Professor of Clinical Genetics, University S Fla College of Medicine
Pediatrics
Dr. Rebecca Sutphen, MD
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Doctor Rebecca Sutphen, MD is an expert in the field of Pediatrics. She went to medical school at Temple University School of Medicine. She has 3 awards "America's Top Doctors", "America's Top Doctors for Cancer" and "Super Doctor". Rebecca Sutphen is a published doctor. She has 50 papers published. The most current publication "t(1;18)(q32.1;q22.1) associated with genitourinary malformations."
Publications
- American BRCA Outcomes and Utilization of Testing (ABOUT) Study: A Pragmatic Research Model that Incorporates Personalized Medicine/Patient-Centered Outcomes in a Real...
- Identification of Cell Membrane Protein Stress-Induced Phosphoprotein 1 as a Potential Ovarian Cancer Biomarker Using Aptamers Selected by Cell Systematic Evolution of...
- Kernel canonical correlation analysis for assessing gene-gene interactions and application to ovarian cancer.
- Inherited variants in regulatory T cell genes and outcome of ovarian cancer.
- The Rare Diseases Clinical Research Network Contact Registry update: features and functionality.
- Improving Reliability of Response Prediction to Platinum-Based Therapy by AdaBoost and Multiple Classifiers.
- Integration of clinical information and gene expression profiles for prediction of chemo-response for ovarian cancer.
- The presence of germ line mosaicism in cleidocranial dysplasia.
- Genotype/phenotype observations in African Americans with Bartter syndrome.
- Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy.
- The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome.
- Severe Lhermitte-Duclos disease with unique germline mutation of PTEN.
- t(1;18)(q32.1;q22.1) associated with genitourinary malformations.
- The genetic basis of Cowden''s syndrome: three novel mutations in PTEN/MMAC1/TEP1.
- Inherited susceptibility to breast and ovarian cancer.
- Expanded phenotype of cranioectodermal dysplasia (Sensenbrenner syndrome)
- Clitoromegaly in neurofibromatosis.
- XXY male with X-linked dominant chondrodysplasia punctata (Happle syndrome)
- Tracheoesophageal anomalies in oculoauriculovertebral (Goldenhar) spectrum.
- Identification of genes associated with ovarian cancer metastasis using microarray expression analysis.
- Genetic/familial high-risk assessment: breast and ovarian.
- BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases.
- Surface-enhanced Raman scattering detection of lysophosphatidic acid.
- Re: Prognostic significance of a short sequence insertion in the MCL-1 promoter in chronic lymphocytic leukemia.
- Genetic linkage of prostate cancer risk to the chromosome 3 region bearing FHIT.
- BRCA1 and BRCA2 mutations in a study of African American breast cancer patients.
- Lysophospholipids are potential biomarkers of ovarian cancer.
- Mismatch repair gene expression defects contribute to microsatellite instability in ovarian carcinoma.
- Current and evolving strategies for colorectal cancer screening.
- Characterization of mutations in 22 females with X-linked dominant chondrodysplasia punctata (Happle syndrome).
- Assessment of hepatocyte growth factor in ovarian cancer mortality.
- MicroRNA Processing and Binding Site Polymorphisms are not Replicated in the Ovarian Cancer Association Consortium.
- LIN28B polymorphisms influence susceptibility to epithelial ovarian cancer.
- Inherited variants in mitochondrial biogenesis genes may influence epithelial ovarian cancer risk.
- The role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testing.
- Improved survival in non-Ashkenazi Jewish ovarian cancer patients with BRCA1 and BRCA2 gene mutations.
- Study of the molecular recognition of aptamers selected through ovarian cancer cell-SELEX.
- A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.
- Real world experience with cancer genetic counseling via telephone.
- Urine collection and processing for protein biomarker discovery and quantification.
- Evaluation of established breast cancer risk factors as modifiers of BRCA1 or BRCA2: a multi-center case-only analysis.
- A risk variant in an miR-125b binding site in BMPR1B is associated with breast cancer pathogenesis.
- Single nucleotide polymorphisms in the TP53 region and susceptibility to invasive epithelial ovarian cancer.
- Determination of cancer risk associated with germ line BRCA1 missense variants by functional analysis.
- Improved survival in BRCA2 carriers with ovarian cancer.
- Association of single nucleotide polymorphisms in glycosylation genes with risk of epithelial ovarian cancer.
- Strong signature of natural selection within an FHIT intron implicated in prostate cancer risk.
- Proteomic contributions to personalized cancer care.
- Sampling strategies for tissue microarrays to evaluate biomarkers in ovarian cancer.
Schools
Temple University School Of Medicine
All Childns Hospital University South Fla College Med
University South Fla College Med
Doctors Specialties
- Clinical Cytogenetics
- Clinical Genetics
- Clinical Molecular Genetics
- Pediatrics
Accepted Insurances
Awards
- America's Top Doctors
- America's Top Doctors for Cancer
- Super Doctor
Education
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Temple University School of Medicine
Hospital
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All Children's Hospital Johns Hopkins Medicine
