MASCIA, ELISABETTA
 Distribuzione geografica
Continente #
EU - Europa 84
AS - Asia 79
NA - Nord America 79
Totale 242
Nazione #
US - Stati Uniti d'America 79
CN - Cina 40
IT - Italia 39
SG - Singapore 36
SE - Svezia 19
RU - Federazione Russa 14
FI - Finlandia 4
IE - Irlanda 3
IN - India 2
PL - Polonia 2
DE - Germania 1
FR - Francia 1
IR - Iran 1
NL - Olanda 1
Totale 242
Città #
Singapore 28
Milan 19
Shanghai 17
Ashburn 14
Boardman 11
New York 8
Washington 7
Budrio 4
Lawrence 4
Princeton 4
Dublin 3
Guangzhou 3
Helsinki 3
Moscow 3
Dallas 2
Ferrara 2
Nola 2
Pavia 2
Pune 2
Rome 2
Seattle 2
Warsaw 2
Amsterdam 1
Beijing 1
Chongqing 1
Fermo 1
Fuzhou 1
Jiaxing 1
Lappeenranta 1
Los Angeles 1
Mozzate 1
Osio Sotto 1
Paris 1
Segrate 1
Wuhan 1
Wuxi 1
Xuzhou 1
Totale 159
Nome #
DNA Methylation in the Anti-Mullerian Hormone Gene and the Risk of Disease Activity in Multiple Sclerosis 33
Combining Clinical and Genetic Data to Predict Response to Fingolimod Treatment in Relapsing Remitting Multiple Sclerosis Patients: A Precision Medicine Approach 22
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis 22
Transcriptional effects of fingolimod treatment on peripheral T cells in relapsing remitting multiple sclerosis patients 19
A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis Susceptibility 18
Exploring the Association of HLA Genetic Risk Burden on Thalamic and Hippocampal Atrophy in Multiple Sclerosis Patients 17
Erratum: Correction to: A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility (Journal of neurology (2022) 269 8 (4510-4522)) 17
Involvement of NINJ2 Protein in Inflammation and Blood-Brain Barrier Transmigration of Monocytes in Multiple Sclerosis 16
Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population 16
Transcriptomic Analysis of Peripheral Monocytes upon Fingolimod Treatment in Relapsing Remitting Multiple Sclerosis Patients 15
Risk HLA Variants Affect the T-Cell Repertoire in Multiple Sclerosis 14
Locus for severity implicates CNS resilience in progression of multiple sclerosis 14
A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility 13
An investigation of the role of common and rare variants in a large italian multiplex family of multiple sclerosis patients 11
Genetic Contribution to Medium-Term Disease Activity in Multiple Sclerosis 9
Broadening the Genetic Spectrum of Painful Small-Fiber Neuropathy through Whole-Exome Study in Early-Onset Cases 7
Vitamin D affects the risk of disease activity in multiple sclerosis 7
Pharmacogenomics of clinical response to Natalizumab in multiple sclerosis: a genome-wide multi-centric association study 5
CHRNA7 Gene and Response to Cholinesterase Inhibitors in an Italian Cohort of Alzheimer's Disease Patients 4
A whole-genome sequencing study associates GRAMD1B with multiple sclerosis risk and disease activity 3
Combining clinical data, genetics, and adverse childhood experiences for suicidality prediction in mood disorders: a machine learning approach 2
Whole-genome epigenomic approach in multiplex families with multiple sclerosis revealed new epigenetic traits involved in the disease 1
A whole-genome epigenomic approach in multiple sclerosis multiplex families revealed new epigenetic traits involved in the disease 1
A whole-exome sequencing approach in multiplex Italian multiple sclerosis families to identify new genes involved in the disease 1
A Whole-Exome Sequencing Study In Multiple Sclerosis Multiplex Families 1
Totale 288
Categoria #
all - tutte 3.778
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 3.778


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20225 0 0 0 0 0 1 2 1 0 1 0 0
2022/202352 9 7 1 1 4 5 4 7 9 2 0 3
2023/2024109 11 2 13 12 5 12 0 18 0 3 13 20
2024/2025122 31 15 19 35 22 0 0 0 0 0 0 0
Totale 288