Author details

Full Name

Martin S Taylor

Affiliation

Institute of Genetics and Cancer, University of Edinburgh

ORCID

Career Start Year

2000

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
35140396	Signatures of TOP1 transcription-associated mutagenesis in cancer and germline.	Nature	2022
35504971	Publisher Correction: Signatures of TOP1 transcription-associated mutagenesis in cancer and germline.	Nature	2022
35379293	The contribution of evolutionarily volatile promoters to molecular phenotypes and human trait variation.	Genome Biol	2022
35140396	Signatures of TOP1 transcription-associated mutagenesis in cancer and germline.	Nature	2022
35074757	In Vivo Modeling of Patient Genetic Heterogeneity Identifies New Ways to Target Cholangiocarcinoma.	Cancer Res	2022
35379293	The contribution of evolutionarily volatile promoters to molecular phenotypes and human trait variation.	Genome Biol	2022
35504971	Publisher Correction: Signatures of TOP1 transcription-associated mutagenesis in cancer and germline.	Nature	2022
35074757	In Vivo Modeling of Patient Genetic Heterogeneity Identifies New Ways to Target Cholangiocarcinoma.	Cancer Res	2022
34417209	Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome.	Genome Res	2021
34417209	Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome.	Genome Res	2021
32275854	Codon Usage and Splicing Jointly Influence mRNA Localization.	Cell Syst	2020
31790603	Seasonal patterns of traumatic brain injury deaths due to traffic-related incidents in the Slovak Republic.	Traffic Inj Prev	2020
32275854	Codon Usage and Splicing Jointly Influence mRNA Localization.	Cell Syst	2020
33128046	Evolutionary dependencies show paths to cancer development.	Nat Genet	2020
32718981	Comparative transcriptomics of primary cells in vertebrates.	Genome Res	2020
31790603	Seasonal patterns of traumatic brain injury deaths due to traffic-related incidents in the Slovak Republic.	Traffic Inj Prev	2020
33128046	Evolutionary dependencies show paths to cancer development.	Nat Genet	2020
32718981	Comparative transcriptomics of primary cells in vertebrates.	Genome Res	2020
31765389	Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions.	PLoS Genet	2019
31765389	Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions.	PLoS Genet	2019
29361513	Manipulation 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 Mech	2018
29361513	Manipulation 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 Mech	2018
29106596	Aberrant ribonucleotide incorporation and multiple deletions in mitochondrial DNA of the murine MPV17 disease model.	Nucleic Acids Res	2017
29284524	Bidirectional transcription initiation marks accessible chromatin and is not specific to enhancers.	Genome Biol	2017
29106596	Aberrant ribonucleotide incorporation and multiple deletions in mitochondrial DNA of the murine MPV17 disease model.	Nucleic Acids Res	2017
29284524	Bidirectional transcription initiation marks accessible chromatin and is not specific to enhancers.	Genome Biol	2017
27490693	Mutational Biases Drive Elevated Rates of Substitution at Regulatory Sites across Cancer Types.	PLoS Genet	2016
27490693	Mutational Biases Drive Elevated Rates of Substitution at Regulatory Sites across Cancer Types.	PLoS Genet	2016
25744449	Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study.	Twin Res Hum Genet	2015
25744449	Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study.	Twin Res Hum Genet	2015
25624100	Lagging-strand replication shapes the mutational landscape of the genome.	Nature	2015
26313479	Genome-wide mapping of embedded ribonucleotides and other noncanonical nucleotides using emRiboSeq and EndoSeq.	Nat Protoc	2015
26228054	The frequent evolutionary birth and death of functional promoters in mouse and human.	Genome Res	2015
26173456	Homozygous loss-of-function variants in European cosmopolitan and isolate populations.	Hum Mol Genet	2015
26313479	Genome-wide mapping of embedded ribonucleotides and other noncanonical nucleotides using emRiboSeq and EndoSeq.	Nat Protoc	2015
26228054	The frequent evolutionary birth and death of functional promoters in mouse and human.	Genome Res	2015
26173456	Homozygous loss-of-function variants in European cosmopolitan and isolate populations.	Hum Mol Genet	2015
25624100	Lagging-strand replication shapes the mutational landscape of the genome.	Nature	2015
24462371	Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects.	Am J Hum Genet	2014
25539843	Quantification of epigenetic biomarkers: an evaluation of established and emerging methods for DNA methylation analysis.	BMC Genomics	2014
25400697	SuRFing the genomics wave: an R package for prioritising SNPs by functionality.	Genome Med	2014
24462371	Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects.	Am J Hum Genet	2014
25038816	Variant detection sensitivity and biases in whole genome and exome sequencing.	BMC Bioinformatics	2014
24763282	FRA2A is a CGG repeat expansion associated with silencing of AFF3.	PLoS Genet	2014
24906020	Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations.	Am J Hum Genet	2014
24670764	A promoter-level mammalian expression atlas.	Nature	2014
25196122	A CGG-repeat expansion mutation in ZNF713 causes FRA7A: association with autistic spectrum disorder in two families.	Hum Mutat	2014
25125236	Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism.	J Med Genet	2014
25091723	Functional analysis of a novel ENU-induced PHD finger 11 (Phf11) mouse mutant.	Mamm Genome	2014
25077174	Loss 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 Med	2014

