Publications by authors named "Fiona Macdonald"

51Publications

School Breakfast Club Programs in Australian Primary Schools, Not Just Addressing Food Insecurity: A Qualitative Study.

Authors:
Kim Jose Fiona MacDonald Miriam Vandenberg Julie Williams Joan Abbott-Chapman Alison Venn Kylie J Smith

Health Educ Behav 2020 Aug 31;47(4):619-630. Epub 2020 May 31.

University of Tasmania, Hobart, Tasmania, Australia.

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August 2020

A randomized trial comparing vascular access strategies for patients receiving chemotherapy with trastuzumab for early-stage breast cancer.

Authors:
Mark Clemons Carol Stober Anne Kehoe Debbie Bedard Fiona MacDonald Marie-Claude Brunet Deanna Saunders Lisa Vandermeer Sasha Mazzarello Arif Awan Bassam Basulaiman Andrew Robinson Ranjeeta Mallick Brian Hutton Dean Fergusson

Support Care Cancer 2020 Oct 30;28(10):4891-4899. Epub 2020 Jan 30.

Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Canada.

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October 2020

A multicentre, randomized pilot trial comparing vascular access strategies for early stage breast cancer patients receiving non-trastuzumab containing chemotherapy.

Authors:
Andrew Robinson Carol Stober Dean Fergusson Anne Kehoe Debbie Bedard Fiona MacDonald Marie-Claude Brunet Deanna Saunders Sasha Mazzarello Lisa Vandermeer Anil A Joy Arif Awan Bassam Basulaiman Ranjeeta Mallick Brian Hutton Mark Clemons

Breast Cancer Res Treat 2019 Nov 7;178(2):337-345. Epub 2019 Aug 7.

Cancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, Canada.

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November 2019

Taking a Gamble for High Rewards? Management Perspectives on the Value of Mental Health Peer Workers.

Authors:
Louise Byrne Helena Roennfeldt Peri O'Shea Fiona Macdonald

Int J Environ Res Public Health 2018 04 13;15(4). Epub 2018 Apr 13.

School of Management, RMIT University, 124 La Trobe St, Melbourne, VIC 3000, Australia.

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April 2018

Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement.

Authors:
Frédéric Brioude Jennifer M Kalish Alessandro Mussa Alison C Foster Jet Bliek Giovanni Battista Ferrero Susanne E Boonen Trevor Cole Robert Baker Monica Bertoletti Guido Cocchi Carole Coze Maurizio De Pellegrin Khalid Hussain Abdulla Ibrahim Mark D Kilby Malgorzata Krajewska-Walasek Christian P Kratz Edmund J Ladusans Pablo Lapunzina Yves Le Bouc Saskia M Maas Fiona Macdonald Katrin Õunap Licia Peruzzi Sylvie Rossignol Silvia Russo Caroleen Shipster Agata Skórka Katrina Tatton-Brown Jair Tenorio Chiara Tortora Karen Grønskov Irène Netchine Raoul C Hennekam Dirk Prawitt Zeynep Tümer Thomas Eggermann Deborah J G Mackay Andrea Riccio Eamonn R Maher

Nat Rev Endocrinol 2018 04 29;14(4):229-249. Epub 2018 Jan 29.

Department of Medical Genetics, University of Cambridge and National Institute for Health Research (NIHR) Cambridge Biomedical Research Centre and Cancer Research UK Cambridge Centre, Cambridge Biomedical Campus, Cambridge, CB2 0QQ, UK.

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April 2018

Non-invasive prenatal diagnosis of spinal muscular atrophy by relative haplotype dosage.

Authors:
Michael Parks Samantha Court Benjamin Bowns Siobhan Cleary Samuel Clokie Julie Hewitt Denise Williams Trevor Cole Fiona MacDonald Mike Griffiths Stephanie Allen

Eur J Hum Genet 2017 04 25;25(4):416-422. Epub 2017 Jan 25.

West Midlands Regional Genetics Laboratory, Birmingham Women's NHS Foundation Trust, Birmingham, UK.

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April 2017

EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome.

