DANIELI, GIAN ANTONIO
 Distribuzione geografica
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Continente #
NA - Nord America 6.546
EU - Europa 1.209
AS - Asia 812
SA - Sud America 5
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
AF - Africa 1
Totale 8.578
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Nazione #
US - Stati Uniti d'America 6.544
CN - Cina 495
IT - Italia 471
FI - Finlandia 181
SG - Singapore 177
SE - Svezia 157
DE - Germania 125
UA - Ucraina 114
VN - Vietnam 113
FR - Francia 74
GB - Regno Unito 40
IN - India 18
NL - Olanda 14
IE - Irlanda 12
BE - Belgio 6
CH - Svizzera 5
BR - Brasile 3
ES - Italia 3
TR - Turchia 3
AU - Australia 2
EU - Europa 2
HK - Hong Kong 2
IR - Iran 2
PT - Portogallo 2
AL - Albania 1
AT - Austria 1
BY - Bielorussia 1
CA - Canada 1
CL - Cile 1
CZ - Repubblica Ceca 1
EC - Ecuador 1
GL - Groenlandia 1
JP - Giappone 1
MA - Marocco 1
NZ - Nuova Zelanda 1
PH - Filippine 1
PL - Polonia 1
Totale 8.578
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Città #
Fairfield 918
Chandler 629
Woodbridge 621
Houston 579
Jacksonville 550
Ann Arbor 469
Ashburn 420
Cambridge 365
Seattle 342
Wilmington 342
Princeton 163
Boardman 138
Singapore 132
Beijing 123
Dong Ket 113
Helsinki 86
Santa Clara 83
San Diego 81
Roxbury 80
Guangzhou 78
Des Moines 68
Nanjing 68
Medford 30
Rome 29
Milan 27
Shenyang 24
Padova 20
Redwood City 20
Jinan 19
Munich 19
Hebei 18
Norwalk 18
Changsha 15
Shanghai 14
Tianjin 14
Jiaxing 13
Dublin 12
London 11
Nanchang 9
Naples 8
Los Angeles 7
Washington 7
Bologna 6
Florence 6
Hefei 6
Kilburn 6
Kunming 6
Napoli 6
New York 6
Bari 5
Cagliari 5
Indiana 5
Lappeenranta 5
Mumbai 5
Waanrode 5
Borås 4
Boves 4
Dallas 4
Haikou 4
Kharkiv 4
Mestre 4
Ogden 4
Taizhou 4
Augusta 3
Campogalliano 3
Crotone 3
Dearborn 3
Ercolano 3
Hangzhou 3
Las Vegas 3
Livorno 3
Monza 3
Palermo 3
Paris 3
Pisa 3
Stanford 3
São Paulo 3
Tappahannock 3
Trento 3
Verona 3
Zhengzhou 3
Amsterdam 2
Aversa 2
Bacoli 2
Bagnacavallo 2
Bengaluru 2
Brescia 2
Cadoneghe 2
Capannori 2
Cassano Magnago 2
Castelnuovo Rangone 2
Castelvetrano 2
Chicago 2
Chiswick 2
Città di Castello 2
Delhi 2
Ferrara 2
Foggia 2
Fuzhou 2
Gargnano 2
Totale 6.978
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Nome #
Screening di mutazioni patogene nei quattro geni più frequentemente implicati nella cardiomiopatia ipertrofica 458
Ricerca di mutazioni patogene in pazienti affetti da cardiomiopatia ipertrofica: risultati dello screening genetico per 12 geni con tecnica di DNA resequencing array. 182
Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy 142
A preliminary transcript map of a human skeletal muscle 141
Ultrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsies. 137
A Comprehensive, high-resolution genomic transcript map of human skeletal muscle. 131
A study on duplications of the dystrophin gene: Evidence of a geographical difference in the distribution of breakpoints by intron 131
Genomic expression during human myelopoiesis. 128
Detecting Seeded Motifs in DNA Sequences 127
Characterization of C14orf4, a novel intronless human gene containing a polyglutamine repeat, mapped to the ARVD1 critical region 122
A NEW LOCUS FOR ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY (ARVD2) MAPS TO CHROMOSOME 1q42-q43 122
Analysis of 22 deletion breakpoints in dystrophin intron 49 119
The p.A897KfsX4 frameshift variation in desmocollin-2 is not a causative mutation in arrhythmogenic right ventricular cardiomyopathy 119
Novel definition files for human GeneChips based on GeneAnnot. 117
TRAM (Transcriptome Mapper): database-driven creation and analysis of transcriptome maps from multiple sources. 116
Identification and characterization of heart-specific splicing of human Neurexin3 mRNA (NRXN3) 113
