Sfoglia per Autore
FOXP2 is not a major susceptibility gene for autism or specific language impairment
2002 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.
Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region
2002 Bonora E.; Bacchelli E.; Levy E.R.; Blasi F.; Marlow A.; Monaco A.P.; Maestrini E.
Analysis of reelin as a candidate gene for autism
2003 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.
Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene
2003 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.
A Greek Family with a Follicular Variant of Familial Papillary Thyroid Carcinoma: TCO, MNG1, fPTC/PRN, and NMTC1 Excluded as Susceptibility Loci
2005 Tsilchorozidou T; Vafiadou E; Yovos JG; Romeo G; McKay J; Lesueur F; Bonora E
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits
2005 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.
Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.
2005 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).
Novel mutations in mitochondrial respiratory complexes and their functional relevance in thyroid oncocytoma.
2005 Porcelli A.M.; Gasparre G.; Bonora E.; Ghelli A.; Iommarini L.; Biondi A.; Baracca A.; Rugolo M.; Lenaz G.; Romeo G.
Mutation screening and association analysis of six candidate genes for autism on chromosome 7q.
2005 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.
mtDNA inherited and somatic variability in Alzheimer Disease
2006 A. Santoro; E. Balducci; F. Rosini; A. Montesanto; S. Salvioli; G. Rose; E. Bellavista; M. Mishto; Gasparre G.; 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
2006 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
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III
2006 BONORA E.; PORCELLI A.M.; GASPARRE G.; BIONDI A.; GHELLI A.; CARELLI V.; BARACCA A.; TALLINI G.; MARTINUZZI A.; LENAZ G.; RUGOLO M.; ROMEO G.
Integrated web-based approach to multigenic diseases
2006 S. Rossi; D. Masotti; C. Nardini; E. Bonora; E. Macii; S. Volinia; L. Benini
Novel germline variants identified in the inner mitochondrial membrane transporter TIMM44 and their role in predisposition to oncocytic thyroid carcinomas.
2006 Bonora E.; Evangelisti C.; Bonichon F.; Tallini G.; Romeo G.
TOM: a web-based integrated approach for identification of candidate disease genes
2006 Rossi S.; Masotti D.; Nardini C.; Bonora E.; Romeo G.; Macii E.; Benini L.; Volinia S.
GSTT1 and M1 polymorphisms in Hurthle thyroid cancer patients
2006 Stankov K; Landi S; Gioia-Patricola L; Bonora E; Volante M; Papotti M; Romeo G
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours.
2007 Gasparre G.; Porcelli A.M.; Bonora E.; Pennisi L.F.; Toller M.; Iommarini L.; Ghelli A.; Moretti M.; Betts C.M.; Martinelli G.N.; Ceroni A.R.; Curcio F.; Carelli V.; Rugolo M.; Tallini G.; Romeo G.
C620R mutation of the murine ret proto-oncogene: loss of function effect in homozygotes and possible gain of function effect in heterozygotes.
2007 Yin L.; Puliti A.; Bonora E.; Evangelisti C.; Conti V.; Tong WM.; Medard JJ.; Lavoué MF.; Forey N.; Wang LC.; Manié S.; Morel G.; Raccurt M.; Wang ZQ.; Romeo G.
Association of the interleukin-4/interleukin-4 receptor genetic variants with hand osteoathrtitis.
2008 Vargiolu M.; Silvestri T.; Bonora E.; Dolzani P.; Pulsatelli L.; Punzi L.; Fioravanti A.; Facchini A.; Romeo G.; Meliconi R.
The FAGenomicH project: a whole candidate gene approach to identify markers associated with fatness traits in pigs and investigate the pig as a model for human obesity
2008 Fontanesi L.; Fronza R.; Scotti E.; Galimberti G.; Calò D.G.; Bonora E.; Vargiolu M.; Colombo M.; Casadio R.; Romeo G.; Russo V.
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| FOXP2 is not a major susceptibility gene for autism or specific language impairment | Newbury D.F.; Bonora E.; Lamb J.A.; Fisher S.E.; Lai C.S.L.; Baird G.; Jannoun L.; Slonims V.; St...ott C.M.; Merricks M.J.; Bolton P.F.; Bailey A.J.; Monaco A.P. | 2002-01-01 | AMERICAN JOURNAL OF HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
| Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region | Bonora E.; Bacchelli E.; Levy E.R.; Blasi F.; Marlow A.; Monaco A.P.; Maestrini E. | 2002-01-01 | MOLECULAR PSYCHIATRY | - | 1.01 Articolo in rivista | - |
| Analysis of reelin as a candidate gene for autism | Bonora E.; Beyer K.S.; Lamb J.A.; Parr J.R.; Klauck S.M.; Benner A.; Paolucci M.; Abbott A.; Rago...ussis I.; Poustka A.; Bailey A.J.; Monaco A.P. | 2003-01-01 | MOLECULAR PSYCHIATRY | - | 1.01 Articolo in rivista | - |
| Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene | Bacchelli E.; Blasi F.; Biondolillo M.; Lamb J.A.; Bonora E.; Barnby G.; Parr J.; Beyer K.S.; Kla...uck S.M.; Poustka A.; Bailey A.J.; Monaco A.P.; Maestrini E. | 2003-01-01 | MOLECULAR PSYCHIATRY | - | 1.01 Articolo in rivista | - |
