008
4-observational
Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease.
PMID 18438406·Nat Genet·2008
4-observational
Psoriasis is associated with pleiotropic susceptibility loci identified in type II diabetes and Crohn disease.
PMID 17993580·J Med Genet·2008
8-other
New links to the pathogenesis of Crohn disease provided by genome-wide association scans.
PMID 17968351·Nat Rev Genet·2008
6-review
Automated immunochemical quantitation of haemoglobin in faeces collected on cards for screening for colorectal cancer.
PMID 18467371·Gut·2008
8-other
Novel isoforms of the CARD8 (TUCAN) gene evade a nonsense mutation.
PMID 18212821·Eur J Hum Genet·2008
8-other
Gender-stratified analysis of DLG5 R30Q in 4707 patients with Crohn disease and 4973 controls from 12 Caucasian cohorts.
PMID 17693570·J Med Genet·2008
8-other
Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility.
PMID 18836448·Nat Genet·2008
8-other
Cancer incidence in relatives of British Fanconi Anaemia patients.
PMID 18786261·BMC Cancer·2008
8-other
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
PMID 18587394·Nat Genet·2008
1-meta
Functional characterization of two novel 5' untranslated exons reveals a complex regulation of NOD2 protein expression.
PMID 18096043·BMC Genomics·2007
8-other
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.
PMID 17200671·Nat Genet·2007
8-other
Identification, evolution, and association study of a novel promoter and first exon of the human NOD2 (CARD15) gene.
PMID 17719742·Genomics·2007
7-preclinical
Investigation of association of the DLG5 gene with phenotypes of inflammatory bowel disease in the British population.
PMID 16944184·Int J Colorectal Dis·2007
8-other
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.
PMID 17200669·Nat Genet·2007
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1300 MAIN ST
RICHMOND, TX 77469 - Phone
- (281) 341-9696
Quick Facts
- NPI
- 1760619894
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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