يعرض 1 - 10 نتائج من 155 نتيجة بحث عن '"Wallis, Mathew"', وقت الاستعلام: 1.26s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals

    المؤلفون: Layo-Carris, Dana E., Lubin, Emily E.Aff1, Aff2, Sangree, Annabel K.Aff1, Aff2, Clark, Kelly J.Aff1, Aff2, Durham, Emily L., Gonzalez, Elizabeth M.Aff1, Aff2, Smith, Sarina, Angireddy, Rajesh, Wang, Xiao Min, Weiss, Erin, Toutain, AnnickAff3, Aff4, Mendoza-Londono, Roberto, Dupuis, Lucie, Damseh, Nadirah, Velasco, Danita, Valenzuela, IreneAff7, Aff8, Codina-Solà, MartaAff7, Aff8, Ziats, Catherine, Have, Jaclyn, Clarkson, Katie, Steel, Dora, Kurian, Manju, Barwick, Katy, Carrasco, Diana, Dagli, Aditi I., Nowaczyk, M. J. M., Hančárová, Miroslava, Bendová, Šárka, Prchalova, Darina, Sedláček, Zdeněk, Baxová, Alica, Nowak, Catherine Bearce, Douglas, Jessica, Chung, Wendy K.Aff18, Aff19, Longo, Nicola, Platzer, Konrad, Klöckner, Chiara, Averdunk, Luisa, Wieczorek, Dagmar, Krey, Ilona, Zweier, ChristianeAff23, Aff24, Reis, Andre, Balci, Tugce, Simon, Marleen, Kroes, Hester Y., Wiesener, Antje, Vasileiou, Georgia, Marinakis, Nikolaos M., Veltra, Danai, Sofocleous, Christalena, Kosma, Konstantina, Traeger Synodinos, Joanne, Voudris, Konstantinos A., Vuillaume, Marie-LaureAff3, Aff4, Aff29, Gueguen, PaulAff3, Aff4, Aff29, Derive, Nicolas, Colin, Estelle, Battault, Clarisse, Au, Billie, Delatycki, MartinAff32, Aff33, Wallis, MathewAff34, Aff35, Gallacher, LyndonAff32, Aff33, Majdoub, FatmaAff36, Aff37, Aff38, Smal, NoorAff36, Aff37, Weckhuysen, SarahAff36, Aff37, Aff39, Aff40, Aff41, Schoonjans, An-SofieAff39, Aff42, Kooy, R. Frank, Meuwissen, MarijeAff42, Aff43, Cocanougher, Benjamin T., Taylor, Kathryn, Pizoli, Carolyn E., McDonald, Marie T., James, Philip, Roeder, Elizabeth R., Littlejohn, Rebecca, Borja, Nicholas A., Thorson, Willa, King, Kristine, Stoeva, Radka, Suerink, Manon, Nibbeling, Esther, Baskin, StephanieAff47, Aff52, L. E. Guyader, Gwenaël, Kaplan, Julie, Muss, Candace, Carere, Deanna Alexis, Bhoj, Elizabeth J. K.Aff1, Aff2, IDs41431024016101_cor87, Bryant, Laura M.Aff1, Aff56

    المصدر: European Journal of Human Genetics. 32(8):928-937

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  2. 2
    دورية أكاديمية
    Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is ageless

    المؤلفون: Wallis, MathewAff1, Aff9, Aff10, Bodek, Simon D.Aff1, Aff16, IDs13023024032975_cor2, Munro, JacobAff2, Aff3, Rafehi, HaloomAff2, Aff3, Bennett, Mark F.Aff2, Aff3, Aff4, Ye, Zimeng, Schneider, Amy, Gardiner, Fiona, Valente, Giulia, Murdoch, Emma, Uebergang, EloiseAff1, Aff7, Hunter, Jacquie, Stutterd, ChloeAff1, Aff6, Aff7, Aff8, Huq, AamiraAff1, Aff18, Salmon, LucindaAff1, Aff11, Scheffer, IngridAff1, Aff4, Aff5, Eratne, DhamidhuAff1, Aff4, Aff12, Meyn, Stephen, Fong, Chun Y., John, TomAff1, Aff16, Aff19, Mullen, SaulAff1, Aff4, White, Susan M.Aff6, Aff7, Aff8, Brown, Natasha J.Aff6, Aff7, Aff8, McGillivray, GeorgeAff6, Aff13, Chen, Jesse, Richmond, Chris, Hughes, AndrewAff1, Aff16, Krzesinski, Emma, Fennell, AndrewAff1, Aff17, Chambers, BrianAff1, Aff16, Santoreneos, ReneeAff1, Aff6, Le Fevre, AnnaAff1, Aff2, Aff6, Hildebrand, Michael S., Bahlo, MelanieAff2, Aff3, Christodoulou, JohnAff6, Aff7, Aff8, Delatycki, MartinAff1, Aff6, Aff7, Aff8, Berkovic, Samuel F.Aff1, Aff4

