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JASMINE GAULT, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1356036073Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
A 2-base pair deletion polymorphism in the partial duplication of the alpha7 nicotinic acetylcholine gene (CHRFAM7A) on chromosome 15q14 is associated with schizophrenia.
PMID 19631623·Brain Res·2009
8-other
Cerebral cavernous malformations: somatic mutations in vascular endothelial cells.
PMID 19574835·Neurosurgery·2009
8-other
Familial cerebral cavernous malformations: Rio de Janeiro study and review of the recommendations for management.
PMID 19099113·Arq Neuropsiquiatr·2008
6-review
Spinal root arteriovenous malformations and same-segment cord cavernous malformation in familial cerebral cavernous malformation. Case report.
PMID 18928219·J Neurosurg Spine·2008
5-case
Mental health, health, and substance abuse service needs for the Native American Rehabilitation Association Northwest (NARA NW) in the Portland, Oregon metropolitan area.
PMID 18286444·Am Indian Alsk Native Ment Health Res·2008
8-other
Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts.
PMID 18060436·Neurogenetics·2008
4-observational
Spectrum of genotype and clinical manifestations in cerebral cavernous malformations.
PMID 17277691·Neurosurgery·2006
8-other
An adult case of leukoencephalopathy with intracranial calcifications and cysts.
PMID 17130435·Neurology·2006
5-case
Characterization of allelic variants at chromosome 15q14 in schizophrenia.
PMID 16417613·Genes Brain Behav·2006
4-observational
Biallelic somatic and germ line CCM1 truncating mutations in a cerebral cavernous malformation lesion.
PMID 15718512·Stroke·2005
8-other
Variations in structural protein expression and endothelial cell proliferation in relation to clinical manifestations of cerebral cavernous malformations.
PMID 15670382·Neurosurgery·2005
8-other
Multiple spinal cavernous malformations with atypical phenotype after prior irradiation: case report.
PMID 15574226·Neurosurgery·2004
5-case
What genes can teach us about human cerebrovascular malformations.
PMID 15571139·Clin Neurosurg·2004
8-other
Pathobiology of human cerebrovascular malformations: basic mechanisms and clinical relevance.
PMID 15214969·Neurosurgery·2004
6-review
Comparison of polymorphisms in the alpha7 nicotinic receptor gene and its partial duplication in schizophrenic and control subjects.
PMID 14582144·Am J Med Genet B Neuropsychiatr Genet·2003
4-observational
Differential gene expression in human cerebrovascular malformations.
PMID 12535382·Neurosurgery·2003
8-other
Association of promoter variants in the alpha7 nicotinic acetylcholine receptor subunit gene with an inhibitory deficit found in schizophrenia.
PMID 12470124·Arch Gen Psychiatry·2002
8-other
Linkage disequilibrium for schizophrenia at the chromosome 15q13-14 locus of the alpha7-nicotinic acetylcholine receptor subunit gene (CHRNA7).
PMID 11424985·Am J Med Genet·2001
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
- 1 BAYLOR PLZ
HOUSTON, TX 77030 - Phone
- (713) 798-4951
Quick Facts
- NPI
- 1356036073
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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