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SUSAN MEAD, PHARMD
PHARMD
Pharmacist Clinician (PhC)/ Clinical Pharmacy Specialist
NPI: 1245479377Individual
Specialties, Licenses & Credentials
Pharmacist Clinician (PhC)/ Clinical Pharmacy SpecialistPrimary
Pharmacist — Pharmacist Clinician (PhC)/ Clinical Pharmacy Specialist
Code: 1835P0018X
10956(CO)
Research & Publications (20)
Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.
PMID 19081515·Lancet Neurol·2009
8-other
Successful amplification of degraded DNA for use with high-throughput SNP genotyping platforms.
PMID 18551557·Hum Mutat·2008
8-other
Creutzfeldt-Jakob disease, prion protein gene codon 129VV, and a novel PrPSc type in a young British woman.
PMID 18071044·Arch Neurol·2007
5-case
Prion protein (PRNP) genotypes in frontotemporal lobar degeneration syndromes.
PMID 16969862·Ann Neurol·2006
8-other
Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity.
PMID 16923955·Brain·2006
8-other
Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics.
PMID 12690204·Science·2003
7-preclinical
Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1.
PMID 11704923·Am J Hum Genet·2001
8-other
A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family members.
PMID 11723204·J Neurol Neurosurg Psychiatry·2001
5-case
Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease.
PMID 10936691·Neurosci Lett·2000
8-other
No association of PGRN 3'UTR rs5848 in frontotemporal lobar degeneration.
PMID 19446372·Neurobiol Aging·2011
8-other
Progressive logopenic/phonological aphasia: erosion of the language network.
PMID 19679189·Neuroimage·2010
8-other
HECTD2 is associated with susceptibility to mouse and human prion disease.
PMID 19214206·PLoS Genet·2009
7-preclinical
Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration.
PMID 19217189·Neurobiol Aging·2009
8-other
Age of onset and death in inherited prion disease are heritable.
PMID 18729123·Am J Med Genet B Neuropsychiatr Genet·2009
8-other
DNA polymerase switching: effects on spontaneous mutagenesis in Escherichia coli.
PMID 19019142·Mol Microbiol·2009
8-other
Seven-year discordance in age at onset in monozygotic twins with inherited prion disease (P102L).
PMID 19207267·Neuropathol Appl Neurobiol·2009
5-case
A small-scale randomized controlled trial of the revised new forest parenting programme for preschoolers with attention deficit hyperactivity disorder.
PMID 19404717·Eur Child Adolesc Psychiatry·2009
2-rct
Association of a null allele of SPRN with variant Creutzfeldt-Jakob disease.
PMID 18805828·J Med Genet·2008
8-other
A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea.
PMID 18849289·Philos Trans R Soc Lond B Biol Sci·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
- Address
- 18TH AND WARDENBURG DRIVE, UNIVERSITY OF COLORADO
BOULDER, CO 80309 - Phone
- (303) 492-8553
Quick Facts
- NPI
- 1245479377
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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