Sfoglia per Autore
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.
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.
DNA variants in the human RAB3A gene are not associated with autism.
2004 D'Adamo P.; Bacchelli E.; Blasi F.; Lipp H.P.; Toniolo D.; Maestrini 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).
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.
Absence of coding mutations in the X-linked genes Neuroligin 3 and Neuroligin 4 in individuals with autism from the IMGSAC collection
2006 Blasi F.; Bacchelli E.; Pesaresi G.; Carone S.; Bailey A.J.; Maestrini E.
Autism spectrum disorders: molecular genetic advances
2006 Bacchelli E.; Maestrini E.
SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample.
2006 Blasi F.; Bacchelli E.; Carone S.; Toma C.; Monaco AP.; Bailey AJ.; Maestrini E.
Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations.
2007 Toma C; Rossi M; Sousa I; Blasi F; Bacchelli E; Alen R; Vanhala R; Monaco AP; Järvelä I; Maestrini E
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
2007 Autism Genome Project Consortium; Szatmari P; Paterson AD; Zwaigenbaum L; Roberts W; Brian J; Liu XQ; Vincent JB; Skaug JL; Thompson AP; Senman L; Feuk L; Qian C; Bryson SE; Jones MB; Marshall CR; Scherer SW; Vieland VJ; Bartlett C; Mangin LV; Goedken R; Segre A; Pericak-Vance MA; Cuccaro ML; Gilbert JR; Wright HH; Abramson RK; Betancur C; Bourgeron T; Gillberg C; Leboyer M; Buxbaum JD; Davis KL; Hollander E; Silverman JM; Hallmayer J; Lotspeich L; Sutcliffe JS; Haines JL; Folstein SE; Piven J; Wassink TH; Sheffield V; Geschwind DH; Bucan M; Brown WT; Cantor RM; Constantino JN; Gilliam TC; Herbert M; Lajonchere C; Ledbetter DH; Lese-Martin C; Miller J; Nelson S; Samango-Sprouse CA; Spence S; State M; Tanzi RE; Coon H; Dawson G; Devlin B; Estes A; Flodman P; Klei L; McMahon WM; Minshew N; Munson J; Korvatska E; Rodier PM; Schellenberg GD; Smith M; Spence MA; Stodgell C; Tepper PG; Wijsman EM; Yu CE; Roge B; Mantoulan C; Wittemeyer K; Poustka A; Felder B; Klauck SM; Schuster C; Poustka F; Bolte S; Feineis-Matthews S; Herbrecht E; Schmotzer G; Tsiantis J; Papanikolaou K; Maestrini E; Bacchelli E; Blasi F; Carone S; Toma C; Van Engeland H; de Jonge M; Kemner C; Koop F; Langemeijer M; Hijimans C; Staal WG; Baird G; Bolton PF; Rutter ML; Weisblatt E; Green J; Aldred C; Wilkinson JA; Pickles A; Le Couteur A; Berney T; McConachie H; Bailey AJ; Francis K; Honeyman G; Hutchinson A; Parr JR; Wallace S; Monaco AP; Barnby G; Kobayashi K; Lamb JA; Sousa I; Sykes N; Cook EH; Guter SJ; Leventhal BL; Salt J; Lord C; Corsello C; Hus V; Weeks DE; Volkmar F; Tauber M; Fombonne E; Shih A.
Analysis of X chromosome inactivation in autism spectrum disorders.
2008 Gong X; Bacchelli E; Blasi F; Toma C; Betancur C; Chaste P; Delorme R; Durand CM; Fauchereau F; Botros HG; Leboyer M; Mouren-Simeoni MC; Nygren G; Anckarsäter H; Rastam M; Gillberg IC; Gillberg C; Moreno-De-Luca D; Carone S; Nummela I; Rossi M; Battaglia A; International Molecular Genetic Study of Autism Consortium (IMGSAC); Jarvela I; Maestrini E; Bourgeron T.
