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AIMEE VERNER, M.D.
M.D.
Cornea and External Diseases Specialist Physician
NPI: 1063859817IndividualAccepts Medicare
Specialties, Licenses & Credentials
Ophthalmology — Cornea and External Diseases Specialist
Code: 207WX0120X
DR.0060488(CO)
CMS Specialties
PrimaryOPHTHALMOLOGY
Education
UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE
Class of 2013
Research & Publications (20)
Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population.
PMID 17805225·Eur J Hum Genet·2008
8-other
Effect of taurine supplementation on growth and development in preterm or low birth weight infants.
PMID 17943882·Cochrane Database Syst Rev·2007
1-meta
Sex-specific linkage to total serum immunoglobulin E in families of children with asthma in Costa Rica.
PMID 17142250·Hum Mol Genet·2007
8-other
Genome-wide linkage analysis of pulmonary function in families of children with asthma in Costa Rica.
PMID 17099076·Thorax·2007
8-other
Influence of maternal diabetes mellitus on fetal iron status.
PMID 17095546·Arch Dis Child Fetal Neonatal Ed·2007
8-other
Genome-wide detection and characterization of positive selection in human populations.
PMID 17943131·Nature·2007
8-other
Significant linkage to airway responsiveness on chromosome 12q24 in families of children with asthma in Costa Rica.
PMID 17024367·Hum Genet·2007
8-other
Spectrum of mutations in mut methylmalonic acidemia and identification of a common Hispanic mutation and haplotype.
PMID 16281286·Hum Mutat·2006
8-other
Mutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome).
PMID 17033958·Am J Hum Genet·2006
7-preclinical
An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22.
PMID 15668823·Hum Genet·2005
8-other
The c.419-420insA in the MTP gene is associated with abetalipoproteinemia among French-Canadians.
PMID 14741197·Mol Genet Metab·2004
8-other
Localisation of a gene for mucopolysaccharidosis IIIC to the pericentromeric region of chromosome 8.
PMID 15591281·J Med Genet·2004
8-other
Genome-wide scan in Portuguese Island families implicates multiple loci in bipolar disorder: fine mapping adds support on chromosomes 6 and 11.
PMID 15108176·Am J Med Genet B Neuropsychiatr Genet·2004
8-other
Genome-wide scan in Portuguese Island families identifies 5q31-5q35 as a susceptibility locus for schizophrenia and psychosis.
PMID 14699422·Mol Psychiatry·2004
8-other
A survey of genetic and epigenetic variation affecting human gene expression.
PMID 14583597·Physiol Genomics·2004
8-other
Chromosome 6q25 is linked to susceptibility to leprosy in a Vietnamese population.
PMID 12577057·Nat Genet·2003
8-other
[Characteristics of mitochondria and myocardium ultrastructure of rats following chronic incorporation of cesium radionuclides 137 Cs].
PMID 12442592·Aviakosm Ekolog Med·2002
7-preclinical
[Mitochondrial oxidation and ultrastructure of the myocardium on a background of incorporation of cesium radionuclides].
PMID 12098951·Aviakosm Ekolog Med·2002
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
- 1400 DRY CREEK DR
LONGMONT, CO 80503 - Phone
- (303) 772-3300
Quick Facts
- NPI
- 1063859817
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 13
- Publications
- 20
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