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Jenny C Taylor
Jenny C Taylor
Other namesJenny Taylor, JC Taylor
Associate Professor Oxford University
Verified email at well.ox.ac.uk
Title
Cited by
Cited by
Year
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas
C Palles, JB Cazier, KM Howarth, E Domingo, AM Jones, P Broderick, ...
Nature genetics 45 (2), 136-144, 2013
10822013
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples
R Walsh, KL Thomson, JS Ware, BH Funke, J Woodley, KJ McGuire, ...
Genetics in Medicine 19 (2), 192-203, 2017
6682017
Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature
K Schwarze, J Buchanan, JC Taylor, S Wordsworth
Genetics in Medicine 20 (10), 1122-1130, 2018
5292018
Factors influencing success of clinical genome sequencing across a broad spectrum of disorders
JC Taylor, HC Martin, S Lise, J Broxholme, JB Cazier, A Rimmer, ...
Nature genetics 47 (7), 717-726, 2015
4012015
DNA polymerase ɛ and δ exonuclease domain mutations in endometrial cancer
DN Church, SEW Briggs, C Palles, E Domingo, SJ Kearsey, JM Grimes, ...
Human molecular genetics 22 (14), 2820-2828, 2013
3922013
Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patterns
A Schuh, J Becq, S Humphray, A Alexa, A Burns, R Clifford, SM Feller, ...
Blood, The Journal of the American Society of Hematology 120 (20), 4191-4196, 2012
3792012
Metabolic modulator perhexiline corrects energy deficiency and improves exercise capacity in symptomatic hypertrophic cardiomyopathy
K Abozguia, P Elliott, W McKenna, TT Phan, G Nallur-Shivu, I Ahmed, ...
Circulation 122 (16), 1562-1569, 2010
3632010
Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1
E Jaeger, S Leedham, A Lewis, S Segditsas, M Becker, PR Cuadrado, ...
Nature genetics 44 (6), 699-703, 2012
2892012
Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis
HC Martin, GE Kim, AT Pagnamenta, Y Murakami, GL Carvill, E Meyer, ...
Human molecular genetics 23 (12), 3200-3211, 2014
2752014
Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation
D Wells, K Kaur, J Grifo, M Glassner, JC Taylor, E Fragouli, S Munne
Journal of medical genetics 51 (8), 553-562, 2014
2702014
SAMHD1 is mutated recurrently in chronic lymphocytic leukemia and is involved in response to DNA damage
R Clifford, T Louis, P Robbe, S Ackroyd, A Burns, AT Timbs, ...
Blood, The Journal of the American Society of Hematology 123 (7), 1021-1031, 2014
2582014
The complete costs of genome sequencing: a microcosting study in cancer and rare diseases from a single center in the United Kingdom
K Schwarze, J Buchanan, JM Fermont, H Dreau, MW Tilley, JM Taylor, ...
Genetics in Medicine 22 (1), 85-94, 2020
2122020
Sequencing of human genomes with nanopore technology
R Bowden, RW Davies, A Heger, AT Pagnamenta, M de Cesare, ...
Nature communications 10 (1), 1869, 2019
2002019
Germline selection shapes human mitochondrial DNA diversity
W Wei, S Tuna, MJ Keogh, KR Smith, TJ Aitman, PL Beales, DL Bennett, ...
Science 364 (6442), eaau6520, 2019
1842019
DNA testing for hypertrophic cardiomyopathy: a cost-effectiveness model
S Wordsworth, J Leal, E Blair, R Legood, K Thomson, A Seller, J Taylor, ...
European heart journal 31 (8), 926-935, 2010
1792010
Whole-genome sequencing of bladder cancers reveals somatic CDKN1A mutations and clinicopathological associations with mutation burden
JB Cazier, SR Rao, CM McLean, AK Walker, BJ Wright, EEM Jaeger, ...
Nature communications 5 (1), 3756, 2014
1662014
Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants
JJ Johnston, JJ van der Smagt, JA Rosenfeld, AT Pagnamenta, A Alswaid, ...
Genetics in Medicine 20 (10), 1175-1185, 2018
1642018
Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease
ME Shanks, SM Downes, RR Copley, S Lise, J Broxholme, KAZ Hudspith, ...
European journal of human genetics 21 (3), 274-280, 2013
1482013
Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project
P Robbe, N Popitsch, SJL Knight, P Antoniou, J Becq, M He, A Kanapin, ...
Genetics in Medicine 20 (10), 1196-1205, 2018
1422018
Presence of multiple recurrent mutations confers poor trial outcome of relapsed/refractory CLL
R Guièze, P Robbe, R Clifford, S De Guibert, B Pereira, A Timbs, ...
Blood, The Journal of the American Society of Hematology 126 (18), 2110-2117, 2015
1352015
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