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JACOB LASALLE, M.D.
M.D.
Pain Medicine (Anesthesiology) Physician
NPI: 1669883484IndividualAccepts Medicare
Specialties, Licenses & Credentials
Pain Medicine (Anesthesiology) PhysicianPrimary
Anesthesiology — Pain Medicine
Code: 207LP2900X
285753(NY)
Education
OTHER
Class of 2013
Research & Publications (20)
The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13.
PMID 18840528·Neurobiol Dis·2010
6-review
Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number.
PMID 18835857·J Med Genet·2009
5-case
Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions.
PMID 19386901·J Neurosci·2009
4-observational
Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism.
PMID 19000991·Hum Mol Genet·2009
7-preclinical
Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size.
PMID 19656775·Hum Mol Genet·2009
7-preclinical
A novel hypomorphic MECP2 point mutation is associated with a neuropsychiatric phenotype.
PMID 18989701·Hum Genet·2009
5-case
MECP2 promoter methylation and X chromosome inactivation in autism.
PMID 19132145·Autism Res·2008
8-other
Gender influences monoallelic expression of ATP10A in human brain.
PMID 18726118·Hum Genet·2008
8-other
Immunologic and neurodevelopmental susceptibilities of autism.
PMID 18394707·Neurotoxicology·2008
6-review
Analysis of protein domains and Rett syndrome mutations indicate that multiple regions influence chromatin-binding dynamics of the chromatin-associated protein MECP2 in vivo.
PMID 18334558·J Cell Sci·2008
7-preclinical
Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15.
PMID 18177502·BMC Genet·2008
5-case
Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes.
PMID 18042715·Proc Natl Acad Sci U S A·2007
8-other
The team approach to diabetes management: partnering with patients.
PMID 17991188·Int J Clin Pract Suppl·2007
6-review
15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders.
PMID 17339270·Hum Mol Genet·2007
7-preclinical
Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome.
PMID 16682435·Hum Mol Genet·2006
7-preclinical
Oral combination therapy with thiazolidinediones in type 2 diabetes.
PMID 17112324·Am J Manag Care·2006
8-other
Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients.
PMID 16859563·BMC Med Genet·2006
7-preclinical
Rett syndrome: a Rosetta stone for understanding the molecular pathogenesis of autism.
PMID 16512349·Int Rev Neurobiol·2005
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 281 BROADWAY, 2ND FLOOR
BROOKLYN, NY 10007 - Phone
- (646) 596-7386
Quick Facts
- NPI
- 1669883484
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 13
- Publications
- 20
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