P63 An exploration of childhood obesity across ethnic groups in Coventry

Autor: M Murphy, RE Johnson, FK Boardman, A Baker, NR Parsons, W Robertson

Publikováno v: Journal of Epidemiology and Community Health. 70:A81.2-A81

Background Research suggests that there is variation in childhood obesity across ethnic groups in the UK, although findings are inconsistent. The influence of other individual, school and neighbourhood characteristics is not well understood. In addit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::316844eeaf9ee21e5e3d80530d7a9595
https://doi.org/10.1136/jech-2016-208064.162

International Perspectives of Extended Genetic Sequencing When Used as Part of Newborn Screening to Identify Cystic Fibrosis.

Autor: Clark CCA; Warwick Medical School, Warwick University, Coventry CV4 7AL, UK., Holder P; Florence Nightingale Faculty of Nursing, Midwifery & Palliative Care, King's College London, London SE5 9PJ, UK., Boardman FK; Warwick Medical School, Warwick University, Coventry CV4 7AL, UK., Moody L; Centre for Arts, Memory and Communities, Coventry University, Coventry CV1 5FB, UK., Cowlard J; Paediatric Respiratory Medicine, Royal London Children's Hospital, London E1 1FR, UK., Allen L; Cystic Fibrosis Trust, London EC3N 1RE, UK., Walter C; Cystic Fibrosis Trust, London EC3N 1RE, UK., Bonham JR; Pharmacy, Diagnostics and Genetics, Sheffield Children's NHS Foundation Trust, Sheffield S10 2TH, UK., Chudleigh J; Florence Nightingale Faculty of Nursing, Midwifery & Palliative Care, King's College London, London SE5 9PJ, UK.

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What is a 'serious' genetic condition? The perceptions of people living with genetic conditions.

Autor: Boardman FK; Warwick Medical School, University of Warwick, CV4 7HL, Coventry, UK. Felicity.Boardman@warwick.ac.uk., Clark CC; Warwick Medical School, University of Warwick, CV4 7HL, Coventry, UK.

Publikováno v: European journal of human genetics : EJHG [Eur J Hum Genet] 2022 Feb; Vol. 30 (2), pp. 160-169. Date of Electronic Publication: 2021 Sep 27.

Attitudes toward population screening among people living with fragile X syndrome in the UK: 'I wouldn't wish him away, I'd just wish his fragile X syndrome away'.

Autor: Boardman FK; Division of Health Sciences, Warwick Medical School, Coventry, UK.

Publikováno v: Journal of genetic counseling [J Genet Couns] 2021 Feb; Vol. 30 (1), pp. 85-97. Date of Electronic Publication: 2020 Nov 12.

Which types of conditions should be included in reproductive genetic carrier screening? Views of parents of children with a genetic condition.

Autor: Thomas LA; Department of Paediatrics, University of Melbourne, Australia; Victorian Clinical Genetics Services, Australia., Lewis S; Department of Paediatrics, University of Melbourne, Australia; Murdoch Children's Research Institute, Australia., Massie J; Department of Paediatrics, University of Melbourne, Australia; Murdoch Children's Research Institute, Australia; Royal Children's Hospital Melbourne, Australia., Kirk EP; Centre for Clinical Genetics, Sydney Children's Hospital, Australia; Randwick Genomics Laboratory, New South Wales Health Pathology, Australia; School of Women's and Children's Health, University of New South Wales, Australia., Archibald AD; Department of Paediatrics, University of Melbourne, Australia; Victorian Clinical Genetics Services, Australia; Murdoch Children's Research Institute, Australia., Barlow-Stewart K; School of Women's and Children's Health, University of New South Wales, Australia; Northern Clinical School, Faculty of Medicine and Health, University of Sydney, Australia., Boardman FK; Warwick Medical School, University of Warwick, UK., Halliday J; Department of Paediatrics, University of Melbourne, Australia; Murdoch Children's Research Institute, Australia., McClaren B; Department of Paediatrics, University of Melbourne, Australia; Murdoch Children's Research Institute, Australia., Delatycki MB; Department of Paediatrics, University of Melbourne, Australia; Victorian Clinical Genetics Services, Australia; Murdoch Children's Research Institute, Australia. Electronic address: martin.delatycki@vcgs.org.au.

Publikováno v: European journal of medical genetics [Eur J Med Genet] 2020 Dec; Vol. 63 (12), pp. 104075. Date of Electronic Publication: 2020 Sep 30.