VAZZA, GIOVANNI
 Distribuzione geografica
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Continente #
NA - Nord America 3.773
EU - Europa 519
AS - Asia 434
OC - Oceania 9
SA - Sud America 2
AF - Africa 1
Totale 4.738
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Nazione #
US - Stati Uniti d'America 3.771
CN - Cina 307
IT - Italia 156
VN - Vietnam 109
SE - Svezia 88
DE - Germania 67
FI - Finlandia 64
GB - Regno Unito 55
UA - Ucraina 35
NL - Olanda 18
IN - India 9
AU - Australia 7
IE - Irlanda 7
FR - Francia 6
BE - Belgio 5
PL - Polonia 5
ES - Italia 3
GR - Grecia 3
TR - Turchia 3
CA - Canada 2
HU - Ungheria 2
IL - Israele 2
JP - Giappone 2
NZ - Nuova Zelanda 2
BG - Bulgaria 1
BR - Brasile 1
CL - Cile 1
CZ - Repubblica Ceca 1
EG - Egitto 1
HK - Hong Kong 1
IR - Iran 1
LT - Lituania 1
LU - Lussemburgo 1
PT - Portogallo 1
Totale 4.738
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Città #
Fairfield 582
Woodbridge 437
Chandler 393
Houston 331
Ann Arbor 278
Seattle 234
Cambridge 217
Wilmington 217
Ashburn 201
Jacksonville 190
Dong Ket 109
Padova 74
Princeton 71
Beijing 61
San Diego 50
Nanjing 46
Des Moines 45
Medford 40
Roxbury 39
Shenyang 24
Boardman 22
Helsinki 21
Dearborn 20
New York 16
Jinan 15
Nanchang 15
Hebei 14
Guangzhou 13
Tianjin 12
Jiaxing 11
Changsha 10
Norwalk 10
Charleston 9
Falls Church 8
Zhengzhou 8
Dublin 7
Hangzhou 7
Hefei 7
Kunming 7
London 7
Ogden 7
Milan 6
Redwood City 6
Haikou 5
Indiana 5
Lanzhou 5
Munich 5
Sydney 5
Waanrode 5
Bergamo 4
Nürnberg 4
Rome 4
Syracuse 4
Taizhou 4
Amsterdam 3
Casier 3
Chiswick 3
Fuzhou 3
Tappahannock 3
Taranto 3
Turin 3
Warsaw 3
Borås 2
Brendola 2
Budapest 2
Chengdu 2
Foligno 2
Herzliya 2
Istanbul 2
Kilburn 2
Ningbo 2
Pisa 2
Simi Valley 2
Southwark 2
Stockholm 2
Tacoma 2
Taiyuan 2
Vicenza 2
Wroclaw 2
Xian 2
Acton 1
Auburn Hills 1
Auckland 1
Bagnatica 1
Baotou 1
Barcelona 1
Belluno 1
Bristol 1
Brno 1
Cairo 1
Catania 1
Charlotte 1
Chicago 1
Edinburgh 1
Florence 1
Frankfurt am Main 1
Groningen 1
Gunzenhausen 1
Hounslow 1
Jinhua 1
Totale 4.027
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Nome #
Paradoxical GH increase during OGTT is associated to first-generation somatostatin analogs responsiveness in acromegaly 154
Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants. 149
Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26 149
Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy 136
Homozygous desmocollin-2 mutations and arrhythmogenic cardiomyopathy 129
MFN2 KNOCKDOWN CAUSES NEUROMUSCULAR ALTERATIONS DURING ZEBRAFISH (DANIO RERIO) DEVELOPMENT: CHARACTERIZATION AND ANALYSIS OF A NEW MODEL FOR CHARCOT-MARIE-TOOTH TYPE 2A NEUROPATHY 128
A novel SACS mutation results in non-ataxic spastic paraplegia and peripheral neuropathy. 124
A locus for migraine without aura maps on chromosome 14q21.2-q22.3 123
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy 121
Zebrafish Tg(hb9:MTS-Kaede): A new in vivo tool for studying the axonal movement of mitochondria 117
Performance of four models for eye color prediction in an Italian population sample 117
Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder. 116
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample 115
Rare Risk Variants Identification by Identity-by-Descent Mapping and Whole-Exome Sequencing Implicates Neuronal Development Pathways in Schizophrenia and Bipolar Disorder 113
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signaling 111
Abstracts of the XXIII rd World Congress of Psychiatric Genetics (WCPG): Poster abstracts 108
A novel 9-bp insertion in the GJB1 gene causing a mild form of X-linked CMT with late onset 106
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. 105
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1 102
Hereditary spastic paraplegia associated with peripheral neuropathy: a distinct clinical and genetic entity 102
Novel mutations in the L1CAM gene support the complexity of L1 syndrome 102
