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MEGAN SORICH, D.O.
D.O.
Orthopaedic Surgery Physician
NPI: 1366705147IndividualAccepts Medicare
Specialties, Licenses & Credentials
Orthopaedic Surgery PhysicianPrimary
Orthopaedic Surgery
Code: 207X00000X
R2230(TX)63573(MN)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Education
OTHER
Class of 2012
Research & Publications (14)
Comparison data sets for benchmarking QSAR methodologies in lead optimization.
PMID 19569715·J Chem Inf Model·2009
4-observational
Partial charge calculation method affects CoMFA QSAR prediction accuracy.
PMID 19239274·J Chem Inf Model·2009
8-other
Effect of steric molecular field settings on CoMFA predictivity.
PMID 18038162·J Mol Model·2008
8-other
In vivo response to methotrexate forecasts outcome of acute lymphoblastic leukemia and has a distinct gene expression profile.
PMID 18416598·PLoS Med·2008
8-other
Recent advances in the in silico modelling of UDP glucuronosyltransferase substrates.
PMID 18220572·Curr Drug Metab·2008
6-review
Thirty-count breathlessness score: reliability, sensitivity, specificity and validity.
PMID 17875062·Respirology·2007
8-other
A critical analysis of barriers to the clinical implementation of pharmacogenomics.
PMID 18473000·Ther Clin Risk Manag·2007
8-other
Multiple pharmacophores for the investigation of human UDP-glucuronosyltransferase isoform substrate selectivity.
PMID 14742671·Mol Pharmacol·2004
8-other
Towards integrated ADME prediction: past, present and future directions for modelling metabolism by UDP-glucuronosyltransferases.
PMID 15182810·J Mol Graph Model·2004
6-review
Predicting human drug glucuronidation parameters: application of in vitro and in silico modeling approaches.
PMID 14744236·Annu Rev Pharmacol Toxicol·2004
6-review
Rapid prediction of chemical metabolism by human UDP-glucuronosyltransferase isoforms using quantum chemical descriptors derived with the electronegativity equalization method.
PMID 15456275·J Med Chem·2004
8-other
Pharmacophore and quantitative structure-activity relationship modeling: complementary approaches for the rationalization and prediction of UDP-glucuronosyltransferase 1A4 substrate selectivity.
PMID 12699380·J Med Chem·2003
8-other
In silico insights: chemical and structural characteristics associated with uridine diphosphate-glucuronosyltransferase substrate selectivity.
PMID 14678246·Clin Exp Pharmacol Physiol·2003
8-other
Pharmacophore and quantitative structure activity relationship modelling of UDP-glucuronosyltransferase 1A1 (UGT1A1) substrates.
PMID 12439224·Pharmacogenetics·2002
8-other
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
- 1715 S FRIENDSWOOD DR FL 4
FRIENDSWOOD, TX 77546 - Phone
- (281) 482-5695
Quick Facts
- NPI
- 1366705147
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 2
- Years in Practice
- 14
- Publications
- 14
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