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NATHAN PRESCOTT, D.O.
D.O.
Emergency Medicine Physician
NPI: 1326367657IndividualAccepts Medicare
Specialties, Licenses & Credentials
General Practice Physician
General Practice
Code: 208D00000X
P9446(TX)
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
P9446(TX)
Education
OTHER
Class of 2010
Research & Publications (20)
Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship.
PMID 19068216·Gastroenterology·2009
8-other
Searching for genotype-phenotype structure: using hierarchical log-linear models in Crohn disease.
PMID 19185283·Am J Hum Genet·2009
8-other
Novel isoforms of the CARD8 (TUCAN) gene evade a nonsense mutation.
PMID 18212821·Eur J Hum Genet·2008
8-other
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
Psoriasis is associated with pleiotropic susceptibility loci identified in type II diabetes and Crohn disease.
PMID 17993580·J Med Genet·2008
8-other
Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease.
PMID 18438406·Nat Genet·2008
4-observational
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
PMID 18587394·Nat Genet·2008
1-meta
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.
PMID 17200669·Nat Genet·2007
8-other
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
IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease.
PMID 17484863·Gastroenterology·2007
4-observational
SH3BP2 is rarely mutated in exon 9 in giant cell lesions outside cherubism.
PMID 17545756·Clin Orthop Relat Res·2007
8-other
Sequence variants in the genes for the interleukin-23 receptor (IL23R) and its ligand (IL12B) confer protection against psoriasis.
PMID 17587057·Hum Genet·2007
4-observational
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
PMID 17684544·PLoS One·2007
8-other
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
PMID 17554261·Nat Genet·2007
7-preclinical
A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5.
PMID 17484864·Gastroenterology·2007
8-other
Bone marrow phospho-STAT5 expression in non-CML chronic myeloproliferative disorders correlates with JAK2 V617F mutation and provides evidence of in vivo JAK2 activation.
PMID 17255768·Am J Surg Pathol·2007
8-other
Combined evidence from three large British Association studies rejects TUCAN/CARD8 as an IBD susceptibility gene.
PMID 17484911·Gastroenterology·2007
8-other
A new rabbit monoclonal antibody (4B5) for the immunohistochemical (IHC) determination of the HER2 status in breast cancer: comparison with CB11, fluorescence in situ hybridization (FISH), and interlaboratory reproducibility.
PMID 17536315·Appl Immunohistochem Mol Morphol·2007
4-observational
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.
PMID 17952073·Nat Genet·2007
2-rct
Loss of breast cancer metastasis suppressor 1 protein expression predicts reduced disease-free survival in subsets of breast cancer patients.
PMID 17121889·Clin Cancer Res·2006
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 1600 HOSPITAL PKWY
BEDFORD, TX 76022 - Phone
- (817) 848-4000
Quick Facts
- NPI
- 1326367657
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 2
- Years in Practice
- 16
- Publications
- 20
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