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NIDA LAURIN, M.D.
M.D.
Neurology Physician
NPI: 1306887963IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
35284(AZ)
CMS Specialties
PrimaryNEUROLOGY
Education
OTHER
Class of 1993
Research & Publications (17)
Chromosome 5 and Gilles de la Tourette syndrome: Linkage in a large pedigree and association study of six candidates in the region.
PMID 18454440·Am J Med Genet B Neuropsychiatr Genet·2009
8-other
Association study for genes at chromosome 5p13-q11 in attention deficit hyperactivity disorder.
PMID 18081024·Am J Med Genet B Neuropsychiatr Genet·2008
8-other
No evidence for genetic association between DARPP-32 (PP1R1B) polymorphisms and attention deficit hyperactivity disorder.
PMID 17948899·Am J Med Genet B Neuropsychiatr Genet·2008
8-other
Investigation of the G protein subunit Galphaolf gene (GNAL) in attention deficit/hyperactivity disorder.
PMID 17166517·J Psychiatr Res·2008
8-other
Association study of the nicotinic acetylcholine receptor alpha4 subunit gene, CHRNA4, in attention-deficit hyperactivity disorder.
PMID 17504247·Genes Brain Behav·2008
8-other
Estrogen receptor-related receptor-alpha (ERR-alpha) is dysregulated in inflammatory arthritis.
PMID 18927192·Rheumatology (Oxford)·2008
7-preclinical
No preferential transmission of paternal alleles at risk genes in attention-deficit hyperactivity disorder.
PMID 17325714·Mol Psychiatry·2007
8-other
Association study of the brain-derived neurotropic factor (BDNF) gene in attention deficit hyperactivity disorder.
PMID 17918236·Am J Med Genet B Neuropsychiatr Genet·2007
8-other
Association of the dopamine receptor D1 gene, DRD1, with inattention symptoms in families selected for reading problems.
PMID 17310237·Mol Psychiatry·2007
8-other
Sequestosome 1: mutation frequencies, haplotypes, and phenotypes in familial Paget's disease of bone.
PMID 17229007·J Bone Miner Res·2006
8-other
Association of the calcyon gene (DRD1IP) with attention deficit/hyperactivity disorder.
PMID 16172615·Mol Psychiatry·2005
3-trial
Human hormone-sensitive lipase (HSL): expression in white fat corrects the white adipose phenotype of HSL-deficient mice.
PMID 15961788·J Lipid Res·2005
7-preclinical
Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone.
PMID 11992264·Am J Hum Genet·2002
8-other
Paget disease of bone: mapping of two loci at 5q35-qter and 5q31.
PMID 11473345·Am J Hum Genet·2001
8-other
The adipose tissue phenotype of hormone-sensitive lipase deficiency in mice.
PMID 11316346·Obes Res·2001
7-preclinical
The hormone-sensitive lipase gene is transcribed from at least five alternative first exons in mouse adipose tissue.
PMID 11063252·Mamm Genome·2000
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 9817 N 95TH ST STE 110
SCOTTSDALE, AZ 85258 - Phone
- (480) 779-3997
Quick Facts
- NPI
- 1306887963
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 33
- Publications
- 17
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