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JASON DEYOUNG, PHARMD
PHARMD
Pharmacist
NPI: 1982248738Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
26021432A(IN)
Research & Publications (20)
Polymorphisms in the GRIA1 gene region in psychotic bipolar disorder.
PMID 18484081·Am J Med Genet B Neuropsychiatr Genet·2009
8-other
A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees.
PMID 19319892·Am J Med Genet B Neuropsychiatr Genet·2009
8-other
Temporal trends and patterns of early clopidogrel use across the spectrum of acute coronary syndromes.
PMID 19332190·Am Heart J·2009
4-observational
Mechanism of extreme ultraviolet photoresist development with a supercritical CO2 compatible salt.
PMID 19466780·Langmuir·2009
8-other
Effect of bar-code-assisted medication administration on medication error rates in an adult medical intensive care unit.
PMID 19498127·Am J Health Syst Pharm·2009
8-other
Phylogenomic analysis of the emergence of GC-rich transcription elements.
PMID 17925442·Proc Natl Acad Sci U S A·2007
7-preclinical
Medication discrepancies affecting senior patients at hospital admission.
PMID 16595814·Am J Health Syst Pharm·2006
8-other
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies.
PMID 16582909·Nat Genet·2006
8-other
Results of a SNP genome screen in a large Costa Rican pedigree segregating for severe bipolar disorder.
PMID 16652356·Am J Med Genet B Neuropsychiatr Genet·2006
8-other
A clinical rating scale for Batten disease: reliable and relevant for clinical trials.
PMID 16043799·Neurology·2005
8-other
Characterization of mutations in ATP8B1 associated with hereditary cholestasis.
PMID 15239083·Hepatology·2004
8-other
Re-screening serotonin receptors for genetic variants identifies population and molecular genetic complexity.
PMID 14681923·Am J Med Genet B Neuropsychiatr Genet·2004
4-observational
PharmGKB update: III. Genetic variants of SLC22A1, solute carrier family 22 (organic cation transporter), member 1.
PMID 15169925·Pharmacol Rev·2004
8-other
Natural variation in human membrane transporter genes reveals evolutionary and functional constraints.
PMID 12719533·Proc Natl Acad Sci U S A·2003
8-other
PharmGKB update: I. Genetic variants of the organic cation transporter 2 (OCT2, SLC22A2).
PMID 12869664·Pharmacol Rev·2003
6-review
Sequence diversity and haplotype structure in the human ABCB1 (MDR1, multidrug resistance transporter) gene.
PMID 12893986·Pharmacogenetics·2003
8-other
SNP analysis and presentation in the Pharmacogenetics of Membrane Transporters Project.
PMID 12603056·Pac Symp Biocomput·2003
7-preclinical
Etchant solutions for the removal of Cu(0) in a supercritical CO2-based "dry" chemical mechanical planarization process for device fabrication.
PMID 12708839·J Am Chem Soc·2003
8-other
Evolutionary conservation predicts function of variants of the human organic cation transporter, OCT1.
PMID 12719534·Proc Natl Acad Sci U S A·2003
7-preclinical
Polymorphisms in a human kidney xenobiotic transporter, OCT2, exhibit altered function.
PMID 12142729·Pharmacogenetics·2002
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
- 5925 W 71ST ST STE B
INDIANAPOLIS, IN 46278 - Phone
- (317) 614-6182
Quick Facts
- NPI
- 1982248738
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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