RAMPAZZO, ALESSANDRA
 Distribuzione geografica
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Continente #
NA - Nord America 6.966
EU - Europa 1.266
AS - Asia 928
SA - Sud America 6
OC - Oceania 5
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
Totale 9.173
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Nazione #
US - Stati Uniti d'America 6.960
CN - Cina 524
IT - Italia 472
SG - Singapore 267
SE - Svezia 186
DE - Germania 157
FI - Finlandia 142
UA - Ucraina 95
FR - Francia 69
VN - Vietnam 63
GB - Regno Unito 51
IN - India 42
NL - Olanda 26
GR - Grecia 18
TR - Turchia 16
RU - Federazione Russa 14
BE - Belgio 11
IE - Irlanda 9
AT - Austria 4
AU - Australia 4
BR - Brasile 4
CA - Canada 4
HK - Hong Kong 4
LB - Libano 4
IR - Iran 3
BY - Bielorussia 2
CH - Svizzera 2
CZ - Repubblica Ceca 2
HR - Croazia 2
PL - Polonia 2
BD - Bangladesh 1
CL - Cile 1
EC - Ecuador 1
ES - Italia 1
EU - Europa 1
ID - Indonesia 1
JP - Giappone 1
KZ - Kazakistan 1
MA - Marocco 1
MX - Messico 1
NI - Nicaragua 1
NZ - Nuova Zelanda 1
PK - Pakistan 1
RO - Romania 1
Totale 9.173
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Città #
Fairfield 1.126
Woodbridge 742
Houston 590
Chandler 547
Ashburn 492
Ann Arbor 474
Seattle 414
Cambridge 374
Wilmington 366
Jacksonville 330
Singapore 203
Santa Clara 166
Princeton 140
Boardman 139
Beijing 122
San Diego 95
Padova 75
Roxbury 71
Nanjing 70
Helsinki 68
Dong Ket 63
Medford 58
Milan 55
Des Moines 54
Guangzhou 48
Jinan 22
New York 22
Changsha 21
Shenyang 20
Redwood City 19
Rome 19
Hebei 16
Jiaxing 15
Norwalk 13
Tianjin 13
Washington 13
Istanbul 11
Zhengzhou 11
Bologna 10
London 10
Shanghai 10
Nanchang 9
Dallas 8
Munich 8
Pune 8
Trieste 8
Waanrode 8
Dearborn 7
Dublin 7
Falls Church 7
Hangzhou 7
Nuremberg 7
Nürnberg 7
Ogden 7
Turin 7
Chennai 6
Kharar 6
Selvazzano Dentro 6
Verona 6
Amersfoort 5
Arlington 5
Kilburn 5
Kunming 5
North Bergen 5
Villafranca Padovana 5
Augusta 4
Beirut 4
Brescia 4
Chicago 4
Fuzhou 4
Los Angeles 4
Naples 4
Stanford 4
Taiyuan 4
Treviso 4
Acton 3
Aprilia 3
Bengaluru 3
Blacksburg 3
Cachan 3
Chengdu 3
Essen 3
Falkenstein 3
Furore 3
Genoa 3
Ghent 3
Grosseto 3
Hounslow 3
Kharkiv 3
Marcallo con Casone 3
Osio Sotto 3
Pescara 3
Surat 3
Taizhou 3
Toronto 3
Vienna 3
Amsterdam 2
Avellino 2
Bari 2
Bitonto 2
Totale 7.397
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Nome #
'Hot phase' clinical presentation in arrhythmogenic cardiomyopathy 270
Cardiomiopatia/displasia aritmogena del ventricolo destro 233
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
Missense mutations in desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro. 164
Arrhythmogenic Cardiomyopathy 152
Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy 146
Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy 144
Ultrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsies. 143
Homozygous desmocollin-2 mutations and arrhythmogenic cardiomyopathy 138
Arrhythmogenic right ventricular cardiomyopathy type 1 (ARVD1): confirmation of locus assignment and mutation screening of four candidate genes. 132
Follow-Up with Exercise Test of Effort-Induced Ventricular Arrhythmias Linked to Ryanodine Receptor Type 2 Gene Mutations. 131
PHENOTYPIC EXPRESSION IS A PREREQUISITE FOR MALIGNANT ARRHYTHMIC EVENTS AND SUDDEN CARDIAC DEATH IN ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 128
A NEW LOCUS FOR ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY (ARVD2) MAPS TO CHROMOSOME 1q42-q43 127
Characterization of C14orf4, a novel intronless human gene containing a polyglutamine repeat, mapped to the ARVD1 critical region 125
The novel S59P mutation in the TNFRSF1A gene identified in an adult onset TNF receptor associated periodic syndrome (TRAPS) constitutively activates NF-κB pathway. 125
New FIG4 gene mutations causing aggressive ALS 124
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
