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 HNRNPH2-Related Disorder. 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.
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
Lance Rodan is a Medical Genetics specialist and a Pediatric Neurologist in Boston, Massachusetts. Dr. Rodan is rated as a Distinguished provider by MediFind in the treatment of HNRNPH2-Related Disorder. His top areas of expertise are Hennekam Syndrome, Increased Head Circumference, Polymicrogyria, Retinopathy Pigmentary Mental Retardation, and Deep Brain Stimulation. Dr. Rodan is currently accepting new patients.
Children's Hospital Pediatric Associates, Inc
Stephanie Sacharow is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Sacharow is rated as a Distinguished provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Cat Eye Syndrome, and Dihydropteridine Reductase Deficiency. Dr. Sacharow is currently accepting new patients.
Children's Hospital Pediatric Associates, Inc
Amy Kritzer is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Kritzer is rated as a Distinguished provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Maternal Hyperphenylalaninemia, Phenylketonuria (PKU), Biotinidase Deficiency, and Smith-Lemli-Opitz Syndrome. Dr. Kritzer is currently accepting new patients.
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.