Publications by Dr Michael Jackson - ePrints

Browsing publications by Dr Michael Jackson.

Newcastle Authors	Title	Year
Ben Whittle Dr Hannah Lowes Dr Dasha Deen Dr Angela Pyle Dr Jonathan Coxhead et al.	Early-stage idiopathic Parkinson's disease is associated with reduced circular RNA expression	2024
Dr Richard Gallon Rachel Phelps Christine Hayes Annabel Kunzemann Martinez Dr Gillian Borthwick et al.	Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair Deficiency	2023
Dr Richard Gallon Dr Mauro Santibanez Koref Dr Michael Jackson Dr Gillian Borthwick	Is HLA type a possible cancer risk modifier in Lynch syndrome?	2023
Dr Michael Jackson Dr Mauro Santibanez Koref	Large-scale benchmarking of circRNA detection tools reveals large differences in sensitivity but not in precision	2023
Maria Rasmussen Peter Sowter Dr Richard Gallon Christine Hayes Dr Mauro Santibanez Koref et al.	Mismatch repair deficiency testing in Lynch syndrome-associated urothelial tumors	2023
Dr Richard Gallon Rachel Phelps Christine Hayes Dr Dino Masic Professor Julie Irving et al.	Detection of constitutional mismatch repair deficiency in children and adolescents with acute lymphoblastic leukemia	2022
Rachel Phelps Dr Richard Gallon Christine Hayes Dr Tom Lee Professor Rakesh Heer et al.	Detection of Microsatellite Instability in Colonoscopic Biopsies and Postal Urine Samples from Lynch Syndrome Cancer Patients Using a Multiplex PCR Assay	2022
Peter Sowter Dr Mauro Santibanez Koref Dr Michael Jackson Dr Gillian Borthwick Professor Neil Rajan et al.	Response to ‘Cutaneous squamous cell carcinoma is associated with Lynch syndrome: widening the spectrum of Lynch syndrome-associated tumours’	2022
Dr Richard Gallon Peter Sowter Rachel Phelps Christine Hayes Dr Gillian Borthwick et al.	How should we test for Lynch syndrome? A review of current guidelines and future strategies	2021
Dr Richard Gallon Dr Steven Cook Dr Mauro Santibanez Koref Dr Michael Jackson Professor Sir John Burn et al.	Sebaceous tumours: a prototypical class of skin tumour for universal germline genetic testing	2021
Dr Richard Gallon Dr Michael Jackson Dr Mauro Santibanez Koref	Constitutional mismatch repair deficiency is the diagnosis in 0.41% of pathogenic NF1/SPRED1 variant negative children suspected of sporadic neurofibromatosis type 1	2020
Dr Richard Gallon Dr Harsh Sheth Christine Hayes Lisa Redford Dr Ghanim Alhilal et al.	Sequencing‐based microsatellite instability testing using as few as six markers for high‐throughput clinical diagnostics	2020
Dr Richard Gallon Dr Harsh Sheth Christine Hayes Dr Gillian Borthwick Professor Sir John Burn et al.	A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes	2019
Dr Carla Jackson Dr Roman Bauer Dr Joseph Collin Dr Birthe Hilgen Dr Darin Zerti et al.	An integrated transcriptional analysis of the developing human retina	2019
Lisa Redford Dr Ghanim Alhilal Dr Stephanie Needham Ottilia O'Brien Julie Coaker et al.	A novel panel of short mononucleotide repeats linked to informative polymorphisms enabling effective high volume low cost discrimination between mismatch repair deficient and proficient tumours	2018
Dr Osagie Izuogu Dr Carla Mellough Dr Joseph Collin Dr Richard Gallon Francesco Kumara Mastrorosa et al.	Analysis of human ES cell differentiation establishes that the dominant isoforms of the lncRNAs RMST and FIRRE are circular	2018
Dr Harsh Sheth Dr Michael Jackson Dr Mauro Santibanez Koref Professor Sir John Burn	Interaction between polymorphisms in aspirin metabolic pathways, regular aspirin use and colorectal cancer risk: A case-control study in unselected white European populations	2018
Dr Jannetta Steyn Professor David Elliott Dr Mauro Santibanez Koref Dr Michael Jackson	Circular RNA enrichment in platelets is a signature of transcriptome degradation	2016
Dr Ginikachukwu Izuogu Dr Mauro Santibanez Koref Professor David Elliott Dr Michael Jackson	Erratum to: PTESFinder: A computational method to identify post-transcriptional exon shuffling (PTES) events [BMC Bioinf. 2016; 17: 31]	2016
Dr Ginikachukwu Izuogu Dr Mauro Santibanez Koref David Elliott Dr Michael Jackson	PTESFinder: a computational method to identify post-transcriptional exon shuffling (PTES) events	2016
Dr Harsh Sheth Dr Michael Jackson Dr John Tyson Professor Ann Daly Professor Sir John Burn et al.	Relevance of genetic factors to warfarin dosing in India	2015