A founder MYBPC3 mutation results in HCM with a high risk of sudden death after the fourth decade of life 120
LGI1 microdeletion in autosomal dominant lateral temporal epilepsy. 117
Arrhythmogenic cardiomyopathy: a disease of intercalated discs. 115
Identification and characterization of heart-specific splicing of human Neurexin3 mRNA (NRXN3) 114
Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substrates. 112
Characterization of a novel human gene containing ANK repeats and ARM domains 112
Advances in Genetics: Dominant Forms 111
Clinical phenotype and diagnosis of arrhythmogenic right ventricular cardiomyopathy in pediatric patients carrying desmosomal gene mutations. 111
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 110
Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia 109
TAIL1: an isthmin-like gene, containing type 1 thrombospondin-repeat and AMOP domain, mapped to ARVD1 critical region. 106
ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm. 106
Denaturing HPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmias 105
Arrhythmogenic right ventricular cardiomyopathy - A still underrecognized clinic entity 105
A novel murine model for arrhythmogenic cardiomyopathy points to a pathogenic role of Wnt signaling and miRNA dysregulation. 105
Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy. 105
Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy 104
Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy. 104
Transcriptomic Characterization of a Human In Vitro Model of Arrhythmogenic Cardiomyopathy Under Topological and Mechanical Stimuli 103
THE GENE FOR ARRHYTHMOGENIC RIGHT-VENTRICULAR CARDIOMYOPATHY MAPS TO CHROMOSOME 14Q23-Q24 98
R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease 97
Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations. 96
Intercalated discs and arrhythmogenic cardiomyopathy. 96
Arrhythmogenic Ventricular Cardiomyopathy Associated With Fibromuscular Dysplasia of Ostial Right Main Coronary Artery. 92
Clinical and Functional Characterization of a Novel Mutation in Lamin A/C Gene in a Multigenerational Family with Arrhythmogenic Cardiac Laminopathy 91
Comparison of clinical features of arrhythmogenic right ventricular cardiomyopathy in men versus women 89
Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy 89
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 89
Molecular Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy 88
Pathogenic Potential of Hic1-Expressing Cardiac Stromal Progenitors 86
Gene symbol: RYR2. Disease: Arrhythmogenic right ventricular cardiomyopathy type 2. 85
Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy 85
Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities. 85
Genetic bases of arrhythmogenic right ventricular cardiomyopathy. 84
Mutation screening in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 83
Molecular genetics of arrhythmogenic right ventricular cardiomyopathy 83
Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy. 83
Desmin mutations and arrhythmogenic right ventricular cardiomyopathy. 82
Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers. 79
Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1. 77
Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy 76
IDENTIFICATION OF MUTATIONS IN THE CARDIAC RYANODINE RECEPTOR GENE IN FAMILIES AFFECTED WITH ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 74
Genetics meets epigenetics: Genetic variants that modulate noncoding RNA in cardiovascular diseases 74
Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death early diagnosis of asymptomatic carriers - Early diagnosis of asymptomatic carriers 73
Novel Missense Variant in MYL2 Gene Associated with Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology 73
From molecular mechanisms of cardiac development to genetic substrate of congenital heart diseases. 72
Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia (vol 55, pg 587, 2010) 71
Is beta-catenin signalling involved in the molecular pathogenesis of arrhythmogenic right ventricular cardiomyopathy? Study on DSG2 transgenic mice 71
Hypertrophic Cardiomyopathy and Primary Restrictive Cardiomyopathy: Similarities, Differences and Phenocopies 70
Arrhythmogenic right-ventricular cardiomyopathy: Molecular genetics into clinical practice in the era of next generation sequencing 69
Is the cause of arrhythmogenic right ventricular cardiomyopathy congenital or acquired? 67
Occurrence of two different intragenic deletions in two male relatives affected with Duchenne muscular dystrophy. 67
Gene symbol: RYR2. Disease: Effort-induced polymorphic ventricular arrhythmias. 65
Arrhythmogenic right ventricular cardiomyopathy: evaluation of the current diagnostic criteria and differential diagnosis 65
Familial effort polymorphic ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy map to chromosome 1q42-43. 64
Diagnosis of arrhythmogenic cardiomyopathy: The Padua criteria 64
Fine mapping and genomic structure of ACTN2, the human gene coding for the sarcomeric fisoform of alpha-Actinin-2, expressed in skeletal and cardiac muscle. 62
Regulatory mutations in transforming growth factor-β3 gene involved in arrhythmogenic right ventricular cardiomyopathy 62
A first insight into molecular genetics of arrhythmogenic right ventricular cardiomyopathy. 60
A DHPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmias. 60
Familial effort polymorphic ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy are linked to chromosome 1q42-43 60
null 59
Study of the molecular pathogenesis of arrhythmogenic cardiomyopathy due to Desmoglein-2 mutations: the zebrafish helps the mouse 59
Genetics of arrhythmogenic right ventricular cardiomyopathy 55
Regulatory mutations in transforming growth factor-beta 3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1 53
Modeling Cardiovascular Diseases with hiPSC-Derived Cardiomyocytes in 2D and 3D Cultures 52
Mutation of the same sequence of the myelin PO gene causing two different phenotypes 51
Circulating miR-185-5p as a Potential Biomarker for Arrhythmogenic Right Ventricular Cardiomyopathy 48
Mutations of the same sequence of the myelin PO gene causing two different phenotypes 47
Evolving Diagnostic Criteria for Arrhythmogenic Cardiomyopathy 46
Clinical profile and long-term follow-up of a cohort of patients with desmoplakin cardiomyopathy 46
Mutations of the same sequence of the myelin PO gene causing two different phenotypes 45
Comparison of knock-in mouse and hiPSC-based models of arrhythmogenic cardiomyopathy carrying the DSG2 p.Q558* mutation 43
Phenotype and Clinical Outcomes in Desmin-Related Arrhythmogenic Cardiomyopathy 42
null 34
Progress in molecular genetics of arrhythmogenic cardiomyopathy of the left ventricle. 32
Progress in molecular genetics of arrhythmogenic cardiomyopathy of the left ventricle 31
Diagnosis of arrhythmogenic cardiomyopathy: The Padua criteria 30
Familial occurrence of arrhythmogenic right ventricular cardiomyopathy 30
Pathogenic variants in plakophilin-2 gene (PKP2) are associated with better survival in arrhythmogenic right ventricular cardiomyopathy 27
Totale 9.165
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Categoria #
all - tutte 34.032
article - articoli 30.589
book - libri 166
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.792
Totale 66.579
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020885 0 0 0 0 0 0 134 184 149 241 97 80
2020/20211.582 47 82 54 105 212 95 61 173 168 269 209 107
2021/20221.504 51 195 165 114 86 96 75 164 103 27 158 270
2022/20231.146 207 147 25 126 188 137 8 90 148 17 36 17
2023/2024681 34 89 68 66 59 90 36 8 26 57 74 74
2024/2025825 15 158 106 111 303 117 15 0 0 0 0 0
Totale 9.296