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SHARON PLON, PHD

PHD

Pediatrics Physician

NPI: 1336229756Individual

Specialties, Licenses & Credentials

Clinical Genetics (M.D.) Physician

Medical Genetics — Clinical Genetics (M.D.)

Code: 207SG0201X

J7630(TX)
Pediatrics PhysicianPrimary

Pediatrics

Code: 208000000X

J7630(TX)

Research & Publications (20)

Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results.
PMID 18951446·Hum Mutat·2008
8-other
A robust estimator of mutation rates.
PMID 19100753·Mutat Res·2009
8-other
The mutation spectrum in RECQL4 diseases.
PMID 18716613·Eur J Hum Genet·2009
8-other
Differential in vitro cytotoxicity does not explain increased host toxicities from chemotherapy in Down syndrome acute lymphoblastic leukemia.
PMID 18718659·Leuk Res·2009
8-other
Prevalence and clinical correlates of JAK2 mutations in Down syndrome acute lymphoblastic leukaemia.
PMID 19120350·Br J Haematol·2009
8-other
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
Locus-specific databases and recommendations to strengthen their contribution to the classification of variants in cancer susceptibility genes.
PMID 18951438·Hum Mutat·2008
8-other
Heterozygous screen in Saccharomyces cerevisiae identifies dosage-sensitive genes that affect chromosome stability.
PMID 18245329·Genetics·2008
8-other
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
Generalized metabolic bone disease in Neurofibromatosis type I.
PMID 18289904·Mol Genet Metab·2008
8-other
Syndromic thrombocytopenia and predisposition to acute myelogenous leukemia caused by constitutional microdeletions on chromosome 21q.
PMID 18487507·Blood·2008
8-other
Multiple tumors in a child with germ-line mutations in TP53 and PTEN.
PMID 18669439·N Engl J Med·2008
5-case
Sensitivity of RECQL4-deficient fibroblasts from Rothmund-Thomson syndrome patients to genotoxic agents.
PMID 18504617·Hum Genet·2008
4-observational
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
A phase 1 study of the proteasome inhibitor bortezomib in pediatric patients with refractory leukemia: a Children's Oncology Group study.
PMID 17332297·Clin Cancer Res·2007
3-trial
Retinoblastoma: review of current management.
PMID 17962617·Oncologist·2007
6-review
Nuclear import and retention domains in the amino terminus of RECQL4.
PMID 17250975·Gene·2007
8-other
Severe dysplasia in children with familial adenomatous polyposis: rare or simply overlooked?
PMID 16567172·J Pediatr Surg·2006
8-other
Multiple endocrine neoplasia type 1 interacts with forkhead transcription factor CHES1 in DNA damage response.
PMID 16951149·Cancer Res·2006
7-preclinical
Defective mitochondrial peroxiredoxin-3 results in sensitivity to oxidative stress in Fanconi anemia.
PMID 17060495·J Cell Biol·2006
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
6701 FANNIN ST
HOUSTON, TX 77030

Location

Practice Location

6701 FANNIN ST, HOUSTON, TX
(832) 822-4240

Quick Facts

NPI
1336229756
Entity Type
Individual
Gender
Female
Medicare
Not confirmed
Specialties
2
Locations
1
Publications
20

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