The 20 Best Chromosome 13q Duplication Doctors in New York, US

Dr. Ronald Wapner is the Director of Reproductive Genetics and Professor of Obstetrics and Gynecology at Columbia University Irving Medical Center. Prior to Columbia University, Dr. Wapner was a Professor of Obstetrics and Gynecology at Drexel University College of Medicine and taught at Thomas Jefferson University for 22 years where he also served as the Director of Maternal Fetal Medicine. Dr. Wapner is an internationally known physician and researcher specializing in reproductive genetics. He pioneered the development of chorionic villus sampling (CVS) and multi-fetal reduction. He has authored or co-authored over 450 publications and he has been an active investigator in the area of Maternal-Fetal Medicine (MFM). Dr. Wapner is rated as a Distinguished provider by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are Preeclampsia, High Blood Pressure in Infants, Gestational Diabetes, Chromosome 13q Duplication, and Hysterectomy.

Rajeevi Madankumar is an Obstetrics and Gynecologist in New Hyde Park, New York. Dr. Madankumar is rated as an Advanced provider by MediFind in the treatment of Chromosome 13q Duplication. Her top areas of expertise are Chromosome 13q Duplication, Trisomy 13, Trisomy 18, and Methimazole Antenatal Exposure.

Susan Klugman, MD, FACOG, FACMG, is Director, Reproductive and Medical Genetics, Program Director, Medical Genetics and Genomics Residency and Professor, Obstetrics & Gynecology and Women’s Health and Pediatrics at Montefiore Einstein. Her clinical focus is on the evaluation of patients and families at risk for genetic disorders including those patients at risk for hereditary cancer syndromes. She also provides evaluations during pregnancy or preconception, including prenatal diagnosis and consultation for patients undergoing assisted reproductive technologies. Dr. Klugman is rated as an Advanced provider by MediFind in the treatment of Chromosome 13q Duplication. Her top areas of expertise are Mosaicism, Chromosome 13q Duplication, Trisomy 13, Holoprosencephaly, and Salpingo-Oophorectomy.

Pe’er Dar, MD, is Director of Fetal Medicine and OBGYN Ultrasound at Montefiore and Professor of Obstetrics and Gynecology and Women’s Health at our Albert Einstein College of Medicine. Dr. Dar’s clinical focus is on the care of women who carry babies with disorders and medical conditions that may affect their lives and he leads the Fetal Medicine and Surgery Team at Montefiore. He particularly specializes in diagnosis and management of medical and structural abnormalities in the fetus and in complicated twin and triplet pregnancies. His expertise include performing detailed ultrasound examination of the fetus including fetal echocardiography (scanning of the fetal heart) and fetal neurosonography (scanning of the fetal brain) as well as performing in-utero fetal surgeries such as fetoscopic laser surgery for monochorionic twins with twin to twin transfusion syndrome, in-utero blood transfusion for fetuses with anemia and in-utero drainage and shunt procedures. Dr. Dar is also experienced in performing amniocentesis, chorionic villous sampling (CVS) and multifetal selective reduction for multiple pregnancies.    Dr. Dar completed his Doctor of Medicine from Tel-Aviv University in Tel-Aviv, Israel in 1986. He started his postgraduate education at Assaf Harofe Medical Center, Tel-Aviv University, with a residency in obstetrics and gynecology and a specialty in high-risk pregnancies from 1992 through 1998. He then came to Montefiore-Einstein, completing a two-year fellowship in medical and reproductive genetics. After spending two years as an attending-specialist in the field of prenatal diagnosis he completed in 2005 three-year residency in obstetrics and gynecology at Montefiore-Einstein. In 2007, he completed additional training in fetal surgery in world-known fetal surgery centers in France and Belgium.  Dr. Dar is very active in research and he is currently the principal investigator in many studies including international multicenter studies. His research focus is in fetal medicine and surgery, non-invasive prenatal screening and placenta accreta spectrum. He has shared his work in many peer-reviewed journals, textbook chapters, abstracts and invited presentations. He is also a reviewer for national and international journals including the American Journal of Obstetrics and Gynecology, Plos one and Prenatal Diagnosis. Dr. Dar is board certified in both Obstetrics and Gynecology and Clinical Genetics and is a member of several professional societies including the Society of Maternal and Fetal Medicine, International Fetal Medicine and Surgery Society and the International Society of Ultrasound in Obstetrics and Gynecology. He has been regularly listed among Castle Connolly Top Doctors for obstetrics and gynecology in the New York Metro area. Dr. Dar is rated as an Advanced provider by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are Placenta Previa, Trisomy 18, Trisomy 13, and Chromosome 13q Duplication.

