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ASHLEY GRIFFITH, PHD
PHD
Psychologist
NPI: 1780306076Individual
Specialties, Licenses & Credentials
PsychologistPrimary
Psychologist
Code: 103T00000X
PSY.0006416(CO)
Research & Publications (20)
Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndrome.
PMID 16885744·Laryngoscope·2006
5-case
Knock-in mouse model for resistance to thyroid hormone (RTH): an RTH mutation in the thyroid hormone receptor beta gene disrupts cochlear morphogenesis.
PMID 12382103·J Assoc Res Otolaryngol·2002
7-preclinical
Improved methods for the extraction and analysis of isoflavones from soy-containing foods and nutritional supplements by reversed-phase high-performance liquid chromatography and liquid chromatography-mass spectrometry.
PMID 11355838·J Chromatogr A·2001
8-other
Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT.
PMID 10903123·Am J Hum Genet·2000
8-other
DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3.
PMID 19603065·Eur J Hum Genet·2010
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
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
Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan.
PMID 19250381·Clin Genet·2009
8-other
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
Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism.
PMID 18952485·Parkinsonism Relat Disord·2009
8-other
Efficient molecular genetic diagnosis of enlarged vestibular aqueducts in East Asians.
PMID 19645628·Genet Test Mol Biomarkers·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
Increased thymus- and decreased parathyroid-fated organ domains in Splotch mutant embryos.
PMID 19135046·Dev Biol·2009
7-preclinical
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
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
PMID 18953341·Nat Genet·2008
7-preclinical
Hedgehog signaling regulates sensory cell formation and auditory function in mice and humans.
PMID 18632939·J Neurosci·2008
4-observational
Evaluation of a mental skills program for serving for an intercollegiate volleyball team.
PMID 18986056·Percept Mot Skills·2008
8-other
Restless legs syndrome: a unique case and essentials of diagnosis and treatment.
PMID 19242602·Medscape J Med·2008
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
- 1700 WHEELING ST
AURORA, CO 80045 - Phone
- (720) 723-6558
Quick Facts
- NPI
- 1780306076
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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