    المصدر: Orphanet Journal of Rare Diseases. 19(1)

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  3. 3
    دورية أكاديمية
    Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals

    المؤلفون: Layo-Carris, Dana E., Lubin, Emily E.Aff1, Aff2, Sangree, Annabel K.Aff1, Aff2, Clark, Kelly J.Aff1, Aff2, Durham, Emily L., Gonzalez, Elizabeth M.Aff1, Aff2, Smith, Sarina, Angireddy, Rajesh, Wang, Xiao Min, Weiss, Erin, Toutain, AnnickAff3, Aff4, Mendoza-Londono, Roberto, Dupuis, Lucie, Damseh, Nadirah, Velasco, Danita, Valenzuela, IreneAff7, Aff8, Codina-Solà, MartaAff7, Aff8, Ziats, Catherine, Have, Jaclyn, Clarkson, Katie, Steel, Dora, Kurian, Manju, Barwick, Katy, Carrasco, Diana, Dagli, Aditi I., Nowaczyk, M. J. M., Hančárová, Miroslava, Bendová, Šárka, Prchalova, Darina, Sedláček, Zdeněk, Baxová, Alica, Nowak, Catherine Bearce, Douglas, Jessica, Chung, Wendy K.Aff18, Aff19, Longo, Nicola, Platzer, Konrad, Klöckner, Chiara, Averdunk, Luisa, Wieczorek, Dagmar, Krey, Ilona, Zweier, ChristianeAff23, Aff24, Reis, Andre, Balci, Tugce, Simon, Marleen, Kroes, Hester Y., Wiesener, Antje, Vasileiou, Georgia, Marinakis, Nikolaos M., Veltra, Danai, Sofocleous, Christalena, Kosma, Konstantina, Synodinos, Joanne Traeger, Voudris, Konstantinos A., Vuillaume, Marie-LaureAff3, Aff4, Aff29, Gueguen, PaulAff3, Aff4, Aff29, Derive, Nicolas, Colin, Estelle, Battault, Clarisse, Au, Billie, Delatycki, MartinAff32, Aff33, Wallis, MathewAff34, Aff35, Gallacher, LyndonAff32, Aff33, Majdoub, FatmaAff36, Aff37, Aff38, Smal, NoorAff36, Aff37, Weckhuysen, SarahAff36, Aff37, Aff39, Aff40, Aff41, Schoonjans, An-SofieAff39, Aff42, Kooy, R. Frank, Meuwissen, MarijeAff42, Aff43, Cocanougher, Benjamin T., Taylor, Kathryn, Pizoli, Carolyn E., McDonald, Marie T., James, Philip, Roeder, Elizabeth R., Littlejohn, Rebecca, Borja, Nicholas A., Thorson, Willa, King, Kristine, Stoeva, Radka, Suerink, Manon, Nibbeling, Esther, Baskin, StephanieAff47, Aff52, Guyader, Gwenaël L. E., Kaplan, Julie, Muss, Candace, Carere, Deanna Alexis, Bhoj, Elizabeth J. K.Aff1, Aff2, IDs4143102401659y_cor87, Bryant, Laura M.Aff1, Aff56

    المصدر: European Journal of Human Genetics. 32(8):1032-1032

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  4. 4
    دورية أكاديمية
    Implementation and Evaluation of a National Multidisciplinary Kidney Genetics Clinic Network Over 10 Years

