Jack Yanovski is a Pediatric Endocrinologist in Bethesda, Maryland. Dr. Yanovski is rated as a Distinguished provider by MediFind in the treatment of Prader-Willi Syndrome. His top areas of expertise are Obesity, Obesity in Children, Congenital Hyperinsulinism, and Prader-Willi Syndrome.

Dr. Stacy Fisher is a cardiologist in Baltimore, Maryland specializing in the care of adult congenital heart disease, pregnancy-related heart disease and congenital heart pulmonary hypertension. She is Associate Director of the Adult Congenital Heart Disease (ACHD) Center at the Johns Hopkins Heart and Vascular Institute and Director of the ACHD Training Program. She is also an Associate Professor of Medicine at the Johns Hopkins University School of Medicine. Her research focus is congenital heart disease in adults including pulmonary hypertension, inherited heart disease and 3D printing translational medicine. She is interested in imaging and using 3D modeling to advance cardiac care and education. Her education includes a Bachelor of Science degree in Microbiology from Miami University in Oxford, Ohio, and a Doctor of Medicine Degree from the University of Maryland School of Medicine in Baltimore, Maryland. She completed an internship and residency in Internal Medicine at Duke University in Durham, North Carolina. Her fellowship in cardiology was at the University of Rochester, Strong Memorial Hospital in Rochester, New York, including serving as the Chief Cardiology Fellow. She was then an Adult Congenital Heart Fellow at the University of Rochester, Strong Memorial Hospital. After completing her fellowship in 2001, she joined a Baltimore cardiology practice and was named Director of Women’s Cardiovascular Services and the Co-Director of the Cardiac Critical Care Unit at Sinai Hospital in Baltimore, positions which she held until 2011. She then joined University of Maryland School of Medicine as Director of Women’s and Complex Heart diseases where she started and directed the Adult Congenital Heart Program and practiced through 2022 when she joined Johns Hopkins. She was recently the President of the American Heart Association’s Greater Maryland Region. Videos Dr. Stacy Fisher. Dr. Fisher is rated as an Advanced provider by MediFind in the treatment of Prader-Willi Syndrome. Her top areas of expertise are Familial Ventricular Tachycardia, Arrhythmias, Ventricular Tachycardia, Aortic Valve Replacement, and Transcatheter Aortic Valve Replacement (TAVR).

Latrica Cook is a primary care provider, practicing in Internal Medicine in Owings Mills, Maryland. Dr. Cook is rated as an Advanced provider by MediFind in the treatment of Prader-Willi Syndrome. Her top areas of expertise are Coffin-Siris Syndrome, Langer Mesomelic Dysplasia, Cornelia De Lange Syndrome, and Russell-Silver Dwarfism. Dr. Cook is currently accepting new patients.

Patrick Shanahan is a primary care provider, practicing in Family Medicine in Chestertown, Maryland. Dr. Shanahan is rated as an Advanced provider by MediFind in the treatment of Prader-Willi Syndrome. His top areas of expertise are Sitosterolemia, Familial Hypertension, Hypertension, and Glucocorticoid-Remediable Aldosteronism. Dr. Shanahan is currently accepting new patients.

Doreen Blake is a primary care provider, practicing in Internal Medicine in Largo, Maryland. Dr. Blake is rated as an Advanced provider by MediFind in the treatment of Prader-Willi Syndrome. Her top areas of expertise are Sitosterolemia, Hypertension, Familial Hypertension, and Glucocorticoid-Remediable Aldosteronism. Dr. Blake is currently accepting new patients.

Dr. Eric Kossoff focuses on the diagnosis and treatment of childhood seizures and epilepsy, particularly treatments other than medications such as diet and neurostimulation. He is one of the world experts on dietary treatment for epilepsy (ketogenic diet) and lectures around the world about this therapy. His specific interests include the ketogenic diet, the modified Atkins diet for children and adults, infantile spasms, benign rolandic epilepsy, the interaction of migraine headaches with epilepsy, and Sturge-Weber syndrome. Dr. Eric Kossoff is also very involved in teaching and is the Director of the Pediatric Neurology Residency Program. He is a professor of neurology and pediatrics at the Johns Hopkins University School of Medicine. He is a co-author of Treatment of Pediatric Neurologic Disorders and the 7th edition of Ketogenic Diet Therapies. Dr. Kossoff sees patients in the Johns Hopkins Outpatient Center (5th floor) in Baltimore on Tuesday afternoons and Thursday mornings. He sees patients at Green Spring Station on Wednesday afternoons. He also participates in telemedicine. Dr. Kossoff received his medical degree from SUNY at Buffalo School of Medicine in New York. He went on to complete a residency in pediatrics at Eastern Virginia Medical School in Norfolk, Virginia. He completed a second residency in child neurology and a fellowship in pediatric epilepsy and clinical neurophysiology at The Johns Hopkins Hospital in Baltimore. Dr. Kossoff is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. His top areas of expertise are Epilepsy, Epilepsy in Children, Seizures, Endovascular Embolization, and Gastrostomy.

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 an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. Her top areas of expertise are Methylmalonic Acidemia, Maple Syrup Urine Disease, Ornithine Transcarbamylase Deficiency, Phenylketonuria (PKU), and Deep Brain Stimulation.

