IRIS Institutional Research Information System - OPENBS Open Archive UniBS

Mazzarotto, Francesco
 Distribuzione geografica
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Continente #
NA - Nord America 1.787
AS - Asia 1.281
EU - Europa 553
SA - Sud America 376
Continente sconosciuto - Info sul continente non disponibili 67
AF - Africa 47
OC - Oceania 5
Totale 4.116
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Nazione #
US - Stati Uniti d'America 1.679
SG - Singapore 489
BR - Brasile 303
CN - Cina 262
HK - Hong Kong 185
VN - Vietnam 124
IT - Italia 115
GB - Regno Unito 90
FR - Francia 76
DE - Germania 68
TR - Turchia 62
CA - Canada 50
IE - Irlanda 45
RU - Federazione Russa 42
BD - Bangladesh 38
IN - India 34
FI - Finlandia 28
AT - Austria 25
AR - Argentina 23
MX - Messico 18
CO - Colombia 15
EC - Ecuador 14
ZA - Sudafrica 13
IQ - Iraq 12
PK - Pakistan 12
SE - Svezia 12
JP - Giappone 10
VE - Venezuela 10
MA - Marocco 8
CR - Costa Rica 7
EG - Egitto 7
ES - Italia 7
GT - Guatemala 7
JM - Giamaica 7
UA - Ucraina 7
HN - Honduras 6
PL - Polonia 6
SA - Arabia Saudita 6
UZ - Uzbekistan 6
AE - Emirati Arabi Uniti 5
AU - Australia 5
CH - Svizzera 5
DZ - Algeria 5
ID - Indonesia 5
NL - Olanda 5
TT - Trinidad e Tobago 5
CZ - Repubblica Ceca 4
LT - Lituania 4
TH - Thailandia 4
AZ - Azerbaigian 3
BO - Bolivia 3
KR - Corea 3
PY - Paraguay 3
SY - Repubblica araba siriana 3
AL - Albania 2
AM - Armenia 2
BB - Barbados 2
BE - Belgio 2
CL - Cile 2
ET - Etiopia 2
IR - Iran 2
JO - Giordania 2
KE - Kenya 2
KH - Cambogia 2
MY - Malesia 2
NG - Nigeria 2
PH - Filippine 2
UY - Uruguay 2
AI - Anguilla 1
AO - Angola 1
BA - Bosnia-Erzegovina 1
BF - Burkina Faso 1
BG - Bulgaria 1
BS - Bahamas 1
CG - Congo 1
CI - Costa d'Avorio 1
DK - Danimarca 1
EE - Estonia 1
GY - Guiana 1
HR - Croazia 1
KG - Kirghizistan 1
KW - Kuwait 1
KZ - Kazakistan 1
LB - Libano 1
LC - Santa Lucia 1
LY - Libia 1
MD - Moldavia 1
MU - Mauritius 1
NO - Norvegia 1
PA - Panama 1
PR - Porto Rico 1
PS - Palestinian Territory 1
PT - Portogallo 1
RO - Romania 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
SV - El Salvador 1
TJ - Tagikistan 1
TN - Tunisia 1
Totale 4.049
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Città #
Singapore 246
San Jose 199
Hong Kong 185
Ashburn 163
The Dalles 99
Council Bluffs 93
Princeton 83
Los Angeles 58
Lauterbourg 57
Fairfield 51
Beijing 47
Istanbul 47
Columbus 44
Dublin 44
Ho Chi Minh City 42
Houston 32
São Paulo 31
Helsinki 28
Dallas 26
Hanoi 25
New York 25
Redondo Beach 25
San Diego 24
Seattle 24
San Francisco 22
North Bergen 20
Santa Clara 19
Wilmington 19
Moscow 18
Nuremberg 16
Brescia 15
Des Moines 15
Elk Grove Village 14
Milan 14
Orem 14
Villa Carcina 14
Atlanta 13
Belo Horizonte 13
Buffalo 13
London 13
Toronto 13
Woodbridge 13
Ann Arbor 12
Vienna 12
Phoenix 11
Brasília 10
Cambridge 10
Denver 10
Montreal 10
Dhaka 9
Düsseldorf 9
Pontassieve 9
Stockholm 9
Brooklyn 8
Chennai 8
Chicago 8
Guangzhou 8
Munich 8
Tianjin 8
Tokyo 8
Boston 7
Curitiba 7
Manchester 7
Portsmouth 7
Quito 7
Baghdad 6
Charlotte 6
Mumbai 6
San José 6
Tashkent 6
Bremen 5
Frankfurt am Main 5
Guatemala City 5
Haiphong 5
Hải Dương 5
Johannesburg 5
Kyiv 5
Lahore 5
Melbourne 5
Mexico City 5
Rio de Janeiro 5
Romola 5
Shanghai 5
Tampa 5
Thái Bình 5
Biên Hòa 4
Bogotá 4
Bologna 4
Caracas 4
Detroit 4
Fortaleza 4
Goiânia 4
Kilburn 4
Kingston 4
Mantova 4
Philadelphia 4
Pittsburgh 4
Poplar 4
Sheffield 4
Uberlândia 4
Totale 2.343
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Nome #
Genome-wide association testing beyond SNPs 153
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death 105
Comparison of long-term outcome in anthracycline-related versus idiopathic dilated cardiomyopathy: a single centre experience 103
Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease 97
Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy 96
Comprehensive sequencing of dilated cardiomyopathy genes reveals additive effects of multiple genes on disease risk and severity 94
Investigation on the high recurrence of the ATTRv-causing transthyretin variant Val142Ile in central Italy 93
Genetic determinants of coping, resilience and self-esteem in schizophrenia suggest a primary role for social factors and hippocampal neurogenesis 93
Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center 93
Advantages and Perils of Clinical Whole-Exome and Whole-Genome Sequencing in Cardiomyopathy 90
Ion channel dysfunction and fibrosis in atrial fibrillation: Two sides of the same coin 90
Disease Progression of Hypertrophic Cardiomyopathy: Modeling Using Machine Learning 88
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy 87
Allele-specific expression analysis: pipelines, applications, challenges, and unmet needs 82
