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Author Details

Martin S Taylor
Institute of Genetics and Cancer, University of Edinburgh
2000
73
37
PMIDPaper TitleJournal TitlePublished Year
35140396Signatures of TOP1 transcription-associated mutagenesis in cancer and germline.Nature2022
35504971Publisher Correction: Signatures of TOP1 transcription-associated mutagenesis in cancer and germline.Nature2022
35379293The contribution of evolutionarily volatile promoters to molecular phenotypes and human trait variation.Genome Biol2022
35140396Signatures of TOP1 transcription-associated mutagenesis in cancer and germline.Nature2022
35074757In Vivo Modeling of Patient Genetic Heterogeneity Identifies New Ways to Target Cholangiocarcinoma.Cancer Res2022
35379293The contribution of evolutionarily volatile promoters to molecular phenotypes and human trait variation.Genome Biol2022
35504971Publisher Correction: Signatures of TOP1 transcription-associated mutagenesis in cancer and germline.Nature2022
35074757In Vivo Modeling of Patient Genetic Heterogeneity Identifies New Ways to Target Cholangiocarcinoma.Cancer Res2022
34417209Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome.Genome Res2021
34417209Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome.Genome Res2021
32275854Codon Usage and Splicing Jointly Influence mRNA Localization.Cell Syst2020
31790603Seasonal patterns of traumatic brain injury deaths due to traffic-related incidents in the Slovak Republic.Traffic Inj Prev2020
32275854Codon Usage and Splicing Jointly Influence mRNA Localization.Cell Syst2020
33128046Evolutionary dependencies show paths to cancer development.Nat Genet2020
32718981Comparative transcriptomics of primary cells in vertebrates.Genome Res2020
31790603Seasonal patterns of traumatic brain injury deaths due to traffic-related incidents in the Slovak Republic.Traffic Inj Prev2020
33128046Evolutionary dependencies show paths to cancer development.Nat Genet2020
32718981Comparative transcriptomics of primary cells in vertebrates.Genome Res2020
31765389Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions.PLoS Genet2019
31765389Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions.PLoS Genet2019
29361513Manipulation of dipeptidylpeptidase 10 in mouse and human <i>in vivo</i> and <i>in vitro</i> models indicates a protective role in asthma.Dis Model Mech2018
29361513Manipulation of dipeptidylpeptidase 10 in mouse and human <i>in vivo</i> and <i>in vitro</i> models indicates a protective role in asthma.Dis Model Mech2018
29106596Aberrant ribonucleotide incorporation and multiple deletions in mitochondrial DNA of the murine MPV17 disease model.Nucleic Acids Res2017
29284524Bidirectional transcription initiation marks accessible chromatin and is not specific to enhancers.Genome Biol2017
29106596Aberrant ribonucleotide incorporation and multiple deletions in mitochondrial DNA of the murine MPV17 disease model.Nucleic Acids Res2017
29284524Bidirectional transcription initiation marks accessible chromatin and is not specific to enhancers.Genome Biol2017
27490693Mutational Biases Drive Elevated Rates of Substitution at Regulatory Sites across Cancer Types.PLoS Genet2016
27490693Mutational Biases Drive Elevated Rates of Substitution at Regulatory Sites across Cancer Types.PLoS Genet2016
25744449Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study.Twin Res Hum Genet2015
25744449Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study.Twin Res Hum Genet2015
25624100Lagging-strand replication shapes the mutational landscape of the genome.Nature2015
26313479Genome-wide mapping of embedded ribonucleotides and other noncanonical nucleotides using emRiboSeq and EndoSeq.Nat Protoc2015
26228054The frequent evolutionary birth and death of functional promoters in mouse and human.Genome Res2015
26173456Homozygous loss-of-function variants in European cosmopolitan and isolate populations.Hum Mol Genet2015
26313479Genome-wide mapping of embedded ribonucleotides and other noncanonical nucleotides using emRiboSeq and EndoSeq.Nat Protoc2015
