IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

CEREDA, CRISTINA
 Distribuzione geografica
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Continente #
AS - Asia 12.347
NA - Nord America 12.069
EU - Europa 10.740
SA - Sud America 1.235
AF - Africa 228
OC - Oceania 155
Continente sconosciuto - Info sul continente non disponibili 7
Totale 36.781
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Nazione #
US - Stati Uniti d'America 11.573
IT - Italia 3.752
CN - Cina 3.349
SG - Singapore 3.263
DE - Germania 1.680
GB - Regno Unito 1.450
HK - Hong Kong 1.282
BD - Bangladesh 1.213
VN - Vietnam 1.145
BR - Brasile 919
RU - Federazione Russa 790
SE - Svezia 532
FR - Francia 517
IN - India 516
NL - Olanda 514
KR - Corea 373
FI - Finlandia 340
CA - Canada 329
IE - Irlanda 289
JP - Giappone 246
ID - Indonesia 216
TR - Turchia 178
AU - Australia 144
ES - Italia 118
AR - Argentina 115
DK - Danimarca 112
IL - Israele 109
PL - Polonia 87
AT - Austria 83
MX - Messico 81
BE - Belgio 73
UA - Ucraina 73
IQ - Iraq 59
CI - Costa d'Avorio 57
CH - Svizzera 53
TW - Taiwan 53
CL - Cile 50
ZA - Sudafrica 47
PH - Filippine 45
EC - Ecuador 44
SA - Arabia Saudita 36
MY - Malesia 35
PK - Pakistan 35
PT - Portogallo 33
CO - Colombia 31
NO - Norvegia 28
IR - Iran 26
MA - Marocco 26
GR - Grecia 24
CZ - Repubblica Ceca 22
AZ - Azerbaigian 21
EU - Europa 21
NP - Nepal 21
RO - Romania 21
DZ - Algeria 20
CR - Costa Rica 19
LT - Lituania 18
HR - Croazia 17
KE - Kenya 17
TH - Thailandia 17
BO - Bolivia 16
HU - Ungheria 15
TN - Tunisia 15
UZ - Uzbekistan 15
AE - Emirati Arabi Uniti 14
EG - Egitto 14
JM - Giamaica 14
PE - Perù 14
PY - Paraguay 14
UY - Uruguay 14
AL - Albania 13
HN - Honduras 13
VE - Venezuela 13
BG - Bulgaria 12
JO - Giordania 12
LU - Lussemburgo 12
RS - Serbia 12
SI - Slovenia 11
MO - Macao, regione amministrativa speciale della Cina 9
NZ - Nuova Zelanda 9
SC - Seychelles 9
NG - Nigeria 8
LV - Lettonia 7
MD - Moldavia 7
PA - Panama 7
SK - Slovacchia (Repubblica Slovacca) 7
SV - El Salvador 7
ET - Etiopia 6
KG - Kirghizistan 6
LB - Libano 6
NI - Nicaragua 6
OM - Oman 6
PS - Palestinian Territory 6
EE - Estonia 5
GT - Guatemala 5
KZ - Kazakistan 5
MT - Malta 5
QA - Qatar 5
CY - Cipro 4
GH - Ghana 4
Totale 36.739
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Città #
Singapore 1.943
Ashburn 1.394
Milan 1.061
Southend 1.003
Hong Kong 993
San Jose 960
Hanover 775
Dallas 724
Council Bluffs 616
Santa Clara 609
Chandler 544
Beijing 477
Los Angeles 471
Hefei 346
New York 330
Frankfurt am Main 315
Ho Chi Minh City 312
Fairfield 311
Hanoi 298
Seattle 284
Dublin 281
Seoul 259
Helsinki 250
Lauterbourg 230
Boardman 227
Princeton 218
Rome 194
Bengaluru 189
Wilmington 180
Moscow 166
Jakarta 165
Shanghai 160
Buffalo 158
Houston 156
Ann Arbor 145
Woodbridge 142
Guangzhou 141
Chicago 134
Toronto 115
Cambridge 112
Munich 108
Tokyo 106
Nanjing 101
Naples 96
Turin 95
Dearborn 90
Des Moines 80
Nuremberg 77
São Paulo 76
Phoenix 74
Cangzhou 72
Istanbul 71
Berlin 70
Atlanta 68
Da Nang 68
The Dalles 68
Redwood City 65
London 63
Hangzhou 60
Abidjan 57
Piscataway 56
Warsaw 55
Bologna 54
Washington 51
Florence 50
Jinan 48
Columbus 47
Haiphong 47
Vienna 47
Amsterdam 46
San Diego 45
Tianjin 44
Genoa 41
Rishon LeTsiyyon 41
Montreal 40
North Bergen 39
Utrecht 39
Catania 36
Orem 36
Philadelphia 36
Dong Ket 35
Medford 35
Redmond 35
Newark 34
Ottawa 34
Pasadena 34
Boston 33
Lappeenranta 33
Mountain View 33
Suzhou 33
Brussels 32
Denver 32
Shenyang 32
Charlotte 31
Mumbai 31
Palermo 31
San Francisco 31
Taipei 31
Bari 30
Fuzhou 30
Totale 20.501
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Nome #
Alzheimer’s, parkinson’s disease and amyotrophic lateral sclerosis gene expression patterns divergence reveals different grade of RNA metabolism involvement 585