The binding of the RyR2 calcium channel to its gating protein FKBP12.6 is oppositely affected by ARVD2 and VTSIP mutations 112
Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substrates. 111
Detection of chromosomal regions showing differential gene expression in human skeletal muscle and in alveolar rhabdomyosarcoma 111
Advances in Genetics: Dominant Forms 109
Prevalence of dystrophin-positive fibers in 85 duchenne muscular dystrophy patients 109
Characterization of a novel human gene containing ANK repeats and ARM domains 109
Motif discovery in promoters of genes co-localized and co-expressed during myeloid cells differentiation 108
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 108
Conservation of a putative AP1 binding site and complete homology to a fetal brain EST in a region upstream of the core muscle promoter in the human dystrophin gene. 108
Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size? 105
A multi-step bioinformatic approach detects putative regulatory elements in gene promoter 105
Heart transplantation in patients with Inherited myopathies associated with end-stage cardiomyopathy: molecular and biochemical defects on cardiac and skeletal muscle 105
Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy 103
A non random genomic distribution of genes expressed in specific human tissues 102
DXS997 localized to intron 48 of dystrophin 102
Mutations in the Cardiac Ryanodine Receptor Gene (hRyR2) underlie catecholaminergic Polymorphic Ventricular Tachycardia 100
ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm. 100
The human SLC8A3 gene and the tissue-specific Na+/Ca2+ exchanger 3 isoforms. 99
Dystrophin-positive fibers in duchenne dystrophy: Origin and correlation to clinical course 97
Heart involvement in muscular dystrophies due to sarcoglycan gene mutations 96
Disease-genes and intracellular protein networks 95
Cardiac involvement in Becker muscular dystrophy 95
Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations. 94
Detecting differentially expressed genes in multiple tag sampling experiments: comparative evaluation of statistical tests 93
Arrhythmogenic right ventricular cardiomyopathy: clinical registry and database, evaluation of therapies, pathology registry, DNA banking 93
A computational framework for the integrated study of the role of promoters similarity and gene clustering in specific regions of the human genome in establishing co-expression of genes: an application to myeloid cells differentiation. 87
Italian population data for D1S1656, D3S1358, D8S1132, D10S2325, VWA, FES/FPS, and F13A01 87
Prognostic factors in mild dystrophinopathies. 87
A computational reconstruction of the adult human heart transcriptional profile 86
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 86
Differential expression of genes coding for ribosomal proteins in different human tissues 85
Towards an in silico analysis of transcription patterns. 85
The human adult skeletal muscle transcriptional profile reconstructed by a novel computational approach 85
Gene symbol: RYR2. Disease: Arrhythmogenic right ventricular cardiomyopathy type 2. 84
Chromosomal assignment of 115 expressed sequence tags (EST's) from human skeletal muscle. 83
Mutation screening in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 82
Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy. 82
Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities. 82
Molecular genetics of arrhythmogenic right ventricular cardiomyopathy 81
REEF: searching REgionally Enriched Features in genomes. 81
Duplication of dystrophin gene and dissimilar clinical phenotype in the same family 80
Chromosomal localisation of the human genes, CPP32, Mch2, Mch3, and Ich-1, involved in cellular apoptosis. 79
Control of the Na+/Ca2+ exchanger 3 promoter by cyclic adenosine monophosphate and Ca2+ in differentiating neurons 78
