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MICHAEL STRATTON, DO
DO
Student in an Organized Health Care Education/Training Program
NPI: 1710169966IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
CMS Specialties
PrimaryANESTHESIOLOGY
Education
OTHER
Class of 2007
Research & Publications (20)
Prevention of venous thromboembolism: adherence to the 1995 American College of Chest Physicians consensus guidelines for surgical patients.
PMID 10668835·Arch Intern Med·2000
4-observational
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.
PMID 19377476·Nat Genet·2009
8-other
Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.
PMID 19330027·Nat Genet·2009
8-other
Younger age-at-diagnosis for familial malignant testicular germ cell tumor.
PMID 19609727·Fam Cancer·2009
4-observational
Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer.
PMID 19330029·Nat Genet·2009
8-other
Brain sex differences and hormone influences: a moving experience?
PMID 19207813·J Neuroendocrinol·2009
6-review
LKB1/KRAS mutant lung cancers constitute a genetic subset of NSCLC with increased sensitivity to MAPK and mTOR signalling inhibition.
PMID 19165201·Br J Cancer·2009
8-other
Lessons learnt from large-scale exon re-sequencing of the X chromosome.
PMID 19297402·Hum Mol Genet·2009
6-review
The Catalogue of Somatic Mutations in Cancer (COSMIC).
PMID 18428421·Curr Protoc Hum Genet·2008
8-other
Subclonal phylogenetic structures in cancer revealed by ultra-deep sequencing.
PMID 18723673·Proc Natl Acad Sci U S A·2008
8-other
Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing.
PMID 18438408·Nat Genet·2008
8-other
In vitro differential sensitivity of melanomas to phenothiazines is based on the presence of codon 600 BRAF mutation.
PMID 18524847·Mol Cancer Ther·2008
8-other
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment.
PMID 18469813·Nat Genet·2008
4-observational
Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation.
PMID 18455129·Am J Hum Genet·2008
8-other
A Ca2+-sensing molecular switch based on alternate frame protein folding.
PMID 18947182·ACS Chem Biol·2008
8-other
Exclusion of biglycan mutations in a cohort of patients with neuromuscular disorders.
PMID 18602826·Neuromuscul Disord·2008
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
- 4502 MEDICAL DR
SAN ANTONIO, TX 78229 - Phone
- (210) 358-2015
Quick Facts
- NPI
- 1710169966
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 19
- Publications
- 20
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