Dr. Odelya H. Kaufman
Overview
Odelya Kaufman, MD, PhD, is an Assistant Professor of Pediatrics at Columbia University Irving Medical Center, Division of Clinical Genetics. Odelya’s clinical expertise is in the diagnosis and management of children and adults with genetic conditions, including various birth defects, developmental disabilities, and pediatric hearing loss or blindness. Odelya attended a combined medical school and graduate program at the Albert Einstein College of Medicine (Bronx, NY) where her PhD studies focused on the functions of RNA binding proteins in ovary development. She subsequently completed her medical residency in Pediatrics and Medical Genetics at Mount Sinai Hospital (New York, NY) where she also participated in research to uncover genetic causes for critically ill infants in the NICU. Her current research interests focus on pediatric rare disease and implementation of genomic medicine.
Dr. Kaufman is board certified in Clinical Genetics And Genomics (MD). She is actively involved in clinical research, co-authoring 7 peer reviewed articles. Dr. Kaufman is currently accepting new patients.
Graduate Institution
Residency
Specialties
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Board Certifications
Languages Spoken
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Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- OTHER MEDICARE PART D
- EPO
- PPO
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
Locations
1111 Westchester Avenue, White Plains, NY 10604
3959 Broadway, New York, NY 10032
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
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Cohen Children's Northwell Health Physician Partners Medical Genetics
Dr. Ian Daniel Krantz, MD, is a renowned physician specializing in Genetics and Pediatrics. He currently sees patients at Cohen Children's Medical Center (CCMC) and Northwell Health Physician Partners Medical Genetics. Dr. Krantz holds certifications in Clinical Genetics, Cytogenetics, and Pediatrics from the American Board of Medical Genetics and the American Board of Pediatrics, respectively.Dr. Krantz completed his BFA at Concordia University in Montreal and his MD at Sackler School of Medicine (Tel Aviv University). He completed his residency in Medical Genetics at Children's Hospital of Philadelphia and his residency in Pediatrics at New York University Medical Center.With an impressive set of academic and administrative titles, Dr. Krantz serves as the Division Chief of Pediatric Genetics and Genomics at Cohen Children's Medical Center and is the System Vice President for Pediatric Genetics at Northwell Health. Additionally, he holds the position of Professor at the Zucker School of Medicine at Northwell Health.Dr. Krantz is recognized for his clinical expertise in isolated and syndromic forms of congenital birth differences and developmental diagnoses, including syndromic and non-syndromic autism. He has a special interest in the genetics of hearing loss and focused expertise in Cornelia de Lange Syndrome, Pallister-Killian syndrome, Alagille syndrome, CHOPS syndrome, among others.Dr. Krantz's research is dedicated to identifying and characterizing the molecular etiology of syndromic and non-syndromic developmental diagnoses. His research lab has made significant contributions in the field, discovering new disease genes and shedding light on critical molecular pathways involved in human developmental disorders.Driven by his commitment to advancing patient care, Dr. Krantz has been at the forefront of integrating genomic technologies into the clinical setting. He has implemented rapid genome sequencing into the NICU and CICU and established biobanks and biorepositories to further research efforts. Through his work, he aims to understand the impact of complex diagnostic information on clinicians and families involved.With his extensive expertise and dedication to advancing genetic research and patient care, Dr. Krantz continues to make significant contributions to the field of Pediatrics and Genetics. Dr. Krantz is highly rated in 15 conditions, according to our data. His clinical expertise encompasses Cornelia De Lange Syndrome, Pallister-Killian Mosaic Syndrome, Mosaicism, and KBG Syndrome.
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Frequently Asked Questions about Dr. Odelya H. Kaufman
How do I make an appointment with Dr. Odelya H. Kaufman?
You can book an appointment with Dr. Odelya H. Kaufman by calling their office at 212-305-6731. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Does Dr. Odelya H. Kaufman accept my insurance?
Dr. Odelya H. Kaufman accepts most major insurance plans, including Cigna and EmblemHealth. We recommend calling the office directly at 212-305-6731 to verify that your specific plan is currently accepted before your visit.
Areas of Expertise
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