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DR. JOY SKAUG MD
MD
Family Medicine Physician
NPI: 1982047379IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
E-9004(AR)
Education
UNIVERSITY OF ARKANSAS COLLEGE OF MEDICINE
Class of 2013
Research & Publications (14)
Structural variation of chromosomes in autism spectrum disorder.
PMID 18252227·Am J Hum Genet·2008
4-observational
Contribution of SHANK3 mutations to autism spectrum disorder.
PMID 17999366·Am J Hum Genet·2007
4-observational
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
PMID 17322880·Nat Genet·2007
4-observational
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia.
PMID 17033973·Am J Hum Genet·2006
5-case
Molecular basis for expression of common and rare fragile sites.
PMID 14517285·Mol Cell Biol·2003
8-other
Identification of a novel lipase gene mutated in lpd mice with hypertriglyceridemia and associated with dyslipidemia in humans.
PMID 12719377·Hum Mol Genet·2003
7-preclinical
A third human carnitine/organic cation transporter (OCTN3) as a candidate for the 5q31 Crohn's disease locus (IBD5).
PMID 12535646·Biochem Biophys Res Commun·2003
7-preclinical
Cloning and characterization of three novel genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: candidate genes for ALS2.
PMID 11161814·Genomics·2001
8-other
Murine phosphatidylserine-specific phospholipase A1 (Ps-pla1) maps to chromosome 16 but is distinct from the lpd (lipid defect) locus.
PMID 11210182·Mamm Genome·2001
7-preclinical
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.
PMID 11586298·Nat Genet·2001
7-preclinical
Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing.
PMID 10973252·Nat Genet·2000
8-other
The human homologue of flamingo, EGFL2, encodes a brain-expressed large cadherin-like protein with epidermal growth factor-like domains, and maps to chromosome 1p13.3-p21.1.
PMID 10907856·DNA Res·2000
7-preclinical
Small GTPase Rac1: structure, localization, and expression of the human gene.
PMID 11062023·Biochem Biophys Res Commun·2000
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
- 1001 W PARKER RD, STE B
JONESBORO, AR 72404 - Phone
- (870) 972-8181
Quick Facts
- NPI
- 1982047379
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 13
- Publications
- 14
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