Bacchelli, Elena; Battaglia, Agatino; Cameli, Cinzia; Lomartire, Silvia; Tancredi, Raffaella; Thomson, Susanne; Sutcliffe, James S.; Maestrini, Elena, Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility, «AMERICAN JOURNAL OF MEDICAL GENETICS. PART A», 2015, 167, pp. 715 - 723 [Scientific article]
Torrico, Bàrbara; Fernàndez-Castillo, Noèlia; Hervás, Amaia; Milà, Montserrat; Salgado, Marta; Rueda, Isabel; Buitelaar, Jan K.; Rommelse, Nanda; Oerlemans, Anoek M.; Bralten, Janita; Freitag, Christine M.; Reif, Andreas; Battaglia, Agatino; Mazzone, Luigi; Maestrini, Elena; Cormand, Bru; Toma, Claudio, Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability, «EUROPEAN JOURNAL OF HUMAN GENETICS», 2015, 23, pp. 1694 - 1701 [Scientific article]
Maier R.; Moser G.; Chen G.-B.; Ripke S.; Coryell W.; Potash J.B.; Scheftner W.A.; Shi J.; Weissman M.M.; Hultman C.M.; Landen M.; Levinson D.F.; Kendler K.S.; Smoller J.W.; Wray N.R.; Lee S.H.; Absher D.; Agartz I.; Akil H.; Amin F.; Andreassen O.A.; Anjorin A.; Anney R.; Arking D.E.; Asherson P.; Azevedo M.H.; Backlund L.; Badner J.A.; Bailey A.J.; Banaschewski T.; Barchas J.D.; Barnes M.R.; Barrett T.B.; Bass N.; Battaglia A.; Bauer M.; Bayes M.; Bellivier F.; Bergen S.E.; Berrettini W.; Betancur C.; Bettecken T.; Biederman J.; Binder E.B.; Black D.W.; Blackwood D.H.R.; Bloss C.S.; Boehnke M.; Boomsma D.I.; Breen G.; Breuer R.; Bruggeman R.; Buccola N.G.; Buitelaar J.K.; Bunney W.E.; Buxbaum J.D.; Byerley W.F.; Caesar S.; Cahn W.; Cantor R.M.; Casas M.; Chakravarti A.; Chambert K.; Choudhury K.; Cichon S.; Robert Cloninger C.; Collier D.A.; Cook E.H.; Coon H.; Cormand B.; Cormican P.; Corvin A.; Coryell W.H.; Craddock N.; Craig D.W.; Craig I.W.; Crosbie J.; Cuccaro M.L.; Curtis D.; Czamara D.; Daly M.J.; Datta S.; Dawson G.; Day R.; De Geus E.J.; Degenhardt F.; Devlin B.; Djurovic S.; Donohoe G.J.; Doyle A.E.; Duan J.; Dudbridge F.; Duketis E.; Ebstein R.P.; Edenberg H.J.; Elia J.; Ennis S.; Etain B.; Fanous A.; Faraone S.V.; Farmer A.E.; Nicol Ferrier I.; Flickinger M.; Fombonne E.; Foroud T.; Frank J.; Franke B.; Fraser C.; Freedman R.; Freimer N.B.; Freitag C.M.; Friedl M.; Frisen L.; Gallagher L.; Gejman P.V.; Georgieva L.; Gershon E.S.; Geschwind D.H.; Giegling I.; Gill M.; Gordon S.D.; Gordon-Smith K.; Green E.K.; Greenwood T.A.; Grice D.E.; Gross M.; Grozeva D.; Guan W.; Gurling H.; De Haan L.; Haines J.L.; Hakonarson H.; Hallmayer J.; Hamilton S.P.; Hamshere M.L.; Hansen T.F.; Hartmann A.M.; Hautzinger M.; Heath A.C.; Henders A.K.; Herms S.; Hickie I.B.; Hipolito M.; Hoefels S.; Holmans P.A.; Holsboer F.; Hoogendijk W.J.; Hottenga J.