Onderzoeker
Rosa Rademakers
- Trefwoorden:Scheikunde
Affiliaties
- VIB CMN - Neurodegeneratieve Hersenziekten (Onderzoeksgroep)
Lid
Vanaf15 jul 2019 → Heden
Publicaties
1 - 10 of 228 results
- Pathological, imaging and genetic characteristics support the existence of distinct TDP-43 types in non-FTLD brains(2019)
Auteurs: Keith A. Josephs, Melissa E. Murray, Nirubol Tosakulwong, Stephen D. Weigand, Amanda M. Serie, Ralph B. Perkerson, Billie J. Matchett, Clifford R., Jr. Jack, David S. Knopman, Ronald C. Petersen, et al.
Pagina's: 227 - 238 - A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity(2019)
Auteurs: Sven J. van der Lee, Olivia J. Conway, Iris Jansen, Minerva M. Carrasquillo, Luca Kleineidam, Erik van den Akker, Isabel Hernandez, Kristel R. van Eijk, Najada Stringa, Jason A. Chen, et al.
Pagina's: 237 - 250 - Ossified blood vessels in primary familial brain calcification elicit a neurotoxic astrocyte response(2019)
Auteurs: Yvette Zarb, Ulrike Weber-Stadlbauer, Daniel Kirschenbaum, Diana Rita Kindler, Juliet Richetto, Daniel Keller, Rosa Rademakers, Dennis W. Dickson, Andreas Pasch, Tatiana Byzova, et al.
Pagina's: 885 - 902 - EIF2AK3 variants in Dutch patients with Alzheimer's disease(2019)
Auteurs: Tsz Hang Wong, Sven J. van der Lee, Jeroen G. J. van Rooij, Lieke H. H. Meeter, Petra Frick, Shamiram Melhem, Harro Seelaar, M. Arfan Ikram, Annemieke J. Rozemuller, Henne Holstege, et al.
Aantal pagina's: 8 - Enhanced phosphorylation of T153 in soluble tau is a defining biochemical feature of the A152T tau risk variant(2019)
Auteurs: Yari Carlomagno, Dah-eun Chloe Chung, Mei Yue, Aishe Kurti, Nicole M. Avendano, Monica Castanedes-Casey, Kelly M. Hinkle, Karen Jansen-West, Lillian M. Daughrity, Jimei Tong, et al.
Aantal pagina's: 13 - Limbic-predominant age-related TDP-43 encephalopathy (LATE): consensus working group report(2019)
Auteurs: Peter T. Nelson, Dennis W. Dickson, John Q. Trojanowski, Clifford R., Jr. Jack, Patricia A. Boyle, Konstantinos Arfanakis, Rosa Rademakers, Irina Alafuzoff, Johannes Attems, Carol Brayne, et al.
Pagina's: 1503 - 1527 - Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD(2019)
Auteurs: Cyril Pottier, Yingxue Ren, Ralph B., III Perkerson, Matt Baker, Gregory D. Jenkins, Marka van Blitterswijk, Mariely DeJesus-Hernandez, Jeroen G. J. van Rooij, Melissa E. Murray, Elizabeth Christopher, et al.
Pagina's: 879 - 899 - Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia(2019)
Auteurs: Luke W. Bonham, Natasha Z. R. Steele, Celeste M. Karch, Iris Broce, Ethan G. Geier, Natalie L. Wen, Parastoo Momeni, John Hardy, Zachary A. Miller, Maria Luisa Gorno-Tempini, et al.
Aantal pagina's: 10 - Heterochromatin anomalies and double-stranded RNA accumulation underlie C9orf72 poly(PR) toxicity(2019)
Auteurs: Yong-Jie Zhang, Lin Guo, Patrick K. Gonzales, Tania F. Gendron, Yanwei Wu, Karen Jansen-West, Aliesha D. O'Raw, Sarah R. Pickles, Mercedes Prudencio, Yari Carlomagno, et al.
Pagina's: 707 - + - Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: results from the GENFI study(2018)
Auteurs: Daniela Galimberti, Giorgio C. Fumagalli, Chiara Fenoglio, Sara M.G. Cioffi, Andrea Arighi, Maria Serpente, Barbara Borroni, Alessandro Padovani, Fabrizio Tagliavini, Mario Masellis, et al.
Pagina's: 245.e9 - 245.e12