A system for developing reasonable adjustments to the application of the National Safety and Quality Health Service Standards for adult patients with intellectual disability in Aus... von Wallace, Robyn A

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ALS-associated TDP-43 induces endoplasmic reticulum stress, which drives cytoplasmic TDP-43 accumulation and stress granule formation von Walker, Adam K, Soo, Kai Y, Sundaramoorthy, Vinod, Parakh, Sonam, Ma, Yi, Farg, Manal A, Wallace, Robyn H, Crouch, Peter J, Turner, Bradley J, Horne, Malcolm K, Atkin, Julie D

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Palliative care for adults with intellectual disability von Wallace, Robyn A.

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National Disability Insurance Scheme, health, hospitals and adults with intellectual disability von Wallace, Robyn A.

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DNA variation in the SNAP25 gene confers risk to ADHD and is associated with reduced expression in prefrontal cortex von Hawi, Ziarih, Matthews, Natasha, Wagner, Joseph, Wallace, Robyn H, Butler, Tim J, Vance, Alasdair, Kent, Lindsey, Gill, Michael, Bellgrove, Mark A

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Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis von Benyamin, Beben, He, Ji, Zhao, Qiongyi, Gratten, Jacob, Garton, Fleur, Leo, Paul J., Liu, Zhijun, Mangelsdorf, Marie, Al-Chalabi, Ammar, Anderson, Lisa, Butler, Timothy J., Chen, Lu, Chen, Xiang-Ding, Cremin, Katie, Deng, Hong-Weng, Devine, Matthew, Edson, Janette, Fifita, Jennifer A., Furlong, Sarah, Han, Ying-Ying, Harris, Jessica, Henders, Anjali K., Jeffree, Rosalind L., Jin, Zi-Bing, Li, Zhongshan, Li, Ting, Li, Mengmeng, Lin, Yong, Liu, Xiaolu, Marshall, Mhairi, McCann, Emily P., Mowry, Bryan J., Ngo, Shyuan T., Pamphlett, Roger, Ran, Shu, Reutens, David C., Rowe, Dominic B., Sachdev, Perminder, Shah, Sonia, Song, Sharon, Tan, Li-Jun, Tang, Lu, van den Berg, Leonard H., van Rheenen, Wouter, Veldink, Jan H., Wallace, Robyn H., Wheeler, Lawrie, Williams, Kelly L., Wu, Jinyu, Wu, Xin, Yang, Jian, Yue, Weihua, Zhang, Zong-Hong, Zhang, Dai, Noakes, Peter G., Blair, Ian P., Henderson, Robert D., McCombe, Pamela A., Visscher, Peter M., Xu, Huji, Bartlett, Perry F., Brown, Matthew A., Wray, Naomi R., Fan, Dongsheng

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Pain management challenges in a patient with mucopolysaccharidosis IVA von Gurgius, Marcus, Donoghue, Sarah, Wallace, Robyn A.

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A Homozygous Mutation in Human PRICKLE1 Causes an Autosomal-Recessive Progressive Myoclonus Epilepsy-Ataxia Syndrome von Bassuk, Alexander G., Wallace, Robyn H., Buhr, Aimee, Buller, Andrew R., Afawi, Zaid, Shimojo, Masahito, Miyata, Shingo, Chen, Shan, Gonzalez-Alegre, Pedro, Griesbach, Hilary L., Wu, Shu, Nashelsky, Marcus, Vladar, Eszter K., Antic, Dragana, Ferguson, Polly J., Cirak, Sebahattin, Voit, Thomas, Scott, Matthew P., Axelrod, Jeffrey D., Gurnett, Christina, Daoud, Azhar S., Kivity, Sara, Neufeld, Miriam Y., Mazarib, Aziz, Straussberg, Rachel, Walid, Simri, Korczyn, Amos D., Slusarski, Diane C., Berkovic, Samuel F., El-Shanti, Hatem I.

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Latent Stem and Progenitor Cells in the Hippocampus Are Activated by Neural Excitation von Walker, Tara L, White, Amanda, Black, Debra M, Wallace, Robyn H, Sah, Pankaj, Bartlett, Perry F

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Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations von Scheffer, Ingrid E., Harkin, Louise A., Grinton, Bronwyn E., Dibbens, Leanne M., Turner, Samantha J., Zielinski, Marta A., Xu, Ruwei, Jackson, Graeme, Adams, Judith, Connellan, Mary, Petrou, Steven, Wellard, R. Mark, Briellmann, Regula S., Wallace, Robyn H., Mulley, John C., Berkovic, Samuel F.

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Non-invasive diffusion tensor imaging detects white matter degeneration in the spinal cord of a mouse model of amyotrophic lateral sclerosis von Underwood, Clare K., Kurniawan, Nyoman D., Butler, Tim J., Cowin, Gary J., Wallace, Robyn H.