26228054The frequent evolutionary birth and death of functional promoters in mouse and human.Genome Res2015
26173456Homozygous loss-of-function variants in European cosmopolitan and isolate populations.Hum Mol Genet2015
25624100Lagging-strand replication shapes the mutational landscape of the genome.Nature2015
24462371Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects.Am J Hum Genet2014
25539843Quantification of epigenetic biomarkers: an evaluation of established and emerging methods for DNA methylation analysis.BMC Genomics2014
25400697SuRFing the genomics wave: an R package for prioritising SNPs by functionality.Genome Med2014
24462371Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects.Am J Hum Genet2014
25038816Variant detection sensitivity and biases in whole genome and exome sequencing.BMC Bioinformatics2014
24763282FRA2A is a CGG repeat expansion associated with silencing of AFF3.PLoS Genet2014
24906020Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations.Am J Hum Genet2014
24670764A promoter-level mammalian expression atlas.Nature2014
25196122A CGG-repeat expansion mutation in ZNF713 causes FRA7A: association with autistic spectrum disorder in two families.Hum Mutat2014
25125236Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism.J Med Genet2014
25091723Functional analysis of a novel ENU-induced PHD finger 11 (Phf11) mouse mutant.Mamm Genome2014
25077174Loss of ALDH18A1 function is associated with a cellular lipid droplet phenotype suggesting a link between autosomal recessive cutis laxa type 3A and Warburg Micro syndrome.Mol Genet Genomic Med2014
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Collaborators

Colin A Semple
Institute of Genetics and Cancer, University of Edinburgh
Co-authored papers 16
Piero Carninci
RIKEN Center for Integrative Medical Sciences
Co-authored papers 10
Alison Meynert
Institute of Genetics and Cancer, University of Edinburgh
Co-authored papers 9
Yoshihide Hayashizaki
Center for Integrative Medical Sciences
Co-authored papers 9
Hideya Kawaji
RIKEN Center for Integrative Medical Sciences
Co-authored papers 8
Alistair R R Forrest
RIKEN Center for Integrative Medical Sciences
Co-authored papers 7
David R FitzPatrick
Institute of Genetics and Cancer, The University of Edinburgh MRC Human Genetics Unit
Co-authored papers 7
Andrew P Jackson
Institute of Genetics and Cancer, University of Edinburgh
Co-authored papers 7
David A Hume
Mater Research Institute-UQ, Translational Research Institute
Co-authored papers 7
Albin Sandelin
University of Copenhagen
Co-authored papers 6
Jun Kawai
RIKEN Center for Integrative Medical Sciences
Co-authored papers 6
Boris Lenhard
MRC London Institute of Medical Sciences
Co-authored papers 6
Harukazu Suzuki
RIKEN Center for Integrative Medical Sciences
Co-authored papers 6
Robert S Young
Usher Institute, University of Edinburgh
Co-authored papers 6
Sean M Grimmond
The University of Melbourne
Co-authored papers 5
Richard Mott
Co-authored papers 5
Shiro Fukuda
Graduate School of Medicine, Osaka University
Co-authored papers 5
Richard R Copley
Co-authored papers 5
Masayoshi Itoh
RIKEN Center for Integrative Medical Sciences
Co-authored papers 5
Timothy Ravasi
Okinawa Institute of Science and Technology Graduate University
Co-authored papers 5
Christine A Wells
The University of Melbourne
Co-authored papers 5
Takeya Kasukawa
RIKEN Center for Integrative Medical Sciences
Co-authored papers 5
Stefano Gustincich
Istituto Italiano di Tecnologia
Co-authored papers 4
Timo Lassmann
Telethon Kids Institute, University of Western Australia
Co-authored papers 4
Geoffrey J Faulkner
Mater Research Institute - University of Queensland
Co-authored papers 4
Yasushi Okazaki
Intractable Disease Research Center, Graduate School of Medicine, Juntendo University
Co-authored papers 4
Vladimir B Bajic
King Abdullah University of Science and Technology (KAUST)
Co-authored papers 4
Claes Wahlestedt
Co-authored papers 4
Matthew E Hurles
Wellcome Sanger Institute
Co-authored papers 4
Carsten O Daub
International Institute of Molecular and Cell Biology in Warsaw
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Release 1.2