IRIS Institutional Research Information System - OPENBS Open Archive UniBS

MAZZAROTTO, Francesco
 Distribuzione geografica
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Continente #
NA - Nord America 301
AS - Asia 152
EU - Europa 129
AF - Africa 3
OC - Oceania 3
SA - Sud America 2
Totale 590
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Nazione #
US - Stati Uniti d'America 296
HK - Hong Kong 98
SG - Singapore 45
IE - Irlanda 43
GB - Regno Unito 25
FI - Finlandia 20
DE - Germania 18
IT - Italia 16
CA - Canada 5
IN - India 4
AU - Australia 3
SE - Svezia 3
TR - Turchia 3
AR - Argentina 1
AT - Austria 1
BR - Brasile 1
CN - Cina 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
ES - Italia 1
MU - Mauritius 1
NG - Nigeria 1
TH - Thailandia 1
ZA - Sudafrica 1
Totale 590
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Città #
Hong Kong 98
Princeton 82
Fairfield 50
Dublin 41
Singapore 36
San Diego 22
Helsinki 20
Houston 19
Wilmington 19
Seattle 18
Des Moines 13
Ann Arbor 12
Woodbridge 12
Ashburn 11
Cambridge 10
London 9
Pontassieve 9
San Francisco 8
Brescia 5
Toronto 5
Kilburn 4
Chiswick 3
Hanover 3
Melbourne 3
New York 3
Wandsworth 2
Acton 1
Bangkok 1
Beijing 1
Brno 1
Cascina 1
Copenhagen 1
Gunzenhausen 1
Hyderabad 1
Oklahoma City 1
Prescot 1
Pune 1
Redmond 1
Southwark 1
Suleja 1
São Paulo 1
Vienna 1
Totale 533
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Nome #
Shared Genetic Predisposition in Peripartum and Dilated Cardiomyopathies 24
FineSplice, enhanced splice junction detection and quantification: a novel pipeline based on the assessment of diverse RNA-Seq alignment solutions 24
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy 21
ZBTB17 (MIZ1) Is Important for the Cardiac Stress Response and a Novel Candidate Gene for Cardiomyopathy and Heart Failure 21
Spatial and Functional Distribution of MYBPC3 Pathogenic Variants and Clinical Outcomes in Patients with Hypertrophic Cardiomyopathy 20
Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease 20
Comprehensive Assessment of Rare Genetic Variation in Dilated Cardiomyopathy Genes in Patients and Controls (vol 101, pg A41, 2015) 19
Sex-related differences in exercise performance and outcome of patients with hypertrophic cardiomyopathy 19
Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy 19
Temporal Trend of Age at Diagnosis in Hypertrophic Cardiomyopathy: An Analysis of the International Sarcomeric Human Cardiomyopathy Registry 19
Contemporary Insights Into the Genetics of Hypertrophic Cardiomyopathy: Toward a New Era in Clinical Testing? 18
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 17
Comparison of long-term outcome in anthracycline-related versus idiopathic dilated cardiomyopathy: a single centre experience 17
Temporal trend in age at diagnosis of hypertrophic cardiomyopathy: an analysis of the share registry 16
INTEGRATED ALLELIC, TRANSCRIPTIONAL, AND PHENOTYPIC DISSECTION OF THE CARDIAC EFFECTS OF TITIN VARIATION IN HEALTH AND DISEASE 16
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples 15
Advantages and Perils of Clinical Whole-Exome and Whole-Genome Sequencing in Cardiomyopathy 15
RE-EVALUATING THE GENETIC CONTRIBUTION OF MONOGENIC DILATED CARDIOMYOPATHY 14
Temporal Trend in Age at Diagnosis of Hypertrophic Cardiomyopathy: An Analysis of the Share Registry 14
EFFECTS OF TRUNCATING VARIANTS IN TITIN ON CARDIAC PHENOTYPE AND LEFT VENTRICULAR REMODELLING IN DILATED CARDIOMYOPATHY 14
Re-evaluating the genetic contribution of monogenic dilated cardiomyopathy 14
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 14
Quantifying evidence toward pathogenicity for rare phenotypes: the case of succinate dehydrogenase genes, SDHB and SDHD 14
Arrhythmogenic potential of myocardial disarray in hypertrophic cardiomyopathy: genetic basis, functional consequences and relation to sudden cardiac death 14
CLINICAL AND GENETIC CHARACTERISTICS OF FAMILIAL DILATED CARDIOMYOPATHY IN A LARGE UK PROSPECTIVE COHORT 13
Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions 13
Evidence-Based Assessment of Genes in Dilated Cardiomyopathy 13
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect 13
Comparison of long-term clinical course and outcome of MYBPC3-versus MYH7-related hypertrophic cardiomyopathy 12
Genetic ancestry analysis of the Italian founder population carrying the cardiac amyloidosis-causing variant Val122Ile in the transthyretin gene 12
Titin-truncating variants affect heart function in disease cohorts and the general population 12
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies 12
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls 12
Comprehensive sequencing of dilated cardiomyopathy genes reveals additive effects of multiple genes on disease risk and severity 11
Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases 11
Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretation 11
Disease Progression of Hypertrophic Cardiomyopathy: Modeling Using Machine Learning 10
Phenotypic Expression and Outcomes in Individuals With Rare Genetic Variants of Hypertrophic Cardiomyopathy 9
A machine learning-based risk stratification model for ventricular tachycardia and heart failure in hypertrophic cardiomyopathy 9
Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy 9
Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: The impact of full-length dystrophin deficiency 9
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death 8
Investigation on the high recurrence of the ATTRv-causing transthyretin variant Val142Ile in central Italy 7
Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies 5
Long-Term Prevalence of Systolic Dysfunction in MYBPC3 Versus MYH7-Related Hypertrophic Cardiomyopathy 4
Slower Calcium Handling Balances Faster Cross-Bridge Cycling in Human MYBPC3 HCM 4
Ion channel dysfunction and fubrosis in atrial fibrillation:Two sides of the same coin 3
Genetic determinants of coping, resilience and self-esteem in schizophrenia suggest a primary role for social factors and hippocampal neurogenesis 2
Totale 642
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Categoria #
all - tutte 14.617
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 14.617
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022330 127 16 2 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
2024/20254 1 3 0 0 0 0 0 0 0 0 0 0
Totale 642