Overview
Olaf Bodamer is a Medical Genetics provider in Boston, Massachusetts. Dr. Bodamer is rated as an Experienced provider by MediFind in the treatment of Hydrops Fetalis. His top areas of expertise are Kabuki Syndrome, Classic Galactosemia, Niemann-Pick Disease, and Mucopolysaccharidoses (MPS). Dr. Bodamer is currently accepting new patients.
His clinical research consists of co-authoring 110 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Hydrops Fetalis.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- OTHER MEDICAID
- STATE MEDICAID
- HMO
- EPO
- HMO
- POS
- PPO
Locations
300 Longwood Ave, Bch3446, Boston, MA 02115
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.
1 Clinical Trials
Children's Hospital Pediatric Associates, Inc
Deborah Marsden is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Marsden is rated as a Distinguished provider by MediFind in the treatment of Hydrops Fetalis. Her top areas of expertise are Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidoses (MPS), Hydrops Fetalis, and Fetal Edema. Dr. Marsden is currently accepting new patients.
Fowzan Alkuraya is a Pediatrics specialist and a Medical Genetics provider in Boston, Massachusetts. Dr. Alkuraya is rated as an Elite provider by MediFind in the treatment of Hydrops Fetalis. His top areas of expertise are Achalasia Microcephaly Syndrome, Microcephaly, Early Infantile Epileptic Encephalopathy, Cortical Dysplasia, and Vitrectomy.
Mary Hitchcock Memorial Hospital
Mary Dinulos is a Medical Genetics specialist and a Pediatrics provider in Manchester, New Hampshire. Dr. Dinulos is rated as an Advanced provider by MediFind in the treatment of Hydrops Fetalis. Her top areas of expertise are Brittle Cornea Syndrome, Vascular Ehlers-Danlos Syndrome (VEDS), 1p36 Deletion Syndrome, and Gingival Fibromatosis with Hypertrichosis.
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
- Elite
- Kabuki SyndromeDr. Bodamer isElite. Learn about Kabuki Syndrome.
- Distinguished
- Achalasia Microcephaly SyndromeDr. Bodamer isDistinguished. Learn about Achalasia Microcephaly Syndrome.
- Classic GalactosemiaDr. Bodamer isDistinguished. Learn about Classic Galactosemia.
- MicrocephalyDr. Bodamer isDistinguished. Learn about Microcephaly.
- Mucopolysaccharidoses (MPS)Dr. Bodamer isDistinguished. Learn about Mucopolysaccharidoses (MPS).
- Niemann-Pick DiseaseDr. Bodamer isDistinguished. Learn about Niemann-Pick Disease.
- Propionic AcidemiaDr. Bodamer isDistinguished. Learn about Propionic Acidemia.
- Advanced
- 3MC SyndromeDr. Bodamer isAdvanced. Learn about 3MC Syndrome.
- Autism Spectrum DisorderDr. Bodamer isAdvanced. Learn about Autism Spectrum Disorder.
- Beckwith-Wiedemann SyndromeDr. Bodamer isAdvanced. Learn about Beckwith-Wiedemann Syndrome.
- Branchio-Oculo-Facial Syndrome (BOFS)
- Cantu SyndromeDr. Bodamer isAdvanced. Learn about Cantu Syndrome.
- Cat Eye SyndromeDr. Bodamer isAdvanced. Learn about Cat Eye Syndrome.
- Experienced
- 15q11.2 MicrodeletionDr. Bodamer isExperienced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Bodamer isExperienced. Learn about 2q37 Deletion Syndrome.
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- 3p Deletion SyndromeDr. Bodamer isExperienced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Bodamer isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Bodamer isExperienced. Learn about Aase Syndrome.