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KEVIN GUNDERSON, DO
DO
Student in an Organized Health Care Education/Training Program
NPI: 1457093635Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Assessment of the performance of the American Urological Association symptom score in 2 distinct patient populations.
PMID 19013602·J Urol·2009
4-observational
Allele-specific gene expression patterns in primary leukemic cells reveal regulation of gene expression by CpG site methylation.
PMID 18997001·Genome Res·2009
8-other
Identification of critical regions for clinical features of distal 10q deletion syndrome.
PMID 19558528·Clin Genet·2009
5-case
Increased LIS1 expression affects human and mouse brain development.
PMID 19136950·Nat Genet·2009
7-preclinical
Single nucleotide polymorphism-based genome-wide chromosome copy change, loss of heterozygosity, and aneuploidy in Barrett's esophagus neoplastic progression.
PMID 19138988·Cancer Prev Res (Phila)·2008
8-other
Comparison of the Agilent, ROMA/NimbleGen and Illumina platforms for classification of copy number alterations in human breast tumors.
PMID 18691401·BMC Genomics·2008
4-observational
Mutations targeting intermodular interfaces or calcium binding destabilize the thrombospondin-2 signature domain.
PMID 18682400·J Biol Chem·2008
7-preclinical
Whole genome genotyping technologies on the BeadArray platform.
PMID 17225249·Biotechnol J·2007
8-other
Characterization of seed-specific benzoyloxyglucosinolate mutations in Arabidopsis thaliana.
PMID 17651367·Plant J·2007
8-other
Mosaic tetrasomy 12p with triplication of 12p detected by array-based comparative genomic hybridization of peripheral blood DNA.
PMID 18000900·Am J Med Genet A·2007
5-case
Genome-wide detection and characterization of positive selection in human populations.
PMID 17943131·Nature·2007
8-other
Characterization of de novo microdeletions involving 17q11.2q12 identified through chromosomal comparative genomic hybridization.
PMID 17916097·Clin Genet·2007
5-case
Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region.
PMID 17666889·Genet Med·2007
5-case
Immunochemical analysis of the structure of the signature domains of thrombospondin-1 and thrombospondin-2 in low calcium concentrations.
PMID 17620335·J Biol Chem·2007
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1431 SW 1ST AVE
OCALA, FL 34471 - Phone
- (352) 401-1000
Quick Facts
- NPI
- 1457093635
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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