IRIS
ROSATO, BARBARA ELENI
 Distribuzione geografica
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Continente #
AS - Asia 1.277
NA - Nord America 1.073
EU - Europa 866
SA - Sud America 171
AF - Africa 53
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 3.445
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Nazione #
US - Stati Uniti d'America 1.037
SG - Singapore 551
RU - Federazione Russa 469
CN - Cina 256
VN - Vietnam 240
IT - Italia 176
BR - Brasile 129
HK - Hong Kong 79
DE - Germania 58
FR - Francia 52
BD - Bangladesh 31
GB - Regno Unito 24
NL - Olanda 23
CI - Costa d'Avorio 22
FI - Finlandia 21
AR - Argentina 20
CA - Canada 20
IN - India 18
JP - Giappone 18
KR - Corea 16
MA - Marocco 13
PH - Filippine 11
IQ - Iraq 9
PK - Pakistan 9
PL - Polonia 8
MX - Messico 7
ZA - Sudafrica 7
VE - Venezuela 6
EC - Ecuador 5
EG - Egitto 5
ID - Indonesia 5
LT - Lituania 5
UZ - Uzbekistan 5
AT - Austria 4
CO - Colombia 4
ES - Italia 4
AE - Emirati Arabi Uniti 3
AU - Australia 3
CL - Cile 3
IE - Irlanda 3
IL - Israele 3
JO - Giordania 3
NI - Nicaragua 3
OM - Oman 3
PE - Perù 3
SE - Svezia 3
TH - Thailandia 3
BE - Belgio 2
CH - Svizzera 2
DZ - Algeria 2
KZ - Kazakistan 2
MY - Malesia 2
NP - Nepal 2
PA - Panama 2
RS - Serbia 2
TR - Turchia 2
TW - Taiwan 2
UA - Ucraina 2
AL - Albania 1
BF - Burkina Faso 1
BN - Brunei Darussalam 1
BS - Bahamas 1
BY - Bielorussia 1
CD - Congo 1
CG - Congo 1
CR - Costa Rica 1
CY - Cipro 1
EE - Estonia 1
EU - Europa 1
GY - Guiana 1
IS - Islanda 1
JM - Giamaica 1
KG - Kirghizistan 1
KW - Kuwait 1
LU - Lussemburgo 1
MK - Macedonia 1
NO - Norvegia 1
RO - Romania 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 3.445
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Città #
Singapore 281
San Jose 259
Moscow 135
Ashburn 94
Hefei 82
Hong Kong 75
Ho Chi Minh City 72
Santa Clara 69
Beijing 68
Chandler 58
Hanoi 58
Naples 57
Los Angeles 33
Lauterbourg 28
The Dalles 23
Munich 21
Amsterdam 18
Boston 17
Frankfurt am Main 16
New York 16
Tokyo 16
Lawrence 15
Millbury 14
Seoul 14
Buffalo 13
Council Bluffs 13
Napoli 13
São Paulo 13
Turku 13
Da Nang 9
Des Moines 9
Redondo Beach 9
Toronto 9
Brooklyn 8
Chicago 8
Dallas 8
London 8
Wilmington 8
Atlanta 7
Casablanca 7
Haiphong 7
Helsinki 7
Nuremberg 7
Tianjin 7
Montreal 6
Belo Horizonte 5
Bexley 5
Fairfield 5
Genoa 5
Islamabad 5
Nanjing 5
Ninh Bình 5
San Francisco 5
Tashkent 5
Warsaw 5
Dong Ket 4
Houston 4
Milan 4
Newark 4
Orem 4
Paris 4
Phoenix 4
Quito 4
Rio de Janeiro 4
Rome 4
Salt Lake City 4
Amman 3
Baghdad 3
Campinas 3
Can Tho 3
Castellammare di Stabia 3
Chennai 3
Curitiba 3
Denver 3
Dublin 3
Falkenstein 3
Guangzhou 3
Kochi 3
Managua 3
Mexico City 3
Mosul 3
Piscataway 3
Poplar 3
Portici 3
Seattle 3
St Louis 3
Stockholm 3
Turin 3
Wroclaw 3
Agadir 2
Biên Hòa 2
Bloomington 2
Brussels 2
Bình Phước 2
Caruaru 2
Columbia 2
Cruz das Almas 2
Detroit 2
Dhaka 2
Fermo 2
Totale 1.913
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Nome #
Common variants at 21q22.3 locus influence MX1 and TMPRSS2 gene expression and susceptibility to severe COVID-19 171
Germline rare variants of lectin pathway genes predispose to asymptomatic SARS-CoV-2 infection in elderly individuals 154
One gene, two opposite phenotypes: a case report of hereditary anemia due to a loss-of-function variant in the EPAS1 gene 148
Complex modes of inheritance in hereditary red blood cell disorders: A case series study of 155 patients 147
