
Overview
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 highly rated in 5 conditions, according to our data. His clinical expertise encompasses Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidoses (MPS), and Williams Syndrome.
He is actively involved in clinical research, co-authoring 25 peer reviewed articles. Dr. Marion is currently accepting new patients.
Specialties
Licenses
Fellowships
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- MEDICARE SNP
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- OTHER MEDICARE
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- EPO
- HMO
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- OTHER MEDICARE PART D
- MANAGED MEDICAID PLAN
- MEDICARE SNP
- HMO
- POS
- HMO
- INDEMNITY
- POS
- PPO
- MEDICARE SNP
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE-MEDICAID PLAN
- EPO
- PPO
- EPO
- HMO
- PPO
- MEDICARE-MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE-MEDICAID PLAN
- EPO
- HMO
- POS
- PPO
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
3415 Bainbridge Avenue, Bronx, NY 10467
1250 Waters Place, Bronx, NY 10461
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.
Cohen Children's Northwell Health Physician Partners Pediatric Orthopaedics
Dr. Sarwahi, heads the Center for Minimally Invasive Scoliosis Surgery and the Center for Advanced Pediatric Orthopedics at Cohens Children s Medical Center, which brings together a dedicated team of fellowship-trained Scoliosis surgeons, neurologists, anesthesiologists, hospitalists, nursing staff and others in state of the art treatment of scoliosis. Few centers in the world offer this technique, technology and team approach.Dr Sarwahi was the Edwin Warner Ryerson Fellow in Pediatric Orthopaedics at Northwestern University Medical School in Chicago. and completed another fellowship in spine deformity at the Hospital for Special Surgery of Cornell University, New York. This extensive training uniquely qualifies him to treat children and adolescents with the expertise of a spine surgeon and the approach of a pediatric orthopaedic surgeon. He is an active member of the Scoliosis Research Society, North American Spine Society and the Society for Minimally Invasive Spine Surgery.Dr Sarwahi has pioneered the minimally invasive scoliosis surgery for idiopathic scoliosis and published the first journal article in the world in the August 2011 issue of Scoliosis and a two-year follow up in the May 2014 issue of the Journal of Spinal Disorders & Techniques. Dr Sarwahi is leading the field again by providing this approach to children with neurological disorders. He is actively involved in basic and clinical science research, and has won numerous national and international awards and nominations. Russell Hibbs science Award (2015, 2013 nomination Scoliosis Research Society),Thomas Whitecloud Award ( 2014, 2014 nomination, 2011 won, Scoliosis Research Society), Young Investigator Research Award- clinical and basic science (2013, 2013 Pediatric Orthopaedic Society of North America), Value Award (North American Spine Society 2013 nomination), Richard D Selznik, MD Award (2013, 2011, 2010, 2009, 2006 Albert Einstein College of Medicine), Louis Goldstein Award (2010 nomination, Scoliosis Research Society), Teacher Of the Year Award 2009, Albert Einstein College Of Medicine, Bronx, New York, Joseph L Posch, MD Award 2004, Best Paper-American Association of Hand Surgeons, 2004 are some of the many. He has co-edited the textbook Spondylolisthesis: Diagnosis, Non-Surgical Management, and Surgical Techniques.Dr Sarwahi is ranked by Becker s Spine review amongst the 12 spine surgeons performing minimally invasive scoliosis surgery in the country. He has been invited by multiple organizations and has presented his technique at a half day course organized by the Scoliosis Research Society at its 47th Annual meeting. His surgical innovations and surgical results have been profiled by NY Daily News, NY1, the Journal News, Sanjay Gupta at www.everydayhealth.com/sanjay-gupta/star-tennis-play etc. He is actively involved in the training of fellows, residents and medical students and annually donates his time to the education of spine surgeons in India. Dr. Sarwahi is highly rated in 8 conditions, according to our data. His clinical expertise encompasses Scoliosis, Adolescent Idiopathic Scoliosis, Kyphosis, Spinal Fusion, and Osteotomy. Dr. Sarwahi is board certified in American Board Of Orthopaedic Surgery. Dr. Sarwahi is currently accepting new patients.
