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Author Details
Full Name
E V Davison
Affiliation
University of Newcastle upon Tyne.
ORCID
Career Start Year
1978
Papers
55
H Index
20
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34758253
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.
N Engl J Med
2021
28126856
Genomics in routine clinical care: what does this mean for primary care?
Br J Gen Pract
2017
20658510
Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis.
Ultrasound Obstet Gynecol
2011
21386874
Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome.
Eur J Hum Genet
2011
21078160
Immunostaining of modified histones defines high-level features of the human metaphase epigenome.
Genome Biol
2010
19388127
Molecular karyotyping of patients with unexplained mental retardation by SNP arrays: a multicenter study.
Hum Mutat
2009
19760623
Microarray based analysis of 3p25-p26 deletions (3p- syndrome).
Am J Med Genet A
2009
17205537
Characterization of a 3;6 translocation associated with renal cell carcinoma.
Genes Chromosomes Cancer
2007
18923927
Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom.
Genomic Med
2007
17499987
Congenital abnormalities and clinical features associated with Wilms' tumour: a comprehensive study from a centre serving a large population.
Eur J Cancer
2007
16872824
Multilocus loss of heterozygosity allelotypes identify a genetic pathway associated with progression from low to high stage disease in neuroblastoma.
Eur J Cancer
2006
17063531
Rapid 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 Diagn
2006
15367911
An excess of chromosome 1 breakpoints in male infertility.
Eur J Hum Genet
2004
12868084
A further case of confined placental mosaicism for trisomy 2 associated with adverse pregnancy outcome.
Prenat Diagn
2003
12466129
Genomic imbalances in pediatric intracranial ependymomas define clinically relevant groups.
Am J Pathol
2002
11422979
First-trimester prenatal diagnosis of a familial subtelomeric translocation.
Ultrasound Obstet Gynecol
2001
11787046
Duplication of chromosome 2 in association with ventriculomegaly - a case report.
Prenat Diagn
2001
11438960
Prenatal testing for uniparental disomy (UPD).
Prenat Diagn
2001
10521826
Prenatal diagnosis of mosaicism for partial trisomy 8: a case report including fetal pathology.
Prenat Diagn
1999
9860296
Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypic characteristics of Wilms' tumour attributable to FWT1.
Hum Genet
1998
9309111
Assessment of chromosome 3 copy number in ocular melanoma using fluorescence in situ hybridization.
Cancer Genet Cytogenet
1997
9267905
Prospective prenatal diagnosis of Prader-Willi syndrome due to maternal disomy for chromosome 15 following trisomic zygote rescue.
Prenat Diagn
1997
8736931
Detection of germinal mosaicism in a DMD family.
Biochem Soc Trans
1996
8953633
Structural chromosome anomalies in congenital diaphragmatic hernia.
Prenat Diagn
1996
8049906
Partial trisomy of C11q and its effect on affective disorder segregating in a three generation family.
Psychiatr Genet
1994
8202034
Cytogenetic abnormalities of small round cell tumours.
Med Pediatr Oncol
1994
8084856
Confined placental mosaicism, IUGR, and adverse pregnancy outcome: a controlled retrospective U.K. collaborative survey.
Prenat Diagn
1994
8469226
Cytogenetic abnormalities in a disseminated medulloblastoma.
Med Pediatr Oncol
1993
8411070
Epidermal mosaicism and Blaschko's lines.
J Med Genet
1993
1640424
Meiotic and sperm chromosome analysis in a male carrier of an inverted insertion (3;10)(q13.2;p14p13).
J Med Genet
1992
1997541
Cytogenetic analysis of a granulocytic sarcoma in a patient without systemic leukaemia.
J Clin Pathol
1991
2009510
Cytogenetic analysis of a congenital fibrosarcoma.
Cancer Genet Cytogenet
1991
2304357
De novo Ph negative T-cell lymphoblastic leukaemia associated with bcr gene rearrangement.
Leuk Res
1990
2525623
Chromosome studies of males in an institution for the mentally handicapped.
J Med Genet
1989
2768519
Chromosome 22 abnormalities in Ewing's sarcoma.
J Clin Pathol
1989
2754723
Prader Willi syndrome with hypothyroidism.
J Ment Defic Res
1989
2732351
Trisomy 11 in acute lymphoblastic leukaemia.
J Clin Pathol
1989
3162393
Translocation t (8;21) associated with marked granulocytic hyperplasia.
Cancer Genet Cytogenet
1988
3203296
Multiple chromosome rearrangements in a childhood ependymoma.
Cancer Genet Cytogenet
1988
3178262
Cytogenetic investigations of solid tumours of children.
Arch Dis Child
1988
2835148
Cytogenetic abnormalities in a primitive neuroectodermal tumor.
Cancer Genet Cytogenet
1988
3624291
Effects of amniocentesis for genetic purposes on the pregnancy and its outcome.
J Biosoc Sci
1987
3693571
Cytogenic investigations in the assessment of response to treatment in neuroblastoma.
J Clin Pathol
1987
3592733
Chromosomes of metastatic retinoblastoma.
Arch Dis Child
1987
3567084
Familial myelodysplasia: progressive disease associated with emergency of monosomy 7.
Br J Haematol
1987
3463203
Karyotypic changes in lymphoblastic transformation of chronic granulocytic leukaemia.
Am J Hematol
1986
3793104
Partial trisomy 20p resulting from a recombination of a familial pericentric inversion.
Hum Genet
1986
3783627
A 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 Genet
1986
3757301
High resolution chromosome results in retinoblastoma families.
Clin Genet
1986
3463406
t(9;11)(p22;q24) in a patient with acute monocytic leukemia.
Cancer Genet Cytogenet
1986
1 - 50 of 55
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row(s) 1 - 30 of 30
Collaborators
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Birmingham Women's and Children's NHS Foundation Trust
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Population Health Sciences Institute, Newcastle University
Co-authored papers
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Sarah Wordsworth
Health Economics Research Centre, University of Oxford
Co-authored papers
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University of Oxford
Co-authored papers
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Co-authored papers
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Cambridge University Hospitals NHS Foundation Trust
Co-authored papers
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1
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Addenbrooke's Hospital
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1
Melissa A Haendel
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
Rita Horvath
School of Clinical Medicine, University of Cambridge
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1
Janice Yip
Co-authored papers
1
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Department of Medicine and Moores Cancer Center, University of California San Diego.
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Eleanor Dewhurst
University of Cambridge
Co-authored papers
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Philip L Beales
UCL Great Ormond Street Institute of Child Health, University College London
Co-authored papers
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Rutendo Mapeta
Cambridge University Hospitals NHS Foundation
Co-authored papers
1
Matthew Welland
Co-authored papers
1
Maureen Cleary
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1
Stephanie Grunewald
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Francesco Muntoni
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Raymond L Stallings
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