IRIS
ROSATO, BARBARA ELENI
 Distribuzione geografica
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Continente #
AS - Asia 1.335
NA - Nord America 1.219
EU - Europa 891
SA - Sud America 173
Continente sconosciuto - Info sul continente non disponibili 60
AF - Africa 53
OC - Oceania 3
Totale 3.734
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Nazione #
US - Stati Uniti d'America 1.169
SG - Singapore 553
RU - Federazione Russa 469
CN - Cina 259
VN - Vietnam 240
IT - Italia 199
BR - Brasile 130
HK - Hong Kong 81
BD - Bangladesh 79
DE - Germania 58
FR - Francia 53
CA - Canada 29
GB - Regno Unito 25
NL - Olanda 23
CI - Costa d'Avorio 22
FI - Finlandia 21
AR - Argentina 20
IN - India 20
JP - Giappone 18
KR - Corea 16
MA - Marocco 13
PH - Filippine 11
IQ - Iraq 9
PK - Pakistan 9
MX - Messico 8
PL - Polonia 8
ZA - Sudafrica 7
ID - Indonesia 6
VE - Venezuela 6
CO - Colombia 5
EC - Ecuador 5
EG - Egitto 5
LT - Lituania 5
UZ - Uzbekistan 5
AT - Austria 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
CR - Costa Rica 2
DZ - Algeria 2
JM - Giamaica 2
KZ - Kazakistan 2
MY - Malesia 2
NP - Nepal 2
PA - Panama 2
PR - Porto Rico 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
CY - Cipro 1
EE - Estonia 1
EU - Europa 1
GY - Guiana 1
IS - Islanda 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 3.676
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Città #
San Jose 290
Singapore 281
Moscow 135
Ashburn 107
Hefei 82
Hong Kong 77
Santa Clara 77
Ho Chi Minh City 72
Beijing 68
Chandler 58
Hanoi 58
Naples 57
Council Bluffs 46
Los Angeles 36
Lauterbourg 28
The Dalles 23
Munich 21
New York 19
Amsterdam 18
Boston 18
Frankfurt am Main 16
Tokyo 16
Buffalo 15
Lawrence 15
Millbury 14
Seoul 14
São Paulo 14
Napoli 13
Phoenix 13
Turku 13
Toronto 12
Dallas 11
Da Nang 9
Des Moines 9
London 9
Redondo Beach 9
Wilmington 9
Brooklyn 8
Chicago 8
Atlanta 7
Casablanca 7
Haiphong 7
Helsinki 7
Milan 7
Nuremberg 7
Tianjin 7
Houston 6
Montreal 6
Belo Horizonte 5
Bexley 5
Fairfield 5
Genoa 5
Islamabad 5
Nanjing 5
Ninh Bình 5
Rome 5
San Francisco 5
Tashkent 5
Warsaw 5
Dong Ket 4
Newark 4
Orem 4
Paris 4
Quito 4
Rio de Janeiro 4
Salt Lake City 4
Turin 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
Philadelphia 3
Piscataway 3
Poplar 3
Portici 3
Seattle 3
St Louis 3
Stockholm 3
Winnipeg 3
Wroclaw 3
Agadir 2
Biên Hòa 2
Bloomington 2
Brussels 2
Bình Phước 2
Calgary 2
Caruaru 2
Columbia 2
Cruz das Almas 2
Totale 2.036
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Nome #
Common variants at 21q22.3 locus influence MX1 and TMPRSS2 gene expression and susceptibility to severe COVID-19 184
RAS signaling pathway is essential in regulating PIEZO1-mediated hepatic iron overload in dehydrated hereditary stomatocytosis 176
Germline rare variants of lectin pathway genes predispose to asymptomatic SARS-CoV-2 infection in elderly individuals 160
Complex modes of inheritance in hereditary red blood cell disorders: A case series study of 155 patients 153
One gene, two opposite phenotypes: a case report of hereditary anemia due to a loss-of-function variant in the EPAS1 gene 150
Kinome multigenic panel identified novel druggable EPHB4-V871I somatic variant in high-risk neuroblastoma 141
PIEZO1-R1864H rare variant accounts for a genetic phenotype-modifier role in dehydrated hereditary stomatocytosis 140
Characterization of two cases of congenital dyserythropoietic anemia type I shed light on the uncharacterized C15orf41 protein 140
Gain-of-function mutations in PIEZO1 directly impair hepatic iron metabolism via the inhibition of the BMP/SMADs pathway 140
Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias 139
Unveiling the genetic landscape of suspected congenital dyserythropoietic anemia type I: A retrospective cohort study of 36 patients 136
Clinical exome-based panel testing for medically actionable secondary findings in a cohort of 383 Italian participants 135
Regulatory noncoding and predicted pathogenic coding variants of ccr5 predispose to severe covid-19 135
Genetics and Genomics Approaches for Diagnosis and Research Into Hereditary Anemias 130
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) 128
PIEZO1 Hypomorphic Variants in Congenital Lymphatic Dysplasia Cause Shape and Hydration Alterations of Red Blood Cells 126
The BMP-SMAD pathway mediates the impaired hepatic iron metabolism associated with the ERFE-A260S variant 126
Rap-011 rescues the disease phenotype in a cellular model of congenital dyserythropoietic anemia type ii by inhibiting the smad2-3 pathway 125
Uridine treatment normalizes the congenital dyserythropoietic anemia type II-like hematological phenotype in a patient with homozygous mutation in the CAD gene 123
Relevance of the E756del common variant in the PIEZO1 gene for haemolytic anaemia and hepatic iron overload 117
Proteome alterations in erythrocytes with PIEZO1 gain-of-function mutations 117
Updates on clinical and laboratory aspects of hereditary dyserythropoietic anemias 114
PIEZO1 mutations impact on early clinical manifestations of myelodysplastic syndromes 113
Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients 113
Hereditary anemia caused by multilocus inheritance of PIEZO1, SLC4A1 and ABCB6 mutations: a diagnostic and therapeutic challenge 108
SEC23B Loss-of-Function Suppresses Hepcidin Expression by Imparing Glycosylation Pathway in Human Hepatic Cells 108
Hereditary Hemolytic Anemia Due to PIEZO1 Red Blood Cell Membrane Defect 99
Evaluation of the main regulators of systemic iron homeostasis in pyruvate kinase deficiency 63
Coinheritance of PIEZO1 variants and multi-locus red blood cell defects account for the symptomatic phenotype in beta-thalassemia carriers 63
Additive effect of multiple genetic variants in SEC23B and PIEZO1 on iron metabolism dyshomeostasis in hereditary anemias 22
Refined classification and phenotype-driven analysis of PIEZO1 variants in hereditary red cell and iron disorders 10
Totale 3.734
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Categoria #
all - tutte 12.136
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 12.136
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022101 0 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
2025/20262.105 234 147 219 179 297 74 278 100 226 147 100 104
2026/2027145 38 67 40 0 0 0 0 0 0 0 0 0
Totale 3.734