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IRENE CARR, PHD, FNP-BC, CNM
PHD, FNP-BC, CNM
Family Nurse Practitioner
NPI: 1801084405Individual
Specialties, Licenses & Credentials
Family Nurse PractitionerPrimary
Nurse Practitioner — Family
Code: 363LF0000X
14827(CA)
Research & Publications (20)
IBDfinder and SNPsetter: tools for pedigree-independent identification of autozygous regions in individuals with recessive inherited disease.
PMID 19405095·Hum Mutat·2009
8-other
Interactive visual analysis of SNP data for rapid autozygosity mapping in consanguineous families.
PMID 16941472·Hum Mutat·2006
8-other
How much gin in the tonic? The problems of writing a provincial medical history,.
PMID 14526792·Can Bull Med Hist·2000
8-other
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response.
PMID 19525956·Nat Genet·2009
8-other
Ketohexokinase: expression and localization of the principal fructose-metabolizing enzyme.
PMID 19365088·J Histochem Cytochem·2009
7-preclinical
Clinical diagnostic utility of IP-10 and LAM antigen levels for the diagnosis of tuberculous pleural effusions in a high burden setting.
PMID 19277111·PLoS One·2009
3-trial
Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta.
PMID 19200525·Am J Hum Genet·2009
8-other
Mutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathy.
PMID 18500342·Nat Genet·2008
4-observational
Clinical and molecular phenotype of Aicardi-Goutieres syndrome.
PMID 17846997·Am J Hum Genet·2007
8-other
Sequence analysis and editing for bisulphite genomic sequencing projects.
PMID 17517768·Nucleic Acids Res·2007
8-other
Homozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndrome and other movement disorders.
PMID 15571623·BMC Neurol·2004
5-case
High-affinity interactions between human alpha1A-adrenoceptor C-terminal splice variants produce homo- and heterodimers but do not generate the alpha1L-adrenoceptor.
PMID 15266013·Mol Pharmacol·2004
8-other
Identification of SATB2 as the cleft palate gene on 2q32-q33.
PMID 12915443·Hum Mol Genet·2003
4-observational
Detection by fluorescence in situ hybridization of microdeletions at 1p36 in lymphomas, unidentified on cytogenetic analysis.
PMID 12660032·Cancer Genet Cytogenet·2003
8-other
Defining "early dementia" and monitoring intervention: what measures are useful in family caregiving?
PMID 12554309·Aging Ment Health·2003
4-observational
Regulation of the avidity of ternary complexes containing the human 5-HT(1A) receptor by mutation of a receptor contact site on the interacting G protein alpha subunit.
PMID 12237254·Br J Pharmacol·2002
8-other
Identification of microcephalin, a protein implicated in determining the size of the human brain.
PMID 12046007·Am J Hum Genet·2002
7-preclinical
BCL10 in malignant lymphomas--an evaluation using fluorescence in situ hybridization.
PMID 11748643·J Pathol·2002
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
- 3020 CHILDRENS WAY
SAN DIEGO, CA 92123 - Phone
- (858) 966-1700
Quick Facts
- NPI
- 1801084405
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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