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KOUSHIK MANTRIPRAGADA, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1265019186Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Genome-wide high-resolution analysis of DNA copy number alterations in NF1-associated malignant peripheral nerve sheath tumors using 32K BAC array.
PMID 19603524·Genes Chromosomes Cancer·2009
8-other
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia.
PMID 19181681·Hum Mol Genet·2009
8-other
High-resolution DNA copy number profiling of malignant peripheral nerve sheath tumors using targeted microarray-based comparative genomic hybridization.
PMID 18281533·Clin Cancer Res·2008
8-other
Telomerase activity is a biomarker for high grade malignant peripheral nerve sheath tumors in neurofibromatosis type 1 individuals.
PMID 18069666·Genes Chromosomes Cancer·2008
8-other
Germline and somatic NF1 gene mutation spectrum in NF1-associated malignant peripheral nerve sheath tumors (MPNSTs).
PMID 17960768·Hum Mutat·2008
8-other
Comprehensive genetic and epigenetic analysis of sporadic meningioma for macro-mutations on 22q and micro-mutations within the NF2 locus.
PMID 17222329·BMC Genomics·2007
8-other
Detection of copy number changes at the NF1 locus with improved high-resolution array CGH.
PMID 17718862·Clin Genet·2007
4-observational
Array-CGH and multipoint FISH to decode complex chromosomal rearrangements.
PMID 17196103·BMC Genomics·2006
8-other
Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH.
PMID 16713171·Genomics·2006
8-other
Microarray-based survey of CpG islands identifies concurrent hyper- and hypomethylation patterns in tissues derived from patients with breast cancer.
PMID 16575877·Genes Chromosomes Cancer·2006
4-observational
Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGH.
PMID 15944227·J Med Genet·2006
8-other
Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH.
PMID 16161042·Int J Cancer·2006
8-other
High-resolution array-CGH profiling of germline and tumor-specific copy number alterations on chromosome 22 in patients affected with schwannomas.
PMID 16078050·Hum Genet·2005
8-other
Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2.
PMID 16287142·Hum Mutat·2005
8-other
Chromosome 22 tiling-path array-CGH analysis identifies germ-line- and tumor-specific aberrations in patients with glioblastoma multiforme.
PMID 15945096·Genes Chromosomes Cancer·2005
8-other
Localization of a putative low-penetrance ependymoma susceptibility locus to 22q11 using a chromosome 22 tiling-path genomic microarray.
PMID 15880457·Genes Chromosomes Cancer·2005
8-other
High-resolution gene copy number and expression profiling of human chromosome 22 in ovarian carcinomas.
PMID 15578687·Genes Chromosomes Cancer·2005
8-other
DNA copy-number analysis of the 22q11 deletion-syndrome region using array-CGH with genomic and PCR-based targets.
PMID 14719134·Int J Mol Med·2004
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
- 22 S GREENE ST
BALTIMORE, MD 21201 - Phone
- (410) 328-6713
Quick Facts
- NPI
- 1265019186
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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