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Page 1
Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease.
Vilariño-Güell C, Zimprich A, Martinelli-Boneschi F, Herculano B, Wang Z, Matesanz F, Urcelay E, Vandenbroeck K, Leyva L, Gris D, Massaad C, Quandt JA, Traboulsee AL, Encarnacion M, Bernales CQ, Follett J, Yee IM, Criscuoli MG, Deutschländer A, Reinthaler EM, Zrzavy T, Mascia E, Zauli A, Esposito F, Alcina A, Izquierdo G, Espino-Paisán L, Mena J, Antigüedad A, Urbaneja-Romero P, Ortega-Pinazo J, Song W, Sadovnick AD. Vilariño-Güell C, et al. Among authors: zauli a. PLoS Genet. 2019 Jun 6;15(6):e1008180. doi: 10.1371/journal.pgen.1008180. eCollection 2019 Jun. PLoS Genet. 2019. PMID: 31170158 Free PMC article.
Analysis of genes, pathways and networks involved in disease severity and age at onset in primary-progressive multiple sclerosis.
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. Giacalone G, et al. Among authors: zauli a. Mult Scler. 2015 Oct;21(11):1431-42. doi: 10.1177/1352458514564590. Epub 2015 Jan 12. Mult Scler. 2015. PMID: 25583839
The burden of multiple sclerosis variants in continental Italians and Sardinians.
Barizzone N, Zara I, Sorosina M, Lupoli S, Porcu E, Pitzalis M, Zoledziewska M, Esposito F, Leone M, Mulas A, Cocco E, Ferrigno P, Guerini FR, Brambilla P, Farina G, Murru R, Deidda F, Sanna S, Loi A, Barlassina C, Vecchio D, Zauli A, Clarelli F, Braga D, Poddie F, Cantello R, Martinelli V, Comi G, Frau J, Lorefice L, Pugliatti M, Rosati G; PROGEMUS (PROgnostic GEnetic factors in MUltiple Sclerosis) Consortium PROGRESSO (Italian network of Primary Progressive Multiple Sclerosis) Consortium; Melis M, Marrosu MG, Cusi D, Cucca F, Martinelli Boneschi F, Sanna S, D'Alfonso S. Barizzone N, et al. Among authors: zauli a. Mult Scler. 2015 Oct;21(11):1385-95. doi: 10.1177/1352458515596599. Mult Scler. 2015. PMID: 26438306
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis.
Mascia E, Clarelli F, Zauli A, Guaschino C, Sorosina M, Barizzone N, Basagni C, Santoro S, Ferrè L, Bonfiglio S, Biancolini D, Pozzato M, Guerini FR, Protti A, Liguori M, Moiola L, Vecchio D, Bresolin N, Comi G, Filippi M, Esposito F, D'Alfonso S, Martinelli-Boneschi F. Mascia E, et al. Among authors: zauli a. J Neuroimmunol. 2022 Jan 15;362:577760. doi: 10.1016/j.jneuroim.2021.577760. Epub 2021 Nov 5. J Neuroimmunol. 2022. PMID: 34922125
A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis Susceptibility.
Esposito F, Osiceanu AM, Sorosina M, Ottoboni L, Bollman B, Santoro S, Bettegazzi B, Zauli A, Clarelli F, Mascia E, Calabria A, Zacchetti D, Capra R, Ferrari M, Provero P, Lazarevic D, Cittaro D, Carrera P, Patsopoulos N, Toniolo D, Sadovnick AD, Martino G, De Jager PL, Comi G, Stupka E, Vilariño-Güell C, Piccio L, Martinelli Boneschi F. Esposito F, et al. Among authors: zauli a. Genes (Basel). 2022 Dec 16;13(12):2392. doi: 10.3390/genes13122392. Genes (Basel). 2022. PMID: 36553660 Free PMC article.
COL6A5 variants in familial neuropathic chronic itch.
Martinelli-Boneschi F, Colombi M, Castori M, Devigili G, Eleopra R, Malik RA, Ritelli M, Zoppi N, Dordoni C, Sorosina M, Grammatico P, Fadavi H, Gerrits MM, Almomani R, Faber CG, Merkies IS, Toniolo D; INGI Network; Cocca M, Doglioni C, Waxman SG, Dib-Hajj SD, Taiana MM, Sassone J, Lombardi R, Cazzato D, Zauli A, Santoro S, Marchi M, Lauria G. Martinelli-Boneschi F, et al. Among authors: zauli a. Brain. 2017 Mar 1;140(3):555-567. doi: 10.1093/brain/aww343. Brain. 2017. PMID: 28073787
Laser capture microdissection for transcriptomic profiles in human skin biopsies.
Santoro S, Lopez ID, Lombardi R, Zauli A, Osiceanu AM, Sorosina M, Clarelli F, Peroni S, Cazzato D, Marchi M, Quattrini A, Comi G, Calogero RA, Lauria G, Martinelli Boneschi F. Santoro S, et al. Among authors: zauli a. BMC Mol Biol. 2018 Jun 19;19(1):7. doi: 10.1186/s12867-018-0108-5. BMC Mol Biol. 2018. PMID: 29921228 Free PMC article.
ASPicDB: a database of annotated transcript and protein variants generated by alternative splicing.
Martelli PL, D'Antonio M, Bonizzoni P, Castrignanò T, D'Erchia AM, D'Onorio De Meo P, Fariselli P, Finelli M, Licciulli F, Mangiulli M, Mignone F, Pavesi G, Picardi E, Rizzi R, Rossi I, Valletti A, Zauli A, Zambelli F, Casadio R, Pesole G. Martelli PL, et al. Among authors: zauli a. Nucleic Acids Res. 2011 Jan;39(Database issue):D80-5. doi: 10.1093/nar/gkq1073. Epub 2010 Nov 4. Nucleic Acids Res. 2011. PMID: 21051348 Free PMC article.
TRAMPLE: the transmembrane protein labelling environment.
Fariselli P, Finelli M, Rossi I, Amico M, Zauli A, Martelli PL, Casadio R. Fariselli P, et al. Among authors: zauli a. Nucleic Acids Res. 2005 Jul 1;33(Web Server issue):W198-201. doi: 10.1093/nar/gki440. Nucleic Acids Res. 2005. PMID: 15980454 Free PMC article.
PONGO: a web server for multiple predictions of all-alpha transmembrane proteins.
Amico M, Finelli M, Rossi I, Zauli A, Elofsson A, Viklund H, von Heijne G, Jones D, Krogh A, Fariselli P, Luigi Martelli P, Casadio R. Amico M, et al. Among authors: zauli a. Nucleic Acids Res. 2006 Jul 1;34(Web Server issue):W169-72. doi: 10.1093/nar/gkl208. Nucleic Acids Res. 2006. PMID: 16844984 Free PMC article.
31 results