Associate Professor of Obstetrics/Gynecology and Human Genetics, University of Chicago Medicine
Obstetrics & Gynecology
Dr. Marion S. Verp, MD
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Marion Verp works in the field of Obstetrics & Gynecology. She went to NYU School of Medicine. She has 5 awards "CMS Meaningful Use Stage 1 Certification", "Chicago Magazine - Women's Health", "Fellow (FACOG)", "Fellow" and "Super Doctor". Doctor Marion S. Verp, MD is a published doctor. She has 55 publications published. The most current publication "Genetic counseling: clinical and ethical challenges." She accepts Medicare payments and is listed with Medicare.gov.
Publications
- Prenatal diagnosis of methotrexate embryopathy.
- A null mutation in HLA-G is not Associated with preeclampsia or intrauterine growth retardation.
- The role of physician preferences in the choice of amniocentesis or chorionic villus sampling for prenatal genetic testing.
- Maternal serum alpha-fetoprotein and anal atresia.
- Cellular response in rabbit eyes after Human fetal RPE cell transplantation.
- Growth of Human fetal retinal pigment epithelium as microspheres.
- Genetic counseling: clinical and ethical challenges.
- Patient or physician preferences for decision analysis: the prenatal genetic testing decision.
- HLA-G1 protein expression is not essential for fetal survival.
- Choroid plexus Cysts: infant and early childhood developmental outcome.
- Prenatal testing for limb reduction defects. How patients' views affect their choice of CVS.
- Analysis of parent of origin specific DNA methylation at SNRPN and PW71 in tissues: implication for prenatal diagnosis.
- Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism.
- Use of decision analysis to evaluate patients' choices of diagnostic prenatal test.
- Maternal-fetal histocompatibility in Intrauterine growth retarded and normal weight babies.
- Cook obstetrics and gynecology catheter multicenter chorionic villus sampling trial: comparison of birth defects With expected rates.
- Posterior urethral valves in successive generations.
- Menetrier Disease in a child of a consanguineous union.
- Gamma delta T cells in Human decidua.
- A cost-effectiveness analysis of amniocentesis and chorionic villus sampling for prenatal genetic testing.
- Preferences of pregnant women for amniocentesis or chorionic villus sampling for prenatal testing: comparison of patients'' choices and those of a decision-analytic mo...
- A prospective trial of prenatal screening for Down syndrome by means of maternal serum alpha-fetoprotein, Human chorionic gonadotropin, and unconjugated estriol.
- Developmental regulation of the catalytic subunit of the apolipoprotein B mRNA editing enzyme (APOBEC-1) in Human small intestine.
- Hypermodal Cells in amniotic fluid cultures: frequency, interpretation, and clinical significance.
- Necessity of formal genetic screening in artificial insemination by donor.
- Heritable aspects of uterine anomalies. I. Three familial aggregates With Müllerian fusion anomalies.
- Hypostatic ulcers in 47,XXY Klinefelter''s syndrome.
- Further comments on amniocentesis in twin gestations.
- Relationship between Y-chromosome length and first-trimester spontaneous abortions.
- Amniocentesis for prenatal diagnosis.
- The prenatal diagnosis of genetic Disorders.
- Linkage analysis in von Willebrand Disease.
- Elevated alpha-fetoprotein and acetylcholinesterase Associated with hydrocele.
- Mosaic trisomy 7 and renal dysplasia.
- Chromosomal mosaicism of trisomy 7 restricted to chorionic villi.
- Inflammatory bowel disease and X chromosome Abnormalities. A case report.
- Abnormal sexual differentiation and neoplasia.
- Parental decision following prenatal diagnosis of fetal chromosome abnormality.
- Growth disadvantage of 45,X and 46,X,del(X)(p11) fibroblasts.
- Fetal urinary tract obstruction and trisomy 18 mosaicism. A case report.
- Urinary tract Abnormalities in hand-foot-genital syndrome.
- Cystic hygroma and 45,X/46,XY mosaicism.
- Pulmonary artery agenesis.
- Non-mosaic trisomy 16 confined to villi.
- Chorionic chromosome Abnormalities and intrauterine growth retardation.
- True hermaphrodite With bilateral ovotestes, bilateral gonadoblastomas and dysgerminomas, 46,XX/46,XY karyotype, and a successful pregnancy.
- Apolipoprotein B messenger RNA editing is developmentally regulated and widely expressed in Human tissues.
- Amniocentesis or chorionic villus sampling for prenatal genetic testing: a decision analysis.
- Chimerism as the etiology of a 46,XX/46,XY fertile true hermaphrodite.
- Delayed diagnosis of pseudohermaphroditism on stored blood spot.
- Genetic risk and early versus late prenatal testing.
- Effect of plasma, steroids, or steroid products on the adhesion of Human opsonized thrombocytes to Human leukocytes.
- Uptake and timing of bilateral prophylactic salpingo-oophorectomy among BRCA1 and BRCA2 mutation carriers.
- Mucopolysaccharidosis type VII as a cause of recurrent non-immune hydrops fetalis.
Schools
NEW YORK UNIV SCH OF MED
Procedures Preformed
- Fluid Contrast Ultrasound
- Gynecologic Cancer Screening
- Hysteroscopy
- Sympathectomy
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Conditions Treated
- Atrophic Vaginitis
- Carcinoma in Situ
- Cervical Polyps
- Endometriosis
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Doctors Specialties
- Clinical Genetics
- Obstetrics
- Gynecology
Accepted Insurances
Awards
- CMS Meaningful Use Stage 1 Certification
- Chicago Magazine - Women's Health
- Fellow (FACOG)
- Fellow
- Super Doctor
Education
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NYU School of Medicine
Hospital
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University of Chicago Medical Center -
MacNeal Hospital
Drug Facts
| NPI NUMBER | 1932145802 | |
| NPPES Provider LastName | VERP | |
| NPPES Provider FirstName | MARION | |
| NPPES Provider ZIPCode | 606371447 | |
| NPPES Provider State | IL | |
| Specialty Description | Obstetrics/Gynecology | |
| Total Claim Count | 32.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1932145802 |
| Last Name Of The Provider | VERP |
| First Name Of The Provider | MARION |
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