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy 82
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect 82
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls 82
Ion channel dysfunction and fubrosis in atrial fibrillation:Two sides of the same coin 81
Shared Genetic Predisposition in Peripartum and Dilated Cardiomyopathies 80
Temporal Trend of Age at Diagnosis in Hypertrophic Cardiomyopathy: An Analysis of the International Sarcomeric Human Cardiomyopathy Registry 79
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies 79
EFFECTS OF TRUNCATING VARIANTS IN TITIN ON CARDIAC PHENOTYPE AND LEFT VENTRICULAR REMODELLING IN DILATED CARDIOMYOPATHY 78
Evidence-Based Assessment of Genes in Dilated Cardiomyopathy 78
A machine learning-based risk stratification model for ventricular tachycardia and heart failure in hypertrophic cardiomyopathy 78
Comprehensive Assessment of Rare Genetic Variation in Dilated Cardiomyopathy Genes in Patients and Controls (vol 101, pg A41, 2015) 77
CLINICAL AND GENETIC CHARACTERISTICS OF FAMILIAL DILATED CARDIOMYOPATHY IN A LARGE UK PROSPECTIVE COHORT 76
Quantifying evidence toward pathogenicity for rare phenotypes: the case of succinate dehydrogenase genes, SDHB and SDHD 75
Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies 74
Genetic and Phenotypic Characterization of Nexilin (NEXN)–Related Cardiomyopathy 74
Contemporary Insights Into the Genetics of Hypertrophic Cardiomyopathy: Toward a New Era in Clinical Testing? 74
Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: The impact of full-length dystrophin deficiency 74
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples 70
Spatial and Functional Distribution of MYBPC3 Pathogenic Variants and Clinical Outcomes in Patients with Hypertrophic Cardiomyopathy 70
Arrhythmogenic potential of myocardial disarray in hypertrophic cardiomyopathy: genetic basis, functional consequences and relation to sudden cardiac death 67
Sex-related differences in exercise performance and outcome of patients with hypertrophic cardiomyopathy 66
Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions 65
FineSplice, enhanced splice junction detection and quantification: a novel pipeline based on the assessment of diverse RNA-Seq alignment solutions 64
Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy 64
Comparison of long-term clinical course and outcome of MYBPC3-versus MYH7-related hypertrophic cardiomyopathy 63
Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases 62
Two decades of genetic testing in hypertrophic cardiomyopathy in a single center: The additive value of extended next-generation sequencing panels lies in the early diagnosis of metabolic mimics 61
Titin-truncating variants affect heart function in disease cohorts and the general population 61
ZBTB17 (MIZ1) Is Important for the Cardiac Stress Response and a Novel Candidate Gene for Cardiomyopathy and Heart Failure 61
Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretation 61
Phenotypic Expression and Outcomes in Individuals With Rare Genetic Variants of Hypertrophic Cardiomyopathy 61
Re-evaluating the genetic contribution of monogenic dilated cardiomyopathy 60
Long-Term Prevalence of Systolic Dysfunction in MYBPC3 Versus MYH7-Related Hypertrophic Cardiomyopathy 59
Temporal Trend in Age at Diagnosis of Hypertrophic Cardiomyopathy: An Analysis of the Share Registry 59
INTEGRATED ALLELIC, TRANSCRIPTIONAL, AND PHENOTYPIC DISSECTION OF THE CARDIAC EFFECTS OF TITIN VARIATION IN HEALTH AND DISEASE 59
Genetic ancestry analysis of the Italian founder population carrying the cardiac amyloidosis-causing variant Val122Ile in the transthyretin gene 58
Temporal trend in age at diagnosis of hypertrophic cardiomyopathy: an analysis of the share registry 55
RE-EVALUATING THE GENETIC CONTRIBUTION OF MONOGENIC DILATED CARDIOMYOPATHY 53
Slower Calcium Handling Balances Faster Cross-Bridge Cycling in Human MYBPC3 HCM 50
Allele-specific expression analysis: pipelines, applications, challenges, and unmet needs 47
An Updated Evidence Assessment of the Genetic Causes of Dilated Cardiomyopathy 20
Pangenomes aid accurate detection of large insertions and deletions from targeted sequencing: the case of cardiomyopathies 13
Totale 4.116
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Categoria #
all - tutte 30.782
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 30.782
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022185 0 0 0 6 0 18 46 8 13 2 13 79
2022/2023107 41 0 1 4 1 42 2 0 6 9 1 0
2023/2024201 1 2 15 15 5 5 5 4 99 2 0 48
2024/2025845 1 6 6 85 88 49 71 84 80 97 183 95
2025/20262.012 191 266 155 322 174 128 273 104 137 139 87 36
2026/2027621 84 68 205 264 0 0 0 0 0 0 0 0
Totale 4.116