Detalhe da pesquisa
1.
DNA Methylation in the Anti-Mullerian Hormone Gene and the Risk of Disease Activity in Multiple Sclerosis.
Ann Neurol
; 2024 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38747444
2.
Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease.
PLoS Genet
; 15(6): e1008180, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31170158
3.
Inverse correlation of genetic risk score with age at onset in bout-onset and progressive-onset multiple sclerosis.
Mult Scler
; 21(11): 1463-7, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25533292
4.
Risk HLA Variants Affect the T-Cell Repertoire in Multiple Sclerosis.
Neurol Neuroimmunol Neuroinflamm
; 10(3)2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36792371
5.
Combining Clinical and Genetic Data to Predict Response to Fingolimod Treatment in Relapsing Remitting Multiple Sclerosis Patients: A Precision Medicine Approach.
J Pers Med
; 13(1)2023 Jan 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36675783
6.
Exploring the Association of HLA Genetic Risk Burden on Thalamic and Hippocampal Atrophy in Multiple Sclerosis Patients.
Genes (Basel)
; 13(11)2022 11 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36421810
7.
Transcriptional effects of fingolimod treatment on peripheral T cells in relapsing remitting multiple sclerosis patients.
Pharmacogenomics
; 23(3): 161-171, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35068175
8.
BDNF Val66Met Polymorphism Is Associated With Motor Recovery After Rehabilitation in Progressive Multiple Sclerosis Patients.
Front Neurol
; 13: 790360, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35265024
9.
Involvement of NINJ2 Protein in Inflammation and Blood-Brain Barrier Transmigration of Monocytes in Multiple Sclerosis.
Genes (Basel)
; 13(11)2022 10 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-36360183
10.
A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis Susceptibility.
Genes (Basel)
; 13(12)2022 12 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36553660
11.
A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility.
J Neurol
; 269(8): 4510-4522, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35545683
12.
Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population.
Front Genet
; 12: 800262, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35047017
13.
An Investigation of the Role of Common and Rare Variants in a Large Italian Multiplex Family of Multiple Sclerosis Patients.
Genes (Basel)
; 12(10)2021 10 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-34681001
14.
Impact of multiple sclerosis risk loci in postinfectious neurological syndromes.
Mult Scler Relat Disord
; 44: 102326, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32615529
15.
Correction to: A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility.
J Neurol
; 269(8): 4523-4524, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35751689
16.
CHRNA7 Gene and Response to Cholinesterase Inhibitors in an Italian Cohort of Alzheimer's Disease Patients.
J Alzheimers Dis
; 52(4): 1203-8, 2016 04 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-27104904
17.
Impact of MS genetic loci on familial aggregation, clinical phenotype, and disease prediction.
Neurol Neuroimmunol Neuroinflamm
; 2(4): e129, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26185776