Familial epilepsy and developmental dysphasia: Description of an Italian pedigree with autosomal dominant inheritance and screening of candidate loci. 101
A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28 101
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy. 98
Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy. 97
Clinical and genetic characterization of an Italian family with slow-channel syndrome 96
Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegia 95
Mutation Analysis of MFN2, GJB1, MPZ and PMP22 in Italian Patients with Axonal Charcot-Marie-Tooth Disease. 95
Efficacy of exome-targeted capture sequencing to detect mutations in known cerebellar ataxia genes 95
Developmental defects and neuromuscular alterations due to mitofusin 2 gene (MFN2) silencing in zebrafish: a new model for Charcot-Marie-Tooth type 2A neuropathy 91
Identification and characterization of C3orf6, a new conserved human gene mapping to chromosome 3q28 89
Familly with two different cases of post- and pre-natal L1 syndrome; When hydrocephaly become "multidisciplinary headache" 89
A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28. 83
Individuation of new mutations in L1CAM gene in patients with L1 diseases. 79
Diagnosis of Primary Ciliary Dyskinesia by a Targeted Next-Generation Sequencing Panel: Molecular and Clinical Findings in Italian Patients 78
The GIP/GIPR axis is functionally linked to GH-secretion increase in a significant proportion of gsp(-) somatotropinomas 75
Evaluation of linkage signals in a subset of families with high recurrence of schizophrenia and bipolar disorder originating from Chioggia 68
c.1392+2T>C mutation in MFN2 gene affects splicing in Charcot-Marie-Tooth (CMT) 2A family. 65
Novel Missense Variant in MYL2 Gene Associated with Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology 65
Zebrafish mitofusin-2 knockdown: a new model for CMT2A neuropathy? 60
High prevalence of chitotriosidase deficiency in Peruvian Amerindians exposed to chitin-bearing food and enteroparasites 60
Studio genetico pilota sulla popolazione di Chioggia: dati preliminari 59
Genome scan for schizophrenia/bipolar disorder supports a susceptibility locus in 15q26 54
NEURO(NO)PATIE MOTORIE DISTALI FAMILIARI 51
Genetic inheritance of schizophrenia and bipolar disorder in an Italian population isolate 50
Novel loss-of-function mutation of the HINT1 gene in a patient with distal motor axonal neuropathy without neuromyotonia. 48
Genetic inheritance of schizophrenia and bipolar disorder in an italian population isolate 46
Novel MFN2 mutations and phenotypic variability in patients with Charcot-Marie-Tooth disease type 2A. 43
Molecular and clinical characterization of a large cohort of Italian patients with Hereditary Spastic Paraplegia (HSP) 36
Clinical and genetic features of a large cohort of Italian SPG4 patients from the D.A.I.S.Y. collaborative network 34
Mfn2 knockdown causes neuromuscular alterations during zebrafish (danio rerio) development: characterization and analysis of a new model for charcot-marie-tooth type 2a neuropathy. 33
Internal validation and improvement of mitochondrial genome sequencing using the Precision ID mtDNA Whole Genome Panel 28
Increasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlations 27
Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia 23
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment 21
Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network 20
The Methylation Analysis of the Glucose-Dependent Insulinotropic Polypeptide Receptor (GIPR) Locus in GH-Secreting Pituitary Adenomas. 15
Totale 4.795
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Categoria #
all - tutte 15.242
article - articoli 13.558
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 28.800
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019243 0 0 0 0 0 0 0 0 0 0 120 123
2019/20201.044 116 41 16 84 97 99 101 113 103 177 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
2023/2024274 20 46 55 32 30 23 30 14 15 9 0 0
Totale 4.795