Underlying genetic variation in familial frontotemporal dementia: sequencing of 198 patients
Mol, Merel O., van Rooij, Jeroen G.J., Wong, Tsz H., Melhem, Shamiram, Verkerk, Annemieke J.M.H., Kievit, Anneke J.A., van Minkelen, Rick, Rademakers, Rosa, Pottier, Cyril, Kaat, Laura Donker, Seelaar, Harro, van Swieten, John C., Dopper, Elise G.P.
Published in Neurobiology of aging (01.01.2021)
Published in Neurobiology of aging (01.01.2021)
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Soft, stretchable, wireless intelligent three‐lead electrocardiograph monitors with feedback functions for warning of potential heart attack
Yiu, Chunki, Liu, Yiming, Zhang, Chao, Zhou, Jingkun, Jia, Huiling, Wong, Tsz H., Huang, Xingcan, Li, Jian, Yao, Kuanming, Yau, Ming K., Zhao, Ling, Li, Hu, Zhang, Binbin, Park, Wooyoung, Zhang, Yuanting, Wang, Zuankai, Yu, Xinge
Published in SmartMat (Beijing, China) (01.12.2022)
Published in SmartMat (Beijing, China) (01.12.2022)
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Novel TUBA4A Variant Associated With Familial Frontotemporal Dementia
Mol, Merel O, Wong, Tsz H, Melhem, Shamiram, Basu, Sreya, Viscusi, Riccardo, Galjart, Niels, Rozemuller, Annemieke J M, Fallini, Claudia, Landers, John E, Kaat, Laura Donker, Seelaar, Harro, van Rooij, Jeroen G J, van Swieten, John C
Published in Neurology. Genetics (01.06.2021)
Published in Neurology. Genetics (01.06.2021)
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A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamics
Nicolas, Gaël, Sévigny, Myriam, Lecoquierre, François, Marguet, Florent, Deschênes, Andréanne, Del Pelaez, Maria Carment, Feuillette, Sébastien, Audebrand, Anaïs, Lecourtois, Magalie, Rousseau, Stéphane, Richard, Anne-Claire, Cassinari, Kévin, Deramecourt, Vincent, Duyckaerts, Charles, Boland, Anne, Deleuze, Jean-François, Meyer, Vincent, Clarimon Echavarria, Jordi, Gelpi, Ellen, Akiyama, Haruhiko, Hasegawa, Masato, Kawakami, Ito, Wong, Tsz H, Van Rooij, Jeroen G J, Van Swieten, John C, Campion, Dominique, Dutchak, Paul A, Wallon, David, Lavoie-Cardinal, Flavie, Laquerrière, Annie, Rovelet-Lecrux, Anne, Sephton, Chantelle F
Published in Acta neuropathologica communications (12.02.2022)
Published in Acta neuropathologica communications (12.02.2022)
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No mutations in hnRNPA1 and hnRNPA2B1 in Dutch patients with amyotrophic lateral sclerosis, frontotemporal dementia, and inclusion body myopathy
Seelen, Meinie, Visser, Anne E, Overste, Daniel J, Kim, Hong J, Palud, A, Wong, Tsz H, van Swieten, John C, Scheltens, Philip, Voermans, Nicol C, Baas, Frank, de Jong, J.M.B.V, van der Kooi, Anneke J, de Visser, Marianne, Veldink, Jan H, Taylor, J. Paul, Van Es, Michael A, van den Berg, Leonard H
Published in Neurobiology of aging (01.08.2014)
Published in Neurobiology of aging (01.08.2014)
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Inside Front Cover: Volume 3 Issue 4
Yiu, Chunki, Liu, Yiming, Zhang, Chao, Zhou, Jingkun, Jia, Huiling, Wong, Tsz H., Huang, Xingcan, Li, Jian, Yao, Kuanming, Yau, Ming K., Zhao, Ling, Li, Hu, Zhang, Binbin, Park, Wooyoung, Zhang, Yuanting, Wang, Zuankai, Yu, Xinge
Published in SmartMat (Beijing, China) (01.12.2022)
Published in SmartMat (Beijing, China) (01.12.2022)
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YIU et al
Yiu, Chunki, Liu, Yiming, Zhang, Chao, Zhou, Jingkun, Jia, Huiling, Wong, Tsz H, Huang, Xingcan, Li, Jian, Yao, Kuanming, Yau, Ming K, Zhao, Ling, Hu, Li, Zhang, Binbin, Park, Wooyoung, Zhang, Yuanting, Wang, Zuankai, Yu, Xinge
Published in SmartMat (Beijing, China) (01.12.2022)
Published in SmartMat (Beijing, China) (01.12.2022)
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Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal dementia and GRN mutations: a genome-wide association study
Pottier, Cyril, Zhou, Xiaolai, Perkerson, Ralph B., Baker, Matt, Jenkins, Gregory D., Serie, Daniel J., Ghidoni, Roberta, Benussi, Luisa, Binetti, Giuliano, de Munain, Adolfo López, Zulaica, Miren, Moreno, Fermin, Le Ber, Isabelle, Pasquier, Florence, Hannequin, Didier, Sánchez-Valle, Raquel, Antonell, Anna, Lladó, Albert, Parsons, Tammee M., Finch, NiCole A., Finger, Elizabeth C., Lippa, Carol F., Huey, Edward D., Neumann, Manuela, Heutink, Peter, Synofzik, Matthis, Wilke, Carlo, Rissman, Robert A., Slawek, Jaroslaw, Sitek, Emilia, Johannsen, Peter, Nielsen, Jørgen E., Ren, Yingxue, van Blitterswijk, Marka, DeJesus-Hernandez, Mariely, Christopher, Elizabeth, Murray, Melissa E., Bieniek, Kevin F., Evers, Bret M., Ferrari, Camilla, Rollinson, Sara, Richardson, Anna, Scarpini, Elio, Fumagalli, Giorgio G., Padovani, Alessandro, Hardy, John, Momeni, Parastoo, Ferrari, Raffaele, Frangipane, Francesca, Maletta, Raffaele, Anfossi, Maria, Gallo, Maura, Petrucelli, Leonard, Suh, EunRan, Lopez, Oscar L., Wong, Tsz H., van Rooij, Jeroen G. J., Seelaar, Harro, Mead, Simon, Caselli, Richard J., Reiman, Eric M., Sabbagh, Marwan Noel, Kjolby, Mads, Nykjaer, Anders, Karydas, Anna M., Boxer, Adam L., Grinberg, Lea T., Grafman, Jordan, Spina, Salvatore, Oblak, Adrian, Mesulam, M-Marsel, Weintraub, Sandra, Geula, Changiz, Hodges, John R., Piguet, Olivier, Brooks, William S., Irwin, David J., Trojanowski, John Q., Lee, Edward B., Josephs, Keith A., Parisi, Joseph E., Ertekin-Taner, Nilüfer, Knopman, David S., Nacmias, Benedetta, Piaceri, Irene, Bagnoli, Silvia, Sorbi, Sandro, Gearing, Marla, Glass, Jonathan, Beach, Thomas G., Black, Sandra E., Masellis, Mario, Rogaeva, Ekaterina, Vonsattel, Jean-Paul, Honig, Lawrence S., Kofler, Julia, Bruni, Amalia C., Snowden, Julie, Mann, David, Pickering-Brown, Stuart
Published in Lancet neurology (30.04.2018)
Published in Lancet neurology (30.04.2018)
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