MINOPOLI, FIORELLA
MINOPOLI, FIORELLA
DIPARTIMENTO DI SCIENZE GINECOLOGICHE, OSTETRICHE E PEDIATRICHE
MINOPOLI F.; Fiorella Minopoli
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
2012 Casey JP; Magalhaes T; Conroy JM; Regan R; Shah N; Anney R; Shields DC; Abrahams BS; Almeida J; Bacchelli E; Bailey AJ; Baird G; Battaglia A; Berney T; Bolshakova N; Bolton PF; Bourgeron T; Brennan S; Cali P; Correia C; Corsello C; Coutanche M; Dawson G; de Jonge M; Delorme R; Duketis E; Duque F; Estes A; Farrar P; Fernandez BA; Folstein SE; Foley S; Fombonne E; Freitag CM; Gilbert J; Gillberg C; Glessner JT; Green J; Guter SJ; Hakonarson H; Holt R; Hughes G; Hus V; Igliozzi R; Kim C; Klauck SM; Kolevzon A; Lamb JA; Leboyer M; Le Couteur A; Leventhal BL; Lord C; Lund SC; Maestrini E; Mantoulan C; Marshall CR; McConachie H; McDougle CJ; McGrath J; McMahon WM; Merikangas A; Miller J; Minopoli F; Mirza GK; Munson J; Nelson SF; Nygren G; Oliveira G; Pagnamenta AT; Papanikolaou K; Parr JR; Parrini B; Pickles A; Pinto D; Piven J; Posey DJ; Poustka A; Poustka F; Ragoussis J; Roge B; Rutter ML; Sequeira AF; Soorya L; Sousa I; Sykes N; Stoppioni V; Tancredi R; Tauber M; Thompson AP; Thomson S; Tsiantis J; Van Engeland H; Vincent JB; Volkmar F; Vorstman JA; Wallace S; Wang K; Wassink TH; White K; Wing K; Wittemeyer K; Yaspan BL; Zwaigenbaum L; Betancur C; Buxbaum JD; Cantor RM; Cook EH; Coon H; Cuccaro ML; Geschwind DH; Haines JL; Hallmayer J; Monaco AP; Nurnberger JI Jr; Pericak-Vance MA; Schellenberg GD; Scherer SW; Sutcliffe JS; Szatmari P; Vieland VJ; Wijsman EM; Green A; Gill M; Gallagher L; Vicente A; Ennis S.
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia.
2010 Pagnamenta AT; Bacchelli E; de Jonge MV; Mirza G; Scerri TS; Minopoli F; Chiocchetti A; Ludwig KU; Hoffmann P; Paracchini S; Lowy E; Harold DH; Chapman JA; Klauck SM; Poustka F; Houben RH; Staal WG; Ophoff RA; O'Donovan MC; Williams J; Nöthen MM; Schulte-Körne G; Deloukas P; Ragoussis J; Bailey AJ; Maestrini E; Monaco AP; International Molecular Genetic Study Of Autism Consortium
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
2012 Leblond C.S.; Heinrich J.; Delorme R.; Proepper C.; Betancur C.; Huguet G.; Konyukh M.; Chaste P| Ey E.; Rastam M.; Anckarsäter H.; Nygren G.; Gillberg IC.; Melke J.; Toro R.; Regnault B.; Fauchereau F.; Mercati O.; Lemière N.; Skuse D.; Poot M.; Holt R.; Monaco A.P.; Järvelä I.; Kantojärvi K.; Vanhala R.; Curran S.; Collier D.A.; Bolton P.; Chiocchetti A.; Klauck S.M.; Poustka F.; Freitag C.M.; Waltes R.; Kopp M.; Duketis E.; Bacchelli E.; Minopoli F.; Ruta L.; Battaglia A.; Mazzone L.; Maestrini E.; Sequeira A.F.; Oliveira B.; Vicente A.; Oliveira G.; Pinto D.; Scherer S.W.; Zelenika D.; Delepine M.; Lathrop M.; Bonneau D.; Guinchat V.; Devillard F.; Assouline B.; Mouren M.C.; Leboyer M.; Gillberg C.; Boeckers T.M.; Bourgeron T.
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.
2010 Maestrini E; Pagnamenta AT; Lamb JA; Bacchelli E; Sykes NH; Sousa I; Toma C; Barnby G; Butler H; Winchester L; Scerri TS; Minopoli F; Reichert J; Cai G; Buxbaum JD; Korvatska O; Schellenberg GD; Dawson G; Bildt AD; Minderaa RB; Mulder EJ; Morris AP; Bailey AJ; Monaco AP.
Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients.