Genome-wide linkage analyses of quantitative and categorical autism subphenotypes.
2008 Liu XQ; Paterson AD; Szatmari P; Autism Genome Project Consortium [..;Maestrini E; ..]
A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12
2009 Asher JE; Lamb JA; Brocklebank D; Cazier JB; Maestrini E; Addis L; Sen M; Baron-Cohen S; Monaco AP.
MET and autism susceptibility: family and case-control studies.
2009 Sousa I; Clark TG; Toma C; Kobayashi K; Choma M; Holt R; Sykes NH; Lamb JA; Bailey AJ; Battaglia A; Maestrini E; Monaco AP.
Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment.
2009 Newbury DF, Warburton PC, Wilson N, Bacchelli E, Carone S; International Molecular Genetic Study of Autism Consortium, Lamb JA, Maestrini E, Volpi EV, Mohammed S, Baird G, Monaco AP.
A genome-wide linkage and association scan reveals novel loci for autism.
2009 WEISS LA, ARKING DE; GENE DISCOVERY PROJECT OF JOHNS HOPKINS & THE AUTISM CONSORTIUM, DALY MJ, CHAKRAVARTI A, BRUNE CW, WEST K, O'CONNOR A, HILTON G, TOMLINSON RL, WEST AB, COOK EH JR, CHAKRAVARTI A, WEISS LA, GREEN T, CHANG SC, GABRIEL S, GATES C, HANSON EM, KIRBY A, KORN J, KURUVILLA F, MCCARROLL S, MORROW EM, NEALE B, PURCELL S, SASANFAR R, SOUGNEZ C, STEVENS C, ALTSHULER D, GUSELLA J, SANTANGELO SL, SKLAR P, TANZI R, DALY MJ, ANNEY R, BAILEY AJ, BAIRD G, BATTAGLIA A, BERNEY T, BETANCUR C, BÖLTE S, BOLTON PF, BRIAN J, BRYSON SE, BUXBAUM JD, CABRITO I, CAI G, CANTOR RM, COOK EH JR, COON H, CONROY J, CORREIA C, CORSELLO C, CRAWFORD EL, CUCCARO ML, DAWSON G, DE JONGE M, DEVLIN B, DUKETIS E, ENNIS S, ESTES A, FARRAR P, FOMBONNE E, FREITAG CM, GALLAGHER L, GESCHWIND DH, GILBERT J, GILL M, GILLBERG C, GOLDBERG J, GREEN A, GREEN J, GUTER SJ, HAINES JL, HALLMAYER JF, HUS V, KLAUCK SM, KORVATSKA O, LAMB JA, LASKAWIEC M, LEBOYER M, COUTEUR AL, LEVENTHAL BL, LIU XQ, LORD C, LOTSPEICH LJ, MAESTRINI E, MAGALHAES T, MAHONEY W, MANTOULAN C, MCCONACHIE H, MCDOUGLE CJ, MCMAHON WM, MARSHALL CR, MILLER J, MINSHEW NJ, MONACO AP, MUNSON J, NURNBERGER JI JR, OLIVEIRA G, PAGNAMENTA A, PAPANIKOLAOU K, PARR JR, PATERSON AD, PERICAK-VANCE MA, PICKLES A, PINTO D, PIVEN J, POSEY DJ, POUSTKA A, POUSTKA F, REGAN R, REICHERT J, RENSHAW K, ROBERTS W, ROGE B, RUTTER ML, SALT J, SCHELLENBERG GD, SCHERER SW, SHEFFIELD V, SUTCLIFFE JS, SZATMARI P, TANSEY K, THOMPSON AP, TSIANTIS J, VAN ENGELAND H, VICENTE AM, VIELAND VJ, VOLKMAR F, WALLACE S, WASSINK TH, WIJSMAN EM, WING K, WITTEMEYER K, YASPAN BL, ZWAIGENBAUM L, MORROW EM, YOO SY, HILL RS, MUKADDES NM, BALKHY S, GASCON G, AL-SAAD S, HASHMI A, WARE J, JOSEPH RM, LECLAIR E, PARTLOW JN, BARRY B, WALSH CA, PAULS D, MOILANEN I, EBELING H, MATTILA ML, KUUSIKKO S, JUSSILA