-J.; Hultman C.M.; Hus V.; Ingason A.; Ising M.; Jamain S.; Jones I.; Jones L.; Kahler A.K.; Kahn R.S.; Kandaswamy R.; Keller M.C.; Kelsoe J.R.; Kendler K.S.; Kennedy J.L.; Kenny E.; Kent L.; Kim Y.; Kirov G.K.; Klauck S.M.; Klei L.; Knowles J.A.; Kohli M.A.; Koller D.L.; Konte B.; Korszun A.; Krabbendam L.; Krasucki R.; Kuntsi J.; Kwan P.; Landen M.; Langstrom N.; Lathrop M.; Lawrence J.; Lawson W.B.; Leboyer M.; Ledbetter D.H.; Lee P.H.; Lencz T.; Lesch K.-P.; Levinson D.F.; Lewis C.M.; Li J.; Lichtenstein P.; Lieberman J.A.; Lin D.-Y.; Linszen D.H.; Liu C.; Lohoff F.W.; Loo S.K.; Lord C.; Lowe J.K.; Lucae S.; MacIntyre D.J.; Madden P.A.F.; Maestrini E.; Magnusson P.K.E.; Mahon P.B.; Maier W.; Malhotra A.K.; Mane S.M.; Martin C.L.; Martin N.G.; Mattheisen M.; Matthews K.; Mattingsdal M.; McCarroll S.A.; McGhee K.A.; McGough J.J.; McGrath P.J.; McGuffin P.; McInnis M.G.; McIntosh A.; McKinney R.; McLean A.W.; McMahon F.J.; McMahon W.M.; McQuillin A.; Medeiros H.; Medland S.E.; Meier S.; Melle I.; Meng F.; Meyer J.; Middeldorp C.M.; Middleton L.; Milanova V.; Miranda A.; Monaco A.P.; Montgomery G.W.; Moran J.L.; Moreno-De-Luca D.; Morken G.; Morris D.W.; Morrow E.M.; Moskvina V.; Mowry B.J.; Muglia P.; Muhleisen T.W.; Muller-Myhsok B.; Murtha M.; Myers R.M.; Myin-Germeys I.; Neale B.M.; Nelson S.F.; Nievergelt C.M.; Nikolov I.; Nimgaonkar V.; Nolen W.A.; Nothen M.M.; Nurnberger J.I.; Nwulia E.A.; Nyholt D.R.; O'Donovan M.C.; O'Dushlaine C.; Oades R.D.; Olincy A.; Oliveira G.; Olsen L.; Ophoff R.A.; Osby U.; Owen M.J.; Palotie A.; Parr J.R.; Paterson A.D.; Pato C.N.; Pato M.T.; Penninx B.W.; Pergadia M.L.; Pericak-Vance M.A.; Perlis R.H.; Pickard B.S.; Pimm J.; Piven J.; Posthuma D.; Potash J.B.; Poustka F.; Propping P.; Purcell S.M.; Puri V.; Quested D.J.; Quinn E.M.; Ramos-Quiroga J.A.; Rasmussen H.B.; Raychaudhuri S.; Rehnstrom K.; Reif A.; Ribases M.; Rice J.P.; Rietschel M.; Ripke S.; Roeder K.; Roeyers H.; Rossin L.; Rothenberger A.; Rouleau G.; Ruderfer D.; Rujescu D.; Sanders A.R.; Sanders S.J.; Santangelo S.L.; Schachar R.; Schalling M.; Schatzberg A.F.; Scheftner W.A.; Schellenb, Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder, «AMERICAN JOURNAL OF HUMAN GENETICS», 2015, 96, pp. 283 - 294 [Scientific article]Open Access
