Graham R Taylor

Graham R Taylor

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Graham R Taylor

Graham R Taylor

Publications by authors named "Graham R Taylor"

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34Publications

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BRAF Inhibition in BRAFV600E-Positive Anaplastic Thyroid Carcinoma.

J Natl Compr Canc Netw 2016 03 8;14(3):249-54. Epub 2016 Mar 8.

Department of Medical Oncology, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia

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http://dx.doi.org/10.6004/jnccn.2016.0030DOI Listing
March 2016

AmpliVar: mutation detection in high-throughput sequence from amplicon-based libraries.

Hum Mutat 2015 Apr 16;36(4):411-8. Epub 2015 Mar 16.

Department of Pathology, The University of Melbourne, Parkville, Victoria, Australia.

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http://dx.doi.org/10.1002/humu.22763DOI Listing
April 2015

Accurately identifying low-allelic fraction variants in single samples with next-generation sequencing: applications in tumor subclone resolution.

Hum Mutat 2013 Oct 11;34(10):1432-8. Epub 2013 Jul 11.

Leeds Institute of Cancer and Pathology, St James's University Hospital, University of Leeds, Leeds, West Yorkshire, LS9 7TF, England.

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http://dx.doi.org/10.1002/humu.22365DOI Listing
October 2013

Illuminator, a desktop program for mutation detection using short-read clonal sequencing.

Genomics 2011 Oct 19;98(4):302-9. Epub 2011 May 19.

Leeds Institute of Molecular Medicine, University of Leeds, UK.

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http://dx.doi.org/10.1016/j.ygeno.2011.05.004DOI Listing
October 2011

GeneScreen: a program for high-throughput mutation detection in DNA sequence electropherograms.

J Med Genet 2011 Feb 30;48(2):123-30. Epub 2010 Oct 30.

Division of Molecular & Translational Medicine, Leeds Institute for Molecular Medicine, University of Leeds, St James's University Hospital, Leeds, UK.

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http://www.tara.tcd.ie/bitstream/handle/2262/53909/PEER_stag
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http://jmg.bmj.com/cgi/doi/10.1136/jmg.2010.082081
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http://dx.doi.org/10.1136/jmg.2010.082081DOI Listing
February 2011

Genetic diagnosis of familial breast cancer using clonal sequencing.

Hum Mutat 2010 Apr;31(4):484-91

University of Leeds Institute of Molecular Medicine, Wellcome Trust Brenner Building, St. James's University Hospital, Beckett Street, Leeds, United Kingdom.

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http://dx.doi.org/10.1002/humu.21216DOI Listing
April 2010

Mutation of the variant alpha-tubulin TUBA8 results in polymicrogyria with optic nerve hypoplasia.

Am J Hum Genet 2009 Nov 5;85(5):737-44. Epub 2009 Nov 5.

Section of Genetics (Leeds Institute of Molecular Medicine [LIMM]), Wellcome Trust Brenner Building, St James's University Hospital, Leeds, LS9 7TF, UK.

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http://dx.doi.org/10.1016/j.ajhg.2009.10.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2775839PMC
November 2009

Planning the human variome project: the Spain report.

