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WILLIAM HIGHSMITH, M.D.
M.D.
Family Medicine Physician
NPI: 1700897600Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
C8440(AR)
Research & Publications (20)
Conversion Technology for the separation of maternal and paternal copies of any autosomal chromosome in somatic cell hybrids.
PMID 18428411·Curr Protoc Hum Genet·2007
7-preclinical
Development of genomic reference materials for cystic fibrosis genetic testing.
PMID 19359498·J Mol Diagn·2009
8-other
Solid phase and solution synthesis of NvocLys(CO(CH2)5NH-NBD)OCH2CN, a trifunctional fluorescent lysine derivative.
PMID 18365133·Amino Acids·2009
8-other
Consensus characterization of 16 FMR1 reference materials: a consortium study.
PMID 18165276·J Mol Diagn·2008
8-other
LOC387715/HTRA1 and complement factor H variants in patients with age-related macular degeneration seen at the mayo clinic.
PMID 18161619·Ophthalmic Genet·2007
8-other
Comparison of three methods for genotyping the UGT1A1 (TA)n repeat polymorphism.
PMID 17459361·Clin Biochem·2007
4-observational
RET proto-oncogene genotyping using unlabeled probes, the masking technique, and amplicon high-resolution melting analysis.
PMID 17384210·J Mol Diagn·2007
8-other
Relationship between age-related macular degeneration-associated variants of complement factor H and LOC387715 with coronary artery disease.
PMID 17352366·Mayo Clin Proc·2007
8-other
A splice-site mutation in CCM1/KRIT1 is associated with retinal and cerebral cavernous hemangioma.
PMID 17148043·Ophthalmic Genet·2006
5-case
Molecular diagnosis of Beckwith-Wiedemann syndrome using quantitative methylation-sensitive polymerase chain reaction.
PMID 17079879·Genet Med·2006
8-other
Diagnosis of alpha-1-antitrypsin deficiency: An algorithm of quantification, genotyping, and phenotyping.
PMID 17053153·Clin Chem·2006
8-other
Mutation scanning of the RET protooncogene using high-resolution melting analysis.
PMID 16391329·Clin Chem·2006
8-other
MYH Y165C and G382D mutations in hepatocellular carcinoma and cholangiocarcinoma patients.
PMID 16292541·J Cancer Res Clin Oncol·2006
8-other
Developing a sustainable process to provide quality control materials for genetic testing.
PMID 16247292·Genet Med·2005
6-review
Cystic fibrosis transmembrane regulator gene carrier status is a risk factor for young onset pancreatic adenocarcinoma.
PMID 16227367·Gut·2005
8-other
A CFTR mutation (D1152H) in a family with mild lung disease and normal sweat chlorides.
PMID 15952991·Clin Genet·2005
8-other
Detection of ultra-low levels of pathologic prion protein in scrapie infected hamster brain homogenates using real-time immuno-PCR.
PMID 15921765·J Virol Methods·2005
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
- 21 OPPORTUNITY DR
SHERIDAN, AR 72150 - Phone
- (870) 942-9835
Quick Facts
- NPI
- 1700897600
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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