Deficit neonatale di vitamina b12 secondario a carenza materna: focus su pattern alimentari e intake nutrizionali in gravidanza 516
HuR interacts with lincBRN1a and lincBRN1b during neuronal stem cells differentiation 508
Transcriptional induction of the heat shock protein B8 mediates the clearance of misfolded proteins responsible for motor neuron diseases 474
Individual risk prediction of high grade prostate cancer based on the combination between total prostate-specific antigen (PSA) and free to total PSA ratio 469
Reference intervals of thyroid hormones and related indices to enhance the assessment of thyroid status in childhood and adolescence 450
Vitamin B12 deficiency in newborns: impact on individual’s health status and healthcare costs 437
Hydrogen peroxide-mediated induction of SOD1 gene transcription is independent from Nrf2 in a cellular model of neurodegeneration 420
HSC70 expression is reduced in lymphomonocytes of sporadic ALS patients and contributes to TDP-43 accumulation 415
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology 350
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways 332
The Chaperone HSPB8 Reduces the Accumulation of Truncated TDP-43 Species in Cells and Protects Against TDP-43-Mediated Toxicity 332
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 329
Oxygen sensing in neurodegenerative diseases: current mechanisms, implication of transcriptional response and pharmacological modulation 325
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis 314
Raman spectroscopy reveals biochemical differences in plasma derived extracellular vesicles from sporadic amyotrophic lateral sclerosis patients 306
RNA molecular signature profiling in PBMCs of sporadic ALS patients: HSP70 overexpression is associated with nuclear SOD1 298
Deficit neonatale e materno di vitamina B12: pattern alimentari e intake nutrizionali durante la gravidanza 297
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis 297
Newborn screening for X-linked adrenoleukodystrophy in Italy: Diagnostic algorithm and disease monitoring 284
Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia 278
The role of Extracellular Vesicles (EVs) in Amyotrophic Lateral Sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) 277
Stroke and Stroke-Like Episodes: Recurrent Manifestations in GLUT1 Deficiency Syndrome 270
Proteostasis and ALS : protocol for a phase II, randomised, double-blind, placebo-controlled, multicentre clinical trial for colchicine in ALS (Co-ALS) 261
Curcumin and Novel Synthetic Analogs in Cell-Based Studies of Alzheimer's Disease 260
Dissecting the Effect of a 3D Microscaffold on the Transcriptome of Neural Stem Cells with Computational Approaches : A Focus on Mechanotransduction 257
Implications for the lncRNA ZEB1-AS1 in sporadic ALS : deregulation in neuronal differentiation and characterization of a novel disease pathway 254
TDP-43 PROTEINOPATHIES: THE ROLE OF EXTRACELLULAR VESICLES 239
Advances in Tissue Engineering and Innovative Fabrication Techniques for 3-D-Structures : Translational Applications in Neurodegenerative Diseases 239
An over-oxidized form of superoxide dismutase found in sporadic amyotrophic lateral sclerosis with bulbar onset shares a toxic mechanism with mutant SOD1 238
Novel frontiers in aicardi-goutières syndrome: association between a rnu7-1 variant and histone dysfunctions 236
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson's disease 233
The role of clinical and neuroimaging features in the diagnosis of CADASIL 229
Biomaterials in Neurodegenerative Disorders : A Promising Therapeutic Approach 229