CUIMC/NewYork-Presbyterian Morgan Stanley Children's Hospital
Joshua Milner is a leader in the field of discovery and immunopathogenesis of genetic diseases that lead to allergic symptoms. Among the disorders he has described and/or found major mechanistic insight are PLAID—an immune disorder that leads to lifelong cold urticaria, the glycosylation disorder PGM3 deficiency, ERBIN mutation, CARD11 dominant negative mutations, STAT3 gain-of-function, Hereditary Alpha Tryptasemia Syndrome, IL-6 receptor deficiency, and others. Dr. Milner graduated with an SB in biology from the Massachusetts Institute of Technology (MIT) in 1995 and an MD with distinction in immunology from the Albert Einstein College of Medicine. He completed his residency in pediatrics at the Children’s National Medical Center in Washington, DC, and, as the recipient of the Pediatric Scientist Development Program Fellowship, did his fellowship in allergy and immunology at NIAID. He completed a postdoctoral fellowship with Dr. William E. Paul, NIAID, examining issues of mouse T-cell receptor repertoires before beginning as an investigator in the Laboratory of Allergic Diseases in the NIAID, where he was eventually named chief.Dr. Milner's vision is to establish how genetic variation can help inform diagnosis and care of all patients with allergic disease—rare and common, severe and mild. This is achieved by performing genetic sequencing on samples from patients with allergic disease of all sorts, as well as performing functional studies on the same patient samples, which together help point to specific immune pathways that may be fundamentally causing disease. This comprehensive analysis, when performed in larger populations, will help personalize medicine so that patients can be better categorized for targeted care. Furthermore, this type of research and care requires a coordinated and comprehensive interdisciplinary approach, taking advantage of the expertise across the department of pediatrics and at multiple outpatient sites. Dr. Milner is highly rated in 11 conditions, according to our data. His clinical expertise encompasses Autosomal Dominant Hyper IgE Syndrome, Hyper IgE Syndrome, Multisystem Inflammatory Syndrome in Children (MIS-C), and Hereditary Alpha-Tryptasemia. Dr. Milner is board certified in Allergy And Immunology. Dr. Milner is currently accepting new patients.
Kings County Hospital Center
Randall Kaye is a Pediatrics provider practicing medicine in Brooklyn, New York. Dr. Kaye is highly rated in 1 condition, according to our data. His clinical expertise encompasses Pseudobulbar Affect.
Frequently Asked Questions about Dr. Robert W. Marion
How do I make an appointment with Dr. Robert W. Marion?
You can book an appointment with Dr. Robert W. Marion by calling their office at 718-741-2323. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Robert W. Marion a top-rated expert for Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Robert W. Marion is classified as an Distinguished expert for Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
What conditions does Dr. Robert W. Marion specialize in?
While Dr. Robert W. Marion is a Pediatrics, they have specific expertise in Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), and Mucopolysaccharidoses (MPS). MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Pediatrics.
Does Dr. Robert W. Marion participate in research or clinical trials?
Yes. Dr. Robert W. Marion has published 25 articles and abstracts on conditions like Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome). You can view a list of Dr. Robert W. Marion's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Robert W. Marion accept my insurance?
Dr. Robert W. Marion accepts most major insurance plans, including Aetna and Anthem BCBS. We recommend calling the office directly at 718-741-2323 to verify that your specific plan is currently accepted before your visit.
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
- Distinguished
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome)
- Advanced
- ChondrodystrophyDr. Marion isAdvanced. Learn about Chondrodystrophy.
- Mucopolysaccharidoses (MPS)Dr. Marion isAdvanced. Learn about Mucopolysaccharidoses (MPS).
- Williams SyndromeDr. Marion isAdvanced. Learn about Williams Syndrome.
- Experienced
- AEC SyndromeDr. Marion isExperienced. Learn about AEC Syndrome.
- CHARGE SyndromeDr. Marion isExperienced. Learn about CHARGE Syndrome.
- Chromosome 13q DuplicationDr. Marion isExperienced. Learn about Chromosome 13q Duplication.
- Early Infantile Epileptic Encephalopathy
- Gorlin-Chaudhry-Moss SyndromeDr. Marion isExperienced. Learn about Gorlin-Chaudhry-Moss Syndrome.
- Immune Defect due to Absence of ThymusDr. Marion isExperienced. Learn about Immune Defect due to Absence of Thymus.
- Koolen De Vries SyndromeDr. Marion isExperienced. Learn about Koolen De Vries Syndrome.
- Microcephaly Deafness SyndromeDr. Marion isExperienced. Learn about Microcephaly Deafness Syndrome.
- Pompe DiseaseDr. Marion isExperienced. Learn about Pompe Disease.
- Trisomy 13Dr. Marion isExperienced. Learn about Trisomy 13.
- Von Gierke DiseaseDr. Marion isExperienced. Learn about Von Gierke Disease.
- Wildervanck SyndromeDr. Marion isExperienced. Learn about Wildervanck Syndrome.