Dr. Garry R. Cutting is a Professor of Pediatrics and Medicine in the McKusick-Nathans Institute of Genetic Medicine of the Johns Hopkins University School of Medicine. He is the Aetna/U.S. Healthcare Professor of Medical Genetics at Johns Hopkins. Dr. Cutting received his undergraduate degree in biology and medical degree from the University of Connecticut. He completed residency training in pediatrics and a fellowship in medical genetics at the Johns Hopkins University School of Medicine. Dr. Cutting is the Medical Director of the DNA Diagnostic Laboratory of Johns Hopkins Genomics. He directed the Medical Genetics Residency Program at Hopkins from 1995 to 2004. Dr. Cutting is the recipient of the Paul di Sant’Agnese Distinguished Scientific Achievement Award from the Cystic Fibrosis Foundation and a MERIT award from the National Institutes of Health. He has published more than 160 peer-reviewed articles. Dr. Cutting was elected to the Society of Pediatric Research (1992), the American Society of Clinical Investigation (1995) and the Association of American Physicians (2017). Dr. Cutting’s primary interests lie in the interpretation of DNA variation and their effect upon human phenotypes. Dr. Cutting’s lab focuses on the effect of common and rare variants in the CFTR gene that cause the single gene disorder cystic fibrosis (CF). His lab operates the CFTR2 database, a resource composed of clinical and genetic data on almost 90,000 individuals with CF world-wide. His laboratory also studies the effect of clinically approved and novel modulators upon CFTR protein bearing disease-causing variants. Dr. Cutting’s laboratory is also leader in the identification and characterization of genetic modifiers of cystic fibrosis. His group is currently collaborating with teams at the University of North Carolina and the University of Washington, Seattle to identify common and rare modifier variants of disease severity by whole genome sequencing of 5200 individuals with CF. Dr. Cutting participates in the clinical translation of variant interpretation as the Medical Director of the DNA Diagnostic Laboratory at Johns Hopkins. Finally, as Editor of the journal Human Mutation Dr. Cutting oversees the review and publication of manuscripts reporting the mechanism, distribution and phenotype consequences of variation in our genomes. Dr. Cutting is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. His top areas of expertise are Exocrine Pancreatic Insufficiency, Sjogren-Larsson Syndrome, Coffin-Siris Syndrome, and Meier-Gorlin Syndrome.

Thomas Traill is a Cardiologist in Baltimore,, Maryland. Dr. Traill is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. His top areas of expertise are Marfan Syndrome, Congenital Contractural Arachnodactyly, Arachnodactyly, and Bicuspid Aortic Valve.

Debra Counts is a Pediatric Endocrinologist and an Endocrinologist in Baltimore, Maryland. Dr. Counts is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. Her top areas of expertise are Idiopathic Short Stature (ISS), Short Stature (Growth Disorders), Klinefelter Syndrome, and Pediatric Growth Hormone Deficiency. Dr. Counts is currently accepting new patients.

Karen Vogt is a Pediatrics specialist and a Pediatric Endocrinologist in Greenbelt, Maryland. Dr. Vogt is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. Her top areas of expertise are Primary Carnitine Deficiency, Prader-Willi Syndrome, Hypotonia, and Obesity.

Sally Radovick is a Pediatric Endocrinologist and a Pediatrics provider in Baltimore, Maryland. Dr. Radovick is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. Her top areas of expertise are Panhypopituitarism, Pediatric Growth Hormone Deficiency, Growth Hormone Deficiency (GHD), and Obesity.

Na Ji is a Child and Adolescent Psychiatrist in Baltimore, Maryland. Dr. Ji is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. Her top area of expertise is Prader-Willi Syndrome.

Hans Bjornsson is a Medical Genetics specialist and a Pediatrics provider in Baltimore, Maryland. Dr. Bjornsson is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. His top areas of expertise are Kabuki Syndrome, Weaver Syndrome, 3MC Syndrome, Coffin-Lowry Syndrome, and Orchiectomy. Dr. Bjornsson is currently accepting new patients.

Marshall Summar is a Medical Genetics specialist and a Pediatrics provider in Chevy Chase, Maryland. Dr. Summar is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. His top areas of expertise are Argininosuccinic Aciduria, Urea Cycle Disorders (UCD), Propionic Acidemia, and Ornithine Translocase Deficiency.

Dr. Ann O'Shea Scheimann is an associate professor of pediatrics at the Johns Hopkins University School of Medicine. Her areas of clinical expertise include pediatric gastroenterology, nutrition and pediatric liver disease including cholestatic liver disease and fatty liver disease. Dr. Scheimann received her B.S. from the University of Dayton. She earned her M.D. from the University of Cincinnati College of Medicine and her M.B.A. from Johns Hopkins. She completed her internship and residency in pediatric medicine and a fellowship in pediatric gastroenterology at the Baylor College of Medicine. In 2000, she joined the Johns Hopkins faculty in pediatrics, where her research focuses on non-alcoholic fatty liver disease, obesity and Prader-Willi syndrome. Prior to joining Johns Hopkins, Dr. Scheimann was an assistant professor of pediatrics at Baylor College of Medicine. In 2005, she developed Weigh Smart, a comprehensive pediatric weight management program funded by the Johns Hopkins Children’s Center, Mt. Washington Pediatric Hospital, and the University of Maryland. She currently serves as the chair of the Pediatric Nutrition Advisory Committee at Johns Hopkins Children's Center. Dr. Scheimann serves on the editorial boards of Pediatrics and Therapeutics, World Journal of Gastroenterology and World Journal of Hepatology. She has received numerous awards and including a grant from the Mt. Washington Pediatric Foundation to start the Weigh Smart program. She has received research support from Agencies including the National Institutes of Health, Foundation for Prader-willi Research and Prader-willi Syndrome Association. She is a member of several professional organizations, including the American Association for the Advancement of the Study of Liver Disease, Obesity Society and the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition. Dr. Scheimann is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. Her top areas of expertise are Delayed Growth, Obesity, Prader-Willi Syndrome, and Non-Alcoholic Fatty Liver Disease.