K, IGNATIUS J, SASANFAR R, TOLOUEI A, GHADAMI M, ROSTAMI M, HOSSEINIPOUR A, VALUJERDI M, SANTANGELO SL, ANDRESEN K, WINKLOSKI B, HADDAD S, KUNKEL L, KOHANE Z, TRAN T, KONG SW, O'NEIL SB, HANSON EM, HUNDLEY R, HOLM I, PETERS H, BARONI E, CANGIALOSE A, JACKSON L, ALBERS L, BECKER R, BRIDGEMOHAN C, FRIEDMAN S, MUNIR K, NAZIR R, PALFREY J, SCHONWALD A, SIMMONS E, RAPPAPORT LA, GAUTHIER J, MOTTRON L, JOOBER R, FOMBONNE E, ROULEAU G, REHNSTROM K, VON WENDT L, PELTONEN L.
Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection.
2009 Sykes NH, Toma C, Wilson N, Volpi EV, Sousa I, Pagnamenta AT, Tancredi R, Battaglia A, Maestrini E, Bailey AJ, Monaco AP; International Molecular Genetic Study of Autism Consortium (IMGSAC).
A genome-wide scan for common alleles affecting risk for autism.
2010 Anney R; Klei L; Pinto D; Regan R; Conroy J; Magalhaes TR; Correia C; Abrahams BS; Sykes N; Pagnamenta AT; Almeida J; Bacchelli E; Bailey AJ; Baird G; Battaglia A; Berney T; Bolshakova N; Bölte S; Bolton PF; Bourgeron T; Brennan S; Brian J; Carson AR; Casallo G; Casey J; Chu SH; Cochrane L; Corsello C; Crawford EL; Crossett A; Dawson G; de Jonge M; Delorme R; Drmic I; Duketis E; Duque F; Estes A; Farrar P; Fernandez BA; Folstein SE; Fombonne E; Freitag CM; Gilbert J; Gillberg C; Glessner JT; Goldberg J; Green J; Guter SJ; Hakonarson H; Heron EA; Hill M; Holt R; Howe JL; Hughes G; Hus V; Igliozzi R; Kim C; Klauck SM; Kolevzon A; Korvatska O; Kustanovich V; Lajonchere CM; Lamb JA; Laskawiec M; Leboyer M; Le Couteur A; Leventhal BL; Lionel AC; Liu XQ; Lord C; Lotspeich L; Lund SC; Maestrini E; Mahoney W; Mantoulan C; Marshall CR; McConachie H; McDougle CJ; McGrath J; McMahon WM; Melhem NM; Merikangas A; Migita O; Minshew NJ; Mirza GK; Munson J; Nelson SF; Noakes C; Noor A; Nygren G; Oliveira G; Papanikolaou K; Parr JR; Parrini B; Paton T; Pickles A; Piven J; Posey DJ; Poustka A; Poustka F; Prasad A; Ragoussis J; Renshaw K; Rickaby J; Roberts W; Roeder K; Roge B; Rutter ML; Bierut LJ; Rice JP; Salt J; Sansom K; Sato D; Segurado R; Senman L; Shah N; Sheffield VC; Soorya L; Sousa I; Stoppioni V; Strawbridge C; Tancredi R; Tansey K; Thiruvahindrapduram B; Thompson AP; Thomson S; Tryfon A; Tsiantis J; Van Engeland H; Vincent JB; Volkmar F; Wallace S; Wang K; Wang Z; Wassink TH; Wing K; Wittemeyer K; Wood S; Yaspan BL; Zurawiecki D; Zwaigenbaum L; Betancur C; Buxbaum JD; Cantor RM; Cook EH; Coon H; Cuccaro ML; Gallagher L; Geschwind DH; Gill M; Haines JL; Miller J; Monaco AP; Nurnberger JI Jr; Paterson AD; Pericak-Vance MA; Schellenberg GD; Scherer SW; Sutcliffe JS; Szatmari P; Vicente AM; Vieland VJ; Wijsman EM; Devlin B; Ennis S; Hallmayer J.
