IRIS
GUERRINI, RENZO
 Distribuzione geografica
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Continente #
EU - Europa 2.647
AS - Asia 559
NA - Nord America 470
SA - Sud America 57
Continente sconosciuto - Info sul continente non disponibili 57
AF - Africa 9
OC - Oceania 1
Totale 3.800
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Nazione #
IT - Italia 2.572
US - Stati Uniti d'America 433
SG - Singapore 173
CN - Cina 131
VN - Vietnam 97
BD - Bangladesh 86
BR - Brasile 38
CA - Canada 15
FR - Francia 15
DE - Germania 14
HK - Hong Kong 14
GB - Regno Unito 12
IQ - Iraq 8
JP - Giappone 8
MX - Messico 8
NL - Olanda 8
ID - Indonesia 7
AR - Argentina 6
IN - India 5
AZ - Azerbaigian 4
CH - Svizzera 4
ZA - Sudafrica 4
CL - Cile 3
EC - Ecuador 3
HN - Honduras 3
PL - Polonia 3
SA - Arabia Saudita 3
TT - Trinidad e Tobago 3
CO - Colombia 2
ES - Italia 2
FI - Finlandia 2
IL - Israele 2
JM - Giamaica 2
JO - Giordania 2
KR - Corea 2
NP - Nepal 2
PE - Perù 2
PK - Pakistan 2
PR - Porto Rico 2
PS - Palestinian Territory 2
RO - Romania 2
RU - Federazione Russa 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
GE - Georgia 1
GT - Guatemala 1
HR - Croazia 1
IE - Irlanda 1
KE - Kenya 1
KZ - Kazakistan 1
LB - Libano 1
LI - Liechtenstein 1
MA - Marocco 1
MD - Moldavia 1
MF - Saint Martin 1
MM - Myanmar 1
MY - Malesia 1
NI - Nicaragua 1
NO - Norvegia 1
OM - Oman 1
PH - Filippine 1
PT - Portogallo 1
PY - Paraguay 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 3.743
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Città #
Genoa 1.448
Genova 434
Rapallo 343
Vado Ligure 257
San Jose 90
Ashburn 81
Singapore 64
Beijing 38
Council Bluffs 31
Ho Chi Minh City 27
Hanoi 25
Hong Kong 14
Lauterbourg 13
New York 13
Frankfurt am Main 12
Bordighera 10
Los Angeles 10
Santa Clara 10
Milan 8
Tokyo 7
Dallas 6
Bologna 5
Haiphong 5
Mexico City 5
Naples 5
Toronto 5
Baku 4
Phoenix 4
Pignataro Maggiore 4
São Paulo 4
Bari 3
Cardiff 3
City of London 3
Florence 3
Garland 3
Montreal 3
Newark 3
Orem 3
Philadelphia 3
Quito 3
Rome 3
The Bronx 3
Vienna 3
Baghdad 2
Blumenau 2
Cagliari 2
Cassopolis 2
Charlotte 2
Chavannes 2
Corona 2
Da Nang 2
Denver 2
Des Moines 2
Detroit 2
Dhaka 2
Hải Dương 2
Indianapolis 2
Inglewood 2
Jeddah 2
Johannesburg 2
Karachi 2
Lake Forest 2
London 2
Manchester 2
Maple Shade Township 2
Mumbai 2
Palermo 2
Paterson 2
Pescara 2
Queens 2
Quận Bình Thạnh 2
San Francisco 2
San Mateo 2
Santa Teresa di Riva 2
Springfield 2
St Louis 2
Thái Nguyên 2
Tianjin 2
Turin 2
Warsaw 2
Wilmington 2
Zurich 2
Abidjan 1
Abilene 1
Abu Dhabi 1
Agadir 1
Ajax 1
Almaty 1
Amman 1
Amsterdam 1
Annapolis 1
Appleton 1
Araure 1
Ariquemes 1
Arujá 1
Baguio City 1
Balneário Piçarras 1
Baltimore 1
Bandung 1
Barataria 1
Totale 3.117
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Nome #
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome 187
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study 170
No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy 164
National survey on the prevalence of single-gene aetiologies for genetic developmental and epileptic encephalopathies in Italy 148
No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1 147
Emerging Role of the Autophagy/Lysosomal Degradative Pathway in Neurodevelopmental Disorders With Epilepsy 139
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study 138
A common SCN1A splice-site polymorphism modifies the effect of carbamazepine on cortical excitability - A pharmacogenetic transcranial magnetic stimulation study 134
Generalized Epilepsy with Febrile Seizures Plus (GEFS+): Clinical Spectrum in Seven Italian Families Unrelated to SCN1A, SCN1B, and GABRG2 Gene Mutations 133
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy 130
Benign Familial Neonatal-Infantile Seizures: Characterization of a New Sodium Channelopathy 119
ATP6V1A is required for synaptic rearrangements and plasticity in murine hippocampal neurons 118
Diagnostic implications of genetic copy number variation in epilepsy plus 113
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications 112
Cortical formation abnormalities on foetal MR imaging: a proposed classification system trialled on 356 cases from Italian and UK centres 110
Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy study 106
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsies 104
Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy 104
Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into Adulthood 103
Atlas of lesion locations and postsurgical seizure freedom in focal cortical dysplasia: A MELD study 99
Event-based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross-sectional data 96
The diagnostic approach to mitochondrial disorders in children in the era of next-generation sequencing: A 4-year cohort study 88
Interpretable surface-based detection of focal cortical dysplasias: a Multi-centre Epilepsy Lesion Detection study 86
The genetics of Dravet syndrome 84
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Epilepsy Patients With KCNC2 Pathogenic Variants 84
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes 80
Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum 75
No evidence of ATP1A2 involvement in 12 multiplex Italian families with benign familial infantile seizures 73
Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression 72
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy 69
Networks Underlie Temporal Onset of Dysplasia-Related Epilepsy: A MELD Study 68
Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis 67
De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies 60
Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses 58
An interconnected data infrastructure to support large-scale rare disease research 58
The Genetic Landscape of Complex Childhood‐Onset Hyperkinetic Movement Disorders 58
Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration 46
Totale 3.800
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Categoria #
all - tutte 13.999
article - articoli 13.999
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 27.998
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/20261.863 181 52 393 160 201 90 200 78 107 131 133 137
2026/2027129 129 0 0 0 0 0 0 0 0 0 0 0
Totale 3.800