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AMANDA GRIFFITH, D.O.
D.O.
Pulmonary Disease Physician
NPI: 1659501633IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
DO1685(NV)
Critical Care Medicine (Internal Medicine) Physician
Internal Medicine — Critical Care Medicine
Code: 207RC0200X
DO1685(NV)
Pulmonary Disease PhysicianPrimary
Internal Medicine — Pulmonary Disease
Code: 207RP1001X
DO1685(NV)
Education
OTHER
Class of 2009
Research & Publications (20)
DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3.
PMID 19603065·Eur J Hum Genet·2010
8-other
Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism.
PMID 18952485·Parkinsonism Relat Disord·2009
8-other
Evaluation of the thyroid in patients with hearing loss and enlarged vestibular aqueducts.
PMID 19620588·Arch Otolaryngol Head Neck Surg·2009
8-other
Increased thymus- and decreased parathyroid-fated organ domains in Splotch mutant embryos.
PMID 19135046·Dev Biol·2009
7-preclinical
Do mutations of the Pendred syndrome gene, SLC26A4, confer resistance to asthma and hypertension?
PMID 19289392·J Med Genet·2009
8-other
Efficient molecular genetic diagnosis of enlarged vestibular aqueducts in East Asians.
PMID 19645628·Genet Test Mol Biomarkers·2009
7-preclinical
Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?
PMID 19204907·Hum Mutat·2009
7-preclinical
Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairment.
PMID 19180119·J Hum Genet·2009
8-other
Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan.
PMID 19250381·Clin Genet·2009
8-other
Segregation of enlarged vestibular aqueducts in families with non-diagnostic SLC26A4 genotypes.
PMID 19578036·J Med Genet·2009
8-other
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis.
PMID 19287372·J Hum Genet·2009
8-other
Exploring gene-environment interactions in Parkinson's disease.
PMID 18210157·Hum Genet·2008
4-observational
Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders.
PMID 18332251·Arch Neurol·2008
4-observational
Anxiety and otovestibular disorders: linking behavioral phenotypes in men and mice.
PMID 17822783·Behav Brain Res·2008
6-review
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
PMID 18953341·Nat Genet·2008
7-preclinical
High-resolution comprehensive radiation hybrid maps of the porcine chromosomes 2p and 9p compared with the human chromosome 11.
PMID 18467842·Cytogenet Genome Res·2008
4-observational
Genetic association between alpha-synuclein and idiopathic Parkinson's disease.
PMID 18404644·Am J Med Genet B Neuropsychiatr Genet·2008
8-other
Hedgehog signaling regulates sensory cell formation and auditory function in mice and humans.
PMID 18632939·J Neurosci·2008
4-observational
A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1.
PMID 18279434·Clin Genet·2008
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 5437 KIETZKE LN
RENO, NV 89511 - Phone
- (775) 322-4550
Quick Facts
- NPI
- 1659501633
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 2
- Years in Practice
- 17
- Publications
- 20
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