ARMAROLI, Annarita
 Distribuzione geografica
Continente #
NA - Nord America 1.567
EU - Europa 724
AS - Asia 256
SA - Sud America 10
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
Totale 2.559
Nazione #
US - Stati Uniti d'America 1.566
PL - Polonia 332
CN - Cina 121
DE - Germania 112
IT - Italia 95
SG - Singapore 61
UA - Ucraina 54
TR - Turchia 47
GB - Regno Unito 46
FI - Finlandia 23
SE - Svezia 23
RU - Federazione Russa 18
BE - Belgio 14
ID - Indonesia 11
CL - Cile 6
BR - Brasile 4
IR - Iran 4
VN - Vietnam 4
ES - Italia 3
KR - Corea 3
NL - Olanda 2
AE - Emirati Arabi Uniti 1
AU - Australia 1
CA - Canada 1
CZ - Repubblica Ceca 1
EU - Europa 1
IN - India 1
KZ - Kazakistan 1
MY - Malesia 1
PH - Filippine 1
RO - Romania 1
Totale 2.559
Città #
Warsaw 332
Fairfield 246
Woodbridge 192
Chandler 147
Ann Arbor 140
Ashburn 102
Houston 88
Cambridge 82
Wilmington 78
Jacksonville 75
Seattle 74
Ferrara 42
Singapore 39
Beijing 34
Izmir 29
New York 29
Milan 22
Bremen 21
Princeton 21
Shanghai 18
Boardman 14
Falls Church 14
Nanjing 14
Shenyang 14
Brussels 12
San Diego 12
Jakarta 11
Helsinki 10
Los Angeles 7
Santa Clara 7
Addison 6
Des Moines 6
Hebei 6
London 6
Changsha 5
Munich 5
Nanchang 5
Rome 5
Santiago 5
Cagliari 4
Dearborn 4
São Paulo 4
Trebaseleghe 4
Dong Ket 3
Jinan 3
Ningbo 3
Redwood City 3
Seocho-gu 3
Tampa 3
Tianjin 3
Zhengzhou 3
Florence 2
Jiaxing 2
Kunming 2
Lanzhou 2
Monmouth Junction 2
Orange 2
Phoenix 2
Redmond 2
Rho 2
Varazze 2
Verona 2
Waanrode 2
Almaty 1
Alpedrete 1
Andover 1
Barcelona 1
Birmingham 1
Bologna 1
Brno 1
Chicago 1
Council Bluffs 1
Edinburgh 1
George Town 1
Guarda Veneta 1
Haikou 1
Hangzhou 1
Hanoi 1
Jurong Town 1
Kilburn 1
Madrid 1
Manila 1
Modena 1
Mountain View 1
Norwalk 1
Palm Bay 1
Prescot 1
Reggio Nell'emilia 1
Sabz 1
San Mateo 1
Sydney 1
Taizhou 1
Toronto 1
Wandsworth 1
Yellow Springs 1
Totale 2.071
Nome #
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy 327
Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression 299
Omics approach and novel biostatistic tools identified RPL3L as potential genetic modifier of clinical severity in female carriers of Duchenne muscle dystrophy 151
Transcriptomics analysis in collagen VI myopathy: Role of circadian genes using novel fluidic card tools 148
Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype 146
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype 143
Paternal germline mosaicism in collagen VI related myopathies 136
Biochemical characterization of patients with in-frame or out-of-frame DMD deletions pertinent to exon 44 or 45 skipping. 129
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: Implications for clinical trials 126
Cyclosporine a in Ullrich congenital muscular dystrophy: Long-term results 118
Early corticosteroid treatment in 4 duchenne muscular dystrophy patients: 14-year follow-up 111
A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation 107
Genetic counseling for women referred for advanced maternal age: a telegenetic approach 106
Huntington's disease-like presentation in Spinocerebellar ataxia type 12 105
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia 105
Becker muscular dystrophy due to an intronic splicing mutation inducing a dual dystrophin transcript 81
Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies 65
Functional characterization of two novel mutations in scn5a associated with brugada syndrome identified in Italian patients 49
Hypospadias prevalence in the Emilia Romagna Region registry: Increasing or methodology? 47
TRANSCRIPTIONAL PROFILING IN DUCHENNE MUSCULAR DYSTROPHY REVEALED A PROFOUND DEREGULATION OF BOTH CIRCADIAN RHYTHM GENES AND GENES INVOLVED IN MUSCLE REGENERATIVE PROCESS AS POSSIBLE NEW DISEASE BIOMARKERS 45
Chromatin configuration, RNA and protein studies identified novel DNA elements that influence the dystrophin transcription dynamics 26
ncRNAs originating from the dystrophin gene as biomarker for assessing antisense therapy 21
TeleNEwCARe: An Italian case-control telegenetics study in patients with Hereditary NEuromuscular and CARdiac diseases 14
Totale 2.605
Categoria #
all - tutte 11.907
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 11.907


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020469 0 0 29 80 42 63 55 47 44 50 36 23
2020/2021385 33 38 22 53 23 48 21 41 9 44 33 20
2021/2022260 19 24 5 9 8 21 31 11 12 23 29 68
2022/2023334 26 44 11 34 65 31 28 30 32 3 19 11
2023/2024197 15 16 17 4 10 51 4 14 4 1 13 48
2024/202583 9 13 61 0 0 0 0 0 0 0 0 0
Totale 2.605