The 20 Best Miller Syndrome Doctors in New York, US

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 an Experienced provider by MediFind in the treatment of Miller Syndrome. His top areas of expertise are Micrognathia, KBG Syndrome, Retinopathy Pigmentary Mental Retardation, and Cardiomyopathic Lentiginosis.

Lakshmi Mehta is a Medical Genetics provider in New York, New York. Dr. Mehta is rated as an Experienced provider by MediFind in the treatment of Miller Syndrome. Her top areas of expertise are Microcephaly, Achalasia Microcephaly Syndrome, Hypotonia, and Acromicric Dysplasia. Dr. Mehta is currently accepting new patients.

Gustavo Maegawa is a Medical Genetics provider in New York, New York. Dr. Maegawa is rated as an Experienced provider by MediFind in the treatment of Miller Syndrome. His top areas of expertise are Krabbe Disease, Acid Sphingomyelinase Deficiency (ASMD), Niemann-Pick Disease, and Gaucher Disease. Dr. Maegawa is currently accepting new patients.

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 an Experienced provider by MediFind in the treatment of Miller Syndrome. His top areas of expertise are Preeclampsia, High Blood Pressure in Infants, Gestational Diabetes, Chromosome 13q Duplication, and Hysterectomy.

Kimihiko Oishi is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Oishi is rated as an Experienced provider by MediFind in the treatment of Miller Syndrome. His top areas of expertise are Micrognathia, Citrullinemia, Urea Cycle Disorders (UCD), and Methylmalonic Acidemia with Homocystinuria.

Chimene Kesserwan is a Medical Genetics provider in New York, New York. Dr. Kesserwan is rated as an Experienced provider by MediFind in the treatment of Miller Syndrome. Her top areas of expertise are Li-Fraumeni Syndrome, Chromosome 7p Deletion, Coffin-Siris Syndrome, and Miller Syndrome.