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ASHA SWAROOP, M.D.
M.D.
Family Medicine Physician
NPI: 1568555266Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
A66375(CA)
Research & Publications (20)
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies.
PMID 19430481·Nat Genet·2009
7-preclinical
Rdh12 activity and effects on retinoid processing in the murine retina.
PMID 19506076·J Biol Chem·2009
7-preclinical
Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome.
PMID 19279158·Hum Mol Genet·2009
7-preclinical
Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa.
PMID 19520207·Am J Hum Genet·2009
8-other
Unraveling a multifactorial late-onset disease: from genetic susceptibility to disease mechanisms for age-related macular degeneration.
PMID 19405847·Annu Rev Genomics Hum Genet·2009
6-review
Geographic atrophy in age-related macular degeneration and TLR3.
PMID 19469037·N Engl J Med·2009
8-other
Canine RD3 mutation establishes rod-cone dysplasia type 2 (rcd2) as ortholog of human and murine rd3.
PMID 19130129·Mamm Genome·2009
7-preclinical
Retinal phenotype of an X-linked pseudo-Usher syndrome in association with the G173R mutation in the RPGR gene.
PMID 18188948·Adv Exp Med Biol·2008
4-observational
Retinitis Pigmentosa GTPase Regulator (RPGR) protein isoforms in mammalian retina: insights into X-linked Retinitis Pigmentosa and associated ciliopathies.
PMID 17904189·Vision Res·2008
7-preclinical
Toll-like receptor polymorphisms and age-related macular degeneration.
PMID 18385087·Invest Ophthalmol Vis Sci·2008
8-other
Inflammation in the pathogenesis of age-related macular degeneration.
PMID 18369057·Br J Ophthalmol·2008
8-other
Discordant phenotypes in fraternal twins having an identical mutation in exon ORF15 of the RPGR gene.
PMID 18332319·Arch Ophthalmol·2008
8-other
Nrl-knockout mice deficient in Rpe65 fail to synthesize 11-cis retinal and cone outer segments.
PMID 18326740·Invest Ophthalmol Vis Sci·2008
7-preclinical
CP110 suppresses primary cilia formation through its interaction with CEP290, a protein deficient in human ciliary disease.
PMID 18694559·Dev Cell·2008
7-preclinical
Rod differentiation factor NRL activates the expression of nuclear receptor NR2E3 to suppress the development of cone photoreceptors.
PMID 18294621·Brain Res·2008
7-preclinical
FGF19 exhibits neuroprotective effects on adult mammalian photoreceptors in vitro.
PMID 18385093·Invest Ophthalmol Vis Sci·2008
7-preclinical
Mutations in TOPORS cause autosomal dominant retinitis pigmentosa with perivascular retinal pigment epithelium atrophy.
PMID 17924349·Am J Hum Genet·2007
8-other
Genetic susceptibility to age-related macular degeneration: a paradigm for dissecting complex disease traits.
PMID 17911160·Hum Mol Genet·2007
6-review
Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations.
PMID 17898302·Invest Ophthalmol Vis Sci·2007
8-other
Hypomorphic CEP290/NPHP6 mutations result in anosmia caused by the selective loss of G proteins in cilia of olfactory sensory neurons.
PMID 17898177·Proc Natl Acad Sci U S A·2007
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
- 3401 W. SUNFLOWER AVE., SUITE 225
SANTA ANA, CA 92704 - Phone
- (714) 619-8777
Quick Facts
- NPI
- 1568555266
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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