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SUNIL ARADHYA, M.D.
M.D.
Emergency Medicine Physician
NPI: 1902164163IndividualAccepts Medicare
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
BP10044219(TX)
CMS Specialties
PrimaryEMERGENCY MEDICINE
Education
UNIVERSITY OF TEXAS MEDICAL BRANCH AT GALVESTON
Class of 2012
Research & Publications (20)
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
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
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
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
Array-based comparative genomic hybridization: clinical contexts for targeted and whole-genome designs.
PMID 17873642·Genet Med·2007
4-observational
Identification of difurocumenonol, a new antimicrobial compound from mango ginger (Curcuma amada Roxb.) rhizome.
PMID 17578425·J Appl Microbiol·2007
8-other
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
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 human secretin gene: fine structure in 11p15.5 and sequence variation in patients with autism.
PMID 12160732·Genomics·2002
8-other
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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 18500 KATY FWY
HOUSTON, TX 77094 - Phone
- (832) 522-1800
Quick Facts
- NPI
- 1902164163
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 14
- Publications
- 20
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