Authors:
Katja Eggermann Jet Bliek Frédéric Brioude Elizabeth Algar Karin Buiting Silvia Russo Zeynep Tümer David Monk Gudrun Moore Thalia Antoniadi Fiona Macdonald Irène Netchine Paolo Lombardi Lukas Soellner Matthias Begemann Dirk Prawitt Eamonn R Maher Marcel Mannens Andrea Riccio Rosanna Weksberg Pablo Lapunzina Karen Grønskov Deborah Jg Mackay Thomas Eggermann

Eur J Hum Genet 2016 10 11;24(10):1377-87. Epub 2016 May 11.

Institut für Humangenetik, RWTH University Aachen, Aachen, Germany.

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October 2016

Non-invasive prenatal diagnosis of Duchenne and Becker muscular dystrophies by relative haplotype dosage.

Authors:
Michael Parks Samantha Court Siobhan Cleary Samuel Clokie Julie Hewitt Denise Williams Trevor Cole Fiona MacDonald Mike Griffiths Stephanie Allen

Prenat Diagn 2016 Apr 23;36(4):312-20. Epub 2016 Feb 23.

West Midlands Regional Genetics Laboratory, Birmingham Women's NHS Foundation Trust, Birmingham, UK.

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April 2016

Role of Aeromonas hydrophila in CRGV in dogs.

Authors:
Fiona A Macdonald

Vet Rec 2015 Dec;177(23):602

Holly Cottage, New Road, Mockbeggar, Ringwood, Hampshire BH24 3NJ, e-mail:

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December 2015

Organism of interest for research into CRGV.

Authors:
Fiona A Macdonald

Vet Rec 2015 May;176(18):469

Holly Cottage, New Road, Mockbeggar, Ringwood, Hampshire BH24 3NJ.

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May 2015

Alcohol brief interventions practice following training for multidisciplinary health and social care teams: a qualitative interview study.

Authors:
Niamh Fitzgerald Heather Molloy Fiona MacDonald Jim McCambridge

Drug Alcohol Rev 2015 Mar 6;34(2):185-93. Epub 2014 Sep 6.

Institute for Social Marketing, UK Centre for Tobacco and Alcohol Studies, School of Health Sciences, University of Stirling, Stirling, FK9 4LA, UK.

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March 2015

Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects.

Authors:
Abdulla Ibrahim Gail Kirby Carol Hardy Renuka P Dias Louise Tee Derek Lim Jonathan Berg Fiona MacDonald Peter Nightingale Eamonn R Maher

Clin Epigenetics 2014 4;6(1):11. Epub 2014 Jun 4.

Department of Medical Genetics, University of Cambridge and NIHR Cambridge Biomedical Research Centre, Cambridge CB2 0QQ, UK ; Centre for Rare Diseases and Personalised Medicine, School of Clinical and Experimental Medicine, College of Medical and Dental Sciences, University of Birmingham, Birmingham B15 2TT, UK.

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July 2014

Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technology.

Authors:
Louise Tee Derek Hk Lim Renuka P Dias Marie-Odile Baudement Amy A Slater Gail Kirby Tom Hancocks Helen Stewart Carol Hardy Fiona Macdonald Eamonn R Maher

Clin Epigenetics 2013 Dec 10;5(1):23. Epub 2013 Dec 10.

Centre for Rare Diseases and Personalised Medicine, School of Clinical and Experimental Medicine, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.

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December 2013

Clinical utility gene card for: von Hippel-Lindau (VHL).

Authors:
Jochen Decker Christine Neuhaus Fiona Macdonald Hiltrud Brauch Eamonn R Maher

Eur J Hum Genet 2014 Apr 28;22(4). Epub 2013 Aug 28.

1] Birmingham Women's Hospital-West Midlands Regional Genetics Laboratory, Birmingham, UK [2] Department of Medical Genetics, University of Cambridge, Cambridge, UK.

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April 2014

Comparison of the clinical scoring systems in Silver-Russell syndrome and development of modified diagnostic criteria to guide molecular genetic testing.

Authors:
Renuka P Dias Peter Nightingale Carol Hardy Gail Kirby Louise Tee Susan Price Fiona Macdonald Timothy G Barrett Eamonn R Maher

J Med Genet 2013 Sep 28;50(9):635-9. Epub 2013 Jun 28.

Centre for Rare Diseases and Personalised Medicine, School of Clinical and Experimental Medicine, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.

