Publications by authors named "Graham R Taylor"

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Clinical Utility of Real-Time Targeted Molecular Profiling in the Clinical Management of Ovarian Cancer: The ALLOCATE Study.
Olga Kondrashova, Gwo-Yaw Ho, George Au-Yeung, Leakhena Leas, Tiffany Boughtwood, Graham R Taylor

JCO Precis Oncol· December 2019

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Exploring the feasibility and utility of exome-scale tumour sequencing in a clinical setting.
Belinda Lee, Ben Tran, Arthur L Hsu, Graham R Taylor, Stephen B Fox

Intern Med J· July 2018

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Circulating tumour cells from patients with colorectal cancer have cancer stem cell hallmarks in culture.
Fanny Grillet, Elsa Bayet, Olivia Villeronce, Luke Zappia, Ebba Louise Lagerqvist, Graham Roy Taylor

Gut· October 2017

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High-Throughput Amplicon-Based Copy Number Detection of 11 Genes in Formalin-Fixed Paraffin-Embedded Ovarian Tumour Samples by MLPA-Seq.
Olga Kondrashova, Clare J Love, Sebastian Lunke, Arthur L Hsu, , Graham R Taylor

PLoS One· June 2016

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BRAF Inhibition in BRAFV600E-Positive Anaplastic Thyroid Carcinoma.
Annette M Lim, Graham R Taylor, Andrew Fellowes, Laird Cameron, Belinda Lee

J Natl Compr Canc Netw· March 2016

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AmpliVar: mutation detection in high-throughput sequence from amplicon-based libraries.
Arthur L Hsu, Olga Kondrashova, Sebastian Lunke, Clare J Love, Cliff Meldrum, Graham R Taylor

Hum Mutat· April 2015

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Robust diagnostic genetic testing using solution capture enrichment and a novel variant-filtering interface.
Christopher M Watson, Laura A Crinnion, Joanne E Morgan, Sally M Harrison, Christine P Diggle, Graham R Taylor

Hum Mutat· April 2014

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Accurately identifying low-allelic fraction variants in single samples with next-generation sequencing: applications in tumor subclone resolution.
Lucy F Stead, Kate M Sutton, Graham R Taylor, Philip Quirke, Pamela Rabbitts

Hum Mutat· October 2013

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Simple and efficient identification of rare recessive pathologically important sequence variants from next generation exome sequence data.
Ian M Carr, Joanne Morgan, Christopher Watson, Svitlana Melnik, Christine P Diggle, Graham R Taylor

Hum Mutat· July 2013

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Mutation detection by clonal sequencing of PCR amplicons and grouped read typing is applicable to clinical diagnostics.
Philip A Chambers, Lucy F Stead, Joanne E Morgan, Ian M Carr, Kate M Sutton, Graham R Taylor

Hum Mutat· January 2013

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Human Variome Project country nodes: documenting genetic information within a country.
George P Patrinos, Timothy D Smith, Heather Howard, Fahd Al-Mulla, Lotfi Chouchane, Graham R Taylor

Hum Mutat· November 2012

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Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration.
Robert K Koenekoop, Hui Wang, Jacek Majewski, Xia Wang, Irma Lopez, Graham R Taylor

Nat Genet· September 2012

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Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta.
David A Parry, Steven J Brookes, Clare V Logan, James A Poulter, Walid El-Sayed, Graham R Taylor

Am J Hum Genet· September 2012

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Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis.
Christine P Diggle, David A Parry, Clare V Logan, Paul Laissue, Carolina Rivera, Graham R Taylor

Hum Mutat· August 2012

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Next-generation sequencing for simultaneous determination of human papillomavirus load, subtype, and associated genomic copy number changes in tumors.
Caroline Conway, Rebecca Chalkley, Alec High, Kenneth Maclennan, Stefano Berri, Graham R Taylor

J Mol Diagn· June 2012

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Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects.
Kamron Khan, Clare V Logan, Martin McKibbin, Eamonn Sheridan, Nursel H Elçioglu, Graham R Taylor

Hum Mol Genet· February 2012

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Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD).
Clare V Logan, Barbara Lucke, Caroline Pottinger, Zakia A Abdelhamed, David A Parry, Graham R Taylor

Nat Genet· November 2011

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Illuminator, a desktop program for mutation detection using short-read clonal sequencing.
Ian M Carr, Joanne E Morgan, Christine P Diggle, Eamonn Sheridan, Alexander F Markham, Graham R Taylor

Genomics· October 2011

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Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte.
David A Parry, Clare V Logan, Bruce E Hayward, Michael Shires, Hanène Landolsi, Graham R Taylor

Am J Hum Genet· September 2011

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Clarity and claims in variation/mutation databasing.
Raymond Dalgleish, William S Oetting, Arleen D Auerbach, Jacques S Beckmann, Anne Cambon-Thomsen, Graham R Taylor

Nat Biotechnol· September 2011

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Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma.
Kamron Khan, Adam Rudkin, David A Parry, Kathryn P Burdon, Martin McKibbin, Graham R Taylor

Am J Hum Genet· September 2011

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GeneScreen: a program for high-throughput mutation detection in DNA sequence electropherograms.
Ian M Carr, Nick Camm, Graham R Taylor, Ruth Charlton, Sian Ellard

J Med Genet· February 2011

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Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens.
Henry M Wood, Ornella Belvedere, Caroline Conway, Catherine Daly, Rebecca Chalkley, Graham R Taylor

Nucleic Acids Res· August 2010

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Genetic diagnosis of familial breast cancer using clonal sequencing.
Joanne E Morgan, Ian M Carr, Eamonn Sheridan, Carol E Chu, Bruce Hayward, Graham R Taylor

Hum Mutat· April 2010

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Mutation of the variant alpha-tubulin TUBA8 results in polymicrogyria with optic nerve hypoplasia.
Mohammad R Abdollahi, Ewan Morrison, Tamara Sirey, Zoltan Molnar, Bruce E Hayward, Graham R Taylor

Am J Hum Genet· November 2009

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