Andrea Gropman is a Pediatric Neurologist and a Neurologist in Memphis, Tennessee. Dr. Gropman is rated as an Elite provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. Her top areas of expertise are Klinefelter Syndrome, Urea Cycle Disorders (UCD), MELAS Syndrome, Ornithine Transcarbamylase Deficiency, and Hormone Replacement Therapy (HRT).

Sharon Cunningham practices in Westmead, Australia. Cunningham is rated as an Elite expert by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. Their top areas of expertise are Ornithine Transcarbamylase Deficiency, Urea Cycle Disorders (UCD), Orotic Aciduria Type 1, and Progressive Familial Intrahepatic Cholestasis Type 3.

Ian Alexander practices in Westmead, Australia. Mr. Alexander is rated as an Elite expert by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. His top areas of expertise are Ornithine Transcarbamylase Deficiency, Urea Cycle Disorders (UCD), Orotic Aciduria Type 1, X-Linked Severe Combined Immunodeficiency, and Liver Transplant.

Johannes Haberle practices in Zurich, Switzerland. Mr. Haberle is rated as an Elite expert by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. His top areas of expertise are Urea Cycle Disorders (UCD), Ornithine Transcarbamylase Deficiency, N-Acetylglutamate Synthase Deficiency, Citrullinemia, and Liver Transplant.

Alexander Laemmle practices in Bern, Switzerland. Mr. Laemmle is rated as an Elite expert by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. His top areas of expertise are Ornithine Transcarbamylase Deficiency, Urea Cycle Disorders (UCD), Vitamin B12 Deficiency, and Hypotonia.

. Dr. Murphy is rated as an Advanced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. His top areas of expertise are Hypertension, Familial Hypertension, Maturity Onset Diabetes of the Young, and Glucocorticoid-Remediable Aldosteronism.

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 Ornithine Transcarbamylase Deficiency. Her top areas of expertise are Methylmalonic Acidemia, Maple Syrup Urine Disease, Ornithine Transcarbamylase Deficiency, Phenylketonuria (PKU), and Deep Brain Stimulation.

. Dr. Gibson is rated as an Experienced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. His top areas of expertise are Acute Cystitis, Morning Sickness, Hospital-Acquired Pneumonia, and Atypical Pneumonia.

Mari Mori is a Medical Genetics specialist and a Pediatrics provider in Maitland, Florida. Dr. Mori is rated as an Advanced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. Her top areas of expertise are Glycogen Storage Disease Type 7, FG Syndrome, Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), and Von Gierke Disease. Dr. Mori is currently accepting new patients.

Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider in Grand Rapids, Michigan. Dr. Priestley has been practicing medicine for over 8 years and is rated as an Advanced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. Her top areas of expertise are Fabry Disease, Ornithine Transcarbamylase Deficiency, Biotinidase Deficiency, and Multiple Sulfatase Deficiency.

Dr. Hilary Vernon is a Professor of Genetic Medicine and pediatrics at the Johns Hopkins University School of Medicine. She is also an attending physician at Kennedy Krieger Institute. Hilary Vernon has expertise in treating inborn errors of metabolism and mitochondrial disorders. She is the director of the Mitochondrial Care Center at The Johns Hopkins Hospital and the Barth Syndrome Interdisciplinary Clinic at the Kennedy Krieger Institute. Her research interests include understanding intermediary metabolism in Barth syndrome and in disorders of branch chain amino acid metabolism. Dr. Vernon also co-directs the Department of Genetic Medicine Clinical Trials Unit, and is the principal investigator on multiple clinical trials for rare diseases. Dr. Vernon received her medical degree and doctorate from Rutgers University, New Brunswick, New Jersey. She completed residencies in genetics and pediatrics at The Johns Hopkins University, and a fellowship in clinical laboratory biochemical genetics at The Johns Hopkins University. Dr. Vernon was recognized with the 2010 Francis F. Schwentker Award for Excellence in Research at Johns Hopkins University and the 2011 James B. Sidbury Jr. Fellowship in Biochemical Genetics at Johns Hopkins University. Dr. Vernon is rated as an Advanced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. Her top areas of expertise are Methylmalonic Acidemia, Propionic Acidemia, Infantile Neutropenia, Progressive External Ophthalmoplegia, and Gastrostomy.