Relazione tra deficit di vitamina B12 evidenziato allo screening neonatale e valori di creatina nella diade -mamma bambino nelle prime epoche di vita 226
HuR’s interaction with lincBRN1a and lincBRN1b is implicated in neuronal stem cells differentiation 226
A pilot study assessing T1-weighted muscle MRI in amyotrophic lateral sclerosis (ALS) 223
Mitophagy dysfunction in PBMCs of sporadic ALS patients 223
Transcriptional characterization of subcutaneous adipose tissue in obesity affected women highlights metabolic dysfunction and implications for lncRNAs 223
Extracellular vesicles and the secretion of TDP species in Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Lobar Degeneration (FTLD) 222
Cobalamin deficiency in the maternal-newborn dyad identified by neonatal screening: preliminary data from an observational study 217
From Neuronal Differentiation of iPSCs to 3D Neuro-Organoids : Modelling and Therapy of Neurodegenerative Diseases 217
Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases 216
C9ORF72 repeat expansion in a large Italian ALS cohort : evidence of a founder effect 215
A Surveillance Function of the HSPB8-BAG3-HSP70 Chaperone complex ensures stress granule integrity and dynamism 215
The mitogenome relationships and phylogeography of barn swallows (Hirundo rustica) 214
RNA-seq Characterization of Sex-Differences in Adipose Tissue of Obesity Affected Patients: Computational Analysis of Differentially Expressed Coding and Non-Coding RNAs 214
Transcriptome Analysis of Subcutaneous Adipose Tissue from Severely Obese Patients Highlights Deregulation Profiles in Coding and Non-Coding Oncogenes 213
Reduction of hRNase H2 activity in Aicardi-Goutières syndrome cells leads to replication stress and genome instability 211
Fast quantification of extracellular vesicles levels in early breast cancer patients by Single Molecule Detection Array (SiMoA) 209
Bioink Composition and Printing Parameters for 3D Modeling Neural Tissue 208
Role of epigenetics and alterations in RNA metabolism in leukodystrophies 207
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis 207
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis : identification of novel mutations 207
Neurodegenerative Disease-Associated TDP-43 Fragments Are Extracellularly Secreted with CASA Complex Proteins 207
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data 206
How PQC inhibition modulates miRNA loading in large and small extracellular vesicles 204
Generation of three iPSC lines from fibroblasts of a patient with Aicardi Goutières Syndrome mutated in TREX1 204
Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia 200
Amino Acid Patterns in Childdren with Autistic Spectrum Disorder: A Preliminary Biochemical Evaluation 199
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia 198
I deficit di vitamina B12 di origine materna nel neonato: sfide attuali e future = Neonatal cobalamin deficiency secondary to maternal causes: today and future challenges 197
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis 197
Transcriptional profiling and functional characterization of three genetic variants in SLC16A2 gene 195
Bisdemethoxycurcumin (BDC)-Loaded H-Ferritin-Nanocages Mediate the Regulation of Inflammation in Alzheimer's Disease Patients 195
Clinical pregenetic screening for stroke monogenic diseases: results from Lombardia GENS registry 195
The absence that makes the difference: choroidal abnormalities in Legius syndrome 194
Extracellular vesicles cooperate with PQC system for the clearance of TDP-43 species associated with ALS and FTD 193
LnRNAs associated with neuronal development and oncogenesis are deregulated in SOD1-G93A murine model of amyotrophic lateral sclerosis 191
Ubiquilin 2 mutations in Italians patients with amyotrophic lateral sclerosis and frontotemporal dementia 190