Stephen Chasen is an Obstetrics and Gynecologist in New York, New York. Dr. Chasen is rated as an Advanced provider by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are Placenta Previa, Trisomy 18, Preeclampsia, Cavernous Lymphangioma, and Hysterectomy.

Fergal Malone is an Obstetrics and Gynecologist in New York, New York. Dr. Malone is rated as an Advanced provider by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are Intrauterine Growth Restriction, Preeclampsia, Twin-To-Twin Transfusion Syndrome, and Chromosome 13q Duplication.

Ashley Roman is a Neonatologist and an Obstetrics and Gynecologist in New York, New York. Dr. Roman is rated as an Advanced provider by MediFind in the treatment of Chromosome 13q Duplication. Her top areas of expertise are Chromosome 13q Duplication, Trisomy 13, Intrauterine Growth Restriction, and Trisomy 18.

Paul Levy, MD, is Director, Center for Inherited Metabolic Disorders and Director, Inherited Metabolic Disease Specialty Care Referral Center at the Children’s Hospital at Montefiore Einstein. He is also Associate Professor, Pediatrics and Pathology at our Albert Einstein College of Medicine. Dr. Levy sees patients with complex medical issues that may have a genetic etiology. He has a special interest in inherited metabolic disorders, including phenylketonuria (PKU), lysosomal storage diseases and urea cycle disorders, and sees newborns referred by the New York State Newborn Screening Program with positive screens. Dr. Levy is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are Krabbe Disease, Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), and N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3.

Gary Fruhman is a Neonatologist and a Medical Genetics provider in Staten Island, New York. Dr. Fruhman is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are Gestational Diabetes, Polyhydramnios, Premature Infant, and Fetal Enterovirus Syndrome.

Dr. Garfield Ashford Dwight Clunie is Director, Maternal-Fetal Medicine at White Plains Hospital. He is board-certified in both Maternal-Fetal Medicine and in Obstetrics & Gynecology. Dr. Clunie is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are Chromosome 13q Duplication, Trisomy 13, Trisomy 18, and Cri-Du-Chat Syndrome.

Nidhi Vohra is a Neonatologist and an Obstetrics and Gynecologist in New Hyde Park, New York. Dr. Vohra is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. Her top areas of expertise are Gestational Diabetes, Fetal Enterovirus Syndrome, Methimazole Antenatal Exposure, and Polyhydramnios.

Oliver Barry is a Pediatrics specialist and a Pediatric Cardiologist in New York, New York. Dr. Barry is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are Pulmonary Valve Stenosis, Total Anomalous Pulmonary Venous Return, Hypoplastic Left Heart Syndrome (HLHS), Congenital Heart Disease (CHD), and Heart Transplant. Dr. Barry is currently accepting new patients.

Vincent Duron, MD is Co-Director of Fetal Therapy, Director of Minimally Invasive Surgery, and Director of Pediatric Trauma and Surgical Critical Care. He practices the full spectrum of pediatric general surgery. He is an expert in minimally invasive surgery, specializing in surgery for congenital anomalies, biliary atresia, lung anomalies, and pectus excavatum. He performs fetal surgery for various conditions, including fetoscopic repair of myelomeningocele/spina bifida and fetoscopic endoluminal tracheal occlusion (FETO) for congenital diaphragmatic hernia. Dr. Duron is a well-funded surgeon-scientist. His research focuses on fluid optimization for critically ill children and fetal and neonatal diagnostics and surgery. He has received multiple research and teaching awards and is a frequently invited speaker, author, and reviewer. He is dedicated to global health and regularly returns to Iquitos, Peru, to train local surgeons in pediatric surgery. Dr. Duron is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are Diaphragmatic Hernia, Congenital Diaphragmatic Hernia, Polyhydramnios, Gastrostomy, and Endoscopy.

