IRIS
PISCOPO, CARMELO
 Distribuzione geografica
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Continente #
EU - Europa 162
NA - Nord America 97
AS - Asia 56
AF - Africa 10
OC - Oceania 3
SA - Sud America 3
Totale 331
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Nazione #
IT - Italia 97
US - Stati Uniti d'America 92
SG - Singapore 46
IE - Irlanda 23
NL - Olanda 14
CI - Costa d'Avorio 8
CN - Cina 8
DE - Germania 7
FI - Finlandia 6
RU - Federazione Russa 6
CA - Canada 5
GB - Regno Unito 4
AU - Australia 3
CH - Svizzera 3
BR - Brasile 2
AT - Austria 1
BE - Belgio 1
CL - Cile 1
HK - Hong Kong 1
NG - Nigeria 1
PK - Pakistan 1
SO - Somalia 1
Totale 331
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Città #
Singapore 37
Naples 23
Dublin 19
Ashburn 17
Amsterdam 11
Santa Clara 8
Milan 6
Catania 5
Rome 5
Chandler 4
Moscow 4
Ottawa 4
Zola Predosa 4
Bari 3
Basel 3
Boardman 3
Boston 3
Casoria 3
Formia 3
Melbourne 3
Munich 3
Americana 2
Bergamo 2
Brognaturo 2
Foggia 2
Lappeenranta 2
Los Angeles 2
Pompei 2
Princeton 2
Washington 2
Bosaso 1
Bournemouth 1
Brussels 1
Casavatore 1
Castellammare di Stabia 1
Chicago 1
Crispano 1
Des Moines 1
Helsinki 1
Hong Kong 1
Jacksonville 1
Kronberg 1
Lagos 1
Lanzhou 1
Lawrence 1
Marcianise 1
Nanchang 1
Nanjing 1
Pisa 1
Richmond 1
Salerno 1
Sant'Anastasia 1
Shenyang 1
Tianjin 1
Vigodarzere 1
Wilmington 1
Totale 215
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Nome #
A first update on mapping the human genetic architecture of COVID-19 79
A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death 40
Germline rare variants of lectin pathway genes predispose to asymptomatic SARS-CoV-2 infection in elderly individuals 34
Clinical heterogeneity of Kabuki syndrome in a cohort of Italian patients and review of the literature 31
Genetic prothrombotic risk factors in children with extrahepatic portal vein obstruction. 27
Genotypes and phenotypes heterogeneity in PIK3CA-related overgrowth spectrum and overlapping conditions: 150 novel patients and systematic review of 1007 patients with PIK3CA pathogenetic variants 20
A Novel Variant in RAD21 in Cornelia De Lange Syndrome Type 4: Case Report and Bioinformatic Analysis 20
Pediatric Portal Vein Thrombosis: More on Thrombophilic Risk Factors. 16
Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry 12
Carriers of ADAMTS13 Rare Variants Are at High Risk of Life-Threatening COVID-19 12
Comprehensive Molecular Analysis of Disease-Related Genes as First-Tier Test for Early Diagnosis, Classification, and Management of Patients Affected by Nonsyndromic Ichthyosis 11
An explainable model of host genetic interactions linked to COVID-19 severity 10
First Case of a Dominant De Novo SEC23A Mutation with Neurological and Psychiatric Features: New Insights into Cranio-Lenticulo-Sutural Dysplasia with Literature Review 10
Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder 9
A Novel De Novo STAG1 Variant in Monozygotic Twins with Neurodevelopmental Disorder: New Insights in Clinical Heterogeneity 8
Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome 8
Totale 347
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Categoria #
all - tutte 2.021
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.021
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201 0 0 0 0 0 0 0 0 0 0 1 0
2021/202213 0 0 0 0 0 0 0 0 4 1 3 5
2022/202352 3 0 1 0 1 2 5 1 16 10 9 4
2023/2024140 7 24 17 16 9 2 7 11 3 4 29 11
2024/2025133 17 27 6 38 45 0 0 0 0 0 0 0
Totale 347