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Association between the ACCN1 gene and multiple sclerosis in Central East Sardinia.
Bernardinelli L, Murgia SB, Bitti PP, Foco L, Ferrai R, Musu L, Prokopenko I, Pastorino R, Saddi V, Ticca A, Piras ML, Cox DR, Berzuini C. Bernardinelli L, et al. Among authors: saddi v. PLoS One. 2007 May 30;2(5):e480. doi: 10.1371/journal.pone.0000480. PLoS One. 2007. PMID: 17534430 Free PMC article.
Investigating the Causal Effect of Brain Expression of CCL2, NFKB1, MAPK14, TNFRSF1A, CXCL10 Genes on Multiple Sclerosis: A Two-Sample Mendelian Randomization Approach.
Fazia T, Nova A, Gentilini D, Beecham A, Piras M, Saddi V, Ticca A, Bitti P, McCauley JL, Berzuini C, Bernardinelli L. Fazia T, et al. Among authors: saddi v. Front Bioeng Biotechnol. 2020 May 5;8:397. doi: 10.3389/fbioe.2020.00397. eCollection 2020. Front Bioeng Biotechnol. 2020. PMID: 32432099 Free PMC article.
Homozygosity Haplotype and Whole-Exome Sequencing Analysis to Identify Potentially Functional Rare Variants Involved in Multiple Sclerosis among Sardinian Families.
Fazia T, Marzanati D, Carotenuto AL, Beecham A, Hadjixenofontos A, McCauley JL, Saddi V, Piras M, Bernardinelli L, Gentilini D. Fazia T, et al. Among authors: saddi v. Curr Issues Mol Biol. 2021 Oct 27;43(3):1778-1793. doi: 10.3390/cimb43030125. Curr Issues Mol Biol. 2021. PMID: 34889895 Free PMC article.
An exome study of Parkinson's disease in Sardinia, a Mediterranean genetic isolate.
Quadri M, Yang X, Cossu G, Olgiati S, Saddi VM, Breedveld GJ, Ouyang L, Hu J, Xu N, Graafland J, Ricchi V, Murgia D, Guedes LC, Mariani C, Marti MJ, Tarantino P, Asselta R, Valldeoriola F, Gagliardi M, Pezzoli G, Ezquerra M, Quattrone A, Ferreira J, Annesi G, Goldwurm S, Tolosa E, Oostra BA, Melis M, Wang J, Bonifati V. Quadri M, et al. Among authors: saddi vm. Neurogenetics. 2015 Jan;16(1):55-64. doi: 10.1007/s10048-014-0425-x. Epub 2014 Oct 8. Neurogenetics. 2015. PMID: 25294124
Mutations in TMEM230 are not a common cause of Parkinson's disease.
Quadri M, Breedveld GJ, Chang HC, Yeh TH, Guedes LC, Toni V, Fabrizio E, De Mari M, Thomas A, Tassorelli C, Rood JP, Saddi V, Chien HF, Kievit AJ, Boon AJ, Stocchi F, Lopiano L, Abbruzzese G, Cortelli P, Meco G, Cossu G, Barbosa ER, Ferreira JJ; International Parkinsonism Genetics Network; Lu CS, Bonifati V. Quadri M, et al. Among authors: saddi v. Mov Disord. 2017 Feb;32(2):302-304. doi: 10.1002/mds.26900. Epub 2017 Jan 16. Mov Disord. 2017. PMID: 28090676 No abstract available.
67 results