IRIS
GUERRINI, RENZO
 Distribuzione geografica
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Continente #
EU - Europa 2.592
AS - Asia 459
NA - Nord America 220
SA - Sud America 55
AF - Africa 9
OC - Oceania 1
Totale 3.336
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Nazione #
IT - Italia 2.526
US - Stati Uniti d'America 201
SG - Singapore 170
CN - Cina 117
VN - Vietnam 96
BR - Brasile 38
FR - Francia 15
DE - Germania 14
HK - Hong Kong 14
GB - Regno Unito 11
IQ - Iraq 8
ID - Indonesia 7
JP - Giappone 7
MX - Messico 7
BD - Bangladesh 5
CA - Canada 5
IN - India 5
NL - Olanda 5
AR - Argentina 4
AZ - Azerbaigian 4
CH - Svizzera 4
ZA - Sudafrica 4
CL - Cile 3
EC - Ecuador 3
SA - Arabia Saudita 3
CO - Colombia 2
FI - Finlandia 2
HN - Honduras 2
IL - Israele 2
JO - Giordania 2
KR - Corea 2
NP - Nepal 2
PE - Perù 2
PK - Pakistan 2
PS - Palestinian Territory 2
RU - Federazione Russa 2
TT - Trinidad e Tobago 2
AE - Emirati Arabi Uniti 1
AT - Austria 1
AU - Australia 1
BO - Bolivia 1
CI - Costa d'Avorio 1
CZ - Repubblica Ceca 1
DO - Repubblica Dominicana 1
ES - Italia 1
GE - Georgia 1
HR - Croazia 1
IE - Irlanda 1
JM - Giamaica 1
KE - Kenya 1
KZ - Kazakistan 1
LB - Libano 1
LI - Liechtenstein 1
MA - Marocco 1
MF - Saint Martin 1
MM - Myanmar 1
MY - Malesia 1
NO - Norvegia 1
OM - Oman 1
PH - Filippine 1
PL - Polonia 1
PT - Portogallo 1
PY - Paraguay 1
RO - Romania 1
SE - Svezia 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
TH - Thailandia 1
TN - Tunisia 1
TR - Turchia 1
TW - Taiwan 1
UA - Ucraina 1
VE - Venezuela 1
Totale 3.336
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Città #
Genoa 1.447
Genova 434
Rapallo 343
Vado Ligure 257
Singapore 61
San Jose 55
Ashburn 50
Council Bluffs 31
Beijing 27
Ho Chi Minh City 27
Hanoi 24
Hong Kong 14
Lauterbourg 13
Frankfurt am Main 12
Bordighera 10
Santa Clara 7
Milan 6
New York 6
Tokyo 6
Haiphong 5
Mexico City 5
Baku 4
São Paulo 4
Cardiff 3
City of London 3
Los Angeles 3
Orem 3
Quito 3
Baghdad 2
Blumenau 2
Bologna 2
Chavannes 2
Da Nang 2
Denver 2
Des Moines 2
Hải Dương 2
Jeddah 2
Johannesburg 2
Karachi 2
London 2
Montreal 2
Mumbai 2
Quận Bình Thạnh 2
Santa Teresa di Riva 2
Thái Nguyên 2
Tianjin 2
Turin 2
Zurich 2
Abidjan 1
Abu Dhabi 1
Agadir 1
Ajax 1
Almaty 1
Amman 1
Amsterdam 1
Araure 1
Ariquemes 1
Arujá 1
Baguio City 1
Balneário Piçarras 1
Bandung 1
Barataria 1
Basra 1
Batumi 1
Bengaluru 1
Biên Hòa 1
Borj el Bey 1
Brasília 1
Bratislava 1
Buenos Aires 1
Bình Phước 1
Bắc Giang 1
Can Tho 1
Canoas 1
Carapicuíba 1
Cariacica 1
Castro 1
Centurion 1
Cesano Maderno 1
Chaguanas 1
Chittagong 1
Ciudad del Este 1
Coaraci 1
Corupá 1
Dakar 1
Delfim Moreira 1
Delhi 1
Denpasar 1
Detroit 1
Dhaka 1
Diamantina 1
Dongguan 1
Dublin 1
Duhok 1
Duque de Caxias 1
Durban 1
El Progreso 1
Elk Grove Village 1
Erbil 1
Evanston 1
Totale 2.955
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Nome #
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome 176
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study 163
No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy 151
No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1 135
Emerging Role of the Autophagy/Lysosomal Degradative Pathway in Neurodevelopmental Disorders With Epilepsy 130
Generalized Epilepsy with Febrile Seizures Plus (GEFS+): Clinical Spectrum in Seven Italian Families Unrelated to SCN1A, SCN1B, and GABRG2 Gene Mutations 127
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study 125
A common SCN1A splice-site polymorphism modifies the effect of carbamazepine on cortical excitability - A pharmacogenetic transcranial magnetic stimulation study 123
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy 118
Diagnostic implications of genetic copy number variation in epilepsy plus 109
ATP6V1A is required for synaptic rearrangements and plasticity in murine hippocampal neurons 108
Benign Familial Neonatal-Infantile Seizures: Characterization of a New Sodium Channelopathy 108
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications 106
Cortical formation abnormalities on foetal MR imaging: a proposed classification system trialled on 356 cases from Italian and UK centres 101
Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy 98
Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy study 97
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsies 90
Event-based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross-sectional data 89
Atlas of lesion locations and postsurgical seizure freedom in focal cortical dysplasia: A MELD study 88
National survey on the prevalence of single-gene aetiologies for genetic developmental and epileptic encephalopathies in Italy 87
The diagnostic approach to mitochondrial disorders in children in the era of next-generation sequencing: A 4-year cohort study 83
Interpretable surface-based detection of focal cortical dysplasias: a Multi-centre Epilepsy Lesion Detection study 81
The genetics of Dravet syndrome 80
Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into Adulthood 74
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Epilepsy Patients With KCNC2 Pathogenic Variants 72
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes 70
No evidence of ATP1A2 involvement in 12 multiplex Italian families with benign familial infantile seizures 66
Networks Underlie Temporal Onset of Dysplasia-Related Epilepsy: A MELD Study 64
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy 64
Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression 62
Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum 58
Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis 56
De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies 55
Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses 50
An interconnected data infrastructure to support large-scale rare disease research 50
The Genetic Landscape of Complex Childhood‐Onset Hyperkinetic Movement Disorders 41
Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration 38
Totale 3.393
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Categoria #
all - tutte 12.494
article - articoli 12.494
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 24.988
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202141 0 0 0 0 0 0 0 0 0 32 1 8
2021/2022177 19 5 1 5 11 14 9 42 8 31 7 25
2022/2023384 19 17 9 49 63 58 17 24 75 6 41 6
2023/2024231 7 34 6 30 27 47 13 18 5 4 10 30
2024/2025732 20 40 2 48 69 106 76 127 33 48 77 86
2025/20261.585 181 52 393 160 201 90 200 78 107 123 0 0
Totale 3.393