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Dr. Ada Hamosh is the Dr. Frank V. Sutland Professor of Pediatric Genetics at the McKusick-Nathans Institute of Genetic Medicine, and a professor in the Department of Epidemiology at Johns Hopkins Bloomberg School of Public Health.
Since 2002, she has served as clinical director of the IGM and scientific director of the Online Mendelian Inheritance in Man® (OMIM), a catalog of more than 12,000 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 2000.
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 70 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 Society for Pediatric Research, the Maryland State Advisory Council on Hereditary & Congenital Disorders and a fellowship at the American College of Medical Genetics.
She serves on the editorial board of 16 different peer-review journals, including the American Journal of Medical Genetics and the Archives of Pediatrics and Adolescent Medicine.
Dr. Hamosh was recognized in Baltimore magazine as one of the region’s top doctors of 2013.
Since 2002, she has served as clinical director of the IGM and scientific director of the Online Mendelian Inheritance in Man® (OMIM), a catalog of more than 12,000 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 2000.
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 70 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 Society for Pediatric Research, the Maryland State Advisory Council on Hereditary & Congenital Disorders and a fellowship at the American College of Medical Genetics.
She serves on the editorial board of 16 different peer-review journals, including the American Journal of Medical Genetics and the Archives of Pediatrics and Adolescent Medicine.
Dr. Hamosh was recognized in Baltimore magazine as one of the region’s top doctors of 2013.
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论文共 119 篇作者统计合作学者相似作者
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medRxiv : the preprint server for health sciences (2023)
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JIMD reportsno. 3 (2023): 233-237
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Genetics in medicine : official journal of the American College of Medical Geneticsno. 2 (2023): 101029-101029
Genetics in Medicine Openno. 1 (2023): 100734-100734
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