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MAERA STRATTON, MD
MD
Neurology with Special Qualifications in Child Neurology Physician
NPI: 1619504875Individual
Specialties, Licenses & Credentials
Pediatrics Physician
Pediatrics
Code: 208000000X
9984(MD)
Neurology with Special Qualifications in Child Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology with Special Qualifications in Child Neurology
Code: 2084N0402X
9984(MD)D0102729(MD)
Research & Publications (20)
Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.
PMID 19330027·Nat Genet·2009
8-other
Lessons learnt from large-scale exon re-sequencing of the X chromosome.
PMID 19297402·Hum Mol Genet·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
Brain sex differences and hormone influences: a moving experience?
PMID 19207813·J Neuroendocrinol·2009
6-review
Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer.
PMID 19330029·Nat Genet·2009
8-other
Younger age-at-diagnosis for familial malignant testicular germ cell tumor.
PMID 19609727·Fam Cancer·2009
4-observational
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.
PMID 19377476·Nat Genet·2009
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
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
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
Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes.
PMID 18404279·Hum Genet·2008
8-other
The Catalogue of Somatic Mutations in Cancer (COSMIC).
PMID 18428421·Curr Protoc Hum Genet·2008
8-other
Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation.
PMID 18455129·Am J Hum Genet·2008
8-other
Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.
PMID 18252223·Am J Hum Genet·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
- 200 N WOLFE ST, STE 2158
BALTIMORE, MD 21287 - Phone
- (410) 955-4259
Quick Facts
- NPI
- 1619504875
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 1
- Publications
- 20
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