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GERALD ROULEAU, MD
MD
Anesthesiology Physician
NPI: 1275110017Individual
Specialties, Licenses & Credentials
Anesthesiology PhysicianPrimary
Anesthesiology
Code: 207L00000X
75426(TN)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
TL.0009418(CO)
Research & Publications (20)
Factors related to quality of life in treatment-adherent, successfully treated HIV patients in France.
PMID 19543547·Open Nurs J·2009
8-other
De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy.
PMID 19557857·Ann Neurol·2009
5-case
Global brain gene expression analysis links glutamatergic and GABAergic alterations to suicide and major depression.
PMID 19668376·PLoS One·2009
7-preclinical
Narcolepsy is strongly associated with the T-cell receptor alpha locus.
PMID 19412176·Nat Genet·2009
7-preclinical
[Mutations in the HSN2 exon of WNK1 cause hereditary sensory neuropathy type II].
PMID 19361385·Med Sci (Paris)·2009
8-other
Recent advances in the genetics of amyotrophic lateral sclerosis.
PMID 19348708·Curr Neurol Neurosci Rep·2009
6-review
A novel TYMP mutation in a French Canadian patient with mitochondrial neurogastrointestinal encephalomyopathy.
PMID 19523753·Clin Neurol Neurosurg·2009
5-case
No association between SRGAP3/MEGAP haploinsufficiency and mental retardation.
PMID 19433673·Arch Neurol·2009
8-other
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.
PMID 19251627·Science·2009
7-preclinical
Greater rupture risk for familial as compared to sporadic unruptured intracranial aneurysms.
PMID 19228834·Stroke·2009
4-observational
No TARDBP mutations in a French Canadian population of patients with Parkinson disease.
PMID 19204172·Arch Neurol·2009
8-other
Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation.
PMID 19196676·N Engl J Med·2009
8-other
Genetic analysis of Factor XII and bradykinin catabolic enzymes in a family with estrogen-dependent inherited angioedema.
PMID 19178938·J Allergy Clin Immunol·2009
8-other
MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels.
PMID 19126776·Hum Mol Genet·2009
8-other
The proportion of mutations predicted to have a deleterious effect differs between gain and loss of function genes in neurodegenerative disease.
PMID 19105188·Hum Mutat·2009
8-other
A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS.
PMID 19321847·Neurology·2009
1-meta
Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis.
PMID 18931000·J Med Genet·2009
8-other
Autosomal-dominant locus for Restless Legs Syndrome in French-Canadians on chromosome 16p12.1.
PMID 18946881·Mov Disord·2009
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
- 1211 Medical Center Dr
Nashville, TN 37232 - Phone
- (615) 343-5860
Quick Facts
- NPI
- 1275110017
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 2
- Publications
- 20
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