RE-BVS – Piemonte Repository

Sfoglia per AUTORE
CLARELLI F
Collezione AOU Novara

Items : 7

Burden of rare coding variants in an Italian cohort of familial multiple sclerosis. in Journal of neuroimmunology / J Neuroimmunol. 2022 Jan 15;362:577760. doi: 10.1016/j.jneuroim.2021.577760. Epub 2021 Nov 5.

2022
AOU Novara

Esposito F; Filippi M; Comi G; Vecchio D; Bresolin N; Moiola L; Protti A; Liguori M; Pozzato M; Guerini FR; Biancolini D; Bonfiglio S; Ferrè L; Santoro S; Basagni C; Barizzone N; Sorosina M; Guaschino C; Zauli A; Mascia E; Clarelli F; D'Alfonso S; Martinelli-Boneschi F;

Correction to: A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility. in Journal of neurology / J Neurol. 2022 Aug;269(8):4523-4524. doi: 10.1007/s00415-022-11216-6.

2022
AOU Novara

Patsopoulos NA; De Jager PL; Filippi M; Leone M; Comi G; Martinelli V; Cusi D; Barlassina C; Zollo A; Ferrè L; Santoro S; Cavalla P; Vecchio D; Zuccalà M; Mascia E; Roostaei T; Bordoni R; Mangano E; Salvi E; Lupoli S; Anand S; Clarelli F; Barizzone N; Sorosina M; De Bellis G; Esposito F; D'Alfonso S; Martinelli Boneschi F;

A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility. in Journal of neurology / J Neurol. 2022 Aug;269(8):4510-4522. doi: 10.1007/s00415-022-11109-8. Epub 2022 May 12.

2022
AOU Novara

An Investigation of the Role of Common and Rare Variants in a Large Italian Multiplex Family of Multiple Sclerosis Patients. in Genes / Genes (Basel). 2021 Oct 13;12(10):1607. doi: 10.3390/genes12101607.

2021
AOU Novara

Barizzone N; Cagliani R; Basagni C; Clarelli F; Mendozzi L; Agliardi C; Forni D; Tosi M; Mascia E; Favero F; Corà D; Corrado L; Sorosina M; Esposito F; Zuccalà M; Vecchio D; Liguori M; Comi C; Comi G; Martinelli V; Filippi M; Leone M; Martinelli-Boneschi F; Caputo D; Sironi M; Guerini FR; D'Alfonso S;

Genomic and functional evaluation of TNFSF14 in multiple sclerosis susceptibility. in Journal of genetics and genomics = Yi chuan xue bao / J Genet Genomics. 2021 Jun 20;48(6):497-507. doi: 10.1016/j.jgg.2021.03.017. Epub 2021 May 25.

2021
AOU San Luigi di Orbassano
AOU Novara

D'Alfonso S; Dianzani U; Martinelli-Boneschi F; Leone M; De Bellis G; Esposito F; Filippi M; Comi G; Cantello R; Martinelli V; Ivashynka A; Solaro C; Ferrante D; Gajofatto A; Perga S; Corsetti E; Martire S; Mangano E; Vecchio D; Clarelli F; Anand S; Bordoni R; Basagni C; Boggio E; Gigliotti L; Sorosina M; Barizzone N; Zuccalà M;

Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population. in Frontiers in genetics / Front Genet. 2022 Jan 3;12:800262. doi: 10.3389/fgene.2021.800262. eCollection 2021.

2021
AOU Novara

Clarelli F; Barizzone N; Mangano E; Zuccalà M; Basagni C; Anand S; Sorosina M; Mascia E; Santoro S; Guerini FR; Virgilio E; Gallo A; Pizzino A; Comi C; Martinelli V; Comi G; De Bellis G; Leone M; Filippi M; Esposito F; Bordoni R; Martinelli Boneschi F; D'Alfonso S;

Analysis of genes, pathways and networks involved in disease severity and age at onset in primary-progressive multiple sclerosis. in Multiple sclerosis (Houndmills, Basingstoke, England) / Mult Scler. 2015 Oct;21(11):1431-42. doi: 10.1177/1352458514564590. Epub 2015 Jan 12.

2015
AOU Novara

Giacalone G; Clarelli F; Osiceanu AM; Guaschino C; Brambilla P; Sorosina M; Liberatore G; Zauli A; Esposito F; Rodegher M; Ghezzi A; Galimberti D; Patti F; Barizzone N; Guerini F; Martinelli V; Leone M; Comi G; D'Alfonso S; Martinelli Boneschi F;