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 [Scientific article]
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 [Scientific article]
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 [Scientific article]
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 [Scientific article]
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) [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 [Scientific article]
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 [Scientific article]
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 [Scientific article]
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 [Scientific article]