Dr. Marion is Executive Director of the Children’s Evaluation and Rehabilitation Center and the University Center of Excellence in Developmental Disabilities at the Rose F. Kennedy Center. He is Chief of the Divisions of Genetics and of Development Medicine at the Children’s Hospital at Montefiore and Director of the Center for Congenital Disorders. A faculty member at Einstein since 1984, Dr. Marion’s interests include the natural history and genetic basis of multiple malformation syndromes. At The Children’s Hospital at Montefiore he has served as Medical Director of the Spina Bifida Center for 20 years, is the founder and Medical Director of the Williams Syndrome Center, and helped organize the Center for CardioG enetics, the Neurofibromatosis Center, and the Center for Excellence in Autism. He has published extensively in the medical literature in these areas and, in addition, is the author of seven books. Dr. Marion is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3, and Mucopolysaccharidoses (MPS).

Georgios Doulaveris, MD, FACOG, is Program Director, Maternal-Fetal Medicine Fellowship Program and Assistant Professor, Obstetrics & Gynecology and Women’s Health at Montefiore Einstein. He specializes in detailed fetal ultrasound for the diagnosis and treatment of fetal malformations, fetal therapy and surgery, prenatal screening for aneuploidy, genetic diagnostic procedures (chorionic villus sampling and amniocentesis), diagnosis and management of fetal growth restriction, multiple gestations and placenta accreta spectrum. He also serves as Director of the Ultrasound Education Program for obstetrics & gynecology residents and as Director of Research of the Fetal Medicine & Ultrasound Division. Dr. Doulaveris is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. His top areas of expertise are High Blood Pressure in Infants, Endometrial Cancer, Small for Gestational Age, Hormone Replacement Therapy (HRT), and Intrauterine Device Insertion.

Dr Levasseur joined the division of Pediatric Cardiology in 2003 after completing her cardiology training at Toronto’s Hospital for Sick Children and a year of advanced echocardiography at Boston’s Children’s Hospital.Dr Levasseur’s passion for the prenatal diagnosis of cardiac anomalies and the support of affected families developed early in her cardiac imaging career. Her practice is dedicated to the care of the most complex patients with congenital heart disease before and after birth. She became director of the Fetal Cardiac Program at Columbia University Medical Center, one of the largest in the country, in 2012 and became director of the noninvasive imaging laboratory (which includes echocardiography, fetal cardiology as well as cardiac magnetic resonance imaging and cardiac computed tomography imaging) in 2016. Dr. Levasseur is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. Her top areas of expertise are Ebstein's Anomaly, Tetralogy of Fallot, Partial Atrioventricular Canal, and Transposition of the Great Arteries.

Kinjal Desai is a Pediatric Cardiologist in New York, New York. Dr. Desai is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. Her top areas of expertise are Kawasaki Disease, Chromosome 13q Duplication, Trisomy 13, and Tricuspid Regurgitation.

Mary D'alton is an Obstetrics and Gynecologist in New York, New York. Dr. D'alton is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. Her top areas of expertise are Preeclampsia, Venous Thromboembolism (VTE), Eclampsia, Hysterectomy, and Intrauterine Device Insertion.

Mariel Turner is a Pediatrics provider in New York,, New York. Dr. Turner is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. Her top areas of expertise are Pulmonary Vein Stenosis, Total Anomalous Pulmonary Venous Return, Hypoplastic Left Heart Syndrome (HLHS), Heart Transplant, and Percutaneous Coronary Intervention (PCI).

Meghana Limaye is a Neonatologist and an Obstetrics and Gynecologist in New York, New York. Dr. Limaye is rated as an Experienced provider by MediFind in the treatment of Chromosome 13q Duplication. Her top areas of expertise are High Blood Pressure in Infants, Cerebral Hypoxia, Newborn Transient Tachypnea, and Chromosome 13q Duplication.