VAZZA, GIOVANNI
 Distribuzione geografica
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Continente #
NA - Nord America 6.355
AS - Asia 3.525
EU - Europa 1.671
SA - Sud America 532
AF - Africa 485
OC - Oceania 50
Continente sconosciuto - Info sul continente non disponibili 18
Totale 12.636
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Nazione #
US - Stati Uniti d'America 6.061
SG - Singapore 1.068
CN - Cina 745
VN - Vietnam 591
IT - Italia 465
BR - Brasile 336
HK - Hong Kong 271
BD - Bangladesh 174
DE - Germania 151
IN - India 121
SE - Svezia 117
FI - Finlandia 116
FR - Francia 115
GB - Regno Unito 107
NL - Olanda 91
PL - Polonia 60
CA - Canada 53
TR - Turchia 51
UA - Ucraina 49
AR - Argentina 45
RU - Federazione Russa 41
JP - Giappone 38
MX - Messico 38
BJ - Benin 32
SA - Arabia Saudita 28
CO - Colombia 27
PH - Filippine 27
PK - Pakistan 26
ZA - Sudafrica 26
ID - Indonesia 25
IQ - Iraq 25
AT - Austria 24
EC - Ecuador 24
JM - Giamaica 24
BE - Belgio 23
ES - Italia 23
MA - Marocco 23
PY - Paraguay 22
UZ - Uzbekistan 22
LA - Repubblica Popolare Democratica del Laos 21
IE - Irlanda 20
JO - Giordania 20
DZ - Algeria 19
GN - Guinea 19
NI - Nicaragua 19
AU - Australia 18
IL - Israele 18
TW - Taiwan 17
VE - Venezuela 17
AL - Albania 16
BY - Bielorussia 16
KR - Corea 16
MU - Mauritius 16
AO - Angola 15
CI - Costa d'Avorio 15
CL - Cile 15
HN - Honduras 15
LV - Lettonia 15
MY - Malesia 15
TH - Thailandia 15
BW - Botswana 14
BZ - Belize 14
CR - Costa Rica 14
CV - Capo Verde 14
CY - Cipro 14
CZ - Repubblica Ceca 14
GR - Grecia 14
KG - Kirghizistan 14
KZ - Kazakistan 14
NP - Nepal 14
PA - Panama 14
TZ - Tanzania 14
UY - Uruguay 14
YT - Mayotte 14
EG - Egitto 13
ET - Etiopia 13
GF - Guiana Francese 13
IR - Iran 13
RS - Serbia 13
TJ - Tagikistan 13
AZ - Azerbaigian 12
KE - Kenya 12
ME - Montenegro 12
NZ - Nuova Zelanda 12
PT - Portogallo 12
SK - Slovacchia (Repubblica Slovacca) 12
UG - Uganda 12
AM - Armenia 11
BA - Bosnia-Erzegovina 11
BO - Bolivia 11
CH - Svizzera 11
GE - Georgia 11
GM - Gambi 11
GT - Guatemala 11
HU - Ungheria 11
LC - Santa Lucia 11
LY - Libia 11
ML - Mali 11
PS - Palestinian Territory 11
SI - Slovenia 11
Totale 12.163
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Città #
Ashburn 693
Singapore 650
Fairfield 582
San Jose 555
Woodbridge 437
Chandler 393
Houston 338
Ann Arbor 278
Hong Kong 249
Seattle 241
Wilmington 219
Cambridge 217
Jacksonville 191
Ho Chi Minh City 173
Santa Clara 159
Beijing 143
Hanoi 116
Dong Ket 109
Padova 95
Los Angeles 92
Boardman 80
New York 79
The Dalles 72
Princeton 71
San Diego 51
Des Moines 46
Nanjing 46
Lauterbourg 45
Milan 43
Medford 40
Munich 39
Roxbury 39
Helsinki 37
Buffalo 36
São Paulo 35
Orem 34
Bytom 31
Cotonou 31
Turku 28
Council Bluffs 27
Shenyang 25
Chennai 24
Da Nang 24
Guangzhou 24
Tokyo 23
Istanbul 21
Rome 21
Dearborn 20
Redondo Beach 20
Stockholm 20
Tashkent 20
Conakry 19
Haiphong 19
Warsaw 19
Atlanta 18
Managua 18
Vientiane 18
Amman 17
Chicago 17
Brooklyn 16
Hefei 16
London 16
Phoenix 16
Abidjan 15
Dallas 15
Dublin 15
Jinan 15
Luanda 15
Mumbai 15
Nanchang 15
Padua 15
Amsterdam 14
Frankfurt am Main 14
Hebei 14
Kingston 14
Montreal 14
Tianjin 14
Vienna 14
Bishkek 13
Biên Hòa 13
Montevideo 13
Praia 13
Riga 13
Changsha 12
Dushanbe 12
Jeddah 12
Johannesburg 12
Lahore 12
Nuremberg 12
Panama City 12
Addis Ababa 11
Baghdad 11
Baku 11
Dar es Salaam 11
Jiaxing 11
Ljubljana 11
Nairobi 11
Naples 11
Rio de Janeiro 11
Accra 10
Totale 7.767
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Nome #
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signaling 365
Paradoxical GH increase during OGTT is associated to first-generation somatostatin analogs responsiveness in acromegaly 338
Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy 306
Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants. 291
Rare Risk Variants Identification by Identity-by-Descent Mapping and Whole-Exome Sequencing Implicates Neuronal Development Pathways in Schizophrenia and Bipolar Disorder 290
The Methylation Analysis of the Glucose-Dependent Insulinotropic Polypeptide Receptor (GIPR) Locus in GH-Secreting Pituitary Adenomas. 286
Performance of four models for eye color prediction in an Italian population sample 286
MFN2 KNOCKDOWN CAUSES NEUROMUSCULAR ALTERATIONS DURING ZEBRAFISH (DANIO RERIO) DEVELOPMENT: CHARACTERIZATION AND ANALYSIS OF A NEW MODEL FOR CHARCOT-MARIE-TOOTH TYPE 2A NEUROPATHY 285
Homozygous desmocollin-2 mutations and arrhythmogenic cardiomyopathy 275
Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26 275
Abstracts of the XXIII rd World Congress of Psychiatric Genetics (WCPG): Poster abstracts 271
A novel SACS mutation results in non-ataxic spastic paraplegia and peripheral neuropathy. 269
Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder. 260
Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegia 257
