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Cristina Cereda
Cristina Cereda
Director of Newborn Screening and Metabolic Diseases, Hospital V. Buzzi - Milan
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Titel
Zitiert von
Zitiert von
Jahr
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
ET Cirulli, BN Lasseigne, S Petrovski, PC Sapp, PA Dion, CS Leblond, ...
SCIENCE, 2015
9892015
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
5892016
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
5792018
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1
YJ Crow, DS Chase, J Lowenstein Schmidt, M Szynkiewicz, GMA Forte, ...
American journal of medical genetics Part A 167 (2), 296-312, 2015
5612015
Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study
GI Rice, G Forte, M Szynkiewicz, DS Chase, A Aeby, MS Abdel-Hamid, ...
The Lancet Neurology 12 (12), 1159-1169, 2013
4222013
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
A surveillance function of the HSPB8-BAG3-HSP70 chaperone complex ensures stress granule integrity and dynamism
M Ganassi, D Mateju, I Bigi, L Mediani, I Poser, HO Lee, SJ Seguin, ...
Molecular cell 63 (5), 796-810, 2016
2942016
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
KP Kenna, PTC van Doormaal, AM Dekker, N Ticozzi, BJ Kenna, ...
NATURE GENETICS, 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
2792021
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
An over-oxidized form of superoxide dismutase found in sporadic amyotrophic lateral sclerosis with bulbar onset shares a toxic mechanism with mutant SOD1
S Guareschi, E Cova, C Cereda, M Ceroni, E Donetti, DA Bosco, D Trotti, ...
Proceedings of the National Academy of Sciences 109 (13), 5074-5079, 2012
1952012
Rivaroxaban or aspirin for patent foramen ovale and embolic stroke of undetermined source: a prespecified subgroup analysis from the NAVIGATE ESUS trial
SE Kasner, B Swaminathan, P Lavados, M Sharma, K Muir, R Veltkamp, ...
The Lancet Neurology 17 (12), 1053-1060, 2018
1832018
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease
CM Lill, A Rengmark, L Pihlstrom, I Fogh, A Shatunov, PM Sleiman, ...
ALZHEIMERS & DEMENTIA, 2015
1752015
GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings
A Caciotti, SC Garman, Y Rivera-Colón, E Procopio, S Catarzi, L Ferri, ...
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1812 (7), 782-790, 2011
1702011
SOD1 transcriptional and posttranscriptional regulation and its potential implications in ALS
P Milani, S Gagliardi, E Cova, C Cereda
Neurology research international 2011, 2011
1682011
SOD1 in amyotrophic lateral sclerosis:“ambivalent” behavior connected to the disease
O Pansarasa, M Bordoni, L Diamanti, D Sproviero, S Gagliardi, C Cereda
International journal of molecular sciences 19 (5), 1345, 2018
1532018
Amyotrophic lateral sclerosis and environmental factors
V Bozzoni, O Pansarasa, L Diamanti, G Nosari, C Cereda, M Ceroni
Functional neurology 31 (1), 7, 2016
1502016
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis
I Fogh, A Ratti, C Gellera, K Lin, C Tiloca, V Moskvina, L Corrado, ...
HUMAN MOLECULAR GENETICS, 2014
1382014
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia
RL McLaughlin, D Schijven, W van Rheenen, KR van Eijk, M O'Brien, ...
NATURE COMMUNICATIONS, 2017
1362017
SOD1 and DJ-1 converge at Nrf2 pathway: a clue for antioxidant therapeutic potential in neurodegeneration
P Milani, G Ambrosi, O Gammoh, F Blandini, C Cereda
Oxidative medicine and cellular longevity 2013, 2013
1332013
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