Authors:
Jim Kaput Richard G H Cotton Lauren Hardman Michael Watson Aida I Al Aqeel Jumana Y Al-Aama Fahd Al-Mulla Santos Alonso Stefan Aretz Arleen D Auerbach Bharati Bapat Inge T Bernstein Jong Bhak Stacey L Bleoo Helmut Blöcker Steven E Brenner John Burn Mariona Bustamante Rita Calzone Anne Cambon-Thomsen Michele Cargill Paola Carrera Lawrence Cavedon Yoon Shin Cho Yeun-Jun Chung Mireille Claustres Garry Cutting Raymond Dalgleish Johan T den Dunnen Carlos Díaz Steven Dobrowolski M Rosário N dos Santos Rosemary Ekong Simon B Flanagan Paul Flicek Yoichi Furukawa Maurizio Genuardi Ho Ghang Maria V Golubenko Marc S Greenblatt Ada Hamosh John M Hancock Ross Hardison Terence M Harrison Robert Hoffmann Rania Horaitis Heather J Howard Carol Isaacson Barash Neskuts Izagirre Jongsun Jung Toshio Kojima Sandrine Laradi Yeon-Su Lee Jong-Young Lee Vera L Gil-da-Silva-Lopes Finlay A Macrae Donna Maglott Makia J Marafie Steven G E Marsh Yoichi Matsubara Ludwine M Messiaen Gabriela Möslein Mihai G Netea Melissa L Norton Peter J Oefner William S Oetting James C O'Leary Ana Maria Oller de Ramirez Mark H Paalman Jillian Parboosingh George P Patrinos Giuditta Perozzi Ian R Phillips Sue Povey Suyash Prasad Ming Qi David J Quin Rajkumar S Ramesar C Sue Richards Judith Savige Dagmar G Scheible Rodney J Scott Daniela Seminara Elizabeth A Shephard Rolf H Sijmons Timothy D Smith María-Jesús Sobrido Toshihiro Tanaka Sean V Tavtigian Graham R Taylor Jon Teague Thoralf Töpel Mollie Ullman-Cullere Joji Utsunomiya Henk J van Kranen Mauno Vihinen Elizabeth Webb Thomas K Weber Meredith Yeager Young I Yeom Seon-Hee Yim Hyang-Sook Yoo

Hum Mutat 2009 Apr;30(4):496-510

Division of Personalised Nutrition and Medicine, FDA/National Center for Toxicological Research, Jefferson, Arkansas 72079, USA.

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http://compbio.berkeley.edu/people/brenner/pubs/kaput-2009-h
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http://doi.wiley.com/10.1002/humu.20972
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http://dx.doi.org/10.1002/humu.20972DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5879779PMC
April 2009

Detecting ligated fragments on oligonucleotide microarrays: optimizing chip design, array multiplex ligation-dependent probe amplification modification, and hybridization parameters.

Methods Mol Biol 2007 ;381:247-65

Regional DNA Lab, Regional Genetics Service, St. James's University Hospital, Leeds, UK.

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http://dx.doi.org/10.1007/978-1-59745-303-5_12DOI Listing
December 2007

Extensive gene conversion at the PMS2 DNA mismatch repair locus.

Hum Mutat 2007 May;28(5):424-30

Leeds Institute of Molecular Medicine, University of Leeds and Yorkshire Regional Genetics Service, St James's University Hospital, Leeds, United Kingdom.

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http://dx.doi.org/10.1002/humu.20457DOI Listing
May 2007

Interactive visual analysis of SNP data for rapid autozygosity mapping in consanguineous families.

Hum Mutat 2006 Oct;27(10):1041-6

Leeds Institute for Molecular Medicine, St James's University Hospital, University of Leeds, Leeds, United Kingdom.

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http://dx.doi.org/10.1002/humu.20383DOI Listing
October 2006

PMS2 mutations in childhood cancer.

J Natl Cancer Inst 2006 Mar;98(5):358-61

University of Leeds, Yorkshire Regional Genetics Service, United Kingdom.

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http://dx.doi.org/10.1093/jnci/djj073DOI Listing
March 2006

Approaches for analyzing human mutations and nucleotide sequence variation: a report from the Seventh International Mutation Detection meeting, 2003.

Hum Mutat 2004 May;23(5):401-5

Department of Medical Sciences, Molecular Medicine, Uppsala University, Sweden.

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http://dx.doi.org/10.1002/humu.20031DOI Listing
May 2004

MLPA and MAPH: new techniques for detection of gene deletions.

Hum Mutat 2004 May;23(5):413-9

Molecular Genetics Laboratory, Genetic Services of Western Australia, Princess Margaret Hospital, Perth, Australia.

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http://dx.doi.org/10.1002/humu.20035DOI Listing
May 2004

Current and emerging techniques for diagnostic mutation detection: an overview of methods for mutation detection.

Methods Mol Med 2004 ;92:9-44

Regional DNA Laboratory, Cancer Research UK Mutation Detection Facility, St James's University Hospital, Leeds.

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http://dx.doi.org/10.1385/1-59259-432-8:9DOI Listing
April 2004