SCOTTON, Chiara
 Distribuzione geografica
Continente #
NA - Nord America 1.933
EU - Europa 1.196
AS - Asia 296
SA - Sud America 1
Totale 3.426
Nazione #
US - Stati Uniti d'America 1.930
PL - Polonia 722
CN - Cina 172
DE - Germania 127
IT - Italia 96
UA - Ucraina 83
TR - Turchia 67
GB - Regno Unito 62
SE - Svezia 29
SG - Singapore 28
FI - Finlandia 22
RU - Federazione Russa 18
BE - Belgio 17
VN - Vietnam 11
ID - Indonesia 9
CZ - Repubblica Ceca 7
NL - Olanda 4
CA - Canada 3
ES - Italia 3
FR - Francia 3
KR - Corea 2
MY - Malesia 2
BD - Bangladesh 1
CL - Cile 1
DK - Danimarca 1
IN - India 1
IR - Iran 1
KZ - Kazakistan 1
MD - Moldavia 1
PH - Filippine 1
RO - Romania 1
Totale 3.426
Città #
Warsaw 722
Fairfield 310
Woodbridge 214
Chandler 163
Ann Arbor 159
Houston 154
Seattle 126
Ashburn 116
Jacksonville 110
Cambridge 97
Wilmington 94
Beijing 45
New York 43
Ferrara 37
Izmir 34
Nanjing 31
Princeton 26
Bremen 25
Boardman 20
Shanghai 20
Shenyang 18
Milan 14
Singapore 13
Brussels 12
Dearborn 12
Falls Church 12
San Diego 12
Dong Ket 10
Nanchang 10
Jakarta 8
Jinan 8
Brno 7
Hebei 6
London 6
Munich 6
Rome 6
Trebaseleghe 6
Helsinki 5
Ningbo 5
Redwood City 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
Kunming 3
Orange 3
Redmond 3
San Mateo 3
Toronto 3
Argenta 2
Austin 2
Biloxi 2
Chicago 2
Haikou 2
Hefei 2
Monmouth Junction 2
Norwalk 2
Pisa 2
Reggio Nell'emilia 2
Shah Alam 2
Tappahannock 2
Varazze 2
Zhengzhou 2
Acton 1
Almaty 1
Alpedrete 1
Andover 1
Augusta 1
Barcelona 1
Bollate 1
Bono 1
Changchun 1
Chengdu 1
Chisinau 1
Council Bluffs 1
Guarda Veneta 1
Hangzhou 1
Hanoi 1
Herk-de-stad 1
Hounslow 1
Kilburn 1
Leawood 1
Los Angeles 1
Madrid 1
Manila 1
Modena 1
Osnabrück 1
Palermo 1
Palm Bay 1
Piacenza 1
Prescot 1
Prineville 1
Sabz 1
Totale 2.842
Nome #
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy 322
POPDC1S201F causes muscular dystrophy and arrhythmia by affecting protein trafficking 303
Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression 296
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. 185
Duchenne muscular dystrophy: From diagnosis to therapy 182
Transcriptomics analysis in collagen VI myopathy: Role of circadian genes using novel fluidic card tools 148
Omics approach and novel biostatistic tools identified RPL3L as potential genetic modifier of clinical severity in female carriers of Duchenne muscle dystrophy 146
Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype 143
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype 140
Paternal germline mosaicism in collagen VI related myopathies 134
Validation of genetic modifiers for Duchenne muscular dystrophy: a multicentre study assessing SPP1 and LTBP4 variants 126
The DMD Locus Harbours Multiple Long Non-Coding RNAs Which Orchestrate and Control Transcription of Muscle Dystrophin mRNA Isoforms 124
Rapid, comprehensive analysis of the dystrophin transcript by a custom micro-fluidic exome array 112
Biomarkers in rare neuromuscular diseases. 108
SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers. 106
A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation 105
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia 102
Muscle Proteomics Reveals Novel Insights into the Pathophysiological Mechanisms of Collagen VI Myopathies 101
Biomarkers in Rare Diseases 100
Complex phenotypes associated with STIM1 mutations in both coiled coil and EF-hand domains 97
null 88
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family 86
The Popeye Domain Containing Genes and their Function in Striated Muscle 76
Report of a novel ATP7A mutation causing distal motor neuropathy 72
NMD CHIP: Un Progetto Europeo per la diagnosi delle patologie neuromuscolari 63
Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3 16
Totale 3.481
Categoria #
all - tutte 11.630
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 11.630


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020958 111 54 51 117 74 103 103 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
2024/20258 8 0 0 0 0 0 0 0 0 0 0 0
Totale 3.481