Linkage and candidate gene studies of autism spectrum disorders in European populations.
2010 Holt R; Barnby G; Maestrini E; Bacchelli E; Brocklebank D; Sousa I; Mulder EJ; Kantojärvi K; Järvelä I; Klauck SM; Poustka F; Bailey AJ; Monaco AP; EU Autism MOLGEN Consortium
ZZOLCHESTRA (cd)
2010 P. Bottacin; V. Canè; E. Cimino; A. Danielli; M. Gollini; G. Gonano; E. Maestrini; A. Polese; A. Rigatti; A. Sodano; G. Tornielli
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| 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 | - |
| 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 | - |
| DNA variants in the human RAB3A gene are not associated with autism. | D'Adamo P.; Bacchelli E.; Blasi F.; Lipp H.P.; Toniolo D.; Maestrini E. | 2004-01-01 | GENES BRAIN AND BEHAVIOR | - | 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 | - |
| 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 | - |
| Absence of coding mutations in the X-linked genes Neuroligin 3 and Neuroligin 4 in individuals with autism from the IMGSAC collection | Blasi F.; Bacchelli E.; Pesaresi G.; Carone S.; Bailey A.J.; Maestrini E. | 2006-01-01 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART B, NEUROPSYCHIATRIC GENETICS | - | 1.01 Articolo in rivista | - |
| Autism spectrum disorders: molecular genetic advances | Bacchelli E.; Maestrini E. | 2006-01-01 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART C, SEMINARS IN MEDICAL GENETICS | - | 1.01 Articolo in rivista | - |
| SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample. | Blasi F.; Bacchelli E.; Carone S.; Toma C.; Monaco AP.; Bailey AJ.; Maestrini E. | 2006-01-01 | EUROPEAN JOURNAL OF HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
| Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations. | Toma C; Rossi M; Sousa I; Blasi F; Bacchelli E; Alen R; Vanhala R; Monaco AP; Järvelä I; Maestrini E | 2007-01-01 | MOLECULAR PSYCHIATRY | - | 1.01 Articolo in rivista | - |
| Mapping autism risk loci using genetic linkage and chromosomal rearrangements | Autism Genome Project Consortium; Szatmari P; Paterson AD; Zwaigenbaum L; Roberts W; Brian J; Liu... XQ; Vincent JB; Skaug JL; Thompson AP; Senman L; Feuk L; Qian C; Bryson SE; Jones MB; Marshall CR; Scherer SW; Vieland VJ; Bartlett C; Mangin LV; Goedken R; Segre A; Pericak-Vance MA; Cuccaro ML; Gilbert JR; Wright HH; Abramson RK; Betancur C; Bourgeron T; Gillberg C; Leboyer M; Buxbaum JD; Davis KL; Hollander E; Silverman JM; Hallmayer J; Lotspeich L; Sutcliffe JS; Haines JL; Folstein SE; Piven J; Wassink TH; Sheffield V; Geschwind DH; Bucan M; Brown WT; Cantor RM; Constantino JN; Gilliam TC; Herbert M; Lajonchere C; Ledbetter DH; Lese-Martin C; Miller J; Nelson