BALDASSARI, SIMONA
 Distribuzione geografica
Continente #
EU - Europa 1.788
AS - Asia 152
SA - Sud America 25
NA - Nord America 20
AF - Africa 4
Totale 1.989
Nazione #
IT - Italia 1.780
SG - Singapore 69
VN - Vietnam 35
CN - Cina 33
US - Stati Uniti d'America 17
AR - Argentina 13
HK - Hong Kong 11
BR - Brasile 10
MX - Messico 3
BD - Bangladesh 2
DE - Germania 2
ET - Etiopia 2
CH - Svizzera 1
EC - Ecuador 1
ES - Italia 1
FI - Finlandia 1
FR - Francia 1
IE - Irlanda 1
IQ - Iraq 1
MU - Mauritius 1
NG - Nigeria 1
PE - Perù 1
RU - Federazione Russa 1
UZ - Uzbekistan 1
Totale 1.989
Città #
Genoa 1.015
Genova 439
Vado Ligure 173
Rapallo 145
Singapore 16
Ashburn 15
Beijing 12
Hong Kong 11
Ho Chi Minh City 10
Hanoi 6
Bordighera 4
Hải Dương 4
Tianjin 4
Haiphong 3
Mexico City 2
Milan 2
Tây Ninh 2
Acaraú 1
Addis Ababa 1
Beau Bassin-Rose Hill 1
Bebedouro 1
Biel/Bienne 1
Biên Hòa 1
Buenos Aires 1
Bukhara 1
Canoas 1
Corrientes 1
Dublin 1
Frankfurt am Main 1
General Rodríguez 1
Graça 1
Helsinki 1
Isidro Casanova 1
Jaguariúna 1
Kirkuk 1
Lanús 1
Lima 1
Lấp Vò 1
Mariano Moreno 1
Nam Định 1
Nazrēt 1
Neuquén 1
Orem 1
Paris 1
Pedras de Fogo 1
Posadas 1
Praia Grande 1
Quito 1
Quảng Ngãi 1
Rafael Castillo 1
Resistencia 1
Río Ceballos 1
San Miguel de Tucumán 1
Santa Teresita 1
Thái Nguyên 1
Tupi Paulista 1
Tuxtla Gutiérrez 1
Việt Hưng 1
Águas Lindas de Goiás 1
Totale 1.905
Nome #
Hyccin, the Molecule Mutated in the Leukodystrophy Hypomyelination and Congenital Cataract (HCC), Is a Neuronal Protein. 161
Hypomyelination and congenital cataract: Identification of novel mutations in two unrelated families. 160
TBC1D24 regulates axonal outgrowth and membrane trafficking at the growth cone in rodent and human neurons 137
Novel FAM126A mutations in hypomyelination and congenital cataract disease. 137
Progress of Induced Pluripotent Stem Cell Technologies to Understand Genetic Epilepsy 133
Optimization of Transcription Factor-Driven Neuronal Differentiation from Human Induced Pluripotent Stem Cells for Disease Modelling and Drug Screening 130
Clinical and Genetic Features in Patients With Reflex Bathing Epilepsy 123
Loss of Wwox Perturbs Neuronal Migration and Impairs Early Cortical Development 111
A Phenotypic-Driven Approach for the Diagnosis of WOREE Syndrome 100
Epilepsy Course and Developmental Trajectories in STXBP1-DEE 92
Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders 87
Allelic heterogeneity and abnormal vesicle recycling in PLAA-related neurodevelopmental disorders 75
Clinical and genetic analysis of patients with segmental overgrowth features and somatic mammalian target of rapamycin (mTOR) pathway disruption: Possible novel clinical issues 66
Generation of an induced pluripotent stem cell line (IGGi002A) from nasal cells of a cystic fibrosis patient homozygous for the G542X-CFTR mutation 65
Vesicular glutamate release from feeder-free hiPSC-derived neurons 65
De novo variants in DENND5B cause a neurodevelopmental disorder 63
Generation of two iPSC lines from Mowat-Wilson syndrome patients carrying heterozygous ZEB2 mutations 57
Expanding the phenotype associated with biallelic SLC20A2 variants 56
Moyamoya Vasculopathy in Neurofibromatosis Type 1 Pediatric Patients: The Role of Rare Variants of RNF213 53
Generation of induced pluripotent stem cell lines from a patient with Sotos syndrome carrying 5q35 microdeletion 41
Multiple Tumors in a Patient with Interleukin-2-Inducible T-Cell Kinase Deficiency: A Case Report 38
Variants in the WDR44 WD40-repeat domain cause a spectrum of ciliopathy by impairing ciliogenesis initiation 37
Functional Characterization of a Novel Intronic Variant in PIEZO2 in a Recessive Form of Distal Arthrogryposis With Impaired Proprioception and Touch (DAIPT) 20
Derivation of the IGGi006-A stem cell line from a patient with CAPRIN1 haploinsufficiency 12
Totale 2.019
Categoria #
all - tutte 7.395
article - articoli 7.395
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 14.790


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202149 0 0 0 0 0 3 4 9 4 16 3 10
2021/2022103 5 5 16 12 4 4 9 22 2 8 7 9
2022/2023177 11 18 2 20 20 26 0 17 27 1 26 9
2023/2024157 4 12 6 23 17 30 11 9 9 5 12 19
2024/2025698 27 27 10 40 37 59 43 179 70 40 94 72
2025/2026537 140 36 88 87 174 12 0 0 0 0 0 0
Totale 2.019