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RABBIA NAEEM, MD
MD
Pediatrics Physician
NPI: 1750776902Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
A153578(CA)
Research & Publications (20)
Overexpression of ZNF342 by juxtaposition with MPO promoter/enhancer in the novel translocation t(17;19)(q23;q13.32) in pediatric acute myeloid leukemia and analysis of ZNF342 expression in leukemia.
PMID 19255975·Genes Chromosomes Cancer·2009
8-other
Quantitation of Aurora kinase A gene copy number in urine sediments and bladder cancer detection.
PMID 18812553·J Natl Cancer Inst·2008
8-other
Syndromic thrombocytopenia and predisposition to acute myelogenous leukemia caused by constitutional microdeletions on chromosome 21q.
PMID 18487507·Blood·2008
8-other
Clear cell sarcoma of soft tissue: diagnostic utility of fluorescence in situ hybridization and reverse transcriptase polymerase chain reaction.
PMID 18333903·J Cutan Pathol·2008
5-case
Clinical utility of array comparative genomic hybridization for detection of chromosomal abnormalities in pediatric acute lymphoblastic leukemia.
PMID 18253961·Pediatr Blood Cancer·2008
8-other
Overexpression of Eg5 causes genomic instability and tumor formation in mice.
PMID 17974955·Cancer Res·2007
7-preclinical
C/EBPbeta suppression by interruption of CUGBP1 resulting from a complex rearrangement of MLL.
PMID 17854664·Cancer Genet Cytogenet·2007
5-case
Deletion of the short arm of chromosome 1 (del 1p) is a strong predictor of poor outcome in myeloma patients undergoing an autotransplant.
PMID 17697969·Biol Blood Marrow Transplant·2007
8-other
A constitutional balanced t(3;8)(p14;q24.1) translocation results in disruption of the TRC8 gene and predisposition to clear cell renal cell carcinoma.
PMID 17539022·Genes Chromosomes Cancer·2007
8-other
Stromal fibroblasts present in invasive human breast carcinomas promote tumor growth and angiogenesis through elevated SDF-1/CXCL12 secretion.
PMID 15882617·Cell·2005
7-preclinical
Microarray-based comparative genomic hybridization of pheochromocytoma cell lines from neurofibromatosis knockout mice reveals genetic alterations similar to those in human pheochromocytomas.
PMID 15860353·Cancer Genet Cytogenet·2005
4-observational
A patient with isochromosome 18q, radial-thumb aplasia, thrombocytopenia, and an unbalanced 10;18 chromosome translocation.
PMID 15637724·Am J Med Genet A·2005
5-case
Loss of heterozygosity occurs via mitotic recombination in Trp53+/- mice and associates with mammary tumor susceptibility of the BALB/c strain.
PMID 15289317·Cancer Res·2004
4-observational
Cytogenetic abnormalities in products of conception: a relationship revisited.
PMID 15214948·Am J Reprod Immunol·2004
8-other
Attenuated phenotype in a child with trisomy for 1q due to unbalanced X;1 translocation [46,X,der(X),t(X;1)(q28;q32.1)].
PMID 15211662·Am J Med Genet A·2004
5-case
Overexpression of MAGE/GAGE genes in paclitaxel/doxorubicin-resistant human cancer cell lines.
PMID 12855658·Clin Cancer Res·2003
8-other
Cloned transchromosomic calves producing human immunoglobulin.
PMID 12172556·Nat Biotechnol·2002
7-preclinical
Role of liver biopsy in the diagnosis of hepatic iron overload in the era of genetic testing.
PMID 12109859·Am J Clin Pathol·2002
8-other
Decisions about amniocentesis by advanced maternal age patients following maternal serum screening may not always correlate clinically with screening results: need for improvement in informed consent process.
PMID 11977174·Am J Med Genet·2002
8-other
Tyrosine kinase activation in breast carcinoma with correlation to HER-2/neu gene amplification and receptor overexpression.
PMID 11774167·Hum Pathol·2001
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 3 locations total
- Address
- 49 Jesse Hill Jr Dr SE Fl 2
Atlanta, GA 30303 - Phone
- (404) 778-1440
Quick Facts
- NPI
- 1750776902
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 3
- Publications
- 20
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