S; Samango-Sprouse CA; Spence S; State M; Tanzi RE; Coon H; Dawson G; Devlin B; Estes A; Flodman P; Klei L; McMahon WM; Minshew N; Munson J; Korvatska E; Rodier PM; Schellenberg GD; Smith M; Spence MA; Stodgell C; Tepper PG; Wijsman EM; Yu CE; Roge B; Mantoulan C; Wittemeyer K; Poustka A; Felder B; Klauck SM; Schuster C; Poustka F; Bolte S; Feineis-Matthews S; Herbrecht E; Schmotzer G; Tsiantis J; Papanikolaou K; Maestrini E; Bacchelli E; Blasi F; Carone S; Toma C; Van Engeland H; de Jonge M; Kemner C; Koop F; Langemeijer M; Hijimans C; Staal WG; Baird G; Bolton PF; Rutter ML; Weisblatt E; Green J; Aldred C; Wilkinson JA; Pickles A; Le Couteur A; Berney T; McConachie H; Bailey AJ; Francis K; Honeyman G; Hutchinson A; Parr JR; Wallace S; Monaco AP; Barnby G; Kobayashi K; Lamb JA; Sousa I; Sykes N; Cook EH; Guter SJ; Leventhal BL; Salt J; Lord C; Corsello C; Hus V; Weeks DE; Volkmar F; Tauber M; Fombonne E; Shih A. | 2007-01-01 | NATURE GENETICS | - | 1.01 Articolo in rivista | - |
| Analysis of X chromosome inactivation in autism spectrum disorders. | Gong X; Bacchelli E; Blasi F; Toma C; Betancur C; Chaste P; Delorme R; Durand CM; Fauchereau F; B...otros HG; Leboyer M; Mouren-Simeoni MC; Nygren G; Anckarsäter H; Rastam M; Gillberg IC; Gillberg C; Moreno-De-Luca D; Carone S; Nummela I; Rossi M; Battaglia A; International Molecular Genetic Study of Autism Consortium (IMGSAC); Jarvela I; Maestrini E; Bourgeron T. | 2008-01-01 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART B, NEUROPSYCHIATRIC GENETICS | - | 1.01 Articolo in rivista | - |
| Genome-wide linkage analyses of quantitative and categorical autism subphenotypes. | Liu XQ; Paterson AD; Szatmari P; Autism Genome Project Consortium [..;Maestrini E; ..] | 2008-01-01 | BIOLOGICAL PSYCHIATRY | - | 1.01 Articolo in rivista | - |
| A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12 | Asher JE; Lamb JA; Brocklebank D; Cazier JB; Maestrini E; Addis L; Sen M; Baron-Cohen S; Monaco AP. | 2009-01-01 | AMERICAN JOURNAL OF HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
| MET and autism susceptibility: family and case-control studies. | Sousa I; Clark TG; Toma C; Kobayashi K; Choma M; Holt R; Sykes NH; Lamb JA; Bailey AJ; Battaglia ...A; Maestrini E; Monaco AP. | 2009-01-01 | EUROPEAN JOURNAL OF HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
| Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment. | Newbury DF, Warburton PC, Wilson N, Bacchelli E, Carone S; International Molecular Genetic Study ...of Autism Consortium, Lamb JA, Maestrini E, Volpi EV, Mohammed S, Baird G, Monaco AP. | 2009-01-01 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART A | - | 1.01 Articolo in rivista | - |
