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Lucy Raymond is Professor of Medical Genetics and Neurodevelopment at the University of Cambridge and Honorary Consultant in Medical Genetics at Cambridge University Hospital, Cambridge Biomedical Campus, UK. Her research interest is understanding the genetic basis of intellectual disability and has identified disease causing genes over the years which have been rapidly translated into clinical service. She is a leader of large collaborative efforts to identify the remaining causes of rare disease genes where intellectual disability, epilepsy or neurological conditions predominate. She is currently Assistant Director of the UK NIHR Rare Diseases Bioresource and Director of the East of England Genomics Medicine Centre that is delivering the 100K Genome Project for Rare Disease and Cancer.
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论文共 243 篇作者统计合作学者相似作者
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American journal of medical genetics. Part App.e63514-e63514, (2024)
Molecular Autismno. 1 (2023): 1-13
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Victoria Patterson,Farid Ullah,Laura Bryant,John N Griffin,Alpa Sidhu, Sheila Saliganan, Mackenzie Blaile,Margarita S Saenz,Rosemarie Smith,Sara Ellingwood,Dorothy K Grange,Xuyun Hu,
Science Advancesno. 17 (2023): eade0631-eade0631
Neurologyno. 12 (2023): E1234-E1247
Genetics in medicine : official journal of the American College of Medical Geneticsno. 11 (2023): 100938-100938
Evelina Carapancea,Marie-Coralie Cornet,Mathieu Milh, Lucrezia De Cosmo,Eric J. Huang,Tiziana Granata,Pasquale Striano,Berten Ceulemans,Anja Stein,Deborah Morris-Rosendahl,Greta Conti, Nipa Mitra,
Neurologyno. 12 (2023)
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Lancet (London, England)no. 10426 (2023): 583-586
American journal of human geneticsno. 8 (2023): 1343-1355
JCPP advancesno. 1 (2023): e12128-e12128
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