Amy Nisselle

Co-design, implementation, and evaluation of plain language genomic test reports

Gemma R Brett, Aisha Ward, Sophie E Bouffler, Elizabeth E Palmer, Kirsten Boggs, Fiona Lynch, Amanda Springer, Amy Nisselle, Zornitza Stark

Journal article  |  2022  |  NPJ GENOMIC MEDICINE

Understanding and communicating genomic results can be challenging for families and health professionals without genetic specialty..

Genetics follow up after rapid genomic sequencing in intensive care: current practices and recommendations for service delivery

Fiona Lynch, Amy Nisselle, Zornitza Stark, Clara L Gaff, Belinda McClaren

Journal article  |  2022  |  EUROPEAN JOURNAL OF HUMAN GENETICS

The delivery of rapid genomic sequencing (rGS) to critically unwell children in intensive care occurs at a time of immense pressur..

Unearthing the Learning of Genomic Medicine in the Workplace: a Qualitative Study

Alice Kim, Amy Nisselle, Jennifer Weller-Newton, Belinda McClaren, Louise Keogh

Journal article  |  2022  |  VOCATIONS AND LEARNING

Workplace learning is fundamental in contextualizing theoretical concepts into practice, making it opportune for professionals to ..

Response to Dwyer et al.

Clara Gaff, Amy Nisselle

Journal article  |  2022  |  Genet Med

Attitudes of Australian dermatologists on the use of genetic testing: A cross-sectional survey with a focus on melanoma.

Clare A Primiero, Amy M Baker, Courtney K Wallingford, Ellie J Maas, Tatiane Yanes, Lindsay Fowles, Monika Janda, Mary-Anne Young, Amy Nisselle, Bronwyn Terrill, Jason M Lodge, Jane M Tiller, Paul Lacaze, Hayley Andersen, Gemma McErlean, Erin Turbitt, H Peter Soyer, Aideen M McInerney-Leo

Journal article  |  2022  |  Front Genet

Background: Melanoma genetic testing reportedly increases preventative behaviour without causing psychological harm. Genetic testi..

Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants

Adam M Bournazos, Lisa G Riley, Shobhana Bommireddipalli, Lesley Ades, Lauren S Akesson, Mohammad Al-Shinnag, Stephen Alexander, Alison D Archibald, Shanti Balasubramaniam, Yemima Berman, Victoria Beshay, Kirsten Boggs, Jasmina Bojadzieva, Natasha J Brown, Samantha J Bryen, Michael F Buckley, Belinda Chong, Mark R Davis, Ruebena Dawes, Martin Delatycki, et al.

Journal article  |  2022  |  GENETICS IN MEDICINE

PURPOSE: Genetic variants causing aberrant premessenger RNA splicing are increasingly being recognized as causal variants in genet..

Theories and models for genomics education and training

M Martyn, A Nisselle, E Lynch, CL Gaff

Book Chapter  |  2022

There is growing evidence that education based on clear theoretical foundations is most effective. The role of learning theories i..

GA4GH: International policies and standards for data sharing across genomic research and healthcare.

Heidi L Rehm, Angela JH Page, Lindsay Smith, Jeremy B Adams, Gil Alterovitz, Lawrence J Babb, Maxmillian P Barkley, Michael Baudis, Michael JS Beauvais, Tim Beck, Jacques S Beckmann, Sergi Beltran, David Bernick, Alexander Bernier, James K Bonfield, Tiffany F Boughtwood, Guillaume Bourque, Sarion R Bowers, Anthony J Brookes, Michael Brudno, et al.

Journal article  |  2021  |  Cell Genom

The Global Alliance for Genomics and Health (GA4GH) aims to accelerate biomedical advances by enabling the responsible sharing of ..

General practitioners' views on genomics, practice and education A qualitative interview study

Marie Brigitte Cusack, Chriselle Hickerton, Amy Nisselle, Belinda McClaren, Bronwyn Terrill, Clara Gaff, Kate Dunlop, Sylvia Metcalfe

Journal article  |  2021  |  AUSTRALIAN JOURNAL OF GENERAL PRACTICE

BACKGROUND AND OBJECTIVES: Genomics is moving rapidly into mainstream medicine through clinical genomic testing and consumer-initi..

Parents' experiences of decision making for rapid genomic sequencing in intensive care

Fiona Lynch, Amy Nisselle, Zornitza Stark, Clara L Gaff, Belinda McClaren

Journal article  |  2021  |  EUROPEAN JOURNAL OF HUMAN GENETICS

The clinical utility of rapid genomic sequencing (rGS) for critically unwell infants and children has been well demonstrated. Pare..