Overview
Peer Dar is an Obstetrics and Gynecologist and a Medical Genetics provider in Bronx, New York. Dr. Dar is rated as an Experienced provider by MediFind in the treatment of Mosaicism. His top areas of expertise are Placenta Previa, Trisomy 18, Trisomy 13, and Chromosome 13q Duplication.
His clinical research consists of co-authoring 5 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- HMO
- POS
- EPO
- HMO
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE-MEDICAID PLAN
- EPO
- HMO
- POS
- PPO
Locations
111 E 210th St, Bronx, NY 10467
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.
2 Clinical Trials
Brynn Levy is a Medical Genetics provider in New York, New York. Dr. Levy is rated as an Advanced provider by MediFind in the treatment of Mosaicism. His top areas of expertise are Mosaicism, Holoprosencephaly, Mosaic Variegated Aneuploidy Syndrome, Mosaic Monosomy 22, and Endoscopy.
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 rated as a Distinguished provider by MediFind in the treatment of Mosaicism. His top areas of expertise are Cornelia De Lange Syndrome, Pallister-Killian Mosaic Syndrome, Mosaicism, and KBG Syndrome.
Ronald Wapner is a Medical Genetics specialist and a Neonatologist in New York, New York. Dr. Wapner is rated as a Distinguished provider by MediFind in the treatment of Mosaicism. His top areas of expertise are Preeclampsia, High Blood Pressure in Infants, Gestational Diabetes, Intraventricular Hemorrhage of the Newborn, and Hysterectomy.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Advanced
- Chromosome 13q DuplicationDr. Dar isAdvanced. Learn about Chromosome 13q Duplication.
- Placenta PreviaDr. Dar isAdvanced. Learn about Placenta Previa.
- Trisomy 13Dr. Dar isAdvanced. Learn about Trisomy 13.
- Trisomy 18Dr. Dar isAdvanced. Learn about Trisomy 18.
- Experienced
- 1p36 Deletion SyndromeDr. Dar isExperienced. Learn about 1p36 Deletion Syndrome.
- Angelman SyndromeDr. Dar isExperienced. Learn about Angelman Syndrome.
- Cat Eye SyndromeDr. Dar isExperienced. Learn about Cat Eye Syndrome.
- Cortical DysplasiaDr. Dar isExperienced. Learn about Cortical Dysplasia.
- Cri-Du-Chat SyndromeDr. Dar isExperienced. Learn about Cri-Du-Chat Syndrome.
- DiGeorge SyndromeDr. Dar isExperienced. Learn about DiGeorge Syndrome.