    المؤلفون: Jayasinghe, Kushani, Biros, Erik, Harris, Trudie, Wood, Alasdair, O’Shea, Rosie, Hill, Lauren, Fowles, Lindsay, Wardrop, Louise, Shalhoub, Carolyn, Hahn, Deirdre, Rangan, Gopala, Kevin, Lucy, Tchan, Michel, Snelling, Paul, Sandow, Rhiannon, Sundaram, Madhivan, Chaturvedi, Swasti, Trnka, Peter, Faull, Randall, Poplawski, Nicola K., Huntley, Vanessa, Garza, Denisse, Wallis, Mathew, Jose, Matthew, Leaver, Anna, Trainer, Alison H., Wilkins, Ella J., White, Sue, Elbaum, Yoni, Prawer, Yael, Krzesinski, Emma, Valente, Giulia, Winship, Ingrid, Ryan, Jessica, Whitlam, John, Nicholls, Kathy, West, Kirsty, Donaldson, Liz, Johnstone, Lilian, Lewit-Mendes, Miranda, Kerr, Peter G., Bodek, Simon, Chakera, Aron, MacShane, Mandi, Mincham, Christine, Stackpoole, Elaine, Willis, Francis, Soraru, Jacqueline, Pachter, Nick, Bennetts, Bruce, Forbes, Thomas A., Mallawaarachchi, Amali, Quinlan, Catherine, Patel, Chirag, McCarthy, Hugh, Goranitis, Illias, Best, Stephanie, Alexander, Stephen, Stark, Zornitza, Mallett, Andrew J.

    المصدر: In Kidney International Reports August 2024 9(8):2372-2385

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  5. 5
    دورية أكاديمية
    Integrated multi-omics for rapid rare disease diagnosis on a national scale

    المؤلفون: Lunke, SebastianAff1, Aff2, Aff3, Bouffler, Sophie E., Patel, Chirag V., Sandaradura, Sarah A.Aff5, Aff6, Wilson, MeredithAff5, Aff6, Pinner, JasonAff7, Aff8, Hunter, Matthew F.Aff9, Aff10, Barnett, Christopher P.Aff11, Aff12, Aff13, Wallis, MathewAff14, Aff15, Kamien, Benjamin, Tan, Tiong Y.Aff1, Aff2, Freckmann, Mary-Louise, Chong, Belinda, Phelan, Dean, Francis, David, Kassahn, Karin S.Aff12, Aff13, Ha, ThuongAff12, Aff18, Aff19, Gao, Song, Arts, PeerAff12, Aff13, Aff18, Aff19, Jackson, Matilda R.Aff3, Aff12, Scott, Hamish S.Aff3, Aff12, Aff13, Aff18, Aff19, Eggers, Stefanie, Rowley, Simone, Boggs, KirstenAff3, Aff5, Aff7, Rakonjac, AnaAff3, Aff5, Aff7, Brett, Gemma R.Aff1, Aff2, de Silva, Michelle G.Aff1, Aff2, Aff20, Springer, AmandaAff9, Aff10, Ward, Michelle, Stallard, Kirsty, Simons, Cas, Conway, Thomas, Halman, Andreas, Van Bergen, Nicole J.Aff2, Aff20, Sikora, Tim, Semcesen, Liana N., Stroud, David A.Aff1, Aff2, Aff20, Compton, Alison G.Aff1, Aff2, Aff20, Thorburn, David R.Aff1, Aff2, Aff20, Bell, Katrina M.Aff1, Aff20, Sadedin, SimonAff1, Aff2, Aff20, North, Kathryn N.Aff2, Aff3, Aff20, Christodoulou, JohnAff2, Aff3, Aff6, Aff20, Stark, ZornitzaAff1, Aff2, Aff3, IDs41591023024019_cor44

    المصدر: Nature Medicine. 29(7):1681-1691

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  6. 6
    دورية أكاديمية
    The clinical utility and costs of whole-genome sequencing to detect cancer susceptibility variants—a multi-site prospective cohort study