Dr Maria Lastowska Hani Al-Afghani Haya AL-Balool Harsh SHETH Dr Jonathan Coxhead et al.	Identification of a neuronal transcription factor network involved in medulloblastoma development	2013
Dr Sushma Grellscheid Caroline Dalgliesh Andy Best Yilei Liu Dr Ingrid Ehrmann et al.	Identification of evolutionarily conserved exons as regulated targets for the splicing activator tra2β in development	2011
Haya AL-Balool Dr Mark Wade Dr Jonathan Coxhead Professor Julie Irving Professor David Elliott et al.	Post-transcriptional exon shuffling events in humans can be evolutionarily conserved and abundant	2011
Dr Ingrid Ehrmann Caroline Dalgliesh Anastasios Tsaousis Dr Ralf Kist Weiping Li et al.	Haploinsufficiency of the germ cell-specific nuclear RNA binding protein hnRNP G-T prevents functional spermatogenesis in the mouse	2008
Dr Katrina Wood Dr Michael Jackson Dr Maria Lastowska Dr Darroch Hall Dr Helen Imrie et al.	Histological profile of tumours from MYCN transgenic mice	2008
Dr Maria Lastowska Dr Michael Jackson	Minimal disease monitoring by QRT–PCR: guidelines for identification and systematic validation of molecular markers prior to evaluation in prospective clinical trials	2008
Dr Maria Lastowska Dr Michael Jackson	Cell lines from MYCN transgenic murine tumours reflect the molecular and biological characteristics of human neuroblastoma	2007
Dr Maria Lastowska Dr Mauro Santibanez Koref Ilka Wappler Dr Heiko Peters Dr Andrew Hall et al.	Identification of candidate genes involved in neuroblastoma progression by combining genomic and expression microarrays with survival data	2007
Dr Julian Venables Dr Lisa Turnbull Dr David Bourn Dr Martha Lucia Diaz Torres Dr Michael Jackson et al.	Atypical haemolytic uraemic syndrome associated with a hybrid complement gene	2006
Dr Michael Jackson Dr Lisa Turnbull Professor Judith Goodship Dr Liz Kemp Professor Tim Goodship et al.	De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome	2006
Dr Michael Jackson Kathryn Creighton Dr Mauro Santibanez Koref	Evidence for widespread reticulate evolution within human duplicons	2005
Jonathan Mudge Dr Michael Jackson	Evolutionary implications of pericentromeric gene expression in humans	2005
Dr Emma Tonkin Pieter Eichhorn Burhan Imamwerdi Emerita Professor Susan Lindsay Dr Michael Jackson et al.	A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3	2004
Dr Maria Lastowska Professor Andrew Pearson Dr Michael Jackson	Regions Syntenic to Human 17q Are Gained in Mouse and Rat Neuroblastoma	2004
Dr Michael Jackson	Duplicate, decouple, disperse: The evolutionary transience of human centromeric regions	2003
Jonathan Mudge Dr Michael Jackson	Neocentromeres in 15q24-26 map to duplicons which flanked an ancestral cantromere in 15q25	2003
Jonathan Mudge Dr Michael Jackson	Neocentromeres in 15q24-26 map to duplicons which flanked an ancestral centromere in 15q25	2003
Dr Maria Lastowska Simon Cotterill Natalie Bown Professor John Lunec Professor Tom Strachan et al.	Breakpoint position on 17q identifies the most aggressive neuroblastoma tumors	2002
Moira Crosier Dr Michael Jackson	Human paralogs of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific duplication mechanisms	2002
Dr Maria Lastowska Simon Cotterill Dr Nicholas Bown Dr Katia Mazzocco Professor Andrew Pearson et al.	Comprehensive genetic and histopathologic study reveals three types of neuroblastoma tumors	2001
Dr Maria Lastowska Dr Nicholas Bown Professor John Lunec Professor Tom Strachan Professor Andrew Pearson et al.	Molecular cytogenetic definition of 17q translocation breakpoints in neuroblastoma	2001
Dr Maria Lastowska Dr Nicholas Bown Professor John Lunec Professor Tom Strachan Professor Andrew Pearson et al.	Molecular cytogenetic definition of 17q translocation breakpoints in neuroblastoma	2001
Dr Michael Jackson Moira Crosier	Characterisation of the heterochromatin/euchromatin boundary at 10q11 and identification of novel transcripts formed by repeat induced instability	1999
Dr Michael Jackson	Oral staphylococci in health and disease	1999
Dr Michael Jackson Dennis Kirk	Sequences flanking the centromere of human chromosome 10 are a complex patchwork of arm-specific sequences, stable duplications and unstable sequences with homologies to telomeric and other centromeric locations	1999
Dr Maria Lastowska Dr Nicholas Bown Professor John Lunec Professor Tom Strachan Professor Andrew Pearson et al.	Molecular cytogenetic delineation of 17q translocation breakpoints in neuroblastoma cell lines	1998