DANIELI, GIAN ANTONIO
 Distribuzione geografica
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Continente #
NA - Nord America 6.283
EU - Europa 1.111
AS - Asia 588
OC - Oceania 3
SA - Sud America 3
Continente sconosciuto - Info sul continente non disponibili 2
AF - Africa 1
Totale 7.991
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Nazione #
US - Stati Uniti d'America 6.281
CN - Cina 451
IT - Italia 434
FI - Finlandia 181
SE - Svezia 157
DE - Germania 123
UA - Ucraina 113
VN - Vietnam 113
GB - Regno Unito 40
FR - Francia 22
IN - India 18
NL - Olanda 12
IE - Irlanda 11
BE - Belgio 6
CH - Svizzera 4
ES - Italia 3
TR - Turchia 3
AU - Australia 2
EU - Europa 2
AL - Albania 1
AT - Austria 1
BR - Brasile 1
BY - Bielorussia 1
CA - Canada 1
CL - Cile 1
CZ - Repubblica Ceca 1
EC - Ecuador 1
GL - Groenlandia 1
IR - Iran 1
JP - Giappone 1
MA - Marocco 1
NZ - Nuova Zelanda 1
PT - Portogallo 1
SG - Singapore 1
Totale 7.991
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Città #
Fairfield 918
Chandler 629
Woodbridge 621
Houston 579
Jacksonville 550
Ann Arbor 469
Ashburn 417
Cambridge 365
Seattle 342
Wilmington 342
Princeton 163
Beijing 123
Dong Ket 113
Helsinki 86
San Diego 81
Roxbury 80
Guangzhou 77
Des Moines 68
Nanjing 68
Boardman 47
Medford 30
Rome 24
Shenyang 23
Redwood City 20
Jinan 19
Milan 19
Hebei 18
Norwalk 18
Padova 18
Munich 17
Changsha 15
Tianjin 14
Jiaxing 13
Shanghai 12
Dublin 11
London 11
Nanchang 9
Naples 8
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
Los Angeles 5
Mumbai 5
Waanrode 5
Borås 4
Boves 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
Tappahannock 3
Trento 3
Verona 3
Zhengzhou 3
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
Gargnano 2
Groningen 2
Hanover 2
Islington 2
La Coruña 2
Lucca 2
Melfi 2
Totale 6.646
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Nome #
Screening di mutazioni patogene nei quattro geni più frequentemente implicati nella cardiomiopatia ipertrofica 412
Ricerca di mutazioni patogene in pazienti affetti da cardiomiopatia ipertrofica: risultati dello screening genetico per 12 geni con tecnica di DNA resequencing array. 179
A preliminary transcript map of a human skeletal muscle 136
Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy 136
Ultrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsies. 133
A Comprehensive, high-resolution genomic transcript map of human skeletal muscle. 123
A study on duplications of the dystrophin gene: Evidence of a geographical difference in the distribution of breakpoints by intron 123
Genomic expression during human myelopoiesis. 121
Detecting Seeded Motifs in DNA Sequences 120
Characterization of C14orf4, a novel intronless human gene containing a polyglutamine repeat, mapped to the ARVD1 critical region 119
The p.A897KfsX4 frameshift variation in desmocollin-2 is not a causative mutation in arrhythmogenic right ventricular cardiomyopathy 116
TRAM (Transcriptome Mapper): database-driven creation and analysis of transcriptome maps from multiple sources. 113
Novel definition files for human GeneChips based on GeneAnnot. 111
Analysis of 22 deletion breakpoints in dystrophin intron 49 110
A NEW LOCUS FOR ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY (ARVD2) MAPS TO CHROMOSOME 1q42-q43 110
Identification and characterization of heart-specific splicing of human Neurexin3 mRNA (NRXN3) 108
Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substrates. 106
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 104
Advances in Genetics: Dominant Forms 103
Prevalence of dystrophin-positive fibers in 85 duchenne muscular dystrophy patients 103
Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size? 102
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. 102
Detection of chromosomal regions showing differential gene expression in human skeletal muscle and in alveolar rhabdomyosarcoma 102
Motif discovery in promoters of genes co-localized and co-expressed during myeloid cells differentiation 101
The binding of the RyR2 calcium channel to its gating protein FKBP12.6 is oppositely affected by ARVD2 and VTSIP mutations 100
Characterization of a novel human gene containing ANK repeats and ARM domains 100
Heart transplantation in patients with Inherited myopathies associated with end-stage cardiomyopathy: molecular and biochemical defects on cardiac and skeletal muscle 98
A non random genomic distribution of genes expressed in specific human tissues 97
A multi-step bioinformatic approach detects putative regulatory elements in gene promoter 97
Mutations in the Cardiac Ryanodine Receptor Gene (hRyR2) underlie catecholaminergic Polymorphic Ventricular Tachycardia 96
Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy 95
DXS997 localized to intron 48 of dystrophin 95
The human SLC8A3 gene and the tissue-specific Na+/Ca2+ exchanger 3 isoforms. 93
ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm. 92
Dystrophin-positive fibers in duchenne dystrophy: Origin and correlation to clinical course 91
Heart involvement in muscular dystrophies due to sarcoglycan gene mutations 90
Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations. 89
Detecting differentially expressed genes in multiple tag sampling experiments: comparative evaluation of statistical tests 89
Cardiac involvement in Becker muscular dystrophy 89