PIEZO1-R1864H rare variant accounts for a genetic phenotype-modifier role in dehydrated hereditary stomatocytosis 139
Gain-of-function mutations in PIEZO1 directly impair hepatic iron metabolism via the inhibition of the BMP/SMADs pathway 136
Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias 133
Kinome multigenic panel identified novel druggable EPHB4-V871I somatic variant in high-risk neuroblastoma 133
Characterization of two cases of congenital dyserythropoietic anemia type I shed light on the uncharacterized C15orf41 protein 132
Unveiling the genetic landscape of suspected congenital dyserythropoietic anemia type I: A retrospective cohort study of 36 patients 131
Clinical exome-based panel testing for medically actionable secondary findings in a cohort of 383 Italian participants 130
Regulatory noncoding and predicted pathogenic coding variants of ccr5 predispose to severe covid-19 130
Genetics and Genomics Approaches for Diagnosis and Research Into Hereditary Anemias 125
Corrigendum: Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein (Frontiers in Physiology, (2019), 10, 10.3389/fphys.2019.00621) 124
RAS signaling pathway is essential in regulating PIEZO1-mediated hepatic iron overload in dehydrated hereditary stomatocytosis 122
The BMP-SMAD pathway mediates the impaired hepatic iron metabolism associated with the ERFE-A260S variant 121
Uridine treatment normalizes the congenital dyserythropoietic anemia type II-like hematological phenotype in a patient with homozygous mutation in the CAD gene 120
PIEZO1 Hypomorphic Variants in Congenital Lymphatic Dysplasia Cause Shape and Hydration Alterations of Red Blood Cells 119
Rap-011 rescues the disease phenotype in a cellular model of congenital dyserythropoietic anemia type ii by inhibiting the smad2-3 pathway 117
Proteome alterations in erythrocytes with PIEZO1 gain-of-function mutations 112
Relevance of the E756del common variant in the PIEZO1 gene for haemolytic anaemia and hepatic iron overload 110
Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients 109
PIEZO1 mutations impact on early clinical manifestations of myelodysplastic syndromes 108
Updates on clinical and laboratory aspects of hereditary dyserythropoietic anemias 107
Hereditary anemia caused by multilocus inheritance of PIEZO1, SLC4A1 and ABCB6 mutations: a diagnostic and therapeutic challenge 106
SEC23B Loss-of-Function Suppresses Hepcidin Expression by Imparing Glycosylation Pathway in Human Hepatic Cells 104
Hereditary Hemolytic Anemia Due to PIEZO1 Red Blood Cell Membrane Defect 72
Evaluation of the main regulators of systemic iron homeostasis in pyruvate kinase deficiency 60
Coinheritance of PIEZO1 variants and multi-locus red blood cell defects account for the symptomatic phenotype in beta-thalassemia carriers 60
Additive effect of multiple genetic variants in SEC23B and PIEZO1 on iron metabolism dyshomeostasis in hereditary anemias 17
Refined classification and phenotype-driven analysis of PIEZO1 variants in hereditary red cell and iron disorders 6
Totale 3.503
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Categoria #
all - tutte 10.673
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 10.673
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202111 0 0 0 0 0 0 0 0 0 0 0 11
2021/2022104 3 0 3 4 3 0 7 8 1 2 36 37
2022/2023152 17 24 8 1 16 10 1 15 28 15 12 5
2023/2024138 6 27 23 11 1 8 4 25 2 4 20 7
2024/2025986 28 42 12 16 19 61 79 80 51 91 401 106
2025/20262.019 234 147 219 179 297 74 278 100 226 147 100 18
Totale 3.503