| A Greek Family with a Follicular Variant of Familial Papillary Thyroid Carcinoma: TCO, MNG1, fPTC/PRN, and NMTC1 Excluded as Susceptibility Loci | Tsilchorozidou T; Vafiadou E; Yovos JG; Romeo G; McKay J; Lesueur F; Bonora E | 2005-01-01 | THYROID | - | 1.01 Articolo in rivista | - |
| Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits | Macdermot, Kay D.; Bonora, Elena; Sykes, Nuala; Coupe, Anne-Marie; Lai, Cecilia S. L.; Vernes, So...nja C.; Vargha-Khadem, Faraneh; Mckenzie, Fiona; Smith, Robert L.; Monaco, Anthony P.; Fisher, Simon E. | 2005-01-01 | AMERICAN JOURNAL OF HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
| Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects. | Lamb J.A.; Barnby G.; Bonora E.; Sykes N.; Bacchelli E.; Blasi F.; Maestrini E.; Broxholme J.; Tz...enova J.; Weeks D.; Bailey A.J.; Monaco A.P.; International Molecular Genetic Study of Autism Consortium (IMGSAC). | 2005-01-01 | JOURNAL OF MEDICAL GENETICS | - | 1.01 Articolo in rivista | - |
| Novel mutations in mitochondrial respiratory complexes and their functional relevance in thyroid oncocytoma. | Porcelli A.M.; Gasparre G.; Bonora E.; Ghelli A.; Iommarini L.; Biondi A.; Baracca A.; Rugolo M.;... Lenaz G.; Romeo G. | 2005-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Mutation screening and association analysis of six candidate genes for autism on chromosome 7q. | Bonora E.; Lamb J.A.; Barnby G.; Sykes N.; Moberly T.; Beyer K.S.; Klauck S.M.; Poustka F.; Bacch...elli 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. | 2005-01-01 | EUROPEAN JOURNAL OF HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
| mtDNA inherited and somatic variability in Alzheimer Disease | A. Santoro; E. Balducci; F. Rosini; A. Montesanto; S. Salvioli; G. Rose; E. Bellavista; M. Mishto...; Gasparre G.; E. Bonora; A. Chiamenti; G. Romeo; C. Gabelli; G. Crepaldi; T. Grune; G. De Benedictis; C. Franceschi | 2006-01-01 | ALZHEIMER'S & DEMENTIA | - | 4.02 Riassunto (Abstract) | - |
| mtDNA inherited and somatic variability in Alzheimer’s disease | 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 | 2006-01-01 | FREE RADICAL RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III | BONORA E.; PORCELLI A.M.; GASPARRE G.; BIONDI A.; GHELLI A.; CARELLI V.; BARACCA A.; TALLINI G.; ...MARTINUZZI A.; LENAZ G.; RUGOLO M.; ROMEO G. | 2006-01-01 | CANCER RESEARCH | - | 1.01 Articolo in rivista | - |
| Integrated web-based approach to multigenic diseases | S. Rossi; D. Masotti; C. Nardini; E. Bonora; E. Macii; S. Volinia; L. Benini | 2006-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Novel germline variants identified in the inner mitochondrial membrane transporter TIMM44 and their role in predisposition to oncocytic thyroid carcinomas. | Bonora E.; Evangelisti C.; Bonichon F.; Tallini G.; Romeo G. | 2006-01-01 | BRITISH JOURNAL OF CANCER | - | 1.01 Articolo in rivista | - |
| TOM: a web-based integrated approach for identification of candidate disease genes | Rossi S.; Masotti D.; Nardini C.; Bonora E.; Romeo G.; Macii E.; Benini L.; Volinia S. | 2006-01-01 | NUCLEIC ACIDS RESEARCH | - | 1.01 Articolo in rivista | NAR2006.pdf |
| GSTT1 and M1 polymorphisms in Hurthle thyroid cancer patients | Stankov K; Landi S; Gioia-Patricola L; Bonora E; Volante M; Papotti M; Romeo G | 2006-01-01 | CANCER LETTERS | - | 1.01 Articolo in rivista | - |
| Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours. | Gasparre G.; Porcelli A.M.; Bonora E.; Pennisi L.F.; Toller M.; Iommarini L.; Ghelli A.; Moretti ...M.; Betts C.M.; Martinelli G.N.; Ceroni A.R.; Curcio F.; Carelli V.; Rugolo M.; Tallini G.; Romeo G. | 2007-01-01 | PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA | - | 1.01 Articolo in rivista | - |
| C620R mutation of the murine ret proto-oncogene: loss of function effect in homozygotes and possible gain of function effect in heterozygotes. | Yin L.; Puliti A.; Bonora E.; Evangelisti C.; Conti V.; Tong WM.; Medard JJ.; Lavoué MF.; Forey N....; Wang LC.; Manié S.; Morel G.; Raccurt M.; Wang ZQ.; Romeo G. | 2007-01-01 | INTERNATIONAL JOURNAL OF CANCER | - | 1.01 Articolo in rivista | - |
| Association of the interleukin-4/interleukin-4 receptor genetic variants with hand osteoathrtitis. | Vargiolu M.; Silvestri T.; Bonora E.; Dolzani P.; Pulsatelli L.; Punzi L.; Fioravanti A.; Facchin...i A.; Romeo G.; Meliconi R. | 2008-01-01 | OSTEOARTHRITIS AND CARTILAGE | - | 4.02 Riassunto (Abstract) | - |
| The FAGenomicH project: a whole candidate gene approach to identify markers associated with fatness traits in pigs and investigate the pig as a model for human obesity | Fontanesi L.; Fronza R.; Scotti E.; Galimberti G.; Calò D.G.; Bonora E.; Vargiolu M.; Colombo M.;... Casadio R.; Romeo G.; Russo V. | 2008-01-01 | - | University of Ljubljana, Biotechnical Faculty | 4.02 Riassunto (Abstract) | - |
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