Meral Gunay-Aygun is a professor of pediatrics and genetic medicine at Johns Hopkins University School of Medicine. Dr. Gunay-Aygun specializes in the diagnosis and treatment of children and adults with inherited metabolic diseases including diagnostic evaluation and follow-up of newborns with abnormal newborn screens for inherited metabolic diseases. After serving 14 years as an attending physician at The Johns Hopkins Hospital in Baltimore, she joined the medical staff of Johns Hopkins All Children’s Hospital in St. Petersburg, Florida in 2022. Dr. Gunay-Aygun earned her medical degree from Hacettepe University School of Medicine, Ankara, Turkey. She completed pediatrics and medical genetics residencies at Case Western Reserve University, Cleveland, Ohio, and a biochemical genetics fellowship at the National Institutes of Health’s National Human Genome Research Institute, Bethesda, Maryland. She has made numerous research contributions, especially in the study of inherited ciliopathies, for which she has earned international recognition. Dr. Gunay-Aygun received the Innovative Leadership Award from Genetic Alliance, as well as the NHGRI Merit Award for her research on Autosomal Recessive Polycystic Kidney Disease/Congenital Hepatic Fibrosis. She is a member of myriad professional organizations, including the American Society of Human Genetics, the American Academy of Pediatrics, the Society of Pediatric Research and the Society for Inherited Metabolic Disorders. Dr. Gunay is rated as an Advanced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. Her top areas of expertise are Phenylketonuria (PKU), Ornithine Translocase Deficiency, Ornithine Transcarbamylase Deficiency, and Argininosuccinic Aciduria.

Raymond Wang is a Medical Genetics provider in Orange, California. Dr. Wang is rated as an Advanced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. His top areas of expertise are Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Pompe Disease, and Adenoidectomy.

Hind Alsharhan is a Medical Genetics provider in Baltimore, Maryland. Dr. Alsharhan is rated as an Advanced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. Her top areas of expertise are ALG3-CDG, Ornithine Transcarbamylase Deficiency, Coenzyme Q Cytochrome C Reductase Deficiency, and Phenylketonuria (PKU).

Berna Seker-Yilmaz practices in Mersin, Turkey. Ms. Seker-Yilmaz is rated as a Distinguished expert by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. Her top areas of expertise are Ornithine Transcarbamylase Deficiency, Urea Cycle Disorders (UCD), Visceromegaly, Short-Chain Acyl-CoA Dehydrogenase Deficiency, and Liver Transplant.

Paul Gissen practices in London, United Kingdom. Mr. Gissen is rated as a Distinguished expert by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. His top areas of expertise are CLN2 Disease, Argininosuccinic Aciduria, Batten Disease, CLN4 Disease, and Liver Transplant.

Kimitoshi Nakamura practices in Chuo, Japan. Nakamura is rated as a Distinguished expert by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. Their top areas of expertise are Fabry Disease, Urea Cycle Disorders (UCD), Ornithine Transcarbamylase Deficiency, Vitrectomy, and Liver Transplant.

Markey Mcnutt is a Medical Genetics specialist and an Endocrinologist in Frisco, Texas. Dr. Mcnutt is rated as a Distinguished provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. His top areas of expertise are Ornithine Translocase Deficiency, Ornithine Transcarbamylase Deficiency, Phenylketonuria (PKU), and Multiple Sulfatase Deficiency.

Karolina Stepien practices in Salford, United Kingdom. Ms. Stepien is rated as a Distinguished expert by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. Her top areas of expertise are Classic Galactosemia, Ornithine Transcarbamylase Deficiency, Mucopolysaccharidoses (MPS), Liver Transplant, and Gastrostomy.

Jessica Scott-Schwoerer is a Pediatrics specialist and an Endocrinologist in Milwaukee, Wisconsin. Dr. Scott-Schwoerer is rated as a Distinguished provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. Her top areas of expertise are Ornithine Transcarbamylase Deficiency, Von Gierke Disease, Propionic Acidemia, and Phenylketonuria (PKU). Dr. Scott-Schwoerer is currently accepting new patients.