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Author Details

Mark T Ross
Illumina Cambridge Ltd.
1990
72
38
PMIDPaper TitleJournal TitlePublished Year
36658389Whole genome sequencing provides comprehensive genetic testing in childhood B-cell acute lymphoblastic leukaemia.Leukemia2023
37216686The genomic landscape of acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21.Blood2023
36550215Integrative genomic analysis of childhood acute lymphoblastic leukaemia lacking a genetic biomarker in the UKALL2003 clinical trial.Leukemia2023
36333502Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features.Nat Genet2022
33632293Clinical-grade whole-genome sequencing and 3' transcriptome analysis of colorectal cancer patients.Genome Med2021
32807235Detection of ctDNA in plasma of patients with clinically localised prostate cancer is associated with rapid disease progression.Genome Med2020
31964840Imaging breast cancer using hyperpolarized carbon-13 MRI.Proc Natl Acad Sci U S A2020
29388947Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project.Genet Med2018
29930474Familial congenital cataract, coloboma, and nystagmus phenotype with variable expression caused by mutation in <i>PAX6</i> in a South African family.Mol Vis2018
27161491The somatic mutation profiles of 2,433 breast cancers refines their genomic and transcriptomic landscapes.Nat Commun2016
27264733Erratum: The somatic mutation profiles of 2,433 breast cancers refine their genomic and transcriptomic landscapes.Nat Commun2016
26192915Whole-genome sequencing provides new insights into the clonal architecture of Barrett's esophagus and esophageal adenocarcinoma.Nat Genet2015
23817176Intraclonal heterogeneity is a critical early event in the development of myeloma and precedes the development of clinical symptoms.Leukemia2014
25587359Assessment of patient-derived tumour xenografts (PDXs) as a discovery tool for cancer epigenomics.Genome Med2014
24857694An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval.Am J Hum Genet2014
24335234SAMHD1 is mutated recurrently in chronic lymphocytic leukemia and is involved in response to DNA damage.Blood2014
23863747Meta-analysis of IDH-mutant cancers identifies EBF1 as an interaction partner for TET2.Nat Commun2013
22674553A validated tumorgraft model reveals activity of dovitinib against renal cell carcinoma.Sci Transl Med2012
22915640Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patterns.Blood2012
22683710BAP1 loss defines a new class of renal cell carcinoma.Nat Genet2012
20016485A comprehensive catalogue of somatic mutations from a human cancer genome.Nature2010
18208332Large-scale population study of human cell lines indicates that dosage compensation is virtually complete.PLoS Genet2008
18987734Accurate whole human genome sequencing using reversible terminator chemistry.Nature2008
17333537Genes flanking Xist in mouse and human are separated on the X chromosome in American marsupials.Chromosome Res2007
17943131Genome-wide detection and characterization of positive selection in human populations.Nature2007
17943122A second generation human haplotype map of over 3.1 million SNPs.Nature2007
16650760The sequences of the human sex chromosomes.Curr Opin Genet Dev2006
16710414The DNA sequence and biological annotation of human chromosome 1.Nature2006
15772651The DNA sequence of the human X chromosome.Nature2005
16241968More on: polymorphism and hemophilia A causing inversions in distal Xq28: a complex picture.J Thromb Haemost2005
16235118Isolation, X location and activity of the marsupial homologue of SLC16A2, an XIST-flanking gene in eutherian mammals.Chromosome Res2005
16380909Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombination.Am J Hum Genet2005
16030148Progressive proximal expansion of the primate X chromosome centromere.Proc Natl Acad Sci U S A2005
15164054The DNA sequence and comparative analysis of human chromosome 10.Nature2004
15591263Position effect on PLP1 may cause a subset of Pelizaeus-Merzbacher disease symptoms.J Med Genet2004
15057823The DNA sequence and analysis of human chromosome 13.Nature2004
12754510Positional cloning of a quantitative trait locus on chromosome 13q14 that influences immunoglobulin E levels and asthma.Nat Genet2003
14574404The DNA sequence and analysis of human chromosome 6.Nature2003
12647244Construction and integration of radiation-hybrid and cytogenetic maps of dog Chromosome X.Mamm Genome2003
11944989An integrated, functionally annotated gene map of the DXS8026-ELK1 interval on human Xp11.3-Xp11.23: potential hotspot for neurogenetic disorders.Genomics2002
11827456Physical and transcript map of the hereditary prostate cancer region at xq27.Genomics2002
11170748A 6.9-Mb high-resolution BAC/PAC contig of human 4p15.3-p16.1, a candidate region for bipolar affective disorder.Genomics2001
11374897A novel poly(A)-binding protein gene (PABPC5) maps to an X-specific subinterval in the Xq21.3/Yp11.2 homology block of the human sex chromosomes.Genomics2001
11237015The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X.Nature2001
11237011Initial sequencing and analysis of the human genome.Nature2001
11780052The DNA sequence and comparative analysis of human chromosome 20.Nature2001
11499681Physical and transcriptional mapping of the X-linked cleft palate and ankyloglossia (CPX) critical region.Hum Genet2001
11401425Identification and characterization of KLHL4, a novel human homologue of the Drosophila Kelch gene that maps within the X-linked cleft palate and Ankyloglossia (CPX) critical region.Genomics2001
11029003An SNP map of human chromosome 22.Nature2000
10049581Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid-induced gene in Xp22.Genomics1999
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Collaborators

Illumina Cambridge Ltd.
Co-authored papers 37
4Wellcome Trust Sanger Institute
Co-authored papers 16
Co-authored papers 12
Tufts University Graduate School of Biomedical Sciences
Co-authored papers 12
The Wellcome Trust Sanger Institute
Co-authored papers 12
Illumina Ltd.
Co-authored papers 11
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European Bioinformatics Institute
Co-authored papers 11
The Wellcome Trust Sanger Institute
Co-authored papers 10
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 9
UCL Cancer Institute, University College London
Co-authored papers 9
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 9
University of Cambridge
Co-authored papers 9
University of Oxford
Co-authored papers 9
Institute of Biotechnology, University of Cambridge
Co-authored papers 9
Co-authored papers 9
University of Cambridge
Co-authored papers 9
The Wellcome Trust Sanger Institute
Co-authored papers 8
Co-authored papers 8
Co-authored papers 8
European Bioinformatics Institute (EMBL-EBI)
Co-authored papers 8
Co-authored papers 7
Co-authored papers 7
Co-authored papers 7
Co-authored papers 7
Inivata Ltd.
Co-authored papers 7
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Co-authored papers 6
Wellcome Sanger Institute
Co-authored papers 6
Wellcome Trust Sanger Institute
Co-authored papers 5