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September 2013

A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma.

Authors:
Eleanor Rattenberry Lindsey Vialard Anna Yeung Hayley Bair Kirsten McKay Mariam Jafri Natalie Canham Trevor R Cole Judit Denes Shirley V Hodgson Richard Irving Louise Izatt Márta Korbonits Ajith V Kumar Fiona Lalloo Patrick J Morrison Emma R Woodward Fiona Macdonald Yvonne Wallis Eamonn R Maher

J Clin Endocrinol Metab 2013 Jul 10;98(7):E1248-56. Epub 2013 May 10.

Centre for Rare Diseases and Personalised Medicine, School of Clinical and Experimental Medicine, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TH, United Kingdom.

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July 2013

Mutation spectrum in RAB3GAP1, RAB3GAP2, and RAB18 and genotype-phenotype correlations in warburg micro syndrome and Martsolf syndrome.

Authors:
Mark T Handley Deborah J Morris-Rosendahl Stephen Brown Fiona Macdonald Carol Hardy Danai Bem Sarah M Carpanini Guntram Borck Loreto Martorell Claudia Izzi Francesca Faravelli Patrizia Accorsi Lorenzo Pinelli Lina Basel-Vanagaite Gabriela Peretz Ghada M H Abdel-Salam Maha S Zaki Anna Jansen David Mowat Ian Glass Helen Stewart Grazia Mancini Damien Lederer Tony Roscioli Fabienne Giuliano Astrid S Plomp Arndt Rolfs John M Graham Eva Seemanova Pilar Poo Angels García-Cazorla Patrick Edery Ian J Jackson Eamonn R Maher Irene A Aligianis

Hum Mutat 2013 May;34(5):686-96

MRC Human Genetics Unit, Medical Research Council and Institute of Genetics and Molecular Medicine, University of Edinburgh, Scotland, UK.

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May 2013

Genotype-phenotype correlation in 153 adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: analysis of the United Kingdom Congenital adrenal Hyperplasia Adult Study Executive (CaHASE) cohort.

Authors:
Nils Krone Ian T Rose Debbie S Willis James Hodson Sarah H Wild Emma J Doherty Stefanie Hahner Silvia Parajes Roland H Stimson Thang S Han Paul V Carroll Gerry S Conway Brian R Walker Fiona MacDonald Richard J Ross Wiebke Arlt

J Clin Endocrinol Metab 2013 Feb 21;98(2):E346-54. Epub 2013 Jan 21.

Centre for Endocrinology, Diabetes, and Metabolism, School of Clinical and Experimental Medicine, University of Birmingham, Birmingham B15 2TT, United Kingdom.

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February 2013

Mutation detection in cholestatic patients using microarray resequencing of ATP8B1 and ABCB11.

Authors:
Kirsten E McKay Christopher K Bruce Jane L Hartley A S Knisely Ulrich Baumann Sonja-Stephanie Bockisch Ekkehard Sturm Christian J Hendriksz Deidre A Kelly Fiona Macdonald Paul Gissen

F1000Res 2013 6;2:32. Epub 2013 Feb 6.

Great Ormond Street Hospital for Children, London, WC1N 3JH, UK.

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March 2014

Evaluation of SDHB, SDHD and VHL gene susceptibility testing in the assessment of individuals with non-syndromic phaeochromocytoma, paraganglioma and head and neck paraganglioma.

Authors:
Mariam Jafri James Whitworth Eleanor Rattenberry Lindsey Vialard Gail Kilby Ajith V Kumar Louise Izatt Fiona Lalloo Paul Brennan Jackie Cook Patrick J Morrison Natalie Canham Ruth Armstrong Carole Brewer Susan Tomkins Alan Donaldson Julian Barwell Trevor R Cole A Brew Atkinson Simon Aylwin Steve G Ball Umasuthan Srirangalingam Shern L Chew Dafydd Gareth R Evans Shirley V Hodgson Richard Irving Emma Woodward Fiona Macdonald Eamonn R Maher

Clin Endocrinol (Oxf) 2013 Jun 6;78(6):898-906. Epub 2013 Apr 6.

Centre for Rare Diseases and Personalised Medicine, School of Clinical and Experimental Medicine, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.

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June 2013