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David Bentley

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Guy Leschziner; Josemir W. Sander; Lucy Kinton; Toby Andrew; David R Bentley; Maria Calafato; Alison J Coffey; Emmanuel Dias-Neto; Sheila P Gregorio; Michael R Johnson
Q8IYL2 is a candidate gene for the familial epilepsy syndrome of Partial Epilepsy with Pericentral Spikes (PEPS).
Guy Leschziner; Andrea L Jorgensen; Toby Andrew; Paula R Williamson; Anthony G Marson; Alison J Coffey; Claire Middleditch; David J Balding; Jane Rogers; David R Bentley; David W Chadwick; Michael R Johnson; Munir Pirmohamed
The association between polymorphisms in RLIP76 and drug response in epilepsy.
Guy Leschziner; Toby Andrew; John Paul Leach; David W Chadwick; Alison J Coffey; David J Balding; David R Bentley; Munir Pirmohamed; Michael R Johnson
Common ABCB1 polymorphisms are not associated with multidrug resistance in epilepsy using a gene-wide tagging approach.

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All Publications

2011: Guy Leschziner; Josemir W. Sander; Lucy Kinton; Toby Andrew; David R Bentley; Maria Calafato; Alison J Coffey; Emmanuel Dias-Neto; Sheila P Gregorio; Michael R Johnson
Q8IYL2 is a candidate gene for the familial epilepsy syndrome of Partial Epilepsy with Pericentral Spikes (PEPS).
Epilepsy research 2011;96(1-2):109-15.
2007: Guy Leschziner; Andrea L Jorgensen; Toby Andrew; Paula R Williamson; Anthony G Marson; Alison J Coffey; Claire Middleditch; David J Balding; Jane Rogers; David R Bentley; David W Chadwick; Michael R Johnson; Munir Pirmohamed
The association between polymorphisms in RLIP76 and drug response in epilepsy.
Pharmacogenomics 2007;8(12):1715-22.
2007: Guy Leschziner; Toby Andrew; John Paul Leach; David W Chadwick; Alison J Coffey; David J Balding; David R Bentley; Munir Pirmohamed; Michael R Johnson
Common ABCB1 polymorphisms are not associated with multidrug resistance in epilepsy using a gene-wide tagging approach.
Pharmacogenetics and genomics 2007;17(3):217-20.
2006: Guy Leschziner; Andrea L Jorgensen; Toby Andrew; Munir Pirmohamed; Paula R Williamson; Anthony G Marson; Alison J Coffey; Claire Middleditch; Jane Rogers; David R Bentley; David W Chadwick; David J Balding; Michael R Johnson
Clinical factors and ABCB1 polymorphisms in prediction of antiepileptic drug response: a prospective cohort study.
Lancet neurology 2006;5(8):668-76.
2006: Mark T Ross; David R Bentley; Chris Tyler-Smith
The sequences of the human sex chromosomes.
Current opinion in genetics & development 2006;16(3):213-8.
2005: Mark T Ross; David R Bentley
More on: polymorphism and hemophilia A causing inversions in distal Xq28: a complex picture.
Journal of thrombosis and haemostasis : JTH 2005;3(11):2600-1.
2005: Xiayi Ke; Marcos M Miretti; John Broxholme; Sarah Hunt; Stephan Beck; David R Bentley; Panos Deloukas; Lon R Cardon
A comparison of tagging methods and their tagging space.
Human molecular genetics 2005;14(18):2757-67.
2005: Marcos M Miretti; Emily C Walsh; Xiayi Ke; Marcos Delgado; Mark Griffiths; Sarah Hunt; Jonathan Morrison; Pamela Whittaker; Eric S Lander; Lon R Cardon; David R Bentley; John D Rioux; Stephan Beck; Panos Deloukas
A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms.
American journal of human genetics 2005;76(4):634-46.
2004: Weihua Zhang; ANDREW COLLINS; Jane Gibson; William Tapper; Sarah Hunt; Panos Deloukas; David R Bentley; Newton E Morton
Impact of population structure, effective bottleneck time, and allele frequency on linkage disequilibrium maps.
Proceedings of the National Academy of Sciences of the United States of America 2004;101(52):18075-80.
