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Author Details

Georgina Hall
The University of Melbourne, The Royal Children's Hospital
2008
38
17
PMIDPaper TitleJournal TitlePublished Year
37169548Gillick competence: an inadequate guide to the ethics of involving adolescents in decision-making.J Med Ethics2024
37831289Reconceiving Reproduction: Removing "Rearing" From the Definition-and What This Means for ART.J Bioeth Inq2024
37055160<i>A little bit pregnant:</i> towards a pluralist account of non-sexual reproduction.J Med Ethics2023
35246174Bi-allelic mutation of CTNNB1 causes a severe form of syndromic microphthalmia, persistent foetal vasculature and vitreoretinal dysplasia.Orphanet J Rare Dis2022
36347604Reproduction misconceived: why there is no right to reproduce and the implications for ART access.J Med Ethics2022
33353976Correction: Clinical utility of genetic testing in 201 preschool children with inherited eye disorders.Genet Med2021
34758253100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.N Engl J Med2021
31848469Clinical utility of genetic testing in 201 preschool children with inherited eye disorders.Genet Med2020
30680631The psychosocial and service delivery impact of genomic testing for inherited retinal dystrophies.J Community Genet2019
31719542Clinical and genetic variability in children with partial albinism.Sci Rep2019
28918392CNVs affecting cancer predisposing genes (CPGs) detected as incidental findings in routine germline diagnostic chromosomal microarray (CMA) testing.J Med Genet2018
28029058Prenatal central nervous system anomaly with skeletal dysplasia associated with a de novo interstitial tandem triplication of chromosome 14.J Obstet Gynaecol2017
28341476Panel-Based Clinical Genetic Testing in 85 Children with Inherited Retinal Disease.Ophthalmology2017
28301457Exploring the feasibility of delivering standardized genomic care using ophthalmology as an example.Genet Med2017
28327572The role of genetic counsellors in genomic healthcare in the United Kingdom: a statement by the Association of Genetic Nurses and Counsellors.Eur J Hum Genet2017
27080487Identifying variation in models of care for the genomic-based diagnosis of inherited retinal dystrophies in the United Kingdom.Eye (Lond)2016
27933154Improving diagnosis for congenital cataract by introducing NGS genetic testing.BMJ Qual Improv Rep2016
27628848The role of small in-frame insertions/deletions in inherited eye disorders and how structural modelling can help estimate their pathogenicity.Orphanet J Rare Dis2016
27208204Molecular findings from 537 individuals with inherited retinal disease.J Med Genet2016
27315345Diagnosing the cause of bilateral paediatric cataracts: comparison of standard testing with a next-generation sequencing approach.Eye (Lond)2016
26872967Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease.Ophthalmology2016
25273951Patient expectations and attitudes towards specialist genetic eye services.J Genet Couns2015
25987160Pinpointing clinical diagnosis through whole exome sequencing to direct patient care: a case of Senior-Loken syndrome.Lancet2015
25802877Genetic counselors and Genomic Counseling in the United Kingdom.Mol Genet Genomic Med2015
25567483Variation in healthcare services for specialist genetic testing and implications for planning genetic services: the example of inherited retinal dystrophy in the English NHS.J Community Genet2015
23845030Genetic testing for inherited ocular disease: delivering on the promise at last?Clin Exp Ophthalmol2014
24464918Chromosomal microarray analysis allows prenatal detection of low level mosaic autosomal aneuploidy.Prenat Diagn2014
23334530Building the genetic counsellor profession in the United Kingdom: two decades of growth and development.J Genet Couns2013
23743435Valuing the benefits of genetic testing for retinitis pigmentosa: a pilot application of the contingent valuation method.Br J Ophthalmol2013
23740962Understanding the expectations of patients with inherited retinal dystrophies.Br J Ophthalmol2013
23811034A clinical molecular genetic service for United Kingdom families with choroideraemia.Eur J Med Genet2013
23403902Understanding the impact of genetic testing for inherited retinal dystrophy.Eur J Hum Genet2013
23512800Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.Ultrasound Obstet Gynecol2013
22570351Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic study.Invest Ophthalmol Vis Sci2012
22581970A paradigm shift in the delivery of services for diagnosis of inherited retinal disease.J Med Genet2012
21951448Role and function of a paediatric clinical ethics service: experiences at the Royal Children's Hospital, Melbourne.J Paediatr Child Health2011
20049518Explaining Mendelian inheritance in genetic consultations: an IPR study of counselor and counselee experiences.J Genet Couns2010
19418904Interview with Norman Ford.Monash Bioeth Rev2008
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Collaborators

Graeme C M Black
Manchester University Hospitals NHS Foundation Trust, St Mary's Hospital
Co-authored papers 23
Jamie M Ellingford
University of Manchester
Co-authored papers 9
Panagiotis I Sergouniotis
University of Manchester
Co-authored papers 8
Jill Clayton-Smith
Institute of Human Development, University of Manchester
Co-authored papers 7
Sofia Douzgou
Haukeland University Hospital
Co-authored papers 7
Dominic J McMullan
Birmingham Women's and Children's NHS Foundation Trust
Co-authored papers 5
Anthony T Moore
UCL Institute of Ophthalmology, University College London
Co-authored papers 5
Andrew R Webster
Institute of Ophthalmology, University College London
Co-authored papers 5
Christine Patch
Queen Mary University of London, United Kingdom Society and Ethics Research
Co-authored papers 4
Anna Middleton
Kavli Centre for Ethics, University of Cambridge
Co-authored papers 2
Dalia Kasperaviciute
Genomics England Ltd.
Co-authored papers 2
Andrea H N??meth
University of Oxford
Co-authored papers 2
Katherine R Smith
Walter and Eliza Hall Institute of Medical Research
Co-authored papers 2
Philip Twiss
Cambridge University Hospitals NHS Foundation Trust
Co-authored papers 1
Rutendo Mapeta
Cambridge University Hospitals NHS Foundation
Co-authored papers 1
Matthew Welland
Co-authored papers 1
Maureen Cleary
Great Ormond Street Hospital for Children NHS Trust
Co-authored papers 1
Stephanie Grunewald
Great Ormond Street Hospital for Children NHS Trust
Co-authored papers 1
Francesco Muntoni
UCL Great Ormond Street Institute of Child Health
Co-authored papers 1
Antonio Rueda Martin
Queen Mary University of London
Co-authored papers 1
Dragana Josifova
Guy's and St Thomas' Hospital
Co-authored papers 1
Douglass M Turnbull
Newcastle University
Co-authored papers 1
Valentina Cipriani
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 1
Christopher Boustred
Co-authored papers 1
Anna de Burca
Oxford University Hospitals NHS Foundation Trust
Co-authored papers 1
Charu Deshpande
Guy's Hospital
Co-authored papers 1
Bishoy Habib
Co-authored papers 1
Gr??inne S Gorman
Newcastle upon Tyne Hospitals NHS Foundation Trust
Co-authored papers 1
No??mi B A Roy
MRC Weatherall Institute of Molecular Medicine, University of Oxford
Co-authored papers 1
Sarju G Mehta
Cambridge University Hospitals NHS Foundation Trust
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Release 1.2