Overview
Nancy Braverman is a Medical Genetics specialist and a Pediatrics provider in Baltimore, Maryland. Dr. Braverman is rated as an Experienced provider by MediFind in the treatment of Liver Failure. Her top areas of expertise are Zellweger Syndrome, Chondrodysplasia Punctata Syndrome, X-Linked Chondrodysplasia Punctata 2, and Acromesomelic Dysplasia.
Her clinical research consists of co-authoring 88 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 3 articles in the study of Liver Failure.
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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.
1 Clinical Trials
Douglas Mogul is a Pediatrics provider in Baltimore, Maryland. Dr. Mogul is rated as an Advanced provider by MediFind in the treatment of Liver Failure. His top areas of expertise are Biliary Atresia, Liver Failure, Traumatic Brain Injury, and Hepatoblastoma.
Nada Yazigi is a Pediatric Gastroenterologist and a Pediatrics provider in Washington, Washington, D.c.. Dr. Yazigi is rated as an Advanced provider by MediFind in the treatment of Liver Failure. Her top areas of expertise are Crigler-Najjar Syndrome, Liver Failure, Biliary Hypoplasia, Liver Transplant, and Pancreas Transplant. Dr. Yazigi is currently accepting new patients.
Rubenstein Child Health Building
Dr. Jill A. Fahrner is an assistant professor in the Departments of Genetic Medicine and Pediatrics at the Johns Hopkins University School of Medicine. Her area of clinical expertise is medical genetics. Dr. Fahrner earned her Ph.D. from Johns Hopkins University and her M.D. from the University of North Carolina. She completed pediatrics residency training at Duke University Medical Center. She joined the McKusick-Nathans Institute of Genetic Medicine as a genetic medicine resident in 2009 and completed her training in 2012. She stayed on as chief resident from 2012-2013 and then joined the faculty as an assistant professor in the Department of Pediatrics within the McKusick-Nathans Institute of Genetic Medicine in 2013. Her current primary appointment is Assistant Professor in the Department of Genetic Medicine, where she is Director of the multidisciplinary Epigenetics and Chromatin Clinic. She is a physician-scientist with a long-standing interest in epigenetic mechanisms of disease. Her clinical focus is on caring for individuals with epigenetic and chromatin disorders, specifically Mendelian disorders of the epigenetic machinery, or chromatin modifying disorders. She has seen hundreds of individuals with congenital disorders involving disrupted epigenetics, most of which exhibit neurodevelopmental disabilities and abnormal growth. Her laboratory research is focused on understanding disease mechanisms and developing therapies for select Mendelian disorders of the epigenetic machinery. She is a member of the American Society of Human Genetics (ASHG), having won an ASHG Reviewer’s Choice Abstract Award for her work on growth retardation in Kabuki syndrome 1. She has received a Johns Hopkins School of Medicine Clinician Scientist Award, a Johns Hopkins School of Medicine Musculoskeletal Pilot and Feasibility Award, a William and Ella Owens Medical Research Foundation Award, the Margaret Ellen Nielsen Fellowship Award, and the Alice and YT Chen Travel Award while at Johns Hopkins. She is the recipient of a prestigious Hartwell Foundation Individual Biomedical Research Award and also has ongoing research funding from the National Institutes of Health. Dr. Fahrner is rated as a Distinguished provider by MediFind in the treatment of Liver Failure. Her top areas of expertise are Weaver Syndrome, Sotos Syndrome, Kabuki Syndrome, and Marshall-Smith 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
- Elite
- AchondrogenesisDr. Braverman isElite. Learn about Achondrogenesis.
- Acromesomelic DysplasiaDr. Braverman isElite. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux Type
- Chondrodysplasia Punctata Syndrome
- Distinguished
- Congenital CataractDr. Braverman isDistinguished. Learn about Congenital Cataract.
- HypotoniaDr. Braverman isDistinguished. Learn about Hypotonia.
- Advanced
- Dubowitz SyndromeDr. Braverman isAdvanced. Learn about Dubowitz Syndrome.
- Malonyl-CoA Decarboxylase DeficiencyDr. Braverman isAdvanced. Learn about Malonyl-CoA Decarboxylase Deficiency.
- Experienced
- Aase SyndromeDr. Braverman isExperienced. Learn about Aase Syndrome.
- Adrenoleukodystrophy (ALD)Dr. Braverman isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Argininosuccinic AciduriaDr. Braverman isExperienced. Learn about Argininosuccinic Aciduria.
- Bietti Crystalline Dystrophy (BCD)Dr. Braverman isExperienced. Learn about Bietti Crystalline Dystrophy (BCD).
- HypermethioninemiaDr. Braverman isExperienced. Learn about Hypermethioninemia.
- Infantile Refsum DiseaseDr. Braverman isExperienced. Learn about Infantile Refsum Disease.
