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Credit Name
Mathew J Wallis
Full Name
Wallis, Mathew J
 
Department
 
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Publications

Results 1-10 of 10 (Search time: 0.008 seconds).

Publication YearTitleAuthor(s)
118-Jan-2021Anhedonia and anergia predict mortality in older Australians living in residential aged care.Greenfield, L; Mathews, S ; Toukhsati, Samia R 
215-Jan-2021The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspective.Eratne, Dhamidhu; Schneider, Amy L ; Lynch, Ella; Martyn, Melissa; Velakoulis, Dennis; Fahey, Michael; Kwan, Patrick; Leventer, Richard; Rafehi, Haloom; Chong, Belinda; Stark, Zornitza; Lunke, Sebastian; Phelan, Dean G; O'Keefe, Melanie; Siemering, Kirby; West, Kirsty; Sexton, Adrienne; Jarmolowicz, Anna; Taylor, Jessica A; Schultz, Joshua; Purvis, Rebecca; Uebergang, Eloise; Chalinor, Heather; Creighton, Belinda; Gelfand, Nikki; Saks, Tamar; Prawer, Yael; Smagarinsky, Yana; Pan, Tianxin; Goranitis, Ilias; Ademi, Zanfina; Gaff, Clara; Huq, Aamira; Walsh, Maie; James, Paul A; Krzesinski, Emma I; Wallis, Mathew J ; Stutterd, Chloe A ; Bahlo, Melanie; Delatycki, Martin B ; Berkovic, Samuel F 
314-Oct-2020Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome.Palencia-Campos, Adrian; Aoto, Phillip C; Machal, Erik M F; Rivera-Barahona, Ana; Soto-Bielicka, Patricia; Bertinetti, Daniela; Baker, Blaine; Vu, Lily; Piceci-Sparascio, Francesca; Torrente, Isabella; Boudin, Eveline; Peeters, Silke; Van Hul, Wim; Huber, Celine; Bonneau, Dominique; Hildebrand, Michael S ; Coleman, Matthew; Bahlo, Melanie; Bennett, Mark F ; Schneider, Amy L ; Scheffer, Ingrid E ; Kibæk, Maria; Kristiansen, Britta S; Issa, Mahmoud Y; Mehrez, Mennat I; Ismail, Samira; Tenorio, Jair; Li, Gaoyang; Skålhegg, Bjørn Steen; Otaify, Ghada A; Temtamy, Samia; Aglan, Mona; Jønch, Aia E; De Luca, Alessandro; Mortier, Geert; Cormier-Daire, Valérie; Ziegler, Alban; Wallis, Mathew J ; Lapunzina, Pablo; Herberg, Friedrich W; Taylor, Susan S; Ruiz-Perez, Victor L
417-Sep-2020Clinical impact of genomic testing in patients with suspected monogenic kidney disease.Jayasinghe, Kushani; Stark, Zornitza; Kerr, Peter G; Gaff, Clara; Martyn, Melissa; Whitlam, John B ; Creighton, Belinda; Donaldson, Elizabeth; Hunter, Matthew; Jarmolowicz, Anna; Johnstone, Lilian; Krzesinski, Emma; Lunke, Sebastian; Lynch, Elly; Nicholls, Kathleen; Patel, Chirag; Prawer, Yael; Ryan, Jessica; See, Emily J ; Talbot, Andrew; Trainer, Alison; Tytherleigh, Rigan; Valente, Giulia M ; Wallis, Mathew J ; Wardrop, Louise; West, Kirsty H; White, Susan M; Wilkins, Ella; Mallett, Andrew J; Quinlan, Catherine
521-Jan-2020Prospective Evaluation of the Utility of Whole Exome Sequencing in Dilated Cardiomyopathy.Ramchand, Jay ; Wallis, Mathew J ; Macciocca, Ivan; Lynch, Elly; Farouque, Omar ; Martyn, Melissa; Phelan, Dean; Chong, Belinda; Lockwood, Siobhan; Weintraub, Robert; Thompson, Tina; Trainer, Alison; Zentner, Dominica; Vohra, Jitendra; Chetrit, Michael; Hare, David L ; James, Paul
6Jan-2020Small interstitial 9p24.3 deletions principally involving KANK1 are likely benign copy number variants.Wallis, Mathew J ; Boys, Amber; Tassano, Elisa; Delatycki, Martin B 
720-Jul-2019Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain size.Le Duc, Diana; Giulivi, Cecilia; Hiatt, Susan M; Napoli, Eleonora; Panoutsopoulos, Alexios; Harlan De Crescenzo, Angelo; Kotzaeridou, Urania; Syrbe, Steffen; Anagnostou, Evdokia; Azage, Meron; Bend, Renee; Begtrup, Amber; Brown, Natasha J; Büttner, Benjamin; Cho, Megan T; Cooper, Gregory M; Doering, Jan H; Dubourg, Christèle; Everman, David B; Hildebrand, Michael S ; Santos, Francis Jeshira Reynoso; Kellam, Barbara; Keller-Ramey, Jennifer; Lemke, Johannes R; Liu, Shuxi; Niyazov, Dmitriy; Payne, Katelyn; Person, Richard; Quélin, Chloé; Schnur, Rhonda E; Smith, Brooke T; Strober, Jonathan; Walker, Susan; Wallis, Mathew J ; Walsh, Laurence; Yang, Sandra; Yuen, Ryan K C; Ziegler, Andreas; Sticht, Heinrich; Pride, Michael C; Orosco, Lori; Martínez-Cerdeño, Verónica; Silverman, Jill L; Crawley, Jacqueline N; Scherer, Stephen W; Zarbalis, Konstantinos S; Jamra, Rami
8Apr-2019A novel approach to offering additional genomic findings-A protocol to test a two-step approach in the healthcare system.Martyn, Melissa; Kanga-Parabia, Anaita; Lynch, Elly; James, Paul A; Macciocca, Ivan; Trainer, Alison H; Halliday, Jane; Keogh, Louise; Wale, Janney; Winship, Ingrid; Bogwitz, Michael; Valente, Giulia M ; Walsh, Maie; Downie, Lilian; Amor, David; Wallis, Mathew J ; Cunningham, Fiona; Burgess, Matthew J; Brown, Natasha J; Jarmolowicz, Anna; Lunke, Sebastian; Goranitis, Ilias; Gaff, Clara L
9Apr-2018Surprisingly good outcome in antenatal diagnosis of severe hydrocephalus related to CCDC88C deficiency.Wallis, Mathew J ; Baumer, Alessandra; Smaili, Wiam; Jaouad, Imane Cherkaoui; Sefiani, Abdelaziz; Jacobson, Erica; Bowyer, Lucy; Mowat, David; Rauch, Anita
10Sep-2017Blake's pouch cyst in 13q deletion syndrome: posterior fossa malformations may occur due to disruption of multiple genesMyers, Kenneth A; Wallis, Mathew J ; Fitt, Gregory J ; Sarnat, Harvey B; Newton, Mark R