Overview
Seth Berger is a Medical Genetics specialist and a Pediatrics provider in Washington, Washington, D.c.. Dr. Berger is rated as an Experienced provider by MediFind in the treatment of Maple Syrup Urine Disease. His top areas of expertise are Fetal Edema, Hydrops Fetalis, Hemolytic Disease of the Newborn, and Alpha Thalassemia.
His clinical research consists of co-authoring 70 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Maple Syrup Urine Disease.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- POS
- PPO
Locations
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.
Nicholas Ah Mew is a Medical Genetics specialist and a Pediatrics provider in Washington, Washington, D.c.. Dr. Ah Mew is rated as a Distinguished provider by MediFind in the treatment of Maple Syrup Urine Disease. His top areas of expertise are Urea Cycle Disorders (UCD), Maple Syrup Urine Disease, Argininosuccinic Aciduria, and Propionic Acidemia.
Rubenstein Child Health Building
Dr. Ada Hamosh is the Dr. Frank V. Sutland Professor of Pediatric Genetics in the Departments of Genetic Medicine and Pediatrics. Since 2002, she has served as clinical director of the McKusick-Nathans Institute of Genetic Medicine, now Department of Genetic Medicine and scientific director of the Online Mendelian Inheritance in Man® (OMIM), a catalog of more than 16,800 human genes and genetic disorders created by Dr. Victor A. McKusick. Her research centers the molecular basis of Mendelian disorders, the integration of genetics into clinical practice and the diagnosis and management of inborn errors of metabolism. Dr. Hamosh earned a bachelor’s degree in biology from Wesleyan University, a medical degree from Georgetown University School of Medicine and a master’s of public health from Johns Hopkins University School of Public Health. She later completed a fellowship in medical and biochemical genetics from the Johns Hopkins School of Medicine, before joining the Johns Hopkins faculty in 1992. Dr. Hamosh began her genetics career focusing on cystic fibrosis, serving as coordinator of the International Cystic Fibrosis Genotype-Phenotype Consortium. She served as chair of the Maryland State Advisory Council for Hereditary & Congenital Disorders from 2001-2009, during which time she also served on the executive committee of the Genetic Counseling Training Program, run by Johns Hopkins University and the National Human Genome Research Institute. Dr. Hamosh has authored more than 128 publications on a variety of topics. In addition, she is a member of 16 professional associations and advisory committees including the American Society of Human Genetics, the Steering Committee of the Global Alliance for Genomics and Health, and the executive board of the Human Genome Organization, of which she will be President from 2023-2025. Dr. Hamosh was recognized in Baltimore magazine as one of the region’s top doctors in 2013, and 2016-2020. Dr. Hamosh is rated as a Distinguished provider by MediFind in the treatment of Maple Syrup Urine Disease. Her top areas of expertise are Methylmalonic Acidemia, Maple Syrup Urine Disease, Ornithine Transcarbamylase Deficiency, Phenylketonuria (PKU), and Deep Brain Stimulation.
Children's Hospital
Natasha Shur is a Medical Genetics specialist and a Pediatrics provider in Washington, Washington, D.c.. Dr. Shur is rated as an Advanced provider by MediFind in the treatment of Maple Syrup Urine Disease. Her top areas of expertise are Pyruvate Carboxylase Deficiency, Phenylketonuria (PKU), Ehlers-Danlos Syndrome (EDS), and Lowe Syndrome.
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
- Alpha ThalassemiaDr. Berger isDistinguished. Learn about Alpha Thalassemia.
- Fetal EdemaDr. Berger isDistinguished. Learn about Fetal Edema.
- Hemolytic Disease of the NewbornDr. Berger isDistinguished. Learn about Hemolytic Disease of the Newborn.
- HoloprosencephalyDr. Berger isDistinguished. Learn about Holoprosencephaly.
- Hydrops FetalisDr. Berger isDistinguished. Learn about Hydrops Fetalis.
- Advanced
- ALG9-CDGDr. Berger isAdvanced. Learn about ALG9-CDG.
- Early Infantile Epileptic Encephalopathy
- MosaicismDr. Berger isAdvanced. Learn about Mosaicism.
- Experienced
- Achalasia Microcephaly SyndromeDr. Berger isExperienced. Learn about Achalasia Microcephaly Syndrome.
- ALG1-CDGDr. Berger isExperienced. Learn about ALG1-CDG.
- Aplasia Cutis CongenitaDr. Berger isExperienced. Learn about Aplasia Cutis Congenita.
- Arthrogryposis Multiplex CongenitaDr. Berger isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Autism Spectrum DisorderDr. Berger isExperienced. Learn about Autism Spectrum Disorder.
- Brittle Cornea SyndromeDr. Berger isExperienced. Learn about Brittle Cornea Syndrome.