Nuclear Phospho-SOD1 Protects DNA from Oxidative Stress Damage in Amyotrophic Lateral Sclerosis 190
Generation of three isogenic induced Pluripotent Stem Cell lines (iPSCs) from fibroblasts of a patient with Aicardi Goutières Syndrome carrying a c.2471G>A dominant mutation in IFIH1 gene 188
Implication of the oncogenic lncRNA ZEB1-AS1 mediated pathway in sporadic ALS pathogenesis 187
Covidarray : A microarray-based assay with high sensitivity for the detection of sars-cov-2 in nasopharyngeal swabs 187
Redox Imbalance in Neurological Disorders in Adults and Children 186
Case Report: Novel Compound Heterozygous RNASEH2B Mutations Cause Aicardi–Goutières Syndrome 186
Genetic variation in DPP6 gene is not associated with susceptibility to Amyotrophic Lateral Sclerosis in two European population 185
Trehalose treatment finely tunes the mitophagy pathway in PBMCs of sALS patients 182
Global deregulation of lncRNAs involved in neuronal development could play a role in ALS 181
MINCR : A long non-coding RNA shared between cancer and neurodegeneration 180
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis 178
HuR’s interaction with lincBRN1a and lincBRN1b is implicated in neuronal stem cells differentiation 178
Establishment of three iPSC lines from fibroblasts of a patient with Aicardi Goutières syndrome mutated in RNaseH2B 176
Effect of the 3D micro-scaffold Nichoid on the transcriptome of Neural Stem Cells 175
C9orf72 repeat expansions are restricted to the ALS-FTD spectrum 172
Pathological Proteins Are Transported by Extracellular Vesicles of Sporadic Amyotrophic Lateral Sclerosis Patients 172
Lysosomes Dysfunction Causes Mitophagy Impairment in PBMCs of Sporadic ALS Patients 172
Doxorubicin and congo red effectiveness on prion infectivity in golden Syrian hamster 171
HuR’s interaction with lincBRN1a and lincBRN1b is implicated in neuronal stem cells differentiation 169
Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis 169
Towards genomic-Newborn Screening: Technical feasibility of Exome Sequencing starting from dried blood spots 166
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS 166
Neural precursor cells expanded inside the 3d micro-scaffold nichoid present different non-coding rnas profiles and transcript isoforms expression : Possible epigenetic modulation by 3d growth 166
The role of extracellular vesicles in the removal of aggregated TDP43 responsible for ALS/FTD diseases 164
Mutation analysis of the VPS54 gene in ALS patients 163
Further insights into Allan-Herndon-Dudley syndrome: a novel SLC16A2 splice site variant 162
The Effect of Healthy Lifestyle Strategies on the Management of Insulin Resistance in Children and Adolescents with Obesity: A Narrative Review 161
Molecular Genetics of GLUT1DS Italian Pediatric Cohort: 10 Novel Disease-Related Variants and Structural Analysis 161
Neural precursors cells expanded in a 3D micro-engineered niche present enhanced therapeutic efficacy in vivo 160
Detection of SARS-CoV-2 genome and whole transcriptome sequencing in frontal cortex of COVID-19 patients 158
Totale 23.927
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Categoria #
all - tutte 109.676
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 109.676
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021249 0 0 0 0 0 0 0 0 0 0 0 249
2021/20222.773 151 109 113 233 260 208 241 213 374 276 189 406
2022/20232.370 249 268 183 174 217 367 114 128 289 66 208 107
2023/20242.599 88 167 152 271 464 220 151 203 140 163 241 339
2024/20256.792 254 590 251 586 443 437 411 632 402 668 909 1.209
2025/202619.198 1.373 1.045 1.569 1.006 1.173 1.206 2.632 1.191 2.541 1.409 2.114 1.939
Totale 38.289