IRIS
CARDIERO, GIOVANNA
 Distribuzione geografica
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Continente #
NA - Nord America 73
EU - Europa 65
AS - Asia 63
AF - Africa 5
Totale 206
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Nazione #
US - Stati Uniti d'America 69
IT - Italia 53
SG - Singapore 43
CN - Cina 14
CI - Costa d'Avorio 5
CA - Canada 4
NL - Olanda 4
VN - Vietnam 4
DE - Germania 3
IE - Irlanda 2
AT - Austria 1
FI - Finlandia 1
GB - Regno Unito 1
HK - Hong Kong 1
IN - India 1
Totale 206
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Città #
Singapore 39
Naples 16
Chandler 11
Santa Clara 8
Boardman 7
Milan 6
Ashburn 5
Marsala 5
Amsterdam 4
Dong Ket 4
Napoli 4
Ottawa 4
Beijing 3
Alcamo 2
Brindisi 2
Des Moines 2
Dublin 2
Hebei 2
Mariglianella 2
Millbury 2
Palermo 2
Rovigo 2
Boston 1
Formia 1
Fort Worth 1
Hong Kong 1
Kronberg 1
Lawrence 1
Munich 1
Nuremberg 1
Princeton 1
Rome 1
Seattle 1
Washington 1
Xi'an 1
Totale 147
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Nome #
Alpha-Thalassemia Associated with Hb Instability: A Tale of Two Features. The Case of Hb Rogliano or alpha1 Cod 108(G15)Thr->Asn and Hb Policoro or alpha2 Cod 124(H7)Ser->Pro. 56
A wide next-generation-sequencing panel improves the molecular diagnosis of dyslipidemias 51
Calprotectin Levels and Neutrophil Count Are Prognostic Markers of Mortality in COVID-19 Patients 22
Assessment of Platelet Aggregation and Thrombin Generation in Patients with Familial Chylomicronemia Syndrome Treated with Volanesorsen: A Cross-Sectional Study 14
Alpha-Thalassemia in Southern Italy: Characterization of Five New Deletions Removing the Alpha-Globin Gene Cluster 12
Functional analysis of three new alpha-thalassemia deletions involving MCS-R2 reveals the presence of an additional enhancer element in the 5' boundary region 11
Impact of 12-SNP and 6-SNP Polygenic Scores on Predisposition to High LDL-Cholesterol Levels in Patients with Familial Hypercholesterolemia 11
Effect of Mutations on mRNA and Globin Stability: The Cases of Hb Bernalda/Groene Hart and Hb Southern Italy 10
mRNA Analysis of Frameshift Mutations with Stop Codon in the Last Exon: The Case of Hemoglobins Campania [α1 cod95 (−C)] and Sciacca [α1 cod109 (−C)] 7
Association of Very Rare NOTCH2 Variants with Clinical Features of Alagille Syndrome 7
Identification and molecular characterization of a novel 163 kb deletion: The Italian (ϵγδβ)(0)-thalassemia 7
Role of nonsense-mediated decay and nonsense-associated altered splicing in the mRNA pattern of two new α-thalassemia mutants 7
Simplified Criteria for Identification of Familial Hypercholesterolemia in Children: Application in Real Life 6
WTAP and BIRC3 are involved in the posttranscriptional mechanisms that impact on the expression and activity of the human lactonase PON2 5
Totale 226
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Categoria #
all - tutte 1.371
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 1.371
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20209 0 0 0 0 0 0 0 0 0 4 2 3
2020/20219 0 0 0 0 0 2 0 1 1 0 0 5
2021/202215 0 0 0 0 0 0 1 0 0 5 4 5
2022/202340 2 3 1 2 5 4 3 5 7 4 3 1
2023/202468 1 5 4 9 1 3 1 9 5 3 15 12
2024/202573 14 16 12 25 6 0 0 0 0 0 0 0
Totale 226