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BRIAN HENDRICKSON, D.O.
D.O.
Internal Medicine Physician
NPI: 1710961412Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
34006558(OH)
Research & Publications (20)
Differences in SMN1 allele frequencies among ethnic groups within North America.
PMID 19625283·J Med Genet·2009
8-other
Anger expression and sleep quality in patients with coronary heart disease: findings from the Heart and Soul Study.
PMID 19251866·Psychosom Med·2009
3-trial
Multiple rare nonsynonymous variants in the adenomatous polyposis coli gene predispose to colorectal adenomas.
PMID 18199528·Cancer Res·2008
8-other
Evidence for common ancestral origin of a recurring BRCA1 genomic rearrangement identified in high-risk Hispanic families.
PMID 17646271·Cancer Epidemiol Biomarkers Prev·2007
8-other
Development of lentiviral vectors with regulated respiratory epithelial expression in vivo.
PMID 17575080·Am J Respir Cell Mol Biol·2007
7-preclinical
Bioinformatics and human identification in mass fatality incidents: the world trade center disaster.
PMID 17524061·J Forensic Sci·2007
8-other
Depression and inflammation in patients with coronary heart disease: findings from the Heart and Soul Study.
PMID 17434456·Biol Psychiatry·2007
8-other
Polymeric immunoglobulin receptor in intestinal immune defense against the lumen-dwelling protozoan parasite Giardia.
PMID 17056558·J Immunol·2006
7-preclinical
Protection against rotavirus shedding after intranasal immunization of mice with a chimeric VP6 protein does not require intestinal IgA.
PMID 16375942·Virology·2006
7-preclinical
Application of embryonic lethal or other obvious phenotypes to characterize the clinical significance of genetic variants found in trans with known deleterious mutations.
PMID 16267036·Cancer Res·2005
8-other
Prevalence of five previously reported and recurrent BRCA1 genetic rearrangement mutations in 20,000 patients from hereditary breast/ovarian cancer families.
PMID 15846789·Genes Chromosomes Cancer·2005
8-other
Single nucleotide polymorphisms in clinical genetic testing: the characterization of the clinical significance of genetic variants and their application in clinical research for BRCA1.
PMID 15829246·Mutat Res·2005
6-review
Genome-wide loss of heterozygosity analysis of WT1-wild-type and WT1-mutant Wilms tumors.
PMID 15761866·Genes Chromosomes Cancer·2005
8-other
A multi-exonic BRCA1 deletion identified in multiple families through single nucleotide polymorphism haplotype pair analysis and gene amplification with widely dispersed primer sets.
PMID 15681486·J Mol Diagn·2005
8-other
The potential for increased clinical sensitivity in genetic testing for polyposis colorectal cancer through the analysis of MYH mutations in North American patients.
PMID 15635083·J Med Genet·2005
8-other
Two rare novel polymorphisms in the D8S1179 and D13S317 markers and method to mitigate their impact on human identification.
PMID 15311419·Croat Med J·2004
8-other
Accurate STR allele designations at the FGA and vWA loci despite primer site polymorphisms.
PMID 15027538·J Forensic Sci·2004
8-other
A biochemical analysis demonstrates that the BRCA1 intronic variant IVS10-2A--> C is a mutation.
PMID 14513821·J Hum Genet·2003
8-other
Gastric inflammation as a feature of ulcerative colitis.
PMID 12960641·J Pediatr Gastroenterol Nutr·2003
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
- 2405 N COLUMBUS ST, SUITE 280
LANCASTER, OH 43130 - Phone
- (740) 689-4470
Quick Facts
- NPI
- 1710961412
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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