Items where authors include "Rademakers, R."

Article

Mizielinska, S., Hautbergue, G.M. orcid.org/0000-0002-1621-261X, Gendron, T.F. et al. (5 more authors) (2025) Amyotrophic lateral sclerosis caused by hexanucleotide repeat expansions in C9orf72: from genetics to therapeutics. The Lancet Neurology, 24 (3). pp. 261-274. ISSN 1474-4422

Louros, N. orcid.org/0000-0002-4030-1022, Wilkinson, M. orcid.org/0000-0001-5490-613X, Tsaka, G. et al. (14 more authors) (2024) Local structural preferences in shaping tau amyloid polymorphism. Nature Communications, 15. 1028. ISSN 2041-1723

Dewan, R. orcid.org/0000-0002-7611-7032, Chia, R. orcid.org/0000-0002-4709-7423, Ding, J. et al. (469 more authors) (2021) Pathogenic huntingtin repeat expansions in patients with frontotemporal dementia and amyotrophic lateral sclerosis. Neuron, 109 (3). 448-460.e4. ISSN 0896-6273

Farhan, S.M.K., Howrigan, D.P., Abbott, L.E. et al. (32 more authors) (2019) Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein. Nature Neuroscience, 22 (12). pp. 1966-1974. ISSN 1097-6256

Dolzhenko, E., van Vugt, J.J.F.A., Shaw, R.J. et al. (42 more authors) (2017) Detection of long repeat expansions from PCR-free whole-genome sequence data. Genome Research , 27. pp. 1895-1903. ISSN 1088-9051

Kenna, K.P., van Doormaal, P.T.C., Dekker, A.M. et al. (92 more authors) (2016) NEK1 variants confer susceptibility to amyotrophic lateral sclerosis. Nature Genetics, 48 (9). pp. 1037-1042. ISSN 1061-4036

Van Deerlin, V.M., Sleiman, P.M.A., Martinez-Lage, M. et al. (97 more authors) (2010) Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP43 inclusions. Nature Genetics, 42 (3). pp. 234-239. ISSN 1061-4036,