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Antonia Ratti
Antonia Ratti
Verified email at unimi.it
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Year
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis
CH Wu, C Fallini, N Ticozzi, PJ Keagle, PC Sapp, K Piotrowska, P Lowe, ...
Nature 488 (7412), 499-503, 2012
7262012
TDP‐43 is recruited to stress granules in conditions of oxidative insult
C Colombrita, E Zennaro, C Fallini, M Weber, A Sommacal, E Buratti, ...
Journal of neurochemistry 111 (4), 1051-1061, 2009
5932009
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
W Van Rheenen, A Shatunov, AM Dekker, RL McLaughlin, FP Diekstra, ...
Nature genetics 48 (9), 1043-1048, 2016
5882016
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1268-1283. e6, 2018
5782018
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS
BN Smith, N Ticozzi, C Fallini, AS Gkazi, S Topp, KP Kenna, EL Scotter, ...
Neuron 84 (2), 324-331, 2014
4112014
Physiological functions and pathobiology of TDP‐43 and FUS/TLS proteins
A Ratti, E Buratti
Journal of neurochemistry 138, 95-111, 2016
4022016
Discovery of a biomarker and lead small molecules to target r (GGGGCC)-associated defects in c9FTD/ALS
Z Su, Y Zhang, TF Gendron, PO Bauer, J Chew, WY Yang, E Fostvedt, ...
Neuron 83 (5), 1043-1050, 2014
3702014
TDP-43 and FUS RNA-binding proteins bind distinct sets of cytoplasmic messenger RNAs and differently regulate their post-transcriptional fate in motoneuron-like cells
C Colombrita, E Onesto, F Megiorni, A Pizzuti, FE Baralle, E Buratti, ...
Journal of Biological Chemistry 287 (19), 15635-15647, 2012
3172012
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
KP Kenna, PTC Van Doormaal, AM Dekker, N Ticozzi, BJ Kenna, ...
Nature genetics 48 (9), 1037-1042, 2016
2832016
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
W Van Rheenen, RAA Van Der Spek, MK Bakker, JJFA Van Vugt, PJ Hop, ...
Nature genetics 53 (12), 1636-1648, 2021
2782021
The long non-coding RNAs in neurodegenerative diseases: novel mechanisms of pathogenesis
P Riva, A Ratti, M Venturin
Current Alzheimer Research 13 (11), 1219-1231, 2016
2582016
High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis
L Corrado, A Ratti, C Gellera, E Buratti, B Castellotti, Y Carlomagno, ...
Human mutation 30 (4), 688-694, 2009
2462009
Poly(GP) proteins are a useful pharmacodynamic marker for C9ORF72-associated amyotrophic lateral sclerosis
TF Gendron, J Chew, JN Stankowski, LR Hayes, YJ Zhang, M Prudencio, ...
Science translational medicine 9 (383), eaai7866, 2017
2232017
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis
L Corrado, R Del Bo, B Castellotti, A Ratti, C Cereda, S Penco, G Sorarù, ...
Journal of medical genetics 47 (3), 190-194, 2010
2152010
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort
N Ticozzi, V Silani, AL LeClerc, P Keagle, C Gellera, A Ratti, F Taroni, ...
Neurology 73 (15), 1180-1185, 2009
1772009
Gene-specific mitochondria dysfunctions in human TARDBP and C9ORF72 fibroblasts
E Onesto, C Colombrita, V Gumina, MO Borghi, S Dusi, A Doretti, ...
Acta neuropathologica communications 4, 1-14, 2016
1742016
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis
BN Smith, SD Topp, C Fallini, H Shibata, HJ Chen, C Troakes, A King, ...
Science translational medicine 9 (388), eaad9157, 2017
1502017
The validation of the Italian Edinburgh cognitive and behavioural ALS screen (ECAS)
B Poletti, F Solca, L Carelli, F Madotto, A Lafronza, A Faini, A Monti, ...
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 17 (7-8), 489-498, 2016
1502016
Genetics of familial Amyotrophic lateral sclerosis
N Ticozzi, C Tiloca, C Morelli, C Colombrita, B Poletti, A Doretti, ...
Archives italiennes de biologie 149 (1), 65-82, 2011
1452011
A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories
C Akimoto, AE Volk, M van Blitterswijk, M Van den Broeck, CS Leblond, ...
Journal of medical genetics 51 (6), 419-424, 2014
1412014
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