| A genome-wide linkage and association scan reveals novel loci for autism. | WEISS LA, ARKING DE; GENE DISCOVERY PROJECT OF JOHNS HOPKINS & THE AUTISM CONSORTIUM, DALY MJ, CH...AKRAVARTI A, BRUNE CW, WEST K, O'CONNOR A, HILTON G, TOMLINSON RL, WEST AB, COOK EH JR, CHAKRAVARTI A, WEISS LA, GREEN T, CHANG SC, GABRIEL S, GATES C, HANSON EM, KIRBY A, KORN J, KURUVILLA F, MCCARROLL S, MORROW EM, NEALE B, PURCELL S, SASANFAR R, SOUGNEZ C, STEVENS C, ALTSHULER D, GUSELLA J, SANTANGELO SL, SKLAR P, TANZI R, DALY MJ, ANNEY R, BAILEY AJ, BAIRD G, BATTAGLIA A, BERNEY T, BETANCUR C, BÖLTE S, BOLTON PF, BRIAN J, BRYSON SE, BUXBAUM JD, CABRITO I, CAI G, CANTOR RM, COOK EH JR, COON H, CONROY J, CORREIA C, CORSELLO C, CRAWFORD EL, CUCCARO ML, DAWSON G, DE JONGE M, DEVLIN B, DUKETIS E, ENNIS S, ESTES A, FARRAR P, FOMBONNE E, FREITAG CM, GALLAGHER L, GESCHWIND DH, GILBERT J, GILL M, GILLBERG C, GOLDBERG J, GREEN A, GREEN J, GUTER SJ, HAINES JL, HALLMAYER JF, HUS V, KLAUCK SM, KORVATSKA O, LAMB JA, LASKAWIEC M, LEBOYER M, COUTEUR AL, LEVENTHAL BL, LIU XQ, LORD C, LOTSPEICH LJ, MAESTRINI E, MAGALHAES T, MAHONEY W, MANTOULAN C, MCCONACHIE H, MCDOUGLE CJ, MCMAHON WM, MARSHALL CR, MILLER J, MINSHEW NJ, MONACO AP, MUNSON J, NURNBERGER JI JR, OLIVEIRA G, PAGNAMENTA A, PAPANIKOLAOU K, PARR JR, PATERSON AD, PERICAK-VANCE MA, PICKLES A, PINTO D, PIVEN J, POSEY DJ, POUSTKA A, POUSTKA F, REGAN R, REICHERT J, RENSHAW K, ROBERTS W, ROGE B, RUTTER ML, SALT J, SCHELLENBERG GD, SCHERER SW, SHEFFIELD V, SUTCLIFFE JS, SZATMARI P, TANSEY K, THOMPSON AP, TSIANTIS J, VAN ENGELAND H, VICENTE AM, VIELAND VJ, VOLKMAR F, WALLACE S, WASSINK TH, WIJSMAN EM, WING K, WITTEMEYER K, YASPAN BL, ZWAIGENBAUM L, MORROW EM, YOO SY, HILL RS, MUKADDES NM, BALKHY S, GASCON G, AL-SAAD S, HASHMI A, WARE J, JOSEPH RM, LECLAIR E, PARTLOW JN, BARRY B, WALSH CA, PAULS D, MOILANEN I, EBELING H, MATTILA ML, KUUSIKKO S, JUSSILA K, IGNATIUS J, SASANFAR R, TOLOUEI A, GHADAMI M, ROSTAMI M, HOSSEINIPOUR A, VALUJERDI M, SANTANGELO SL, ANDRESEN K, WINKLOSKI B, HADDAD S, KUNKEL L, KOHANE Z, TRAN T, KONG SW, O'NEIL SB, HANSON EM, HUNDLEY R, HOLM I, PETERS H, BARONI E, CANGIALOSE A, JACKSON L, ALBERS L, BECKER R, BRIDGEMOHAN C, FRIEDMAN S, MUNIR K, NAZIR R, PALFREY J, SCHONWALD A, SIMMONS E, RAPPAPORT LA, GAUTHIER J, MOTTRON L, JOOBER R, FOMBONNE E, ROULEAU G, REHNSTROM K, VON WENDT L, PELTONEN L. | 2009-01-01 | NATURE | - | 1.01 Articolo in rivista | - |
| Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection. | Sykes NH, Toma C, Wilson N, Volpi EV, Sousa I, Pagnamenta AT, Tancredi R, Battaglia A, Maestrini ...E, Bailey AJ, Monaco AP; International Molecular Genetic Study of Autism Consortium (IMGSAC). | 2009-01-01 | EUROPEAN JOURNAL OF HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
