Sally M. Harrison

University of Leeds — United Kingdom

Medicine · Health Sciences

18h-index844citations27works0.02yr avg
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Research Topics

Viral gastroenteritis research and epidemiology(6), Genomic variations and chromosomal abnormalities(5), Animal Virus Infections Studies(5), Genomics and Rare Diseases(4), Virus-based gene therapy research(3)

Publications27 total

Novel avian paramyxovirus isolated from gulls in Caspian seashore in Kazakhstan
PLoS ONE·2017· 19 citedOpen Access
How to analyse the spatiotemporal tumour samples needed to investigate cancer evolution: A case study using paired primary and recurrent glioblastoma
International Journal of Cancer·2017· 9 citedOpen Access
m6aViewer: software for the detection, analysis, and visualization of<i>N</i><sup>6</sup>-methyladenosine peaks from m<sup>6</sup>A-seq/ME-RIP sequencing data
RNA·2017· 39 citedOpen Access
Upregulated WEE1 protects endothelial cells of colorectal cancer liver metastases
Oncotarget·2017· 10 citedOpen Access
P08.40 RNAseq of paired primary and recurrent glioblastoma samples
Neuro-Oncology·2016Open Access
A Chromosome 7 Pericentric Inversion Defined at Single-Nucleotide Resolution Using Diagnostic Whole Genome Sequencing in a Patient with Hand-Foot-Genital Syndrome
PLoS ONE·2016· 39 citedOpen Access
Complete Genome Sequence of a Novel Avian Paramyxovirus (APMV-13) Isolated from a Wild Bird in Kazakhstan
Genome Announcements·2016· 26 citedOpen Access
Exploring the surfaceome of Ewing sarcoma identifies a new and unique therapeutic target
Proceedings of the National Academy of Sciences·2016· 59 citedOpen Access
Whole genome sequencing improved case ascertainment in an outbreak of Shiga toxin-producing <i>Escherichia coli</i> O157 associated with raw drinking milk
Epidemiology and Infection·2016· 49 citedOpen Access
Deficiency of the myogenic factor MyoD causes a perinatally lethal fetal akinesia
Journal of Medical Genetics·2016· 22 citedOpen Access
Enhanced diagnostic yield in Meckel-Gruber and Joubert syndrome through exome sequencing supplemented with split-read mapping
BMC Medical Genetics·2016· 91 citedOpen Access
OVA: integrating molecular and physical phenotype data from multiple biomedical domain ontologies with variant filtering for enhanced variant prioritization
Bioinformatics·2015· 24 citedOpen Access
Rapid Detection of Rare Deleterious Variants by Next Generation Sequencing with Optional Microarray SNP Genotype Data
Human Mutation·2015· 16 citedOpen Access
Detection of somatic mutations in tumors using unaligned clonal sequencing data
Laboratory Investigation·2014· 3 cited
Diagnostic whole genome sequencing and split‐read mapping for nucleotide resolution breakpoint identification in CNTNAP2 deficiency syndrome
American Journal of Medical Genetics Part A·2014· 33 citedOpen Access
Robust Diagnostic Genetic Testing Using Solution Capture Enrichment and a Novel Variant‐Filtering Interface
Human Mutation·2013· 37 citedOpen Access
Simple and Efficient Identification of Rare Recessive Pathologically Important Sequence Variants from Next Generation Exome Sequence Data
Human Mutation·2013· 7 cited
Kaposi's Sarcoma-Associated Herpesvirus RTA Promotes Degradation of the Hey1 Repressor Protein through the Ubiquitin Proteasome Pathway
Journal of Virology·2009· 86 citedOpen Access
Mapping the minimal regions within the ORF73 protein required for herpesvirus saimiri episomal persistence
Journal of General Virology·2008· 6 cited
Kaposi's sarcoma‐associated herpesvirus (KSHV) Rta and cellular HMGB1 proteins synergistically transactivate the KSHV <i>ORF50</i> promoter
FEBS Letters·2008· 31 cited
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Frequent Co-authors

Ian Carr(12), Christopher M. Watson(10), David T. Bonthron(10), Laura A. Crinnion(9), Carolina Lascelles(6), Agne Antanaviciute(5), Julian A. Hiscox(5), Alexander F. Markham(5), Adrian Whitehouse(4), Lucy F. Stead(4), Eamonn Sheridan(4), Brian K. Dove(3), Ruth Charlton(2), Ian Tarpey(2), Lisa Rothwell(2), Pete Kaiser(2), Mark L. Reed(2), Joanne Morgan(2), Christine P. Diggle(2), Graham R. Taylor(2)