Computational reconstruction of the human skeletal muscle secretome 78
Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy 78
Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers. 77
Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1. 76
Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy 75
Novel genes possibly relevant for molecular diagnosis or therapy of human rhabdomyosarcoma, detected by genomic expression profiling 73
The preliminary transcript map of a human skeletal muscle 73
IDENTIFICATION OF MUTATIONS IN THE CARDIAC RYANODINE RECEPTOR GENE IN FAMILIES AFFECTED WITH ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 72
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 72
Geographic distribution of hereditary myopathies in Northeast Italy 72
Tissue expression and fine mapping of the human Endothelin-1 Converting Enzyme (hECE-1) by FISH, monochromosomal and radiation hybrids 71
A novel resource for the study of genes expressed in the adult human retina 71
Corrigenda: DXS997 localized to intron 48 of dystrophin (Human Molecular Genetics (1993) 2 (2199)) 71
Investigating the mechanism of chromosomal deletion: Characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene 70
Is the cause of arrhythmogenic right ventricular cardiomyopathy congenital or acquired? 66
CORRELATION BETWEEN CARDIAC INVOLVEMENT AND CTG TRINUCLEOTIDE REPEAT LENGTH IN MYOTONIC DYSTROPHY 66
Gene symbol: RYR2. Disease: Effort-induced polymorphic ventricular arrhythmias. 63
Mutations in the cardiac Ryanodine receptor gene (hRYR2) underlie Catecholaminergic Polymorphic Ventricular Tachycardia 63
Fine mapping of five skeletal muscle genes: alpha-tropomyosin, beta-tropomyosin, troponin-I slow twitch, troponin-I fast-twitch and troponin-C fast. 63
Stephen J. Gould: The Scientific Legacy 62
Cardiac transplantation in a Duchenne muscular dystrophy carrier 61
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. 59
Allele frequency distributions for D1S1656, D8S1132, D10S2325, D18S51, and D21S11 loci in a Northern-Italy population 59
null 59
Familial effort polymorphic ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy are linked to chromosome 1q42-43 59
Mutations in the Cardiac Ryanodine Receptor Gene cause Catecholaminergic Polymorphic Ventricular Tachicardia 57
DNA resequencing array for mutation detection in hypertrophic cardiomyopathy 56
A DHPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmias. 56
Genetics of arrhythmogenic right ventricular cardiomyopathy 54
Myocardial involvement is very frequent among patients affected with subclinical muscular dystrophy 41
Association between human polymorphic DNA markers and hypoxia adaptation in sherpa detected by a preliminary genome scan 32
Progress in molecular genetics of arrhythmogenic cardiomyopathy of the left ventricle. 31
Progress in molecular genetics of arrhythmogenic cardiomyopathy of the left ventricle 30
Could utrophin rescue the myocardium of pateints with dystrophin gene mutations? 27
DUCHENNE CARRIER DETECTION 25
Genotype-phenotype correlation in arrhythmogenic right-ventricular cardiomyopathy linked to desmoplakin mutation (ARVD8) 21
Totale 8.613
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Categoria #
all - tutte 29.326
article - articoli 24.504
book - libri 156
conference - conferenze 0
curatela - curatele 279
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 949
Totale 55.214
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.194 0 0 0 0 156 134 140 199 135 227 111 92
2020/20211.258 52 92 20 169 113 106 34 115 170 106 133 148
2021/20221.339 23 142 205 101 56 85 78 138 65 15 192 239
2022/20231.301 221 178 37 180 193 187 25 79 118 15 54 14
2023/2024511 19 83 61 42 53 56 24 19 28 28 53 45
2024/2025485 4 111 87 70 213 0 0 0 0 0 0 0
Totale 8.613