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个人简介
Dr Suzanne Nevin is a Post-doctoral Researcher at the Sydney Children’s Hospital and the Behavioural Sciences Unit, UNSW Sydney. She has a Bachelor of Psychology (Honours) and completed her PhD within the School of Clinical Medicine, UNSW. Her research is focussed on co-developing psychosocial resources to improve psychological outcomes among caregivers and children living with severe and rare neurodevelopmental conditions. Through her PhD research Suzanne co-designed with families a world-first evidence-based suite of audio-visual positive psychology resources to promote adaptive coping-based skills among parents of children with rare and severe neurogenetic conditions, which is available online and for download.
研究兴趣
论文共 21 篇作者统计合作学者相似作者
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Lauren Ha,Suzanne M. Nevin,Claire E. Wakefield, Jacqueline Jacovou,David Mizrahi,Christina Signorelli
Journal of Cancer Survivorshippp.1-16, (2024)
Clarissa E. Schilstra,Ursula M. Sansom-Daly,Sarah J. Ellis,Antoinette C. Anazodo,Toby N. Trahair,Toni Lindsay, Azhani Amiruddin, Cath O'Dwyer,Fiona Maguire,Suzanne Nevin,Robert Battisti,Joanna E. Fardell
Emily A. Innes,Fleur Annette Le Marne,Rebecca Macintosh,Suzanne M. Nevin,Nancy E. Briggs, Sinthu Vivekanandarajah, Richard Webster,Rani K. Sachdev,Ann M. E. Bye
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY (2024): 1-13
Emily A Innes,Fleur Annette Le Marne,Rebecca Macintosh,Suzanne M. Nevin,Nancy E Briggs, Sinthu Vivekanandarajah, Richard I Webster,Rani K Sachdev,Ann M E Bye
Seizure: European Journal of Epilepsy (2024): 1-13
Suzanne M. Nevin, Fleur A. Le Marne, Erin Beavis, Rebecca Macintosh, Elizabeth E. Palmer, Rani Sachdev,Kenneth Nunn, Ann Bye
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2024)
Emily A Innes,Fleur Annette Le Marne,Rebecca Macintosh,Suzanne M Nevin,Nancy E Briggs, Sinthu Vivekanandarajah, Richard I Webster,Rani K Sachdev,Ann M E Bye
Eden Robertson,Lauren Kelada,Stephanie Best,Ilias Goranitis, Kris Pierce,Natalie Grainger,Suzanne Nevin,Rebecca Macintosh,Fleur Le Marne, Erin Beavins,Rani Sachdev,Annie Bye,
EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 325-326
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Orphanet journal of rare diseasesno. 1 (2023): 1-32
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