1 - 50 of 146

Marta Gut

Universitat de Barcelona (UB)

Career Start Year 2010

Number of shared co-authors 19

Martin Kircher

Berlin Institute of Health (BIH) at Charite-Universitatsmedizin Berlin

Career Start Year 2008

Number of shared co-authors 11

David L Corcoran

The University of North Carolina at Chapel Hill

Career Start Year 2005

Number of shared co-authors 2

Shyam Prabhakar

Genome Institute of Singapore (GIS)

Career Start Year 2004

Number of shared co-authors 7

Jochen Hecht

The Barcelona Institute of Science and Technology

Career Start Year 2003

Number of shared co-authors 5

Valer Gotea

National Human Genome Research Institute, National Institutes of Health

Career Start Year 2003

Number of shared co-authors 10

Eric Haugen

Altius Institute for Biomedical Sciences

Career Start Year 2003

Number of shared co-authors 43

Manolis Kellis

Massachusetts Institute of Technology

Career Start Year 2003

Number of shared co-authors 48

John A Capra

Bakar Computational Health Sciences Institute, University of California san francisco

Career Start Year 2003

Number of shared co-authors 2

Christie L Kovar

Baylor College of Medicine

Career Start Year 2002

Number of shared co-authors 55

Tarjei S Mikkelsen

Harvard University, USA Broad Institute, USA Harvard Stem Cell Institute

Career Start Year 2001

Number of shared co-authors 37

Michael D Wilson

SickKids Research Institute

Career Start Year 2000

Number of shared co-authors 9

Shawn Levy

HudsonAlpha Institute for Biotechnology

Career Start Year 1999

Number of shared co-authors 12

Paul Flicek

European Bioinformatics Institute

Career Start Year 1999

Number of shared co-authors 94

Nadav Ahituv

University of California san francisco

Career Start Year 1998

Number of shared co-authors 6

Sarah J Wheelan

National Human Genome Research Institute, National Institutes of Health

Career Start Year 1998

Number of shared co-authors 13

Edwin Cuppen

Hartwig Medical Foundation

Career Start Year 1997

Number of shared co-authors 21

Jay Shendure

University of Washington

Career Start Year 1996

Number of shared co-authors 25

Len A Pennacchio

Lawrence Berkeley National Laboratory

Career Start Year 1995

Number of shared co-authors 16

Jared C Roach

Institute for Systems Biology

Career Start Year 1995

Number of shared co-authors 6

Ping Liang

College of Chemistry and Chemical Engineering, Hunan University

Career Start Year 1995

Number of shared co-authors 1

Lucinda Fulton

McDonnell Genome Institute, Washington University School of Medicine

Career Start Year 1994

Number of shared co-authors 81

Samuel Levy

Bluestar Genomics Inc.

Career Start Year 1991

Number of shared co-authors 21

Thomas J Hudson

Ontario Institute for Cancer Research

Career Start Year 1991

Number of shared co-authors 49

Gustavo Glusman

Institute for Systems Biology

Career Start Year 1988

Number of shared co-authors 46

James C Mullikin

National Human Genome Research Institute, National Institutes of Health

Career Start Year 1985

Number of shared co-authors 79

Richard K Wilson

The Ohio State University

Career Start Year 1983

Number of shared co-authors 94

Stephan Beck

UCL Cancer Institute, University College London

Career Start Year 1983

Number of shared co-authors 70

Richard M Myers

HudsonAlpha Institute for Biotechnology

Career Start Year 1980

Number of shared co-authors 67

Kelly A Frazer

University of California, USA Institute for Genomic Medicine

Career Start Year 1967

Number of shared co-authors 23

row(s) 1 - 30 of 30

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

Co-authored papers 4

1 - 30

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