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Author Details

E V Davison
University of Newcastle upon Tyne.
1978
55
20
PMIDPaper TitleJournal TitlePublished Year
34758253100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.N Engl J Med2021
28126856Genomics in routine clinical care: what does this mean for primary care?Br J Gen Pract2017
20658510Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis.Ultrasound Obstet Gynecol2011
21386874Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome.Eur J Hum Genet2011
21078160Immunostaining of modified histones defines high-level features of the human metaphase epigenome.Genome Biol2010
19388127Molecular karyotyping of patients with unexplained mental retardation by SNP arrays: a multicenter study.Hum Mutat2009
19760623Microarray based analysis of 3p25-p26 deletions (3p- syndrome).Am J Med Genet A2009
17205537Characterization of a 3;6 translocation associated with renal cell carcinoma.Genes Chromosomes Cancer2007
18923927Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom.Genomic Med2007
17499987Congenital abnormalities and clinical features associated with Wilms' tumour: a comprehensive study from a centre serving a large population.Eur J Cancer2007
16872824Multilocus loss of heterozygosity allelotypes identify a genetic pathway associated with progression from low to high stage disease in neuroblastoma.Eur J Cancer2006
17063531Rapid prenatal diagnosis of common trisomies: discordant results between QF-PCR analysis and karyotype analysis on long-term culture for a case of trisomy 18 detected in CVS.Prenat Diagn2006
15367911An excess of chromosome 1 breakpoints in male infertility.Eur J Hum Genet2004
12868084A further case of confined placental mosaicism for trisomy 2 associated with adverse pregnancy outcome.Prenat Diagn2003
12466129Genomic imbalances in pediatric intracranial ependymomas define clinically relevant groups.Am J Pathol2002
11422979First-trimester prenatal diagnosis of a familial subtelomeric translocation.Ultrasound Obstet Gynecol2001
11787046Duplication of chromosome 2 in association with ventriculomegaly - a case report.Prenat Diagn2001
11438960Prenatal testing for uniparental disomy (UPD).Prenat Diagn2001
10521826Prenatal diagnosis of mosaicism for partial trisomy 8: a case report including fetal pathology.Prenat Diagn1999
9860296Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypic characteristics of Wilms' tumour attributable to FWT1.Hum Genet1998
9309111Assessment of chromosome 3 copy number in ocular melanoma using fluorescence in situ hybridization.Cancer Genet Cytogenet1997
9267905Prospective prenatal diagnosis of Prader-Willi syndrome due to maternal disomy for chromosome 15 following trisomic zygote rescue.Prenat Diagn1997
8736931Detection of germinal mosaicism in a DMD family.Biochem Soc Trans1996
8953633Structural chromosome anomalies in congenital diaphragmatic hernia.Prenat Diagn1996
8049906Partial trisomy of C11q and its effect on affective disorder segregating in a three generation family.Psychiatr Genet1994
8202034Cytogenetic abnormalities of small round cell tumours.Med Pediatr Oncol1994
8084856Confined placental mosaicism, IUGR, and adverse pregnancy outcome: a controlled retrospective U.K. collaborative survey.Prenat Diagn1994
8469226Cytogenetic abnormalities in a disseminated medulloblastoma.Med Pediatr Oncol1993
8411070Epidermal mosaicism and Blaschko's lines.J Med Genet1993
1640424Meiotic and sperm chromosome analysis in a male carrier of an inverted insertion (3;10)(q13.2;p14p13).J Med Genet1992
1997541Cytogenetic analysis of a granulocytic sarcoma in a patient without systemic leukaemia.J Clin Pathol1991
2009510Cytogenetic analysis of a congenital fibrosarcoma.Cancer Genet Cytogenet1991
2304357De novo Ph negative T-cell lymphoblastic leukaemia associated with bcr gene rearrangement.Leuk Res1990
2525623Chromosome studies of males in an institution for the mentally handicapped.J Med Genet1989
2768519Chromosome 22 abnormalities in Ewing's sarcoma.J Clin Pathol1989
2754723Prader Willi syndrome with hypothyroidism.J Ment Defic Res1989
2732351Trisomy 11 in acute lymphoblastic leukaemia.J Clin Pathol1989
3162393Translocation t (8;21) associated with marked granulocytic hyperplasia.Cancer Genet Cytogenet1988
3203296Multiple chromosome rearrangements in a childhood ependymoma.Cancer Genet Cytogenet1988
3178262Cytogenetic investigations of solid tumours of children.Arch Dis Child1988
2835148Cytogenetic abnormalities in a primitive neuroectodermal tumor.Cancer Genet Cytogenet1988
3624291Effects of amniocentesis for genetic purposes on the pregnancy and its outcome.J Biosoc Sci1987
3693571Cytogenic investigations in the assessment of response to treatment in neuroblastoma.J Clin Pathol1987
3592733Chromosomes of metastatic retinoblastoma.Arch Dis Child1987
3567084Familial myelodysplasia: progressive disease associated with emergency of monosomy 7.Br J Haematol1987
3463203Karyotypic changes in lymphoblastic transformation of chronic granulocytic leukaemia.Am J Hematol1986
3793104Partial trisomy 20p resulting from a recombination of a familial pericentric inversion.Hum Genet1986
3783627A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndrome.J Med Genet1986
3757301High resolution chromosome results in retinoblastoma families.Clin Genet1986
3463406t(9;11)(p22;q24) in a patient with acute monocytic leukemia.Cancer Genet Cytogenet1986
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Collaborators

Birmingham Women's and Children's NHS Foundation Trust
Co-authored papers 6
Population Health Sciences Institute, Newcastle University
Co-authored papers 4
Health Economics Research Centre, University of Oxford
Co-authored papers 2
University of Oxford
Co-authored papers 2
Health Economics Research Centre, University of Oxford
Co-authored papers 2
Cambridge University Hospitals NHS Foundation Trust
Co-authored papers 1
Radboud University Medical Center
Co-authored papers 1
Addenbrooke's Hospital
Co-authored papers 1
American Medical Informatics Association, Oregon Health and Science University, Oregon State University, University of Colorado Anschutz Medical Campus, University of North Carolina at Chapel Hill, University of Wisconsin-Madison
Co-authored papers 1
School of Clinical Medicine, University of Cambridge
Co-authored papers 1
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Department of Medicine and Moores Cancer Center, University of California San Diego.
Co-authored papers 1
University of Cambridge
Co-authored papers 1
UCL Great Ormond Street Institute of Child Health, University College London
Co-authored papers 1
Cambridge University Hospitals NHS Foundation
Co-authored papers 1
Co-authored papers 1
Great Ormond Street Hospital for Children NHS Trust
Co-authored papers 1
Great Ormond Street Hospital for Children NHS Trust
Co-authored papers 1
UCL Great Ormond Street Institute of Child Health
Co-authored papers 1
Royal College of Surgeons in Ireland
Co-authored papers 1
Queen Mary University of London
Co-authored papers 1
Guy's and St Thomas' Hospital
Co-authored papers 1
Newcastle University
Co-authored papers 1
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 1
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Oxford University Hospitals NHS Foundation Trust
Co-authored papers 1
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Guy's Hospital
Co-authored papers 1
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Newcastle upon Tyne Hospitals NHS Foundation Trust
Co-authored papers 1