IRIS
SANGIUOLO, FEDERICA CARLA
 Distribuzione geografica
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Continente #
NA - Nord America 1.149
EU - Europa 311
AS - Asia 83
AF - Africa 12
SA - Sud America 10
Totale 1.565
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Nazione #
US - Stati Uniti d'America 1.130
IT - Italia 80
FR - Francia 67
DE - Germania 56
CN - Cina 21
GB - Regno Unito 20
IE - Irlanda 19
IN - India 19
SE - Svezia 19
AE - Emirati Arabi Uniti 15
HN - Honduras 11
RU - Federazione Russa 9
ZA - Sudafrica 9
CZ - Repubblica Ceca 8
KR - Corea 8
CA - Canada 7
NL - Olanda 7
FI - Finlandia 6
JP - Giappone 6
VN - Vietnam 6
CL - Cile 5
ES - Italia 5
BR - Brasile 3
UA - Ucraina 3
AR - Argentina 2
AT - Austria 2
DK - Danimarca 2
PT - Portogallo 2
TR - Turchia 2
TW - Taiwan 2
BE - Belgio 1
GH - Ghana 1
IR - Iran 1
KE - Kenya 1
LK - Sri Lanka 1
LT - Lituania 1
MK - Macedonia 1
MX - Messico 1
NO - Norvegia 1
PH - Filippine 1
PL - Polonia 1
SC - Seychelles 1
SI - Slovenia 1
TH - Thailandia 1
Totale 1.565
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Città #
Woodbridge 168
Houston 120
Santa Cruz 106
Fairfield 104
Buffalo 60
Seattle 57
Ashburn 56
Wilmington 56
Cambridge 35
Rome 24
Ann Arbor 19
Chicago 19
Dublin 19
Stockholm 16
Mountain View 14
Las Vegas 11
Clearwater 9
University Park 9
Kannur 8
Muizenberg 8
San Diego 8
Centro 7
Los Angeles 7
Saint Petersburg 7
San Francisco 7
Beijing 6
Dong Ket 6
Milan 6
Phoenix 6
Riva 6
Boardman 5
Dallas 5
Helsinki 5
Nepi 5
New York 5
Ottawa 5
Pietra Ligure 5
Guangzhou 4
Pirmasens 4
Amsterdam 3
Atlanta 3
Auburn 3
Chennai 3
Council Bluffs 3
Easton 3
Nürnberg 3
Paris 3
Provo 3
Tegucigalpa 3
Tucson 3
Wuhan 3
Annapolis Junction 2
Büdelsdorf 2
Columbus 2
Dorchester 2
Frankfurt am Main 2
Fremont 2
Henderson 2
Kochi 2
Madrid 2
Mutters 2
Nam-gu 2
Portland 2
Recife 2
Santiago 2
Scarsdale 2
Sezze 2
Taipei 2
Yellow Springs 2
Zagarolo 2
Anderson 1
Andover 1
Austin 1
Bad Vilbel 1
Baltimore 1
Bayreuth 1
Bengaluru 1
Bergamo 1
Bisceglie 1
Brescia 1
Brno 1
Buenos Aires 1
Cagayan de Oro 1
Cardiff 1
Changsha 1
Chongqing 1
Chuoku 1
Coimbra 1
Coventry 1
Crugers 1
Denver 1
Des Moines 1
Fleming Island 1
Frankfurt 1
Fujita 1
Ghent 1
Goose Creek 1
Guildford 1
Gunzenhausen 1
Huntsville 1
Totale 1.131
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Nome #
Cerebral cavernous malformations associated to meningioma: High penetrance in a novel family mutated in the PDCD10 gene, file e291c0d5-f6db-cddb-e053-3a05fe0aa144 212
A perturbed MicroRNA expression pattern characterizes embryonic neural stem cells derived from a severe mouse model of spinal muscular atrophy (SMA), file e291c0d4-f7df-cddb-e053-3a05fe0aa144 202
Identification and characterization of 5' CCG interruptions in complex DMPK expanded alleles, file e291c0d6-2b4c-cddb-e053-3a05fe0aa144 189
Early hippocampal i-LTP and LOX-1 overexpression induced by anoxia: A potential role in neurodegeneration in NPC mouse model, file e291c0d6-d28e-cddb-e053-3a05fe0aa144 148
Coexistence of Two Novel Mutations in CDKN2A and PMS1 Genes in a Single Patient Identifies a New and Severe Cancer Predisposition Syndrome, file e291c0d7-42f7-cddb-e053-3a05fe0aa144 137
SMA human iPSC-derived motor neurons show perturbed differentiation and reduced miR-335-5P expression, file e291c0d8-2720-cddb-e053-3a05fe0aa144 93
