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Stanislas Lyonnet is a French geneticist. As of 2012 he was Professor of genetics at Paris Descartes University, and a clinical geneticist in the Department of Medical Genetics at the Hôpital Necker - Enfants Malades. His research is aimed at isolating the genes that cause congenital malformation and birth defects. ==Biography== Lyonnet studied Paediatrics and Genetics at the Pierre-and-Marie-Curie University. He obtained his Doctorate in Medicine, specializing in Pediatrics, in 1989. He obtained a Master of Science degree from the Institut Cochin and a PhD in Genetics from Necker in 1992. In 1995 he was made a Full Professor in the Genetic Department of the Paris Descartes Medical School. He was responsible for the Rare Disease Research Program of the French national agency for research (ANR). Lyonnet has been a member of the board of the European Society of Human Genetics and its scientific program committee. He is a section editor of the ''European Journal of Human Genetics'', and is on the editorial boards of ''Human Molecular Genetics'' and ''Clinical Dysmorphology''. He teaches in the European Master of Genetics program at the Paris Descartes and Paris Diderot universities. He is also a member of the INSERM Scientific Advisory Board. 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Stanislas Lyonnet」の詳細全文を読む スポンサード リンク
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