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Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy von Lower, Karen M, Lütcherath, Viggo, Gécz, Jozef, Frints, Suzanna G.M, Partington, Michael, Strømme, Petter, Scheffer, Ingrid E, Gedeon, Ági K, Lewis, Suzanne M.E, Turner, Gillian, Fryns, Jean-Pierre, Sutherland, Grant R, Wallace, Robyn H, Mangelsdorf, Marie E, Shaw, Marie A, Mulley, John C, Bruyere, Helene

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Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese von Gratten, Jacob, Zhao, Qiongyi, Benyamin, Beben, Garton, Fleur, He, Ji, Leo, Paul J, Mangelsdorf, Marie, Anderson, Lisa, Zhang, Zong-Hong, Chen, Lu, Chen, Xiang-Ding, Cremin, Katie, Deng, Hong-Weng, Edson, Janette, Han, Ying-Ying, Harris, Jessica, Henders, Anjali K, Jin, Zi-Bing, Li, Zhongshan, Lin, Yong, Liu, Xiaolu, Marshall, Mhairi, Mowry, Bryan J, Ran, Shu, Reutens, David C, Song, Sharon, Tan, Li-Jun, Tang, Lu, Wallace, Robyn H, Wheeler, Lawrie, Wu, Jinyu, Yang, Jian, Xu, Huji, Visscher, Peter M, Bartlett, Perry F, Brown, Matthew A, Wray, Naomi R, Fan, Dongsheng

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Clinical audit of gastrointestinal conditions occurring among adults with Down syndrome attending a specialist clinic von Wallace, Robyn A.

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Truncation of the GABAA-Receptor γ2 subunit in a family with generalized epilepsy with febrile seizures plus von HARKIN, Louise A, BOWSER, David N, SCHEFFER, Ingrid E, PETROU, Steven, DIBBENS, Leanne M, SINGH, Rita, PHILLIPS, Fiona, WALLACE, Robyn H, RICHARDS, Michaella C, WILLIAMS, David A, MULLEY, John C, BERKOVIC, Samuel F

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A Methodological Approach to Small Area Estimation for the Behavioral Risk Factor Surveillance System von Pierannunzi, Carol, Xu, Fang, Wallace, Robyn C, Garvin, William, Greenlund, Kurt J, Bartoli, William, Ford, Derek, Eke, Paul, Town, G Machell

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Transgenic mice overexpressing mutant TDP-43 show aberrant splicing of neurological disorders-associated gene Zmynd11 prior to onset of motor symptoms von Narayanan, Ramesh K, Panwar, Ajay, Butler, Tim J, Cutrupi, Anthony N, Kennerson, Marina, Vucic, Steve, Ashokkumar, Balasubramaniem, Mangelsdorf, Marie, Wallace, Robyn H

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A high density linkage disequilibrium mapping in 14 noradrenergic genes: evidence of association between SLC6A2, ADRA1B and ADHD von Hawi, Ziarih, Matthews, Natasha, Barry, Edwina, Kirley, Aiveen, Wagner, Joseph, Wallace, Robyn H., Heussler, Helen S., Vance, Alasdair, Gill, Michael, Bellgrove, Mark A.

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Multiplex families with epilepsy: Success of clinical and molecular genetic characterization von Afawi, Zaid, Oliver, Karen L, Kivity, Sara, Mazarib, Aziz, Blatt, Ilan, Neufeld, Miriam Y, Helbig, Katherine L, Goldberg-Stern, Hadassa, Misk, Adel J, Straussberg, Rachel, Walid, Simri, Mahajnah, Muhammad, Lerman-Sagie, Tally, Ben-Zeev, Bruria, Kahana, Esther, Masalha, Rafik, Kramer, Uri, Ekstein, Dana, Shorer, Zamir, Wallace, Robyn H, Mangelsdorf, Marie, MacPherson, James N, Carvill, Gemma L, Mefford, Heather C, Jackson, Graeme D, Scheffer, Ingrid E, Bahlo, Melanie, Gecz, Jozef, Heron, Sarah E, Corbett, Mark, Mulley, John C, Dibbens, Leanne M, Korczyn, Amos D, Berkovic, Samuel F

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PGRMC1 effects on metabolism, genomic mutation and CpG methylation imply crucial roles in animal biology and disease von Thejer, Bashar M, Adhikary, Partho P, Teakel, Sarah L, Fang, Johnny, Weston, Paul A, Gurusinghe, Saliya, Anwer, Ayad G, Gosnell, Martin, Jazayeri, Jalal A, Ludescher, Marina, Gray, Lesley-Ann, Pawlak, Michael, Wallace, Robyn H, Pant, Sameer D, Wong, Marie, Fischer, Tamas, New, Elizabeth J, Fehm, Tanja N, Neubauer, Hans, Goldys, Ewa M, Quinn, Jane C, Weston, Leslie A, Cahill, Michael A

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