Samantha Turner

Contact categoryResearcher (past)
Job titleSessional Academic
Research instituteSchool of Allied Health
Faculty of Health Sciences

Research outputs

Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40
Morgan, Angela, Scerri, T.S., Vogel, Adam P., Reid, Christopher A., Quach, Mara, Jackson, Victoria, McKenzie, Chaseley, Burrows, Emma L., Bennett, Mark F., Turner, Samantha, Reilly, Sheena, Horton, Sarah E., Block, Susan, Kefalianos, Elaina, Frigerio-Domingues, Carlos and et. al.. (2023). Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40. Brain. 146(12), pp. 5086-5097. https://doi.org/10.1093/brain/awad314

Journal article

In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2
Morison, Lottie D., Meffert, Elisabeth, Stampfer, Miriam, Steiner-Wilke, Irene, Vollmer, Brigitte, Schulze, Katrin, Briggs, Tracy, Braden, Ruth, Vogel, Adam, Thompson-Lake, Daisy G. Y, Patel, Chirag, Blair, Edward, Goel, Himanshu, Turner, Samantha, Moog, Ute, Riess, Angelika, Liegeois, Frederique, Koolen, David A, Amor, David J., ... Morgan, Angela T.. (2023). In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2. Journal of Medical Genetics. 60(6), pp. 597-607. https://doi.org/10.1136/jmg-2022-108734

Journal article

Atypical development of Broca's area in a large family with inherited stuttering
Thompson-Lake, Daisy G. Y, Scerri, Thomas S., Block, Susan, Turner, Samantha J., Reilly, Sheena, Kefalianos, Elaina, Bonthrone, Alexandra F., Helbig, Ingo, Bahlo, Melanie, Scheffer, Ingrid E., Hildebrand, Michael S., Liégeois, Frédérique J. and Morgan, Angela T.. (2022). Atypical development of Broca's area in a large family with inherited stuttering. Brain. 145(3), pp. 1177-1188. https://doi.org/10.1093/brain/awab364

Journal article

Speech in children with cerebral palsy
Mei, Cristina, Reilly, Sheena, Bickerton, Molly, Mensah, Fiona, Turner, Samantha, Kumaranayagam, Dhanooshini, Pennington, Lindsay, Reddihough, Dinah and Morgan, Angela T.. (2020). Speech in children with cerebral palsy. Developmental Medicine and Child Neurology. 62(12), pp. 1374-1382. https://doi.org/10.1111/dmcn.14592

Journal article

Severe childhood speech disorder : Gene discovery highlights transcriptional dysregulation
Hildebrand, Michael S., Jackson, Victoria E., Scerri, Thomas S., Van Reyk, Olivia, Coleman, Matthew, Braden, Ruth O., Turner, Samantha, Rigbye, Kristin A., Boys, Amber, Barton, Sarah, Webster, Richard, Fahey, Michael, Saunders, Kerryn, Parry-Fielder, Bronwyn, Paxton, Georgia, Hayman, Michael, Coman, David, Goel, Himanshu, Baxter, Anne, ... Morgan, Angela T.. (2020). Severe childhood speech disorder : Gene discovery highlights transcriptional dysregulation. Neurology. 94(20), pp. e2148-e2167. https://doi.org/10.1212/WNL.0000000000009441

Journal article

Looking to the future : Speech, language, and academic outcomes in an adolescent with childhood apraxia of speech
Turner, Samantha J., Vogel, Adam P., Parry-Fielder, Bronwyn, Campbell, Rhonda, Scheffer, Ingrid E. and Morgan, Angela T.. (2019). Looking to the future : Speech, language, and academic outcomes in an adolescent with childhood apraxia of speech. Folia Phoniatrica et Logopaedica. 71(5-6), pp. 203-215. https://doi.org/10.1159/000500554

Journal article

Dorsal language stream anomalies in an inherited speech disorder
Liégeois, Frédérique J., Turner, Samantha J., Mayes, Angela, Bonthrone, Alexandra F., Boys, Amber, Smith, Libby, Parry-Fielder, Bronwyn, Mandelstam, Simone, Spencer-Smith, Megan, Bahlo, Melanie, Scerri, Tom S., Hildebrand, Michael S., Scheffer, Ingrid E., Connelly, Alan and Morgan, Angela T.. (2019). Dorsal language stream anomalies in an inherited speech disorder. Brain: a journal of neurology. 142(4), pp. 966-977. https://doi.org/10.1093/brain/awz018

Journal article

Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations
Corbett, Mark A., Turner, Samantha J., Gardner, Alison, Silver, Jeremy, Stankovich, Jim, Leventer, Richard J., Derry, Christopher P., Carroll, Renee, Ha, Thuong, Scheffer, Ingrid E., Bahlo, Melanie, Jackson, Graeme D., Mackey, David A., Berkovic, Samuel F. and Gecz, Jozef. (2017). Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations. European Journal of Medical Genetics. 60(8), pp. 437-443. https://doi.org/10.1016/j.ejmg.2017.06.002

Journal article

Dysarthria and broader motor speech deficits in Dravet syndrome
Turner, Samantha J., Brown, Amy, Arpone, Marta, Anderson, Vicki, Morgan, Angela T. and Scheffer, Ingrid E.. (2017). Dysarthria and broader motor speech deficits in Dravet syndrome. Neurology. 88(8), pp. 743-749. https://doi.org/10.1212/WNL.0000000000003635

Journal article

Early neuroimaging markers of FOXP2 intragenic deletion
Liégeois, Frédérique J., Hildebrand, Michael S., Bonthrone, Alexandra, Turner, Samantha J., Scheffer, Ingrid E., Bahlo, Melanie, Connelly, Alan and Morgan, Angela T.. (2016). Early neuroimaging markers of FOXP2 intragenic deletion. Scientific Reports. 6, p. Article: 35192. https://doi.org/10.1038/srep35192

Journal article

GRIN2A : An aptly named gene for speech dysfunction
Turner, Samantha, Mayes, Angela K., Verhoeven, Andrea, Mandelstam, Simone A., Morgan, Angela and Scheffer, Ingrid E.. (2015). GRIN2A : An aptly named gene for speech dysfunction. Neurology. 84(6), pp. 586-593. https://doi.org/10.1212/WNL.0000000000001228

Journal article

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