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个人简介
Professor Baralle leads a group that investigates the role of RNA and splicing in genetic disease, new methods for genetic diagnostic testing, and the causes of rare disease syndromes. She is clinical specialty lead for Genetics for the Wessex CRN. Her group comprises both clinical and non-clinical scientists and students.
研究兴趣
论文共 196 篇作者统计合作学者相似作者
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Yuyang Chen,Ruebena Dawes, Hyung Chul Kim, Sarah L Stenton,Susan Walker,Alicia Ljungdahl, Jenny Lord, Vijay S Ganesh, Jialan Ma,Alexandra C Martin-Geary, Gabrielle Lemire, Elston N D'Souza,
medRxiv : the preprint server for health sciences (2024)
JOURNAL OF MEDICAL GENETICSno. 3 (2024): 294-297
Archives of disease in childhoodno. 3 (2024): 177-178
Rebekah Penrice-Randal,Fabio Strazzeri,Benoit Ernst, Brice Van Eeckhout,Julien Guiot,Anna Julie Peired,Cosimo Nardi, Erika Parkinson,Monique Henket, Alicia Staderoli, Elora Guglielmi, Anne-Francoise Dive,
medrxiv(2024)
Eleanor G Seaby,Gary Leggatt,Guo Cheng,N Simon Thomas,James J Ashton,Imogen Stafford,Diana Baralle,Heidi L Rehm,Anne O'Donnell-Luria,Sarah Ennis, Genomics England Research Consortium
Genetics in medicine : official journal of the American College of Medical Geneticsno. 4 (2024): 101073-101073
medRxiv : the preprint server for health sciences (2023)
Nature Geneticsno. 9 (2023): 1598-1607
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Suly Saray Villa Vasquez, Lama Al-Abdi,Rob Ewing, Fowzan Alkuraya,Reuben Pengelly,David Ian Wilson,Diana Baralle,Gabrielle Wheway
EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 649-649
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