2004: Xiayi Ke; Caroline Durrant; Andrew P Morris; Sarah Hunt; David R Bentley; Panos Deloukas; Lon R Cardon
Efficiency and consistency of haplotype tagging of dense SNP maps in multiple samples.
Human molecular genetics 2004;13(21):2557-65.
2004: David R Bentley
Genomes for medicine.
Nature 2004;429(6990):440-5.
2004: Gil McVean; Simon R Myers; Sarah Hunt; Panos Deloukas; David R Bentley; Peter Donnelly
The fine-scale structure of recombination rate variation in the human genome.
Science (New York, N.Y.) 2004;304(5670):581-4.
2003: David R Bentley
DNA sequence variation of Homo sapiens.
Cold Spring Harbor symposia on quantitative biology 2003;68():55-63.
2002: Elisabeth Dawson; Goncalo Abecasis; Suzannah Bumpstead; Yuan Chen; Sarah Hunt; David M Beare; Jagjit Pabial; Thomas Dibling; Emma Tinsley; Susan Kirby; David Carter; Marianna Papaspyridonos; Simon Livingstone; Rocky Ganske; Elin Lõhmussaar; Jana Zernant; Neeme Tõnisson; Maido Remm; Reedik Mägi; Tarmo Puurand; Jaak Vilo; Ants Kurg; Kate Rice; Panos Deloukas; Richard Mott; Andres Metspalu; David R Bentley; Lon R Cardon; Carl Bruder
A first-generation linkage disequilibrium map of human chromosome 22.
Nature 2002;418(6897):544-8.
2002: Berthold Göttgens; Linda M Barton; Michael A Chapman; Angus M Sinclair; Bjarne Knudsen; Darren Grafham; James G R Gilbert; Jane Rogers; David R Bentley; Anthony R Green
Transcriptional regulation of the stem cell leukemia gene (SCL)--comparative analysis of five vertebrate SCL loci.
Genome research 2002;12(5):749-59.
2001: Kathryn L Evans; Stéphanie Le Hellard; stewart morris; D Lawson; Claire Whitton; Colin Semple; Judy A Fantes; Helen S Torrance; M Pat Malloy; John Maule; Sean Humphray; Mark T Ross; David R Bentley; Walter J Muir; D H R Blackwood; David J Porteous
A 6.9-Mb high-resolution BAC/PAC contig of human 4p15.3-p16.1, a candidate region for bipolar affective disorder.
Genomics 2001;71(3):315-23.
2001: Berthold Göttgens; James G R Gilbert; Linda M Barton; Darren Grafham; Jane Rogers; David R Bentley; Anthony R Green
Long-range comparison of human and mouse SCL loci: localized regions of sensitivity to restriction endonucleases correspond precisely with peaks of conserved noncoding sequences.
Genome research 2001;11(1):87-97.
2000: David R Bentley
Decoding the human genome sequence.
Human molecular genetics 2000;9(16):2353-8.
2000: Anthony J Bench; Elisabeth P Nacheva; T L Hood; J L Holden; L French; Soheila Swanton; KM Champion; Juan Li; Pamela Whittaker; George Stavrides; A R Hunt; Brian J P Huntly; Lynda J Campbell; David R Bentley; Panos Deloukas; Anthony R Green
Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes. UK Cancer Cytogenetics Group (UKCCG).
Oncogene 2000;19(34):3902-13.
2000: Charles J Shaw-Smith; Alison J Coffey; Elizabeth J Huckle; J Durham; Elizabeth A Campbell; T C Freeman; Julian R F Walters; David R Bentley
Improved method for detecting differentially expressed genes using cDNA indexing.
BioTechniques 2000;28(5):958-64.
2000: David R Bentley
The Human Genome Project--an overview.
Medicinal research reviews 2000;20(3):189-96.
2000: Berthold Göttgens; Linda M Barton; James G R Gilbert; Anthony J Bench; Maria-Jose Sanchez; Sabine Bahn; S Mistry; Darren Grafham; A McMurray; Mark Vaudin; Enrique Amaya; David R Bentley; Anthony R Green; Angus M Sinclair
Analysis of vertebrate SCL loci identifies conserved enhancers.
