SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

SCOTTON, Chiara
 Distribuzione geografica
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Continente #
NA - Nord America 2.047
EU - Europa 1.242
AS - Asia 447
SA - Sud America 38
AF - Africa 6
Totale 3.780
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Nazione #
US - Stati Uniti d'America 2.042
PL - Polonia 722
CN - Cina 191
SG - Singapore 143
DE - Germania 131
IT - Italia 104
UA - Ucraina 83
GB - Regno Unito 70
TR - Turchia 68
BR - Brasile 33
FI - Finlandia 31
SE - Svezia 29
BE - Belgio 27
RU - Federazione Russa 18
ID - Indonesia 17
VN - Vietnam 11
CZ - Repubblica Ceca 7
NL - Olanda 6
CA - Canada 5
ES - Italia 3
FR - Francia 3
IQ - Iraq 3
AR - Argentina 2
AT - Austria 2
CL - Cile 2
KR - Corea 2
MA - Marocco 2
MY - Malesia 2
PK - Pakistan 2
ZA - Sudafrica 2
AO - Angola 1
BD - Bangladesh 1
DK - Danimarca 1
DZ - Algeria 1
EC - Ecuador 1
HU - Ungheria 1
IN - India 1
IR - Iran 1
KZ - Kazakistan 1
LT - Lituania 1
LV - Lettonia 1
MD - Moldavia 1
NP - Nepal 1
PH - Filippine 1
QA - Qatar 1
RO - Romania 1
TW - Taiwan 1
Totale 3.780
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Città #
Warsaw 722
Fairfield 310
Woodbridge 214
Chandler 163
Ann Arbor 159
Houston 154
Seattle 126
Ashburn 116
Jacksonville 110
Singapore 98
Cambridge 97
Wilmington 94
Santa Clara 80
Beijing 45
New York 43
Ferrara 37
Izmir 34
Nanjing 31
Princeton 26
Bremen 25
Shanghai 23
Brussels 22
Boardman 20
Shenyang 18
Jakarta 16
Milan 16
Helsinki 14
Dearborn 12
Falls Church 12
San Diego 12
London 11
Dong Ket 10
Nanchang 10
Jinan 9
Munich 9
Brno 7
Hebei 6
Rome 6
Trebaseleghe 6
Ningbo 5
Redwood City 5
Toronto 5
Addison 4
Cagliari 4
Des Moines 4
Jiaxing 4
Lanzhou 4
Mountain View 4
Phoenix 4
Tianjin 4
Waanrode 4
Bologna 3
Changsha 3
Haikou 3
Kunming 3
Los Angeles 3
Orange 3
Redmond 3
San Mateo 3
Argenta 2
Austin 2
Biloxi 2
Chicago 2
Hefei 2
Johannesburg 2
Monmouth Junction 2
Naples 2
Norwalk 2
Pisa 2
Reggio Nell'emilia 2
San Giovanni Rotondo 2
Shah Alam 2
Tappahannock 2
Varazze 2
Zhengzhou 2
Acton 1
Agadir 1
Algiers 1
Almaty 1
Alpedrete 1
Amsterdam 1
Andover 1
Araguari 1
Augusta 1
Baghdad 1
Barcelona 1
Barra Bonita 1
Barra do Corda 1
Belo Horizonte 1
Bollate 1
Bono 1
Campos dos Goytacazes 1
Capâo Bonito 1
Carlos Barbosa 1
Carmo da Cachoeira 1
Catu 1
Changchun 1
Chengdu 1
Chisinau 1
Council Bluffs 1
Totale 3.055
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Nome #
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy 336
POPDC1S201F causes muscular dystrophy and arrhythmia by affecting protein trafficking 314
Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression 307
STUDIO DELL’ESOMA MEDIANTE TECNOLOGIE DI GENOTIPIZZAZIONE AD ALTA EFFICIENZA: SEQUENZIAMENTO DI NUOVA GENERAZIONE (NGS) e IBRIDAZIONE GENOMICA COMPARATIVA (CGH), PER L’IDENTIFICAZIONE DI NUOVI GENI MALATTIA IN PATOLOGIE NEUROMUSCOLARI. 197
Duchenne muscular dystrophy: From diagnosis to therapy 195
Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype 182
Transcriptomics analysis in collagen VI myopathy: Role of circadian genes using novel fluidic card tools 181
Omics approach and novel biostatistic tools identified RPL3L as potential genetic modifier of clinical severity in female carriers of Duchenne muscle dystrophy 158
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype 153
Paternal germline mosaicism in collagen VI related myopathies 148
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia 146
Validation of genetic modifiers for Duchenne muscular dystrophy: a multicentre study assessing SPP1 and LTBP4 variants 136
The DMD Locus Harbours Multiple Long Non-Coding RNAs Which Orchestrate and Control Transcription of Muscle Dystrophin mRNA Isoforms 133
Rapid, comprehensive analysis of the dystrophin transcript by a custom micro-fluidic exome array 122
SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers. 118
Biomarkers in rare neuromuscular diseases. 116
A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation 112
Biomarkers in Rare Diseases 110
Muscle Proteomics Reveals Novel Insights into the Pathophysiological Mechanisms of Collagen VI Myopathies 109
Complex phenotypes associated with STIM1 mutations in both coiled coil and EF-hand domains 109
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family 101
null 88
The Popeye Domain Containing Genes and their Function in Striated Muscle 84
Report of a novel ATP7A mutation causing distal motor neuropathy 83
NMD CHIP: Un Progetto Europeo per la diagnosi delle patologie neuromuscolari 75
Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3 22
Totale 3.835
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Categoria #
all - tutte 14.900
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 14.900
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020551 0 0 0 0 0 103 103 83 78 89 54 41
2020/2021578 48 44 42 57 32 60 41 57 26 77 66 28
2021/2022309 15 32 10 14 13 15 28 16 12 27 26 101
2022/2023348 31 47 7 49 75 41 16 21 27 3 12 19
2023/2024189 14 16 11 8 8 52 2 12 7 1 0 58
2024/2025362 10 7 65 49 128 103 0 0 0 0 0 0
Totale 3.835