Overview
Eva Morava is a Medical Genetics provider in New York, New York. Dr. Morava is rated as an Experienced provider by MediFind in the treatment of KBG Syndrome. Her top areas of expertise are MELAS Syndrome, ALG6-CDG, Phenylketonuria (PKU), and Glutaric Acidemia Type 1.
Her clinical research consists of co-authoring 16 peer reviewed articles and participating in 6 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:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
1428 Madison Ave, New York, NY 10029
Additional Areas of Focus
Dr. Morava has provided the following conditions as areas of focus. Please note that we may not have enough data to validate their experience in some of these conditions.
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.
6 Clinical Trials
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 KBG Syndrome. His top areas of expertise are Cornelia De Lange Syndrome, Pallister-Killian Mosaic Syndrome, Mosaicism, and KBG Syndrome.
Erica Fernandes is a Medical Genetics specialist and a Pediatrics provider in New Hyde Park, New York. Dr. Fernandes is rated as an Advanced provider by MediFind in the treatment of KBG Syndrome. Her top areas of expertise are Microcephaly, Chromosome 13q Deletion, Acrodermatitis Enteropathica, and CHARGE Syndrome.
Mafalda Cabral-Dos is a Medical Genetics provider in New York, New York. Dr. Cabral-Dos is rated as an Advanced provider by MediFind in the treatment of KBG Syndrome. Her top areas of expertise are Snyder-Robinson Syndrome, Caudal Appendage Deafness, Acrodermatitis Enteropathica, and Trichorhinophalangeal Syndrome Type 2.
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
- ALG6-CDGDr. Morava isAdvanced. Learn about ALG6-CDG.
- MELAS SyndromeDr. Morava isAdvanced. Learn about MELAS Syndrome.
- Experienced
- 2q37 Deletion SyndromeDr. Morava isExperienced. Learn about 2q37 Deletion Syndrome.
- 47 XYY SyndromeDr. Morava isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Morava isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Morava isExperienced. Learn about Abruzzo-Erickson Syndrome.
- Acrodermatitis EnteropathicaDr. Morava isExperienced. Learn about Acrodermatitis Enteropathica.
- Acrorenal Mandibular SyndromeDr. Morava isExperienced. Learn about Acrorenal Mandibular Syndrome.