Nature biotechnology 2000;18(2):181-6.
2000: Charles J Shaw-Smith; Alison J Coffey; MA Leversha; T C Freeman; David R Bentley; Julian R F Walters
Characterisation of a novel murine intestinal serine protease, DISP.
Biochimica et biophysica acta 2000;1490(1-2):131-6.
1999: H E Steingruber; A Dunham; Alison J Coffey; SM Clegg; Gareth R Howell; GL Maslen; Carol E Scott; Rhian Gwilliam; P J Hunt; E C Sotheran; Elizabeth J Huckle; SE Hunt; Pawandeep Dhami; CA Soderlund; MA Leversha; David R Bentley; Mark T Ross
High-resolution landmark framework for the sequence-ready mapping of Xq23-q26.1.
Genome research 1999;9(8):751-62.
1998: David R Bentley; Kim D Pruitt; Panos Deloukas; G D Schuler; James Ostell
Coordination of human genome sequencing via a consensus framework map.
Trends in genetics : TIG 1998;14(10):381-4.
1998: Anthony J Bench; M A Aldred; Sean Humphray; KM Champion; James G R Gilbert; FA Asimakopoulos; Panos Deloukas; Rhian Gwilliam; David R Bentley; Anthony R Green
A detailed physical and transcriptional map of the region of chromosome 20 that is deleted in myeloproliferative disorders and refinement of the common deleted region.
Genomics 1998;49(3):351-62.
1997: Simon G Gregory; Gareth R Howell; David R Bentley
Genome mapping by fluorescent fingerprinting.
Genome research 1997;7(12):1162-8.
1997: SM Walpole; A Nicolaou; Gareth R Howell; A Whittaker; David R Bentley; Mark T Ross; J R W Yates; Dorothy Trump
High-resolution physical map of the X-linked retinoschisis interval in Xp22.
Genomics 1997;44(3):300-8.
1996: Andrew Mungall; C A Edwards; S A Ranby; Sean Humphray; R W Heathcott; C M Clee; C L East; E Holloway; A P Butler; C F Langford; Rhian Gwilliam; K M Rice; G L Maslen; Nigel P Carter; Mark T Ross; Panos Deloukas; David R Bentley; Carl Bruder
Physical mapping of chromosome 6: a strategy for the rapid generation of sequence-ready contigs.
DNA sequence : the journal of DNA sequencing and mapping 1996;7(1):47-9.
1996: S A Forbes; L Brennan; M Richardson; A Coffey; C G Cole; S G Gregory; David R Bentley; S Mumm; Gudrun E Moore; Philip Stanier
Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3.
Genomics 1996;31(1):36-43.
1994: Galit Rotman; Kinneret Savitsky; Yehiel Ziv; C G Cole; Michael J Higgins; I Bar-Am; Carl Bruder; Anat Bar-Shira; L Vanagaite; S Qin; J Zhang; N J Nowak; Settara C Chandrasekharappa; H Lehrach; Lydia Avivi; T B Shows; Francis S Collins; David R Bentley; Yosef Shiloh
A YAC contig spanning the ataxia-telangiectasia locus (groups A and C) at 11q22-q23.
Genomics 1994;24(2):234-42.
1994: Igor Vorechovský; David Vetrie; J Holland; David R Bentley; K Thomas; J N Zhou; L D Notarangelo; A Plebani; G Fontán; H D Ochs
Isolation of cosmid and cDNA clones in the region surrounding the BTK gene at Xq21.3-q22.
Genomics 1994;21(3):517-24.
1994: I I Haris; Peter M Green; David R Bentley; Francesco Giannelli
Mutation detection by fluorescent chemical cleavage: application to hemophilia B.
PCR methods and applications 1994;3(5):268-71.
1994: David Vetrie; E Kendall; A Coffey; S Hassock; J Collins; C Todd; Hans Lehrach; Martin Bobrow; David R Bentley; A Harris
A 6.5-Mb yeast artificial chromosome contig incorporating 33 DNA markers on the human X chromosome at Xq22.
Genomics 1994;19(1):42-7.
1993: Roland Roberts; A J Coffey; Martin Bobrow; David R Bentley
Exon structure of the human dystrophin gene.
