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SWAROOP ARADHYA, PH.D.

PH.D.

NPI: 1801343215Individual

Specialties, Licenses & Credentials

Ph.D. Medical GeneticsPrimary

Medical Genetics, Ph.D. Medical Genetics

Code: 170100000X

DRN01001207(CA)

Research & Publications (20)

Array-based comparative genomic hybridization: clinical contexts for targeted and whole-genome designs.
PMID 17873642·Genet Med·2007
4-observational
Whole-genome array-CGH identifies novel contiguous gene deletions and duplications associated with developmental delay, mental retardation, and dysmorphic features.
PMID 17568414·Am J Med Genet A·2007
8-other
Mutations in the calcium-related gene IL1RAPL1 are associated with autism.
PMID 18801879·Hum Mol Genet·2008
5-case
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.
PMID 18628315·J Med Genet·2008
8-other
Genetic analysis of attractin homologs.
PMID 18064672·Genesis·2007
7-preclinical
Identification of difurocumenonol, a new antimicrobial compound from mango ginger (Curcuma amada Roxb.) rhizome.
PMID 17578425·J Appl Microbiol·2007
8-other
In vitro studies on the binding, antioxidant, and cytotoxic actions of punicalagin.
PMID 17243704·J Agric Food Chem·2007
8-other
Isolation and characterization of antioxidant and antibacterial compound from mango ginger (Curcuma amada Roxb.) rhizome.
PMID 17223394·J Chromatogr B Analyt Technol Biomed Life Sci·2007
8-other
Nablus mask-like facial syndrome is caused by a microdeletion of 8q detected by array-based comparative genomic hybridization.
PMID 16691576·Am J Med Genet A·2006
5-case
A mouse keratin 1 mutation causes dark skin and epidermolytic hyperkeratosis.
PMID 16528356·J Invest Dermatol·2006
7-preclinical
The DNA sequence of the human X chromosome.
PMID 15772651·Nature·2005
7-preclinical
The human secretin gene: fine structure in 11p15.5 and sequence variation in patients with autism.
PMID 12160732·Genomics·2002
8-other
Physical and genetic characterization reveals a pseudogene, an evolutionary junction, and unstable loci in distal Xq28.
PMID 11827455·Genomics·2002
7-preclinical
Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes.
PMID 11709543·Hum Mol Genet·2001
7-preclinical
Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndrome.
PMID 11673821·Am J Hum Genet·2001
5-case
A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutations.
PMID 11590134·Hum Mol Genet·2001
8-other
NF-kappaB signaling and human disease.
PMID 11377967·Curr Opin Genet Dev·2001
6-review
Atypical forms of incontinentia pigmenti in male individuals result from mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma).
PMID 11179023·Am J Hum Genet·2001
8-other
Filamin (FLN1), plexin (SEX), major palmitoylated protein p55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2.
PMID 10982489·Am J Med Genet·2000
8-other
Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium.
PMID 10839543·Nature·2000
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
3375 HILLVIEW AVE, MOLECULAR GENETICS LABORATORY
PALO ALTO, CA 94304

Location

Practice Location

3375 HILLVIEW AVE, PALO ALTO, CA
(650) 723-9232

Quick Facts

NPI
1801343215
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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