The efficacy of mindfulness-based therapy for anxiety, social skills, and aggressive behaviors in children and young people with Autism Spectrum Disorder: A systematic review

por Loftus, Tundi, Mathersul, Danielle C., Ooi, Michelle, Yau, Shu H.
Publicado 2023

Case study: auditory brain responses in a minimally verbal child with autism and cerebral palsy

por Yau, Shu H., McArthur, Genevieve, Badcock, Nicholas A., Brock, Jon
Publicado 2015

Machine learning algorithms for mode-of-action classification in toxicity assessment

por Zhang, Yile, Wong, Yau Shu, Deng, Jian, Anton, Cristina, Gabos, Stephan, Zhang, Weiping, Huang, Dorothy Yu, Jin, Can
Publicado 2016

Post-mortem Characterisation of a Case With an ACTG1 Variant, Agenesis of the Corpus Callosum and Neuronal Heterotopia

por Vontell, Regina, Supramaniam, Veena G., Davidson, Alice, Thornton, Claire, Marnerides, Andreas, Holder-Espinasse, Muriel, Lillis, Suzanne, Yau, Shu, Jansson, Mattias, Hagberg, Henrik E., Rutherford, Mary A.
Publicado 2019

A hemizygous mutation in the FOXP3 gene (IPEX syndrome) resulting in recurrent X-linked fetal hydrops: a case report

por Shangaris, Panicos, Ho, Alison, Marnerides, Andreas, George, Simi, AlAdnani, Mudher, Yau, Shu, Jansson, Mattias, Hoyle, Jacqueline, Ahn, Joo Wook, Ellard, Sian, Irving, Melita, Wellesley, Diana, Pasupathy, Dharmintra, Holder-Espinasse, Muriel
Publicado 2021

Diagnostic yield of rare skeletal dysplasia conditions in the radiogenomics era

por Sabir, Ataf H., Morley, Elizabeth, Sheikh, Jameela, Calder, Alistair D., Beleza-Meireles, Ana, Cheung, Moira S., Cocca, Alessandra, Jansson, Mattias, Lillis, Suzanne, Patel, Yogen, Yau, Shu, Hall, Christine M., Offiah, Amaka C., Irving, Melita
Publicado 2021

A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies

por Bovolenta, Matteo, Neri, Marcella, Fini, Sergio, Fabris, Marina, Trabanelli, Cecilia, Venturoli, Anna, Martoni, Elena, Bassi, Elena, Spitali, Pietro, Brioschi, Simona, Falzarano, Maria S, Rimessi, Paola, Ciccone, Roberto, Ashton, Emma, McCauley, Joanne, Yau, Shu, Abbs, Stephen, Muntoni, Francesco, Merlini, Luciano, Gualandi, Francesca, Ferlini, Alessandra
Publicado 2008

ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies

por Cirak, Sebahattin, Foley, Aileen Reghan, Herrmann, Ralf, Willer, Tobias, Yau, Shu, Stevens, Elizabeth, Torelli, Silvia, Brodd, Lina, Kamynina, Alisa, Vondracek, Petr, Roper, Helen, Longman, Cheryl, Korinthenberg, Rudolf, Marrosu, Gianni, Nürnberg, Peter, Michele, Daniel E., Plagnol, Vincent, Hurles, Matt, Moore, Steven A., Sewry, Caroline A., Campbell, Kevin P., Voit, Thomas, Muntoni, Francesco
Publicado 2013

Recessive mutations in EPG5 cause Vici syndrome, a multisystem disorder with defective autophagy

por Cullup, Thomas, Kho, Ay L., Dionisi-Vici, Carlo, Brandmeier, Birgit, Smith, Frances, Urry, Zoe, Simpson, Michael A., Yau, Shu, Bertini, Enrico, McClelland, Verity, Al-Owain, Mohammed, Koelker, Stefan, Koerner, Christian, Hoffmann, Georg F., Wijburg, Frits A., Hoedt, Amber E. ten, Rogers, Curtis, Manchester, David, Miyata, Rie, Hayashi, Masaharu, Said, Elizabeth, Soler, Doriette, Kroisel, Peter M., Windpassinger, Christian, Filloux, Francis M., Al-Kaabi, Salwa, Hertecant, Jozef, Del Campo, Miguel, Buk, Stefan, Bodi, Istvan, Goebel, Hans-Hilmar, Sewry, Caroline A., Abbs, Stephen, Mohammed, Shehla, Josifova, Dragana, Gautel, Mathias, Jungbluth, Heinz
Publicado 2012