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Bio
Jenny Taylor is Co-Theme Leader of the Oxford Biomedical Research Centre's Genomic Medicine Theme, a translational programme funded by the UK’s National Institute of Health Research based at the University of Oxford’s Wellcome Centre for Human Genetics.
Jenny’s research currently focuses on the application of targeted and whole genome sequencing (WGS) to the diagnosis of rare diseases and cancer, and investigation of novel genes emerging applying a range of functional approaches. She was a coinvestigator on the WGS500 project, which was a forerunner to the UK’s 100,000 Genomes Project and also led a team to establish the clinical framework and infrastructure for WGS within the Oxford hospital setting. She continues to participate in the Genomics England programme through its Clinical Interpretation Partnerships.
Research Interests
Papers共 226 篇Author StatisticsCo-AuthorSimilar Experts
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Vincenzo Salpietro, Reza Maroofian,Maha S. Zaki,Jamie Wangen,Andrea Ciolfi,Sabina Barresi,Stephanie Efthymiou,Angelique Lamaze,Gabriel N. Aughey,Fuad Al Mutairi,Aboulfazl Rad,Clarissa Rocca,
AMERICAN JOURNAL OF HUMAN GENETICSno. 1 (2024): 200-210
Gabriel Aughey,Elisa Cali, Reza Maroofian,Maha S Zaki,Alistair T Pagnamenta,Fatima Rahman, Lara Menzies, Anum Shafique,Mohnish Suri, Emmanuel Roze, Mohammed Aguennouz,Zouiri Ghizlane,
medRxiv : the preprint server for health sciences (2024)
Jing Yu,Alistair Pagnamenta,Susan Walker,Benito Banos-Pinero, Mark Rogers,Jackie Cook,Mohamed Wafik, Ellie Hay,Detlef Bockenhauer,Adam Jackson,Emma Clement,Louise Wilson,
EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 56-57
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B.P. Fairfax,C. Taylor,R.A. Watson, W. Ye, O. Tong, F. Matos Santo, N.A. Coupe, M.R. Middleton, M. Payne
Annals of Oncology (2023): S676-S676
Alistair T Pagnamenta, Rebecca S Belles,Bonnie Anne Salbert,Ingrid M Wentzensen,Maria J Guillen Sacoto,Francis Jeshira Reynoso Santos,Alesky Caffo,Matteo Ferla,Benito Banos-Pinero, Karolina Pawliczak, Mina Makvand,Hossein Najmabadi,
JOURNAL OF MEDICAL GENETICSno. 12 (2023): 1235-1244
Clinical Geneticsno. 3 (2023): 390-392
EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 284-285
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