O'Dushlaine, C; Rossin, L; Lee, Ph; Duncan, L; Parikshak, Nn; Newhouse, S; Ripke, S; Neale, Bm; Purcell, Sm; Posthuma, D; Nurnberger, Ji; Lee, Sh; Faraone, Sv; Perlis, Rh; Mowry, Bj; Thapar, A; Goddard, Me; Witte, Js; Absher, D; Agartz, I; Akil, H; Amin, F; Andreassen, Oa; Anjorin, A; Anney, R; Anttila, V; Arking, De; Asherson, P; Azevedo, Mh; Backlund, L; Badner, Ja; Bailey, Aj; Banaschewski, T; Barchas, Jd; Barnes, Mr; Barrett, Tb; Bass, N; Battaglia, A; Bauer, M; Bayés, M; Bellivier, F; Bergen, Se; Berrettini, W; Betancur, C; Bettecken, T; Biederman, J; Binder, Eb; Black, Dw; Blackwood, Dh; Bloss, Cs; Boehnke, M; Boomsma, Di; Breuer, R; Bruggeman, R; Cormican, P; Buccola, Ng; Buitelaar, Jk; Bunney, We; Buxbaum, Jd; Byerley, Wf; Byrne, Em; Caesar, S; Cahn, W; Cantor, Rm; Casas, M; Chakravarti, A; Chambert, K; Choudhury, K; Cichon, S; Mattheisen, M; Cloninger, Cr; Collier, Da; Cook, Eh; Coon, H; Cormand, B; Corvin, A; Coryell, Wh; Craig, Dw; Craig, Iw; Crosbie, J; Cuccaro, Ml; Curtis, D; Czamara, D; Datta, S; Dawson, G; Day, R; De Geus, Ej; Degenhardt, F; Djurovic, S; Donohoe, Gj; Doyle, Ae; Duan, J; Dudbridge, F; Duketis, E; Ebstein, Rp; Edenberg, Hj; Elia, J; Ennis, S; Etain, B; Fanous, A; Farmer, Ae; Ferrier, In; Flickinger, M; Fombonne, E; Foroud, T; Frank, J; Franke, B; Fraser, C; Freedman, R; Freimer, Nb; Freitag, Cm; Friedl, M; Frisén, L; Gallagher, L; Gejman, Pv; Georgieva, L; Gershon, Es; Giegling, I; Gill, M; Gordon, Sd; Gordon-Smith, K; Green, Ek; Greenwood, Ta; Grice, De; Gross, M; Grozeva, D; Guan, W; Gurling, H; De Haan, L; Haines, Jl; Hakonarson, H; Hallmayer, J; Hamilton, Sp; Hamshere, Ml; Hansen, Tf; Hartmann, Am; Hautzinger, M; Heath, Ac; Henders, Ak; Herms, S; Hickie, Ib; Hipolito, M; Hoefels, S; Holsboer, F; Hoogendijk, Wj; Hottenga, Jj; Hultman, Cm; Hus, V; Ingason, A; Ising, M; Jamain, S; Jones, Eg; Jones, I; Jones, L; Tzeng, Jy; Kähler, Ak; Kahn, Rs; Kandaswamy, R; Keller, Mc; Kennedy, Jl; Kenny, E; Kent, L; Kim, Y; Kirov, Gk; Klauck, Sm; Klei, L; Knowles, Ja; Kohli, Ma; Koller, Dl; Konte, B; Korszun, A; Krabbendam, L; Krasucki, R; Kuntsi, J; Kwan, P; Landén, M; Längström, N; Lathrop, M; Lawrence, J; Lawson, Wb; Leboyer, M; Ledbetter, Dh; Lencz, T; Lesch, Kp; Levinson, Df; Lewis, Cm; Li, J; Lichtenstein, P; Lieberman, Ja; Lin, Dy; Linszen, Dh; Liu, C; Lohoff, Fw; Loo, Sk; Lord, C; Lowe, Jk; Lucae, S; Macintyre, Dj; Madden, Pa; Maestrini, E; Magnusson, Pk; Mahon, Pb; Maier, W; Malhotra, Ak; Mane, Sm; Martin, Cl; Martin, Ng; Matthews, K; Mattingsdal, M; Mccarroll, Sa; Mcghee, Ka; Mcgough, Jj; Mcgrath, Pj; Mcguffin, P; Mcinnis, Mg; Mcintosh, A; Mckinney, R; Mclean, Aw; Mcmahon, Fj; Mcmahon, Wm; Mcquillin, A; Medeiros, H; Medland, Se; Meier, S; Melle, I; Meyer, J; Middeldorp, Cm; Middleton, L; Milanova, V; Miranda, A; Monaco, A; Montgomery, Gw; Moran, Jl; Moreno-De-Luca, D; Morken, G; Morris, Dw; Morrow, Em; Moskvina, V; Muglia, P; Mühleisen, Tw; Muir, Wj; Müller-Myhsok, B; Murtha, M; Myers, Rm; Myin-Germeys, I; Neale, Mc; Nelson, Sf; Nievergelt, Cm; Nikolov, I; Nimgaonkar, V; Nolen, Wa; Nöthen, Mm; Nwulia, Ea; Nyholt, Dr; Oades, Rd; Olincy, A; Oliveira, G; Olsen, L; Ophoff, Ra; Osby, U; Owen, Mj; Palotie, A; Parr, Jr; Paterson, Ad; Pato, Cn; Pato, Mt; Penninx, Bw; Pergadia, Ml; Pericak-Vance, Ma; Pickard, Bs; Pimm, J; Piven, J; Potash, Jb; Poustka, F; Propping, P; Puri, V; Quested, Dj; Quinn, Em; Ramos-Quiroga, Ja; Rasmussen, Hb; Raychaudhuri, S; Rehnström, K; Reif, A; Ribasés, M; Rice, Jp; Rietschel, M; Roeder, K; Roeyers, H; Rothenberger, A; Rouleau, G; Ruderfer, D; Rujescu, D; Sanders, Ar; Sanders, Sj; Santangelo, Sl; Sergeant, Ja; Schachar, R; Schalling, M; Schatzberg, Af; Scheftner, Wa; Schellenberg, Gd; Scherer, Sw; Schork, Nj; Schulze, Tg; Schumacher, J; Schwarz, M; Scolnick, E; Scott, Lj; Shi, J; Shilling, Pd; Shyn, Si; Silverman, Jm; Slager, Sl; Smalley, Sl; Smit, Jh; Smith, En; Sonuga-Barke, Ej; St Clair, D; State, M; Steffens, M; Steinhausen, Hc;, Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways, «NATURE NEUROSCIENCE», 2015, 18, pp. 199 - 209 [Scientific article]
Bacchelli E;Ceroni F;Pinto D;Lomartire S;Giannandrea M;D'Adamo P;Bonora E;Parchi P;Tancredi R;Battaglia A;Maestrini E, A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder., «JOURNAL OF NEURODEVELOPMENTAL DISORDERS», 2014, 6, Article number: 17 , pp. 1 - 11 [Scientific article]Open Access
Ceroni F;Sagar A;Simpson NH;Gawthrope AJ;Newbury DF;Pinto D;Francis SM;Tessman DC;Cook EH;Monaco AP;Maestrini E;Pagnamenta AT;Jacob S, A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthma., «AUTISM RESEARCH», 2014, 7, pp. 254 - 263 [Scientific article]
Pinto D; Delaby E; Merico D; Barbosa M; Merikangas A; Klei L; Thiruvahindrapuram B; Xu X; Ziman R; Wang Z; Vorstman JA; Thompson A; Regan R; Pilorge M; Pellecchia G; Pagnamenta AT; Oliveira B; Marshall CR; Magalhaes TR; Lowe JK; Howe JL; Griswold AJ; Gilbert J; Duketis E; Dombroski BA; De Jonge MV; Cuccaro M; Crawford EL; Correia CT; Conroy J; Conceição IC; Chiocchetti AG; Casey JP; Cai G; Cabrol C; Bolshakova N; Bacchelli E; Anney R; Gallinger S; Cotterchio M; Casey G; Zwaigenbaum L; Wittemeyer K; Wing K; Wallace S; van Engeland H; Tryfon A; Thomson S; Soorya L; Rogé B; Roberts W; Poustka F; Mouga S; Minshew N; McInnes LA; McGrew SG; Lord C; Leboyer M; Le Couteur AS; Kolevzon A; Jiménez González P; Jacob S; Holt R; Guter S; Green J; Green A; Gillberg C; Fernandez BA; Duque F; Delorme R; Dawson G; Chaste P; Café C; Brennan S; Bourgeron T; Bolton PF; Bölte S; Bernier R; Baird G; Bailey AJ; Anagnostou E; Almeida J; Wijsman EM; Vieland VJ; Vicente AM; Schellenberg GD; Pericak-Vance