    المؤلفون: Davidson, Aimee L.Aff1, Aff2, Dressel, Uwe, Norris, Sarah, Canson, Daffodil M.Aff1, Aff2, Glubb, Dylan M.Aff1, Aff2, Fortuno, CristinaAff1, Aff2, Hollway, Georgina E., Parsons, Michael T., Vidgen, Miranda E.Aff1, Aff4, Holmes, Oliver, Koufariotis, Lambros T., Lakis, Vanessa, Leonard, Conrad, Wood, Scott, Xu, Qinying, McCart Reed, Amy E., Pickett, Hilda A., Al-Shinnag, Mohammad K.Aff2, Aff7, Austin, Rachel L.Aff4, Aff7, Burke, Jo, Cops, Elisa J., Nichols, Cassandra B., Goodwin, AnnabelAff11, Aff12, Harris, Marion T.Aff13, Aff14, Higgins, Megan J., Ip, Emilia L., Kiraly-Borri, Catherine, Lau, ChiyanAff2, Aff17, Mansour, Julia L., Millward, Michael W., Monnik, Melissa J., Pachter, Nicholas S.Aff10, Aff19, Ragunathan, Abiramy, Susman, Rachel D., Townshend, Sharron L., Trainer, Alison H.Aff9, Aff21, Troth, Simon L., Tucker, Katherine M.Aff22, Aff23, Wallis, Mathew J.Aff8, Aff24, Walsh, Maie, Williams, Rachel A.Aff22, Aff23, Winship, Ingrid M.Aff21, Aff25, Newell, Felicity, Tudini, EmmaAff1, Aff4, Pearson, John V., Poplawski, Nicola K.Aff18, Aff26, Mar Fan, Helen G.Aff2, Aff7, James, Paul A.Aff9, Aff27, Spurdle, Amanda B.Aff1, Aff2, IDs13073023012231_cor49, Waddell, NicolaAff1, Aff2, Ward, Robyn L.Aff2, Aff3, IDs13073023012231_cor51

    المصدر: Genome Medicine. 15(1)

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  7. 7
    دورية أكاديمية
    Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development

    المؤلفون: Kaspi, AntonyAff1, Aff2, Hildebrand, Michael S.Aff2, Aff3, Jackson, Victoria E.Aff1, Aff2, Braden, Ruth, van Reyk, Olivia, Howell, Tegan, Debono, Simone, Lauretta, Mariana, Morison, Lottie, Coleman, Matthew J.Aff2, Aff3, Webster, Richard, Coman, DavidAff5, Aff6, Goel, Himanshu, Wallis, MathewAff8, Aff9, Dabscheck, GabrielAff2, Aff10, Downie, LilianAff2, Aff10, Baker, Emma K.Aff2, Aff3, Parry-Fielder, Bronwyn, Ballard, Kirrie, Harrold, Eva, Ziegenfusz, Shaun, Bennett, Mark F.Aff1, Aff2, Robertson, ErandeeAff1, Aff2, Wang, LongfeiAff1, Aff2, Boys, Amber, Fisher, Simon E.Aff14, Aff15, Amor, David J.Aff2, Aff3, Aff10, Scheffer, Ingrid E., Bahlo, MelanieAff1, Aff2, Morgan, Angela T.Aff2, Aff3, Aff6, Aff10, IDs41380022017648_cor30

    المصدر: Molecular Psychiatry. 28(4):1647-1663

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  8. 8
    دورية أكاديمية
    A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship

