Research in Fetal Medicine 
The Fetal Medicine team  members are very active in both clinical and bench research and are frequent  presenters at national meetings. We have a broad range of on-going research  projects 
and members of our team regularly present their research at national  and international meetings, 
such as the Society for Maternal-Fetal Medicine  (SMFM), International Fetal Medicine and Surgery Society (IFMSS), International  Society of Ultrasound 
in Obstetrics and Gynecology (ISUOG), the Society 
for  Gynecologic Investigation (SGI) and the world congress of the Fetal Medicine Foundation (FMF).  
Past important research projects:
FASTER (First and second trimester evailation of risk for anepolidy): This important study has  been a milestone in non-invasive screening for chromosomal problems in early  pregnancy. Results were published in the New England Journal of Medicine and  several additional publications in other journals.
Clinical experience with  Non-Invasive Prenatal Screening: Demonstrating the success  of this non-invasive technology in the routine practice. Results were published in  the American Journal of Obstetrics and Gynecology
PROCHIEVE study: Demonstrating the benefits of progesterone for the prevention of Preterm  delivery.  Results published in the  journal of Ultrasound in Obstetrics and Gynecology. 
Chromosomal microarray  versus karyotyping for prenatal diagnosis: Demonstrating the  advantages of chromosomal microarray in improving detection of genetic  syndromes especially in cases of fetal anomalies.  Results were published in the New England Journal  of Medicine
Current ongoing studies:
The SMART (SNP- based Microdeletion and  Aneuploidy RegistTry) study: A  multicenter study to assess prevalence of the 22q11 microdeletion syndrome  (DiGeorge) and NIPS performance for prenatal screening for this syndrome 
Fetoscopic  Surgery for the management of Twin-Twin Transfusion Syndrome: to assess performance  utilizing the Solomon technique
Sonographic, laboratory and histologic assessment of the uterine scar: implications for early screening for pregnancy Morbidly Adherent  Placenta (MAP): Placenta accrete is one of the most severe complications in  patients who had a prior cesarean delivery. This study will assess criteria for  early detection of the complication
Epigenetic  Dysregulation and Fetal Origins of Age-Related Diseases: This research focuses on  understanding the mechanism by which maternal nutrition and exercise during  pregnancy ultimately affects the long-term health of the developing child to  identify strategies to prevent or ameliorate early progression of age-related  diseases.
Sexual  Dimorphism in Offspring Exposed to Adverse Maternal Diet Mediated by  Modifications in DNA Methylation: Focusing on sexual differences, in response to  maladaptive intrauterine conditions that ultimately lead to premature aging,  may provide sex specific biomarkers to help identify infants at higher risk for  chronic diseases later in life.
Ductus Arteriosus changes with gestational age: to assess the in-utero normal changes in one of the most important  shunts in the fetal circulation
The PERFECT study  (PAP for Evaluation and REtrieval of fetal Cells Trial): Assessing  improvement of screening for fetal genetics conditions by assessing fetal cells  retrieved from the maternal cervical canal. 
Sleep apnea in  the obese gravida and perinatal outcome: To assess the impact of sleep apnea in  obese patients on fetal growth and other perinatal outcome parameters 
Sonographic  evaluation of 3-dimensional inter-villus blood flow as a marker of impending  preeclampsia: A new technology for improving early  detection of preeclampsia 
Universal screening or short cervix at routine anatomy sonogram: To assess changes in detection of patients at risk for preterm birth  and their outcome 
Epigenetic  Modifications Associated with Abnormal Growth In Utero: To study the effect of the intra  uterine environment on the genetic structure of the growth restricted fetus
Prediction  of intrauterine growth restriction: Prenatal stratification of risk factors  associated with undiagnosed growth restriction 
Epigenetic  alterations associated with pre-eclampsia in the placenta: To study the placental genetic changes  associated with preeclampisa