Disease-genes and intracellular protein networks 88
Italian population data for D1S1656, D3S1358, D8S1132, D10S2325, VWA, FES/FPS, and F13A01 84
Arrhythmogenic right ventricular cardiomyopathy: clinical registry and database, evaluation of therapies, pathology registry, DNA banking 83
Prognostic factors in mild dystrophinopathies. 82
Towards an in silico analysis of transcription patterns. 81
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 81
Gene symbol: RYR2. Disease: Arrhythmogenic right ventricular cardiomyopathy type 2. 80
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. 80
Mutation screening in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) 79
Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy. 79
Chromosomal assignment of 115 expressed sequence tags (EST's) from human skeletal muscle. 78
Differential expression of genes coding for ribosomal proteins in different human tissues 78
The human adult skeletal muscle transcriptional profile reconstructed by a novel computational approach 78
A computational reconstruction of the adult human heart transcriptional profile 77
Computational reconstruction of the human skeletal muscle secretome 77
Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities. 77
Molecular genetics of arrhythmogenic right ventricular cardiomyopathy 75
Chromosomal localisation of the human genes, CPP32, Mch2, Mch3, and Ich-1, involved in cellular apoptosis. 75
REEF: searching REgionally Enriched Features in genomes. 75
Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1. 73
Duplication of dystrophin gene and dissimilar clinical phenotype in the same family 73
Mutations in desmoglein-2 gene are associated 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 70
Control of the Na+/Ca2+ exchanger 3 promoter by cyclic adenosine monophosphate and Ca2+ in differentiating neurons 69
The preliminary transcript map of a human skeletal muscle 69
Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy 69
Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers. 69
Novel genes possibly relevant for molecular diagnosis or therapy of human rhabdomyosarcoma, detected by genomic expression profiling 68
Tissue expression and fine mapping of the human Endothelin-1 Converting Enzyme (hECE-1) by FISH, monochromosomal and radiation hybrids 67
IDENTIFICATION OF MUTATIONS IN THE CARDIAC RYANODINE RECEPTOR GENE IN FAMILIES AFFECTED WITH ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 66
A novel resource for the study of genes expressed in the adult human retina 66
Geographic distribution of hereditary myopathies in Northeast Italy 66
Corrigenda: DXS997 localized to intron 48 of dystrophin (Human Molecular Genetics (1993) 2 (2199)) 63
Investigating the mechanism of chromosomal deletion: Characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene 62
CORRELATION BETWEEN CARDIAC INVOLVEMENT AND CTG TRINUCLEOTIDE REPEAT LENGTH IN MYOTONIC DYSTROPHY 60
Gene symbol: RYR2. Disease: Effort-induced polymorphic ventricular arrhythmias. 59
Mutations in the cardiac Ryanodine receptor gene (hRYR2) underlie Catecholaminergic Polymorphic Ventricular Tachycardia 59
Fine mapping of five skeletal muscle genes: alpha-tropomyosin, beta-tropomyosin, troponin-I slow twitch, troponin-I fast-twitch and troponin-C fast. 59
null 59
Is the cause of arrhythmogenic right ventricular cardiomyopathy congenital or acquired? 59
Stephen J. Gould: The Scientific Legacy 57
Cardiac transplantation in a Duchenne muscular dystrophy carrier 56
Familial effort polymorphic ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy are linked to chromosome 1q42-43 55
Mutations in the Cardiac Ryanodine Receptor Gene cause Catecholaminergic Polymorphic Ventricular Tachicardia 54
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. 53
Allele frequency distributions for D1S1656, D8S1132, D10S2325, D18S51, and D21S11 loci in a Northern-Italy population 53
Genetics of arrhythmogenic right ventricular cardiomyopathy 48
DNA resequencing array for mutation detection in hypertrophic cardiomyopathy 46
A DHPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmias. 45
Myocardial involvement is very frequent among patients affected with subclinical muscular dystrophy 35
Association between human polymorphic DNA markers and hypoxia adaptation in sherpa detected by a preliminary genome scan 28
Progress in molecular genetics of arrhythmogenic cardiomyopathy of the left ventricle. 24
Could utrophin rescue the myocardium of pateints with dystrophin gene mutations? 23
Progress in molecular genetics of arrhythmogenic cardiomyopathy of the left ventricle 23
DUCHENNE CARRIER DETECTION 20
Genotype-phenotype correlation in arrhythmogenic right-ventricular cardiomyopathy linked to desmoplakin mutation (ARVD8) 18
Totale 8.026
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Categoria #
all - tutte 24.565
article - articoli 20.642
book - libri 118
conference - conferenze 0
curatela - curatele 228
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 787
Totale 46.340
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019642 0 0 0 0 0 0 0 0 0 139 267 236
2019/20201.615 250 44 28 99 156 134 140 199 135 227 111 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
2023/2024409 19 83 61 42 53 56 24 19 28 24 0 0
Totale 8.026