Professor of Obstetrics and Gynecology, FIU College of Medicine
Obstetrics & Gynecology
Dr. Joe L. Simpson, MD
Joe L. Simpson, MD practices Obstetrics & Gynecology. He attended Duke University School of Medicine. Duke University School of Medicine is a top medical college. Duke University School of Medicine has a rank of 8 in research and a 29 in primary care He received awards:"Elected Member", "Whos Who in Medicine and Healthcare" and "Super Doctor". Simpson is also a published doctor. He has 59 paper published. The most recent paper is: Genetics of primary ovarian insufficiency: new developments and opportunities.
Publications
- Genetics of primary ovarian insufficiency: new developments and opportunities.
- Impact of an academic-community partnership in medical education on community health: evaluation of a novel student-based home visitation program.
- Birth defects and assisted reproductive technologies.
- Cell-free fetal DNA and maternal serum analytes for monitoring embryonic and fetal status.
- Next generation sequencing for preimplantation genetic diagnosis.
- Prenatal diagnosis and 47,XXY.
- Preventing preterm births: analysis of trends and potential reductions with interventions in 39 countries with very high human development index.
- Xq;autosome translocation in POF: Xq27.2 deletion resulting in haploinsufficiency for SPANX.
- Fetal surgery for myelomeningocele?
- Novel Non-invasive Prenatal Diagnosis as Related to Congenital Adrenal Hyperplasia.
- The illusory "level playing field".
- Florida International University Herbert Wertheim College of Medicine.
- Plasma cell-free DNA in ovarian cancer: an independent prognostic biomarker.
- Preface: Genetic screening and counseling.
- Florida International University: development and accreditation of Miami's Public College of Medicine.
- Mutation analysis of NOBOX homeodomain in Chinese women with premature ovarian failure.
- Oocyte-specific G-protein-coupled receptor 3 (GPR3): no perturbations found in 82 women with premature ovarian failure (first report).
- Transcription factor FIGLA is mutated in patients with premature ovarian failure.
- Developing a national collaborative study system for rare genetic diseases.
- Analysis of LHX8 mutation in premature ovarian failure.
- Genetic and phenotypic heterogeneity in ovarian failure: overview of selected candidate genes.
- Mutation analysis of NANOS3 in 80 Chinese and 88 Caucasian women with premature ovarian failure.
- Analyses of GDF9 mutation in 100 Chinese women with premature ovarian failure.
- In vitro fertilization with preimplantation genetic screening.
- Substandard application of preimplantation genetic screening may interfere with its clinical success.
- NOBOX homeobox mutation causes premature ovarian failure.
- Workshop report: evaluation of genetic and epigenetic risks associated with assisted reproductive technologies and Infertility.
- The FMR1 premutation and reproduction.
- Causes of fetal wastage.
- Growth differentiating factor-9 mutations may be associated with premature ovarian failure.
- Circulating cell-free DNA: a novel biomarker for response to therapy in ovarian carcinoma.
- Quantity versus quality: optimal methods for cell-free DNA isolation from plasma of pregnant women.
- Hypoxia-induced membrane-bound apoptotic DNA particles: potential mechanism of fetal DNA in maternal plasma.
- Quantification of total plasma cell-free DNA in ovarian cancer using real-time PCR.
- Professional self-regulation for preimplantation genetic diagnosis: experience of the American Society for Reproductive Medicine and other professional societies.
- Choosing the best prenatal screening protocol.
- Quantitative DNA perturbations of p53 in endometriosis: analysis of American and Icelandic cases.
- Preimplantation genetic diagnosis reduces pregnancy loss in women aged 35 years and older with a history of recurrent miscarriages.
- Elevated pregnancy losses at high and low extremes of maternal glucose in early normal and diabetic pregnancy: evidence for a protective adaptation in diabetes.
- Where are the genes that cause endometriosis?
- Preimplantation genetic diagnosis (PGD) for heritable neoplasia.
- Protein expression profiling of endometriosis: validation of 2-mm tissue microarrays.
- Genetic basis of endometriosis.
- Over a decade of experience with preimplantation genetic diagnosis.
- Over a decade of experience with preimplantation genetic diagnosis: a multicenter report.
- Pregnancy-associated plasma protein A, free beta-hCG, nuchal translucency, and risk of pregnancy loss.
- Cell-free fetal DNA in maternal blood: evolving clinical applications.
- Interlaboratory comparison of fetal male DNA detection from common maternal plasma samples by real-time PCR.
- Klinefelter syndrome: expanding the phenotype and identifying new research directions.
- Genetics of endometriosis.
- Genetic counseling in translocations.
- A general approach to genetic counseling.
- Genetic screening for cystic fibrosis.
- Heritability and molecular genetic studies of endometriosis.
- Prenatal diagnosis of chromosomal abnormalities using maternal blood.
- Celebrating preimplantation genetic diagnosis of p53 mutations in Li-Fraumeni syndrome.
- Spatial Positioning of All 24 Chromosomes in the Lymphocytes of Six Subjects: Evidence of Reproducible Positioning and Spatial Repositioning following DNA Damage with ...
- Genetics of Female infertility due to anomalies of the ovary and mullerian ducts.
Schools
Duke University
Conditions Treated
- Female Infertility
- Intrauterine Growth Restriction
Doctors Specialties
- Clinical Genetics
- Obstetrics
- Gynecology
Accepted Insurances
Awards
- Elected Member
- Whos Who in Medicine and Healthcare
- Super Doctor
Education
-
New York Presbyterian Hospital - Cornell Campus -
Duke University School of Medicine
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