BALDASSARI, SIMONA
 Distribuzione geografica
Continente #
EU - Europa 1.781
AS - Asia 89
SA - Sud America 18
NA - Nord America 7
AF - Africa 2
Totale 1.897
Nazione #
IT - Italia 1.778
CN - Cina 32
SG - Singapore 30
VN - Vietnam 12
HK - Hong Kong 11
AR - Argentina 8
BR - Brasile 8
US - Stati Uniti d'America 4
MX - Messico 3
BD - Bangladesh 2
CH - Svizzera 1
EC - Ecuador 1
ET - Etiopia 1
FR - Francia 1
IQ - Iraq 1
MU - Mauritius 1
PE - Perù 1
RU - Federazione Russa 1
UZ - Uzbekistan 1
Totale 1.897
Città #
Genoa 1.013
Genova 439
Vado Ligure 173
Rapallo 145
Beijing 11
Hong Kong 11
Singapore 10
Ashburn 4
Bordighera 4
Tianjin 4
Ho Chi Minh City 3
Haiphong 2
Hanoi 2
Hải Dương 2
Mexico City 2
Milan 2
Acaraú 1
Beau Bassin-Rose Hill 1
Bebedouro 1
Biel/Bienne 1
Bukhara 1
Canoas 1
Corrientes 1
General Rodríguez 1
Graça 1
Kirkuk 1
Lanús 1
Lima 1
Lấp Vò 1
Nazrēt 1
Neuquén 1
Paris 1
Pedras de Fogo 1
Praia Grande 1
Quito 1
Rafael Castillo 1
Resistencia 1
Río Ceballos 1
San Miguel de Tucumán 1
Tuxtla Gutiérrez 1
Tây Ninh 1
Việt Hưng 1
Águas Lindas de Goiás 1
Totale 1.854
Nome #
Hyccin, the Molecule Mutated in the Leukodystrophy Hypomyelination and Congenital Cataract (HCC), Is a Neuronal Protein. 158
Hypomyelination and congenital cataract: Identification of novel mutations in two unrelated families. 156
Novel FAM126A mutations in hypomyelination and congenital cataract disease. 135
TBC1D24 regulates axonal outgrowth and membrane trafficking at the growth cone in rodent and human neurons 132
Progress of Induced Pluripotent Stem Cell Technologies to Understand Genetic Epilepsy 127
Optimization of Transcription Factor-Driven Neuronal Differentiation from Human Induced Pluripotent Stem Cells for Disease Modelling and Drug Screening 123
Clinical and Genetic Features in Patients With Reflex Bathing Epilepsy 118
Loss of Wwox Perturbs Neuronal Migration and Impairs Early Cortical Development 106
A Phenotypic-Driven Approach for the Diagnosis of WOREE Syndrome 97
Epilepsy Course and Developmental Trajectories in STXBP1-DEE 89
Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders 85
Allelic heterogeneity and abnormal vesicle recycling in PLAA-related neurodevelopmental disorders 71
Clinical and genetic analysis of patients with segmental overgrowth features and somatic mammalian target of rapamycin (mTOR) pathway disruption: Possible novel clinical issues 63
Generation of an induced pluripotent stem cell line (IGGi002A) from nasal cells of a cystic fibrosis patient homozygous for the G542X-CFTR mutation 62
Vesicular glutamate release from feeder-free hiPSC-derived neurons 62
De novo variants in DENND5B cause a neurodevelopmental disorder 56
Expanding the phenotype associated with biallelic SLC20A2 variants 53
Moyamoya Vasculopathy in Neurofibromatosis Type 1 Pediatric Patients: The Role of Rare Variants of RNF213 51
Generation of two iPSC lines from Mowat-Wilson syndrome patients carrying heterozygous ZEB2 mutations 49
Generation of induced pluripotent stem cell lines from a patient with Sotos syndrome carrying 5q35 microdeletion 37
Multiple Tumors in a Patient with Interleukin-2-Inducible T-Cell Kinase Deficiency: A Case Report 37
Variants in the WDR44 WD40-repeat domain cause a spectrum of ciliopathy by impairing ciliogenesis initiation 33
Functional Characterization of a Novel Intronic Variant in PIEZO2 in a Recessive Form of Distal Arthrogryposis With Impaired Proprioception and Touch (DAIPT) 18
Derivation of the IGGi006-A stem cell line from a patient with CAPRIN1 haploinsufficiency 9
Totale 1.927
Categoria #
all - tutte 7.240
article - articoli 7.240
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 14.480


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202150 0 0 0 0 1 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
2025/2026445 140 36 88 87 94 0 0 0 0 0 0 0
Totale 1.927