Back to Search
BRYAN TRAYNOR, M.D.
M.D.
Neurology Physician
NPI: 1588693584Individual
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
D63874(MD)
Research & Publications (20)
No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort.
PMID 19632744·Neurobiol Aging·2011
8-other
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis.
PMID 19193627·Hum Mol Genet·2009
8-other
SNCA variants are associated with increased risk for multiple system atrophy.
PMID 19475667·Ann Neurol·2009
8-other
Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration.
PMID 19217189·Neurobiol Aging·2009
8-other
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation.
PMID 19450904·Neurobiol Aging·2009
8-other
Extended tracts of homozygosity identify novel candidate genes associated with late-onset Alzheimer's disease.
PMID 19271249·Neurogenetics·2009
8-other
Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.
PMID 18084291·Nat Genet·2008
8-other
Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues.
PMID 18079297·J Neurol Neurosurg Psychiatry·2008
6-review
Amyotrophic lateral sclerosis and soccer: a different epidemiological approach strengthen the previous findings.
PMID 17996254·J Neurol Sci·2008
8-other
A genome-wide association study of sporadic ALS in a homogenous Irish population.
PMID 18057069·Hum Mol Genet·2008
4-observational
Epidemiology and clinical features of amyotrophic lateral sclerosis in Ireland between 1995 and 2004.
PMID 17634215·J Neurol Neurosurg Psychiatry·2008
8-other
Current and future directions in genomics of amyotrophic lateral sclerosis.
PMID 18625410·Phys Med Rehabil Clin N Am·2008
6-review
A common haplotype within the PON1 promoter region is associated with sporadic ALS.
PMID 18618303·Amyotroph Lateral Scler·2008
8-other
TDP-43 is not a common cause of sporadic amyotrophic lateral sclerosis.
PMID 18545701·PLoS One·2008
8-other
Genotype, haplotype and copy-number variation in worldwide human populations.
PMID 18288195·Nature·2008
8-other
The heterogeneity of amyotrophic lateral sclerosis: a possible explanation of treatment failure.
PMID 18220753·Curr Med Chem·2007
6-review
Amyotrophic lateral sclerosis: an emerging era of collaborative gene discovery.
PMID 18060051·PLoS One·2007
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
- 600 N WOLFE ST
BALTIMORE, MD 21287 - Phone
- (410) 955-5000
Quick Facts
- NPI
- 1588693584
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile