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214:. These technologies – which can check 20,000 genes at the same as opposed to checking individual genes sequentially – offer hope for patients with rare diseases. Accurate diagnoses can enable physicians to select the correct medication or to set up the appropriate levels of support for people with learning disabilities. In 2013, she was elected a
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After graduating she joined a start-up company focusing on the genetics of diseases. In 2002, Taylor moved to the Oxford
Genetics Knowledge Park. She was Director of the Oxford Biomedical Research Centre Genetics Theme, which is supported by the
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to show that in whole genome sequencing could be used to diagnose patients with genetic disorders with a greater sensitivity than conventional
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569:"Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas"
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Dixon AL; Liang L; Moffatt MF; et al. (October 2007). "A genome-wide association study of global gene expression".
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639:"Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples"
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Reassessment of
Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples
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153:. Taylor is the Director of the Oxford Biomedical Research Centre Genetics Theme. Her research considers
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affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas
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Claire Palles; Jean-Baptiste Cazier; Kimberley M Howarth; et al. (February 2013).
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that take place in various medical conditions. She worked in collaboration with
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Roddy Walsh; Kate
Thomson; James Ware; et al. (17 August 2016).
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of
Professor of Translational Genomics by the University of Oxford.
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173:. She remained in Oxford for her doctoral research, joining the
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282:"Jenny Taylor, Fellow by Special Election in Human Genetics"
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A genome-wide association study of global gene expression
198:. In particular, she has developed novel ways to perform
423:"Project brings whole genome sequencing into the clinic"
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308:"Women Inspire: An Introduction to the Exhibition"
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328:Taylor, Jenny Carmeron (1997).
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482:publications indexed by the
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448:"Recognition of Distinction"
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237:Her publications include:
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486:bibliographic database.
391:"Professor Jenny Taylor"
288:. St Edmund Hall, Oxford
165:Early life and education
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196:National Health Service
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155:whole genome sequencing
397:. University of Oxford
171:St Edmund Hall, Oxford
70:Translational genomics
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143:Jenny Carmeron Taylor
42:Jenny Carmeron Taylor
644:Genetics in Medicine
421:University, Oxford.
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84:University of Oxford
52:University of Oxford
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705:Categories
261:References
192:physicians
147:geneticist
691:Q37424109
665:1098-3600
626:(erratum)
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