Towards population screening for Cerebral Visual Impairment: Validity of the Five Questions and the CVI Questionnaire by Gorrie, Fiona, Goodall, Karen, Rush, Robert, Ravenscroft, John

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The development of linguistic prediction: Predictions of sound and meaning in 2- to 5-year-olds by Gambi, Chiara, Gorrie, Fiona, Pickering, Martin J., Rabagliati, Hugh

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Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance by Pfeffer, Gerald, Gorman, Gráinne S, Griffin, Helen, Kurzawa-Akanbi, Marzena, Blakely, Emma L., Wilson, Ian, Sitarz, Kamil, Moore, David, Murphy, Julie L., Alston, Charlotte L., Pyle, Angela, Coxhead, Jon, Payne, Brendan, Gorrie, George H., Longman, Cheryl, Hadjivassiliou, Marios, McConville, John, Dick, David, Imam, Ibrahim, Hilton, David, Norwood, Fiona, Baker, Mark R., Jaiser, Stephan R., Yu-Wai-Man, Patrick, Farrell, Michael, McCarthy, Allan, Lynch, Timothy, McFarland, Robert, Schaefer, Andrew M., Turnbull, Douglass M., Horvath, Rita, Taylor, Robert W., Chinnery, Patrick F.

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Transthyretin Cardiac Amyloidosis in Australia and New Zealand–A Multi-Site Snapshot for 2022 by Geenty, Paul, Davidson, Nicholas, Gorrie, Natasha, Bart, Nicole, Baumwol, Jay, Sutton, Timothy, Kwok, Fiona, Hare, James L., Peck, Kah Yong, Korczyk, Dariusz, Gibbs, Simon D.J., Thomas, Liza

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Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing by Hocking, Lynne J, Andrews, Claire, Armstrong, Christine, Ansari, Morad, Baty, David, Berg, Jonathan, Bradley, Therese, Clark, Caroline, Diamond, Austin, Doherty, Jill, Lampe, Anne, McGowan, Ruth, Moore, David J, O'Sullivan, Dawn, Purvis, Andrew, Santoyo-Lopez, Javier, Westwood, Paul, Abbott, Michael, Williams, Nicola, Aitman, Timothy J, Miedzybrodzka, Zosia

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