Genomics 1993;16(2):536-8.
1993: J Holland; A J Coffey; Francesco Giannelli; David R Bentley
Vertical integration of cosmid and YAC resources for interval mapping on the X-chromosome.
Genomics 1993;15(2):297-304.
1993: R H Flomen; E P Green; Peter M Green; David R Bentley; Francesco Giannelli
Determination of the organisation of coding sequences within the iduronate sulphate sulphatase (IDS) gene.
Human molecular genetics 1993;2(1):5-10.
1993: Roland Roberts; David R Bentley; Martin Bobrow
Infidelity in the structure of ectopic transcripts: a novel exon in lymphocyte dystrophin transcripts.
Human mutation 1993;2(4):293-9.
1993: Igor Vorechovský; J Holland; Paschalis Sideras; Carl Bruder; Lennart Hammarström; C I Edvard Smith; David R Bentley; David Vetrie
Isolation of cDNA clones mapping around DXS178: a search for human X-linked agammaglobulinaemia gene using yeast artificial chromosomes, cosmids and direct cDNA selection.
Immunodeficiency 1993;4(1-4):221-4.
1992: John E Collins; L A Everett; David R Bentley; Carl Bruder
A panel of human chromosome 22-specific sequence tagged sites.
Genomics 1992;14(4):1098-103.
1992: C G Cole; K Patel; J Shipley; Denise Sheer; Martin Bobrow; David R Bentley; Carl Bruder
Identification of region-specific yeast artificial chromosomes using pools of Alu element-mediated polymerase chain reaction probes labeled via linear amplification.
Genomics 1992;14(4):931-8.
1992: C G Cole; Carl Bruder; A J Coffey; Mark T Ross; S Meier-Ewert; Martin Bobrow; David R Bentley
A random STS strategy for construction of YAC contigs spanning defined chromosomal regions.
Genomics 1992;14(2):256-62.
1992: Francesco Giannelli; S Saad; A J Montandon; David R Bentley; Peter M Green
A new strategy for the genetic counselling of diseases of marked mutational heterogeneity: haemophilia B as a model.
Journal of medical genetics 1992;29(9):602-7.
1992: Roland Roberts; A J Coffey; Martin Bobrow; David R Bentley
Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCR.
Genomics 1992;13(4):942-50.
1992: R H Flomen; Peter M Green; David R Bentley; Francesco Giannelli; E P Green
Detection of point mutations and a gross deletion in six Hunter syndrome patients.
Genomics 1992;13(3):543-50.
1992: A J Montandon; Peter M Green; David R Bentley; Rolf Ljung; S Kling; IM Nilsson; Francesco Giannelli
Direct estimate of the haemophilia B (factor IX deficiency) mutation rate and of the ratio of the sex-specific mutation rates in Sweden.
Human genetics 1992;89(3):319-22.
1992: Johan T den Dunnen; P M Grootscholten; J G Dauwerse; A P Walker; Anthony P Monaco; R Butler; R Anand; A J Coffey; David R Bentley; H Yde Steensma
Reconstruction of the 2.4 Mb human DMD-gene by homologous YAC recombination.
Human molecular genetics 1992;1(1):19-28.
1992: Roland Roberts; Martin Bobrow; David R Bentley
Point mutations in the dystrophin gene.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(6):2331-5.
1992: David R Bentley; C Todd; J Collins; J Holland; Carl Bruder; S Hassock; A Bankier; Francesco Giannelli
The development and application of automated gridding for efficient screening of yeast and bacterial ordered libraries.
Genomics 1992;12(3):534-41.
1992: A J Coffey; Roland Roberts; Eric Green; C G Cole; R Butler; R Anand; Francesco Giannelli; David R Bentley
Construction of a 2.6-Mb contig in yeast artificial chromosomes spanning the human dystrophin gene using an STS-based approach.
Genomics 1992;12(3):474-84.
1991: S C Yau; Roland Roberts; David R Bentley; Christopher G Mathew; Martin Bobrow
A MseI polymorphism in exon 48 of the dystrophin gene.
Nucleic acids research 1991;19(20):5803.
