A. Santoro; E. Balducci; F. Rosini; A. Montesanto; S. Salvioli; G. Rose; E. Bellavista; M. Mishto; G. Gasparre; E. Bonora; A. Chiamenti; G. Romeo; C. Gabelli; G. Crepaldi; T. Grune; G. De Benedictis; C. Franceschi, mtDNA inherited and somatic variability in Alzheimer’s disease, in: FREE RADICAL RESEARCH, «FREE RADICAL RESEARCH», 2006, 40, pp. S46 - S46 (atti di: Free Radicals in the Aging Process—The 'Free Radical Theory of Aging' 50 years after, Davos (CH), Sept 2006) [atti di convegno-abstract]
Bonora E.; Evangelisti C.; Bonichon F.; Tallini G.; Romeo G., Novel germline variants identified in the inner mitochondrial membrane transporter TIMM44 and their role in predisposition to oncocytic thyroid carcinomas., «BRITISH JOURNAL OF CANCER», 2006, 95, pp. 1529 - 1536 [articolo]
Rossi S.; Masotti D.; Nardini C.; Bonora E.; Romeo G.; Macii E.; Benini L.; Volinia S., TOM: a web-based integrated approach for identification of candidate disease genes, «NUCLEIC ACIDS RESEARCH», 2006, 34, pp. W285 - W292 [articolo]Open Access
Tsilchorozidou T; Vafiadou E; Yovos JG; Romeo G; McKay J; Lesueur F; Bonora E, A Greek Family with a Follicular Variant of Familial Papillary Thyroid Carcinoma: TCO, MNG1, fPTC/PRN, and NMTC1 Excluded as Susceptibility Loci, «THYROID», 2005, 15, pp. 1349 - 1354 [articolo]
Lamb J.A.; Barnby G.; Bonora E.; Sykes N.; Bacchelli E.; Blasi F.; Maestrini E.; Broxholme J.; Tzenova J.; Weeks D.; Bailey A.J.; Monaco A.P.; International Molecular Genetic Study of Autism Consortium (IMGSAC)., Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects., «JOURNAL OF MEDICAL GENETICS», 2005, 42, pp. 132 - 137 [articolo]
Macdermot, Kay D.; Bonora, Elena; Sykes, Nuala; Coupe, Anne-Marie; Lai, Cecilia S. L.; Vernes, Sonja C.; Vargha-Khadem, Faraneh; Mckenzie, Fiona; Smith, Robert L.; Monaco, Anthony P.; Fisher, Simon E., Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits, «AMERICAN JOURNAL OF HUMAN GENETICS», 2005, 76, pp. 1074 - 1080 [articolo]
Bonora E.; Lamb J.A.; Barnby G.; Sykes N.; Moberly T.; Beyer K.S.; Klauck S.M.; Poustka F.; Bacchelli E.; Blasi F.; Maestrini E.; Battaglia A.; Haracopos D.; Pedersen L.; Isager T.; Eriksen G.; Viskum B.; Sorensen E.U.; Brondum-Nielsen K.; Cotterill R.; Engeland H.; Jonge M.; Kemner C.; Steggehuis K.; Scherpenisse M.; Rutter M.; Bolton P.F.; Parr J.R.; Poustka A.; Bailey A.J.; Monaco A.P.; International Molecular Genetic Study of Austism Consortium., Mutation screening and association analysis of six candidate genes for autism on chromosome 7q., «EUROPEAN JOURNAL OF HUMAN GENETICS», 2005, 13, pp. 198 - 207 [articolo]
Porcelli A.M.; Gasparre G.; Bonora E.; Ghelli A.; Iommarini L.; Biondi A.; Baracca A.; Rugolo M.; Lenaz G.; Romeo G., Novel mutations in mitochondrial respiratory complexes and their functional relevance in thyroid oncocytoma., in: Molecular Insight to Physiology and Pathology, s.l, s.n, 2005, pp. SC5.21 - SC5.21 (atti di: International Conference on Mitochondria, Bari, Italy, 17-22 December 2005) [atti di convegno-abstract]
Bonora E.; Beyer K.S.; Lamb J.A.; Parr J.R.; Klauck S.M.; Benner A.; Paolucci M.; Abbott A.; Ragoussis I.; Poustka A.; Bailey A.J.; Monaco A.P., Analysis of reelin as a candidate gene for autism, «MOLECULAR PSYCHIATRY», 2003, 8, pp. 885 - 892 [articolo]
Bacchelli E.; Blasi F.; Biondolillo M.; Lamb J.A.; Bonora E.; Barnby G.; Parr J.; Beyer K.S.; Klauck S.M.; Poustka A.; Bailey A.J.; Monaco A.P.; Maestrini E., Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene, «MOLECULAR PSYCHIATRY», 2003, 8, pp. 916 - 924 [articolo]
Newbury D.F.; Bonora E.; Lamb J.A.; Fisher S.E.; Lai C.S.L.; Baird G.; Jannoun L.; Slonims V.; Stott C.M.; Merricks M.J.; Bolton P.F.; Bailey A.J.; Monaco A.P., FOXP2 is not a major susceptibility gene for autism or specific language impairment, «AMERICAN JOURNAL OF HUMAN GENETICS», 2002, 70, pp. 1318 - 1327 [articolo]
Bonora E.; Bacchelli E.; Levy E.R.; Blasi F.; Marlow A.; Monaco A.P.; Maestrini E., Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region, «MOLECULAR PSYCHIATRY», 2002, 7, pp. 289 - 301 [articolo]
Barbieri, L.; Valbonesi, P.; Bonora, E.; Gorini, P.; Bolognesi, A.; Stirpe, F., Polynucleotide:adenosine glycosidase activity of ribosome-inactivating proteins: Effect on DNA, RNA and poly(A), «NUCLEIC ACIDS RESEARCH», 1997, 25, pp. 518 - 522 [articolo]
