Biography and Research Interest

Publications

Non-Zebrafish Publications

Boaretto F*, Vettori A*, Casarin A,Vazza G, Muglia M, Rossetto MG, Cavallaro T, Rizzuto N, Carelli V, Salviati L, Mostacciuolo ML, Martinuzzi A. Severe CMT type 2 with fatal encephalopathy associated with a novel mfn2 splicing mutation. Neurology. 2010 Jun 8;74(23):1919-21.

Millino C, Fanin M, Vettori A, Laveder P, Mostacciuolo ML, Angelini C, Lanfranchi G. Different atrophy-hypertrophy transcription pathways in muscles affected by severe and mild spinal muscular atrophy. BMC Med. 2009 Apr 7;7:14.

Bovo G, Diani E, Bisulli F, Di Bonaventura C, Striano P, Gambardella A, Ferlazzo E, Egeo G, Mecarelli O, Elia M, Bianchi A, Bortoluzzi S, Vettori A, Aguglia U, Binelli S, De Falco A, Coppola G, Gobbi G, Sofia V, Striano S, Tinuper P, Giallonardo AT, Michelucci R, Nobile C. Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy. Neurosci Lett. 2008 May 2;436(1):23-6.

Vazza G, Bertolin C, Scudellaro E, Vettori A, Boaretto F, Rampinelli S, De Sanctis G, Perini G, Peruzzi P, Mostacciuolo ML. Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26. Mol Psychiatry. 2007 Jan;12(1):87-93.

Simonati A, Boaretto F, Vettori A, Dabrilli P, Criscuolo L, Rizzuto N, Mostacciuolo ML. A novel missense mutation in the l1cam gene in a boy with L1 disease. Neurol Sci. 2006 Jun;27(2):114-7.

Pilichou K, Nava A, Basso A, Beffagna A, Bauce B, Lorenzon A, Frigo G, Vettori A, Valente M, Towbin J, Thiene G, Danieli GA, Ramazzo A. Mutations in desmoglein-2 gene cause arrhythmogenic right ventricular cardiomyopathy. Circulation. 2006 Mar 7;113(9):1171-9.

Velayos-Baeza A* Vettori A* Copley RR, Dobson-Stone C, Monaco AP. Analysis of the human VSP13 gene family. Genomics. 2004 Sep; 84(3):536-49.

Opocher G, Schiavi F, Vettori A, Pampinella F, Vitiello L, Murgia A, Martella M, Taccaliti A, Mantero F, Mostacciuolo M.L. Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma. Clin Endocrino (Oxf). 2003 Dec; 59(6): 707-715.

Pegoraro E, Vettori A, Valentino ML, Molon A, Mostacciuolo ML, Howell N, Carelli V. X-Inactivation pattern in multiple tissues from two leber's hereditary optic neuropathy (LHON) patients. Am J Med Genet. 2003 May; 15,119A(1):37-40.

Soragna D*, Vettori A*, Carraro G, Marchioni E, Vazza G, Bellini S, Tupler R, Savoldi F, Mostacciuolo ML. A locus for migraine without aura maps on chromosome 14q21.2-q22.3. Am J Hum Genet. 2003 Jan; 72(1):161-167.

Zortea M, Vettori A, Trevisan CP, Bellini S, Vazza G, Armani M, Simonati A, Mostacciuolo ML. Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1. J Med Genet. 2002 Jun; 39(6):387-90.