2014 Bonora E;Graziano C;Minopoli F;Bacchelli E;Magini P;Diquigiovanni C;Lomartire S;Bianco F;Vargiolu M;Parchi P;Marasco E;Mantovani V;Rampoldi L;Trudu M;Parmeggiani A;Battaglia A;Mazzone L;Tortora G;Maestrini E;Seri M;Romeo G;IMGSAC
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. | Casey JP; Magalhaes T; Conroy JM; Regan R; Shah N; Anney R; Shields DC; Abrahams BS; Almeida J; B...acchelli E; Bailey AJ; Baird G; Battaglia A; Berney T; Bolshakova N; Bolton PF; Bourgeron T; Brennan S; Cali P; Correia C; Corsello C; Coutanche M; Dawson G; de Jonge M; Delorme R; Duketis E; Duque F; Estes A; Farrar P; Fernandez BA; Folstein SE; Foley S; Fombonne E; Freitag CM; Gilbert J; Gillberg C; Glessner JT; Green J; Guter SJ; Hakonarson H; Holt R; Hughes G; Hus V; Igliozzi R; Kim C; Klauck SM; Kolevzon A; Lamb JA; Leboyer M; Le Couteur A; Leventhal BL; Lord C; Lund SC; Maestrini E; Mantoulan C; Marshall CR; McConachie H; McDougle CJ; McGrath J; McMahon WM; Merikangas A; Miller J; Minopoli F; Mirza GK; Munson J; Nelson SF; Nygren G; Oliveira G; Pagnamenta AT; Papanikolaou K; Parr JR; Parrini B; Pickles A; Pinto D; Piven J; Posey DJ; Poustka A; Poustka F; Ragoussis J; Roge B; Rutter ML; Sequeira AF; Soorya L; Sousa I; Sykes N; Stoppioni V; Tancredi R; Tauber M; Thompson AP; Thomson S; Tsiantis J; Van Engeland H; Vincent JB; Volkmar F; Vorstman JA; Wallace S; Wang K; Wassink TH; White K; Wing K; Wittemeyer K; Yaspan BL; Zwaigenbaum L; Betancur C; Buxbaum JD; Cantor RM; Cook EH; Coon H; Cuccaro ML; Geschwind DH; Haines JL; Hallmayer J; Monaco AP; Nurnberger JI Jr; Pericak-Vance MA; Schellenberg GD; Scherer SW; Sutcliffe JS; Szatmari P; Vieland VJ; Wijsman EM; Green A; Gill M; Gallagher L; Vicente A; Ennis S. | 2012-01-01 | HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
| Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. | Pagnamenta AT; Bacchelli E; de Jonge MV; Mirza G; Scerri TS; Minopoli F; Chiocchetti A; Ludwig KU...; Hoffmann P; Paracchini S; Lowy E; Harold DH; Chapman JA; Klauck SM; Poustka F; Houben RH; Staal WG; Ophoff RA; O'Donovan MC; Williams J; Nöthen MM; Schulte-Körne G; Deloukas P; Ragoussis J; Bailey AJ; Maestrini E; Monaco AP; International Molecular Genetic Study Of Autism Consortium | 2010-01-01 | BIOLOGICAL PSYCHIATRY | - | 1.01 Articolo in rivista | - |
| Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders. | Leblond C.S.; Heinrich J.; Delorme R.; Proepper C.; Betancur C.; Huguet G.; Konyukh M.; Chaste P|... Ey E.; Rastam M.; Anckarsäter H.; Nygren G.; Gillberg IC.; Melke J.; Toro R.; Regnault B.; Fauchereau F.; Mercati O.; Lemière N.; Skuse D.; Poot M.; Holt R.; Monaco A.P.; Järvelä I.; Kantojärvi K.; Vanhala R.; Curran S.; Collier D.A.; Bolton P.; Chiocchetti A.; Klauck S.M.; Poustka F.; Freitag C.M.; Waltes R.; Kopp M.; Duketis E.; Bacchelli E.; Minopoli F.; Ruta L.; Battaglia A.; Mazzone L.; Maestrini E.; Sequeira A.F.; Oliveira B.; Vicente A.; Oliveira G.; Pinto D.; Scherer S.W.; Zelenika D.; Delepine M.; Lathrop M.; Bonneau D.; Guinchat V.; Devillard F.; Assouline B.; Mouren M.C.; Leboyer M.; Gillberg C.; Boeckers T.M.; Bourgeron T. | 2012-01-01 | PLOS GENETICS | - | 1.01 Articolo in rivista | - |
| High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility. | Maestrini E; Pagnamenta AT; Lamb JA; Bacchelli E; Sykes NH; Sousa I; Toma C; Barnby G; Butler H; ...Winchester L; Scerri TS; Minopoli F; Reichert J; Cai G; Buxbaum JD; Korvatska O; Schellenberg GD; Dawson G; Bildt AD; Minderaa RB; Mulder EJ; Morris AP; Bailey AJ; Monaco AP. | 2010-01-01 | MOLECULAR PSYCHIATRY | - | 1.01 Articolo in rivista | - |
| Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients. | Bonora E;Graziano C;Minopoli F;Bacchelli E;Magini P;Diquigiovanni C;Lomartire S;Bianco F;Vargiolu... M;Parchi P;Marasco E;Mantovani V;Rampoldi L;Trudu M;Parmeggiani A;Battaglia A;Mazzone L;Tortora G;Maestrini E;Seri M;Romeo G;IMGSAC | 2014-01-01 | EMBO MOLECULAR MEDICINE | - | 1.01 Articolo in rivista | Bonora.pdf |