VAZZA, GIOVANNI
 Distribuzione geografica
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Continente #
NA - Nord America 4.083
AS - Asia 788
EU - Europa 700
SA - Sud America 15
OC - Oceania 9
AF - Africa 6
Totale 5.601
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Nazione #
US - Stati Uniti d'America 4.078
CN - Cina 360
SG - Singapore 282
IT - Italia 235
VN - Vietnam 109
DE - Germania 96
SE - Svezia 88
FI - Finlandia 69
GB - Regno Unito 56
UA - Ucraina 35
FR - Francia 32
NL - Olanda 25
RU - Federazione Russa 23
BR - Brasile 12
HK - Hong Kong 10
IN - India 10
BE - Belgio 9
IE - Irlanda 8
AU - Australia 7
TW - Taiwan 6
CA - Canada 5
PL - Polonia 5
AT - Austria 4
CI - Costa d'Avorio 4
ES - Italia 3
GR - Grecia 3
TR - Turchia 3
HU - Ungheria 2
IL - Israele 2
JP - Giappone 2
LT - Lituania 2
NZ - Nuova Zelanda 2
BG - Bulgaria 1
CL - Cile 1
CO - Colombia 1
CZ - Repubblica Ceca 1
DZ - Algeria 1
EG - Egitto 1
IQ - Iraq 1
IR - Iran 1
LU - Lussemburgo 1
PH - Filippine 1
PK - Pakistan 1
PT - Portogallo 1
RO - Romania 1
VE - Venezuela 1
Totale 5.601
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Città #
Fairfield 582
Woodbridge 437
Chandler 393
Houston 331
Ann Arbor 278
Seattle 235
Cambridge 217
Wilmington 217
Ashburn 209
Jacksonville 190
Singapore 165
Santa Clara 123
Dong Ket 109
Padova 92
Boardman 78
Princeton 71
Beijing 61
San Diego 50
Nanjing 46
Des Moines 45
Medford 40
Roxbury 39
Helsinki 26
Shenyang 24
Dearborn 20
Milan 17
New York 16
Guangzhou 15
Jinan 15
Nanchang 15
Hebei 14
Tianjin 12
Jiaxing 11
Changsha 10
Norwalk 10
Charleston 9
Hong Kong 9
Zhengzhou 9
Dublin 8
Falls Church 8
Hangzhou 8
Hefei 8
London 8
Kunming 7
Ogden 7
Nuremberg 6
Redwood City 6
Amsterdam 5
Haikou 5
Indiana 5
Lanzhou 5
Mogliano Veneto 5
Munich 5
Rome 5
Sydney 5
Turin 5
Waanrode 5
Abidjan 4
Bergamo 4
Brussels 4
Nürnberg 4
Syracuse 4
Taizhou 4
Casier 3
Chiswick 3
East District 3
Falkenstein 3
Frankfurt am Main 3
Fuzhou 3
Kaohsiung City 3
Tappahannock 3
Taranto 3
Toronto 3
Warsaw 3
Agrigento 2
Bari 2
Borås 2
Brendola 2
Budapest 2
Catania 2
Chengdu 2
Codognè 2
Cologne 2
Foligno 2
Herzliya 2
Istanbul 2
Kilburn 2
Modena 2
Ningbo 2
Nizhniy Novgorod 2
Pisa 2
Shanghai 2
Shenzhen 2
Simi Valley 2
Southwark 2
Stockholm 2
Tacoma 2
Taiyuan 2
Vicenza 2
Vienna 2
Totale 4.465
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Nome #
Paradoxical GH increase during OGTT is associated to first-generation somatostatin analogs responsiveness in acromegaly 180
Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26 167
Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants. 160
Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy 152
MFN2 KNOCKDOWN CAUSES NEUROMUSCULAR ALTERATIONS DURING ZEBRAFISH (DANIO RERIO) DEVELOPMENT: CHARACTERIZATION AND ANALYSIS OF A NEW MODEL FOR CHARCOT-MARIE-TOOTH TYPE 2A NEUROPATHY 148
A novel SACS mutation results in non-ataxic spastic paraplegia and peripheral neuropathy. 143
Homozygous desmocollin-2 mutations and arrhythmogenic cardiomyopathy 139
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy 138
Zebrafish Tg(hb9:MTS-Kaede): A new in vivo tool for studying the axonal movement of mitochondria 137
A locus for migraine without aura maps on chromosome 14q21.2-q22.3 136
Abstracts of the XXIII rd World Congress of Psychiatric Genetics (WCPG): Poster abstracts 135
Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder. 133
Rare Risk Variants Identification by Identity-by-Descent Mapping and Whole-Exome Sequencing Implicates Neuronal Development Pathways in Schizophrenia and Bipolar Disorder 131
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample 126
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signaling 126
Performance of four models for eye color prediction in an Italian population sample 126
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1 123
A novel 9-bp insertion in the GJB1 gene causing a mild form of X-linked CMT with late onset 121
A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28 120
Novel mutations in the L1CAM gene support the complexity of L1 syndrome 118
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy. 115
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. 113
Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegia 112
Clinical and genetic characterization of an Italian family with slow-channel syndrome 112
Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy. 109
Developmental defects and neuromuscular alterations due to mitofusin 2 gene (MFN2) silencing in zebrafish: a new model for Charcot-Marie-Tooth type 2A neuropathy 109
Familial epilepsy and developmental dysphasia: Description of an Italian pedigree with autosomal dominant inheritance and screening of candidate loci. 108
Hereditary spastic paraplegia associated with peripheral neuropathy: a distinct clinical and genetic entity 108
Efficacy of exome-targeted capture sequencing to detect mutations in known cerebellar ataxia genes 107
Familly with two different cases of post- and pre-natal L1 syndrome; When hydrocephaly become "multidisciplinary headache" 102
Mutation Analysis of MFN2, GJB1, MPZ and PMP22 in Italian Patients with Axonal Charcot-Marie-Tooth Disease. 101
Individuation of new mutations in L1CAM gene in patients with L1 diseases. 100
Identification and characterization of C3orf6, a new conserved human gene mapping to chromosome 3q28 96
A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28. 95
Diagnosis of Primary Ciliary Dyskinesia by a Targeted Next-Generation Sequencing Panel: Molecular and Clinical Findings in Italian Patients 91
Novel Missense Variant in MYL2 Gene Associated with Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology 89
Evaluation of linkage signals in a subset of families with high recurrence of schizophrenia and bipolar disorder originating from Chioggia 88
The GIP/GIPR axis is functionally linked to GH-secretion increase in a significant proportion of gsp(-) somatotropinomas 85
Studio genetico pilota sulla popolazione di Chioggia: dati preliminari 83
Zebrafish mitofusin-2 knockdown: a new model for CMT2A neuropathy? 79
c.1392+2T>C mutation in MFN2 gene affects splicing in Charcot-Marie-Tooth (CMT) 2A family. 78
High prevalence of chitotriosidase deficiency in Peruvian Amerindians exposed to chitin-bearing food and enteroparasites 72
Genome scan for schizophrenia/bipolar disorder supports a susceptibility locus in 15q26 71
Genetic inheritance of schizophrenia and bipolar disorder in an Italian population isolate 69
The Methylation Analysis of the Glucose-Dependent Insulinotropic Polypeptide Receptor (GIPR) Locus in GH-Secreting Pituitary Adenomas. 64
NEURO(NO)PATIE MOTORIE DISTALI FAMILIARI 61
Genetic inheritance of schizophrenia and bipolar disorder in an italian population isolate 61
Novel loss-of-function mutation of the HINT1 gene in a patient with distal motor axonal neuropathy without neuromyotonia. 56
Novel MFN2 mutations and phenotypic variability in patients with Charcot-Marie-Tooth disease type 2A. 55
Clinical and genetic features of a large cohort of Italian SPG4 patients from the D.A.I.S.Y. collaborative network 51
Mfn2 knockdown causes neuromuscular alterations during zebrafish (danio rerio) development: characterization and analysis of a new model for charcot-marie-tooth type 2a neuropathy. 48
Molecular and clinical characterization of a large cohort of Italian patients with Hereditary Spastic Paraplegia (HSP) 45
Internal validation and improvement of mitochondrial genome sequencing using the Precision ID mtDNA Whole Genome Panel 40
Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia 38
Increasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlations 34
Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network 33
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment 32
Totale 5.669
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Categoria #
all - tutte 20.810
article - articoli 18.350
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 39.160
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020377 0 0 0 0 0 0 0 0 103 177 48 49
2020/2021823 25 48 38 58 64 38 17 68 99 129 105 134
2021/2022850 25 98 110 44 55 44 45 78 41 18 103 189
2022/2023675 134 77 62 57 94 95 3 46 61 8 27 11
2023/2024342 20 46 55 32 30 23 30 14 15 9 27 41
2024/2025806 4 110 70 78 242 46 75 127 54 0 0 0
Totale 5.669