Hereditary spastic paraplegia associated with peripheral neuropathy: a distinct clinical and genetic entity 253
Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy. 252
Diagnosis of Primary Ciliary Dyskinesia by a Targeted Next-Generation Sequencing Panel: Molecular and Clinical Findings in Italian Patients 249
Zebrafish Tg(hb9:MTS-Kaede): A new in vivo tool for studying the axonal movement of mitochondria 248
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample 245
Efficacy of exome-targeted capture sequencing to detect mutations in known cerebellar ataxia genes 243
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1 239
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. 235
A locus for migraine without aura maps on chromosome 14q21.2-q22.3 234
Novel mutations in the L1CAM gene support the complexity of L1 syndrome 228
A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28 219
Novel Missense Variant in MYL2 Gene Associated with Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology 218
Developmental defects and neuromuscular alterations due to mitofusin 2 gene (MFN2) silencing in zebrafish: a new model for Charcot-Marie-Tooth type 2A neuropathy 218
A novel 9-bp insertion in the GJB1 gene causing a mild form of X-linked CMT with late onset 216
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy 213
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy. 209
Familly with two different cases of post- and pre-natal L1 syndrome; When hydrocephaly become "multidisciplinary headache" 206
Clinical and genetic characterization of an Italian family with slow-channel syndrome 205
Familial epilepsy and developmental dysphasia: Description of an Italian pedigree with autosomal dominant inheritance and screening of candidate loci. 198
Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia 189
The GIP/GIPR axis is functionally linked to GH-secretion increase in a significant proportion of gsp(-) somatotropinomas 188
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment 188
c.1392+2T>C mutation in MFN2 gene affects splicing in Charcot-Marie-Tooth (CMT) 2A family. 186
Mfn2 knockdown causes neuromuscular alterations during zebrafish (danio rerio) development: characterization and analysis of a new model for charcot-marie-tooth type 2a neuropathy. 181
Internal validation and improvement of mitochondrial genome sequencing using the Precision ID mtDNA Whole Genome Panel 181
Individuation of new mutations in L1CAM gene in patients with L1 diseases. 178
Identification and characterization of C3orf6, a new conserved human gene mapping to chromosome 3q28 178
High prevalence of chitotriosidase deficiency in Peruvian Amerindians exposed to chitin-bearing food and enteroparasites 177
Evaluation of linkage signals in a subset of families with high recurrence of schizophrenia and bipolar disorder originating from Chioggia 172
Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network 172
Mutation Analysis of MFN2, GJB1, MPZ and PMP22 in Italian Patients with Axonal Charcot-Marie-Tooth Disease. 170
Studio genetico pilota sulla popolazione di Chioggia: dati preliminari 168
Clinical and genetic features of a large cohort of Italian SPG4 patients from the D.A.I.S.Y. collaborative network 164
A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28. 161
Zebrafish mitofusin-2 knockdown: a new model for CMT2A neuropathy? 160
Genome scan for schizophrenia/bipolar disorder supports a susceptibility locus in 15q26 157
Novel loss-of-function mutation of the HINT1 gene in a patient with distal motor axonal neuropathy without neuromyotonia. 150
Increasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlations 147
NEURO(NO)PATIE MOTORIE DISTALI FAMILIARI 143
Exploring the tumor suppressor role of RIN1 in familial thyroid carcinoma 142
Genetic inheritance of schizophrenia and bipolar disorder in an Italian population isolate 138
Novel MFN2 mutations and phenotypic variability in patients with Charcot-Marie-Tooth disease type 2A. 136
Mutated sigma-1R disrupts cell homeostasis in dHMN patient cells 123
Genetic inheritance of schizophrenia and bipolar disorder in an italian population isolate 116
Molecular and clinical characterization of a large cohort of Italian patients with Hereditary Spastic Paraplegia (HSP) 113
GIPR in GH-PitNETs: molecular and functional insights 87
PitNET tissue deconvolution: tracing normal tissue residues and immune dynamics 61
Totale 12.708
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Categoria #
all - tutte 35.186
article - articoli 30.768
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 65.954
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2024/20251.563 4 110 70 78 242 46 75 127 108 58 252 393
2025/20266.150 337 458 689 883 589 275 919 483 620 361 278 258
2026/2027132 132 0 0 0 0 0 0 0 0 0 0 0
Totale 12.708