1991: Roland Roberts; T F Barby; E Manners; Martin Bobrow; David R Bentley
Direct detection of dystrophin gene rearrangements by analysis of dystrophin mRNA in peripheral blood lymphocytes.
American journal of human genetics 1991;49(2):298-310.
1991: Peter M Green; A J Montandon; David R Bentley; Francesco Giannelli
Genetics and molecular biology of haemophilias A and B.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 1991;2(4):539-65.
1991: C G Cole; P N Goodfellow; Martin Bobrow; David R Bentley
Generation of novel sequence tagged sites (STSs) from discrete chromosomal regions using Alu-PCR.
Genomics 1991;10(3):816-26.
1991: Peter M Green; A J Montandon; Rolf Ljung; David R Bentley; IM Nilsson; S Kling; Francesco Giannelli
Haemophilia B mutations in a complete Swedish population sample: a test of new strategy for the genetic counselling of diseases with high mutational heterogeneity.
British journal of haematology 1991;78(3):390-7.
1991: A J Montandon; Peter M Green; David R Bentley; Rolf Ljung; IM Nilsson; Francesco Giannelli
A new strategy for carrier and prenatal diagnosis and molecular studies in haemophilia B.
Current studies in hematology and blood transfusion 1991;(58):88-93.
1990: Roland Roberts; David R Bentley; T F Barby; E Manners; Martin Bobrow
Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNA.
Lancet 1990;336(8730):1523-6.
1990: Stephen Abbs; Roland Roberts; Christopher G Mathew; David R Bentley; Martin Bobrow
Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy gene.
Genomics 1990;7(4):602-6.
1990: A J Montandon; Peter M Green; David R Bentley; Rolf Ljung; IM Nilsson; Francesco Giannelli
Two factor IX mutations in the family of an isolated haemophilia B patient: direct carrier diagnosis by amplification mismatch detection (AMD).
Human genetics 1990;85(2):200-4.
1990: Peter M Green; A J Montandon; David R Bentley; Rolf Ljung; IM Nilsson; Francesco Giannelli
The incidence and distribution of CpG----TpG transitions in the coagulation factor IX gene. A fresh look at CpG mutational hotspots.
Nucleic acids research 1990;18(11):3227-31.
1990: Roland Roberts; Martin Bobrow; David R Bentley
A MaeIII polymorphism near the dystrophin gene promoter by restriction of amplified DNA.
Nucleic acids research 1990;18(5):1315.
1989: Roland Roberts; A J Montandon; Martin Bobrow; David R Bentley
Detection of novel genetic markers by mismatch analysis.
Nucleic acids research 1989;17(15):5961-71.
1989: T C Tsang; David R Bentley; IM Nilsson; Francesco Giannelli
The use of DNA amplification for genetic counselling related diagnosis in haemophilia B.
Thrombosis and haemostasis 1989;61(3):343-7.
1989: A J Montandon; Peter M Green; Francesco Giannelli; David R Bentley
Direct detection of point mutations by mismatch analysis: application to haemophilia B.
Nucleic acids research 1989;17(9):3347-58.
1989: Peter M Green; David R Bentley; R S Mibashan; IM Nilsson; Francesco Giannelli
Molecular pathology of haemophilia B.
The EMBO journal 1989;8(4):1067-72.
1989: Roland Roberts; C G Cole; K A Hart; Martin Bobrow; David R Bentley
Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy.
Nucleic acids research 1989;17(2):811.
1988: T C Tsang; David R Bentley; R S Mibashan; Francesco Giannelli
A factor IX mutation, verified by direct genomic sequencing, causes haemophilia B by a novel mechanism.
The EMBO journal 1988;7(10):3009-15.
1988: T C Tsang; David R Bentley
An improved sequencing method using Sequenase that is independent of template concentration.
Nucleic acids research 1988;16(13):6238.
1988: A Harris; David R Bentley
Separation of episomal Epstein-Barr virus from Burkitt's lymphoma host cell DNA in pulse field gels.
Nucleic acids research 1988;16(9):4172.
1988: Peter M Green; David R Bentley; R S Mibashan; Francesco Giannelli
Partial deletion by illegitimate recombination of the factor IX gene in a haemophilia B family with two inhibitor patients.
Molecular biology & medicine 1988;5(2):95-106.