    المؤلفون: Ades, Lesley, Enriquez, Annabel, McLean, Alison, Smyth, Renee, Alankarage, Dimithu, Fatkin, Diane, McNamara, James, Soka, Magdalena, Morgan almog, Fear, Vanessa, Medi, Caroline, Stark, Zornitza, Al-Shinnag, Mohammad, Fine, Miriam, Metke, Alejandro, Sy, Raymond, Atherton, John J., Finlay, Keri, Milnes, Di, Tang, Dotti, Austin, Rachel, Garza, Denisse, Milward, Michael, Taylor, Jessica, Bagnall, Richard D., Giannoulatou, Eleni, Morrish, Ansley, Taylor, Shelby, Barnett, Chris, Gongolidis, Laura, Morwood, Jim, Tchan, Michel, Blue, Gillian M., Gray, Belinda, Mountain, Helen, Thompson, Tina, Bodek, Simon, Greer, Cassie, Mowat, David, Thorpe, Jordan, Boggs, Kirsten, Haan, Eric, Ng, Chai-Ann, Trainer, Alison, Bogwitz, Michael, Haas, Mathilda, Nowak, Natalie, Trivedi, Gunjan, Boughtwood, Tiffany, Hanna, Bernadette, Martinez, Noelia Nunez, Valente, Giulia, Bray, Alessandra, Harvey, Richard, Ohanian, Monique, van Spaendonck-Zwarts, Karin, Brion, Marie-Jo, Hayward, Janette, O’Sullivan, Sinead, Vandenberg, Jamie, Brown, Jaye, Herrera, Carmen, Overkov, Angela, Verma, Kunal, Richardson, Rob Bryson, Hill, Adam, Pachter, Nicholas, Vidgen, Miranda, Burnett, Leslie, Hollingsworth, Georgie, Patel, Chirag, Vohra, Jitendra, Burns, Charlotte, Hollway, Georgina, Perrin, Mark, Waddel-Smith, Kathryn, Cao, Michelle, Horton, Ari E., Perry, Matthew, Wallis, Mathew, Carr, Will, Howting, Denise, Pflaumer, Andreas, Weintraub, Robert G., Casauria, Sarah, Ingles, Jodie, Phillips, Peta, Wilson, Meredith, Chalinor, Heather, Isbister, Joanne, Phuong, Thuan, Winlaw, David, Chang, Yuchen, Jackson, Matilda, Pope-Couston, Rachel, Worgan, Lisa, Chapman, Gavin, James, Paul, Poplawski, Nicola K., Wornham, Linda, Charitou, Theosodia, Jane-Pantaleo, Sarah, Punni, Preeti, Wu, Kathy, Chong, Belinda, Johnson, Renee, Quinn, Michael C.J., Yeates, Laura, Collins, Felicity, Kelly, Andrew, Quinn, Michael, Zentner, Dominica, Correnti, Gemma, King-Smith, Sarah, Rajagopalan, Sulekha, Cox, Kathy, Kirk, Edwin, Raju, Hariharan, Cunningham, Fiona, Kummerfeld, Sarah, Rath, Emma M., Das, Debjani, Lassman, Timo, Regan, Matthew, Davis, Jason, Lipton, Jonathon, Rogers, Jonathan, Davis, Andrew, Lunke, Sebastian, Ryan, Mark, De Fazio, Paul, Macciocca, Ivan, Sandaradura, Sarah, de Silva, Michelle, MacIntyre, Paul, Schonrock, Nicole, Den Elzen, Nicola, Madelli, Evanthia O., Scuffham, Paul, Devery, Sophie, Mallawaarachchi, Amali, Semsarian, Chris, Dobbins, Julia, Mansour, Julia, Sherburn, Isabella, Dunwoodie, Sally L., Martin, Ellenore, Sherlock, Mary-Clare, Dwyer, Nathan, Mathew, Jacob, Singer, Emma, Elbracht-Leong, Stefanie, Mattiske, Tessa, Smerdon, Carla, Elliott, David, McGaughran, Julie, Smith, Janine, Brown, Jaye S., Haas, Matilda, Pantaleo, Sarah-Jane

    المصدر: In Genetics in Medicine Open 2024 2

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  9. 9
    دورية أكاديمية
    Correction: Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development

    المؤلفون: Kaspi, AntonyAff1, Aff2, Hildebrand, Michael S.Aff2, Aff3, Jackson, Victoria E.Aff1, Aff2, Braden, Ruth, van Reyk, Olivia, Howell, Tegan, Debono, Simone, Lauretta, Mariana, Morison, Lottie, Coleman, Matthew J.Aff2, Aff3, Webster, Richard, Coman, DavidAff5, Aff6, Goel, Himanshu, Wallis, MathewAff8, Aff9, Dabscheck, GabrielAff2, Aff10, Downie, LilianAff2, Aff10, Baker, Emma K.Aff2, Aff3, Parry-Fielder, Bronwyn, Ballard, Kirrie, Harrold, Eva, Ziegenfusz, Shaun, Bennett, Mark F.Aff1, Aff2, Robertson, ErandeeAff1, Aff2, Wang, LongfeiAff1, Aff2, Boys, Amber, Fisher, Simon E.Aff14, Aff15, Amor, David J.Aff2, Aff3, Aff10, Scheffer, Ingrid E., Bahlo, MelanieAff1, Aff2, Morgan, Angela T.Aff2, Aff3, Aff6, Aff10, IDs4138002201879y_cor30

    المصدر: Molecular Psychiatry. 28(4):1664-1666

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  10. 10
    دورية أكاديمية

    لا يتم عرض هذه النتيجة على الضيوف.

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