| A genome-wide scan for common alleles affecting risk for autism. | Anney R; Klei L; Pinto D; Regan R; Conroy J; Magalhaes TR; Correia C; Abrahams BS; Sykes N; Pagna...menta AT; Almeida J; Bacchelli E; Bailey AJ; Baird G; Battaglia A; Berney T; Bolshakova N; Bölte S; Bolton PF; Bourgeron T; Brennan S; Brian J; Carson AR; Casallo G; Casey J; Chu SH; Cochrane L; Corsello C; Crawford EL; Crossett A; Dawson G; de Jonge M; Delorme R; Drmic I; Duketis E; Duque F; Estes A; Farrar P; Fernandez BA; Folstein SE; Fombonne E; Freitag CM; Gilbert J; Gillberg C; Glessner JT; Goldberg J; Green J; Guter SJ; Hakonarson H; Heron EA; Hill M; Holt R; Howe JL; Hughes G; Hus V; Igliozzi R; Kim C; Klauck SM; Kolevzon A; Korvatska O; Kustanovich V; Lajonchere CM; Lamb JA; Laskawiec M; Leboyer M; Le Couteur A; Leventhal BL; Lionel AC; Liu XQ; Lord C; Lotspeich L; Lund SC; Maestrini E; Mahoney W; Mantoulan C; Marshall CR; McConachie H; McDougle CJ; McGrath J; McMahon WM; Melhem NM; Merikangas A; Migita O; Minshew NJ; Mirza GK; Munson J; Nelson SF; Noakes C; Noor A; Nygren G; Oliveira G; Papanikolaou K; Parr JR; Parrini B; Paton T; Pickles A; Piven J; Posey DJ; Poustka A; Poustka F; Prasad A; Ragoussis J; Renshaw K; Rickaby J; Roberts W; Roeder K; Roge B; Rutter ML; Bierut LJ; Rice JP; Salt J; Sansom K; Sato D; Segurado R; Senman L; Shah N; Sheffield VC; Soorya L; Sousa I; Stoppioni V; Strawbridge C; Tancredi R; Tansey K; Thiruvahindrapduram B; Thompson AP; Thomson S; Tryfon A; Tsiantis J; Van Engeland H; Vincent JB; Volkmar F; Wallace S; Wang K; Wang Z; Wassink TH; Wing K; Wittemeyer K; Wood S; Yaspan BL; Zurawiecki D; Zwaigenbaum L; Betancur C; Buxbaum JD; Cantor RM; Cook EH; Coon H; Cuccaro ML; Gallagher L; Geschwind DH; Gill M; Haines JL; Miller J; Monaco AP; Nurnberger JI Jr; Paterson AD; Pericak-Vance MA; Schellenberg GD; Scherer SW; Sutcliffe JS; Szatmari P; Vicente AM; Vieland VJ; Wijsman EM; Devlin B; Ennis S; Hallmayer J. | 2010-01-01 | HUMAN MOLECULAR GENETICS | - | 1.01 Articolo in rivista | - |
| Linkage and candidate gene studies of autism spectrum disorders in European populations. | Holt R; Barnby G; Maestrini E; Bacchelli E; Brocklebank D; Sousa I; Mulder EJ; Kantojärvi K; Järv...elä I; Klauck SM; Poustka F; Bailey AJ; Monaco AP; EU Autism MOLGEN Consortium | 2010-01-01 | EUROPEAN JOURNAL OF HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
| ZZOLCHESTRA (cd) | P. Bottacin; V. Canè; E. Cimino; A. Danielli; M. Gollini; G. Gonano; E. Maestrini; A. Polese; A. ...Rigatti; A. Sodano; G. Tornielli | 2010-01-01 | - | - | 7.10 Prodotto artistico e spettacolare: Manufatto | - |
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