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SHAWN MCCANDLESS, MD
MD
Clinical Genetics (M.D.) Physician
NPI: 1285650150IndividualAccepts Medicare
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
35-074339(OH)0059942(CO)
CMS Specialties
PrimaryMEDICAL GENETICS AND GENOMICS
Additional
PEDIATRIC MEDICINE
Education
TEMPLE UNIVERSITY SCHOOL OF MEDICINE
Class of 1988
Research & Publications (15)
Clinical outcomes after long-term treatment with alglucosidase alfa in infants and children with advanced Pompe disease.
PMID 19287243·Genet Med·2009
3-trial
The Clinical Utility of the Behavior Rating Inventory of Executive Function (BRIEF) in the diagnosis of ADHD.
PMID 17449837·J Atten Disord·2007
8-other
A phase I/II clinical trial of enzyme replacement therapy in mucopolysaccharidosis II (Hunter syndrome).
PMID 17185020·Mol Genet Metab·2007
3-trial
The tandem mass spectrometry newborn screening experience in North Carolina: 1997-2005.
PMID 16601872·J Inherit Metab Dis·2006
8-other
A clinical report of a patient with two abnormal cell lines: 46,XX,del(21)(q22.1) and 47,XX,+3.
PMID 15580640·Am J Med Genet A·2005
5-case
The Y42H mutation in medium-chain acyl-CoA dehydrogenase, which is prevalent in babies identified by MS/MS-based newborn screening, is temperature sensitive.
PMID 15479234·Eur J Biochem·2004
4-observational
A primer on expanded newborn screening by tandem mass spectrometry.
PMID 15331249·Prim Care·2004
6-review
The burden of genetic disease on inpatient care in a children's hospital.
PMID 14681831·Am J Hum Genet·2004
8-other
Evaluation of 3-methylcrotonyl-CoA carboxylase deficiency detected by tandem mass spectrometry newborn screening.
PMID 12872837·J Inherit Metab Dis·2003
8-other
Infantile hypermethioninemia and hyperhomocysteinemia due to high methionine intake: a diagnostic trap.
PMID 12765841·Mol Genet Metab·2003
5-case
Metachromatic leukodystrophy in the Navajo: fallout of the American-Indian wars of the nineteenth century.
PMID 11424134·Am J Med Genet·2001
8-other
Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency.
PMID 11349232·Am J Hum Genet·2001
8-other
Betaine-homocysteine methyltransferase-2: cDNA cloning, gene sequence, physical mapping, and expression of the human and mouse genes.
PMID 11087663·Genomics·2000
7-preclinical
Adult with an interstitial deletion of chromosome 10 [del(10)(q25. 1q25.3)]: overlap with Coffin-Lowry syndrome.
PMID 11078556·Am J Med Genet·2000
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 13123 E 16TH AVE
AURORA, CO 80045 - Phone
- (848) 777-1234
Quick Facts
- NPI
- 1285650150
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 38
- Publications
- 15
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