CALORE, MARTINA
 Distribuzione geografica
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Continente #
NA - Nord America 1.667
EU - Europa 357
AS - Asia 296
OC - Oceania 2
Continente sconosciuto - Info sul continente non disponibili 1
SA - Sud America 1
Totale 2.324
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Nazione #
US - Stati Uniti d'America 1.666
IT - Italia 143
CN - Cina 135
SG - Singapore 80
SE - Svezia 58
DE - Germania 44
FI - Finlandia 35
VN - Vietnam 32
IN - India 29
FR - Francia 16
HK - Hong Kong 15
GB - Regno Unito 14
GR - Grecia 14
NL - Olanda 12
AT - Austria 6
BE - Belgio 5
UA - Ucraina 5
JP - Giappone 4
RU - Federazione Russa 3
AU - Australia 1
CA - Canada 1
CZ - Repubblica Ceca 1
EC - Ecuador 1
ES - Italia 1
EU - Europa 1
NZ - Nuova Zelanda 1
TR - Turchia 1
Totale 2.324
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Città #
Fairfield 290
Woodbridge 172
Houston 155
Ashburn 146
Seattle 123
Chandler 114
Ann Arbor 113
Cambridge 89
Wilmington 87
Singapore 65
Santa Clara 50
Boardman 47
Beijing 37
Padova 33
Dong Ket 32
Helsinki 23
Princeton 23
Medford 21
Des Moines 18
San Diego 18
Nanjing 15
Milan 14
Central 13
Roxbury 13
Jacksonville 11
Chennai 10
Washington 9
Redwood City 8
Cagliari 6
New York 6
Amersfoort 5
Changsha 5
Nanchang 5
Vienna 5
Guangzhou 4
Hangzhou 4
Jinan 4
Naples 4
Nürnberg 4
Pordenone 4
Shenyang 4
Treviso 4
Dallas 3
Dearborn 3
Ghent 3
Jiaxing 3
Kharar 3
Ogden 3
Surat 3
Zhengzhou 3
Acton 2
Campobasso 2
Cardiff 2
Casa Sampieri-Lunardi 2
Chester 2
Cinisello Balsamo 2
Florence 2
Frankfurt am Main 2
Hefei 2
Ivrea 2
Kilburn 2
Monmouth Junction 2
Muggiò 2
Munich 2
Nuremberg 2
Pune 2
Rimini 2
San Giorgio Ionico 2
San Pancrazio Salentino 2
Shanghai 2
Taiyuan 2
Tianjin 2
Tokyo 2
Tuen Mun 2
Turin 2
Villafranca Padovana 2
Waanrode 2
Altopascio 1
Amsterdam 1
Bagnatica 1
Bari 1
Bengaluru 1
Bochum 1
Bologna 1
Borås 1
Brno 1
Camponogara 1
Chicago 1
Ciudad-rodrigo 1
Ercolano 1
Grado 1
Groningen 1
Haikou 1
Hebei 1
Indiana 1
Indianapolis 1
Inverigo 1
Kharkiv 1
Kunming 1
Lanzhou 1
Totale 1.914
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Nome #
A targeted next-generation gene panel reveals a novel heterozygous nonsense variant in the TP63 gene in patients with arrhythmogenic cardiomyopathy 190
Large Genomic Rearrangements of Desmosomal Genes in Italian Arrhythmogenic Cardiomyopathy Patients 168
Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy 146
Homozygous desmocollin-2 mutations and arrhythmogenic cardiomyopathy 138
Identification of a novel gene involved in Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia 130
Wnt/b-catenin pathway in arrhythmogenic cardiomyopathy 122
The p.A897KfsX4 frameshift variation in desmocollin-2 is not a causative mutation in arrhythmogenic right ventricular cardiomyopathy 122
Mutations in the area composita protein alphaT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy 121
Arrhythmogenic cardiomyopathy: a disease of intercalated discs. 115
Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy. 105
Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy. 104
A novel murine model for arrhythmogenic cardiomyopathy points to a pathogenic role of Wnt signaling and miRNA dysregulation. 104
Intercalated discs and arrhythmogenic cardiomyopathy. 96
Clinical and Functional Characterization of a Novel Mutation in Lamin A/C Gene in a Multigenerational Family with Arrhythmogenic Cardiac Laminopathy 91
Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy 89
Desmin mutations and arrhythmogenic right ventricular cardiomyopathy. 82
Genetics meets epigenetics: Genetic variants that modulate noncoding RNA in cardiovascular diseases 74
Novel Missense Variant in MYL2 Gene Associated with Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology 73
Arrhythmogenic right-ventricular cardiomyopathy: Molecular genetics into clinical practice in the era of next generation sequencing 69
Modeling Cardiovascular Diseases with hiPSC-Derived Cardiomyocytes in 2D and 3D Cultures 52
Circulating miR-185-5p as a Potential Biomarker for Arrhythmogenic Right Ventricular Cardiomyopathy 48
Comparison of knock-in mouse and hiPSC-based models of arrhythmogenic cardiomyopathy carrying the DSG2 p.Q558* mutation 43
Heart transcriptome profile of a novel transgenic mouse model for arrhythmogenic cardiomyopathy 26
Recent advances in crispr/cas9-based genome editing tools for cardiac diseases 21
Animal Models and Molecular Pathogenesis of Arrhythmogenic Cardiomyopathy Associated with Pathogenic Variants in Intercalated Disc Genes 9
Cardiac remodeling and pre-eclampsia: an overview of microRNA expression patterns 7
Chromatin remodelling and epigenetic state regulation by non-coding RNAs in the diseased heart 6
Metabolic Alterations in Inherited Cardiomyopathies 6
The PRKAG2 gene and hypertrophic cardiomyopathy: An energetically imbalanced relationship 6
Longing for Naiades in Heart Failure 6
Epigenetics and microRNAs in cardiovascular diseases. 5
Generation of a human induced pluripotent stem cell line UGENTi002-A from an arrhythmogenic cardiomyopathy patient carrying the c.817C>T DSP heterozygous variant and isogenic control using CRISPR/Cas9 editing 5
MicroRNAs in Cardiac Diseases 5
Therapeutic Delivery of miR-148a Suppresses Ventricular Dilation in Heart Failure 4
Totale 2.388
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Categoria #
all - tutte 9.664
article - articoli 8.747
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 18.411
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020220 0 0 0 0 0 0 36 49 38 56 24 17
2020/2021409 13 17 21 17 52 23 5 28 42 93 55 43
2021/2022376 20 50 45 23 23 29 16 46 18 12 24 70
2022/2023240 49 21 0 25 41 30 4 14 25 7 18 6
2023/2024269 14 22 25 10 27 49 16 21 7 21 22 35
2024/2025261 18 38 40 28 95 41 1 0 0 0 0 0
Totale 2.388