Improving diagnosis for rare diseases: the experience of the Italian undiagnosed Rare diseases network, file e291c0d9-30a6-cddb-e053-3a05fe0aa144 88
Targeting LOX-1 inhibits colorectal cancer metastasis in an animal model, file e291c0d7-d21a-cddb-e053-3a05fe0aa144 72
Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy, file e291c0d8-be75-cddb-e053-3a05fe0aa144 61
Generation and Neuronal Differentiation of hiPSCs From Patients With Myotonic Dystrophy Type 2, file e291c0d8-9e4d-cddb-e053-3a05fe0aa144 60
An enormous Italian pedigree of Marfan syndrome with a novel mutation in the FBN1 gene, file e291c0d9-4a19-cddb-e053-3a05fe0aa144 59
A preliminary analysis of volatile metabolites of human induced pluripotent stem cells along the in vitro differentiation, file e291c0d8-1119-cddb-e053-3a05fe0aa144 53
The lectin-like oxidized LDL receptor-1: A new potential molecular target in colorectal cancer, file e291c0d7-c1ec-cddb-e053-3a05fe0aa144 52
Application of CRISPR/Cas9 to human-induced pluripotent stem cells: from gene editing to drug discovery, file e291c0d9-4f9c-cddb-e053-3a05fe0aa144 50
Application of Next Generation Sequencing for personalized medicine for sudden cardiac death, file e291c0d9-6969-cddb-e053-3a05fe0aa144 48
Pro-oncogenic action of LOX-1 and its splice variant LOX-1Δ4 in breast cancer phenotypes, file e291c0d9-2dfe-cddb-e053-3a05fe0aa144 39
Two Different Therapeutic Approaches for SARS-CoV-2 in hiPSCs-Derived Lung Organoids, file 3566af21-6248-4ce1-bb34-5ef3ed95f083 29
Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies. Front Immunol. 2019 Apr 11;10:316. doi: 10.3389/fimmu.2019.00316. eCollection 2019. Erratum in: Front Immunol. 2019 May 31;10:1184., file e291c0d8-0134-cddb-e053-3a05fe0aa144 19
Cutaneous and metabolic defects associated with nuclear abnormalities in a transgenic mouse model expressing R527H lamin A mutation causing mandibuloacral dysplasia type A (MADA) syndrome, file e291c0d9-134a-cddb-e053-3a05fe0aa144 16
A 14-Year Italian Experience in DM2 Genetic Testing: Frequency and Distribution of Normal and Premutated CNBP Alleles, file f3887b88-7002-4130-93c7-cc12ba00266a 14
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies, file e291c0d7-88d3-cddb-e053-3a05fe0aa144 11
A rare but fatal behçet variant: the hughes–stovin syndrome—successful case report and new evidence from literature review, file 36c5e086-677a-43af-a5c8-a00a79767d9e 3
Assessing individual risk for AMD with genetic counseling, family history, and genetic testing, file e291c0d6-e4a5-cddb-e053-3a05fe0aa144 2
Modelling the pathogenesis of Myotonic Dystrophy type 1 cardiac phenotype through human iPSC-derived cardiomyocytes, file e291c0d7-692a-cddb-e053-3a05fe0aa144 2
Reliable and versatile immortal muscle cell models from healthy and myotonic dystrophy type 1 primary human myoblasts, file e291c0d6-0d9b-cddb-e053-3a05fe0aa144 1
Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experience, file e291c0d8-8821-cddb-e053-3a05fe0aa144 1
Totale 1.661
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Categoria #
all - tutte 4.743
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 4.743
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201982 0 0 0 0 0 0 0 0 0 0 46 36
2019/2020211 21 20 13 18 24 17 17 21 20 19 9 12
2020/2021295 11 21 11 17 26 13 13 25 27 60 39 32
2021/2022333 33 19 14 10 17 22 23 10 19 18 109 39
2022/2023293 7 11 82 53 12 35 14 20 16 14 20 9
2023/2024158 17 7 9 8 15 10 32 27 27 4 2 0
Totale 1.661