M; Paterson AD; Parr JR; Oliveira G; Nurnberger JI; Monaco AP; Maestrini E; Klauck SM; Hakonarson H; Haines JL; Geschwind DH; Freitag CM; Folstein SE; Ennis S; Coon H; Battaglia A; Szatmari P; Sutcliffe JS; Hallmayer J; Gill M; Cook EH; Buxbaum JD; Devlin B; Gallagher L; Betancur C; Scherer SW., Convergence of genes and cellular pathways dysregulated in autism spectrum disorders., «AMERICAN JOURNAL OF HUMAN GENETICS», 2014, 94, pp. 677 - 694 [Scientific article]
Ceroni F; Simpson NH; Francks C; Baird G; Conti-Ramsden G; Clark A; Bolton PF; Hennessy ER; Donnelly P; Bentley DR; Martin H; Parr J; Pagnamenta AT; Maestrini E; Bacchelli E; Fisher SE; Newbury DF, Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment., «EUROPEAN JOURNAL OF HUMAN GENETICS», 2014, 22, pp. 1165 - 1171 [Scientific article]
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, Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients., «EMBO MOLECULAR MEDICINE», 2014, 6, pp. 795 - 809 [Scientific article]Open Access
Leblond CS;Nava C;Polge A;Gauthier J;Huguet G;Lumbroso S;Giuliano F;Stordeur C;Depienne C;Mouzat K;Pinto D;Howe J;Lemière N;Durand CM;Guibert J;Ey E;Toro R;Peyre H;Mathieu A;Amsellem F;Rastam M;Gillberg IC;Rappold GA;Holt R;Monaco AP;Maestrini E;Galan P;Heron D;Jacquette A;Afenjar A;Rastetter A;Brice A;Devillard F;Assouline B;Laffargue F;Lespinasse J;Chiesa J;Rivier F;Bonneau D;Regnault B;Zelenika D;Delepine M;Lathrop M;Sanlaville D;Schluth-Bolard C;Edery P;Perrin L;Tabet AC;Schmeisser MJ;Boeckers TM;Coleman M;Sato D;Szatmari P;Scherer SW;Rouleau GA;Betancur C;Leboyer M;Gillberg C;Delorme R;Bourgeron T, Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments., «PLOS GENETICS», 2014, 10, Article number: e1004580 , pp. 1 - 15 [Scientific article]
Lee SH;Ripke S;Neale BM;Faraone SV;Purcell SM;Perlis RH;Mowry BJ;Thapar A;Goddard ME;Witte JS;Absher D;Agartz I;Akil H;Amin F;Andreassen OA;Anjorin A;Anney R;Anttila V;Arking DE;Asherson P;Azevedo MH;Backlund L;Badner JA;Bailey AJ;Banaschewski T;Barchas JD;Barnes MR;Barrett TB;Bass N;Battaglia A;Bauer M;Bayés M;Bellivier F;Bergen SE;Berrettini W;Betancur C;Bettecken T;Biederman J;Binder EB;Black DW;Blackwood DH;Bloss CS;Boehnke M;Boomsma DI;Breen G;Breuer R;Bruggeman R;Cormican P;Buccola NG;Buitelaar JK;Bunney WE;Buxbaum JD;Byerley WF;Byrne EM;Caesar S;Cahn W;Cantor RM;Casas M;Chakravarti A;Chambert K;Choudhury K;Cichon S;Cloninger CR;Collier DA;Cook EH;Coon H;Cormand B;Corvin A;Coryell WH;Craig DW;Craig IW;Crosbie J;Cuccaro ML;Curtis D;Czamara D;Datta S;Dawson G;Day R;De Geus EJ;Degenhardt F;Djurovic S;Donohoe GJ;Doyle AE;Duan J;Dudbridge F;Duketis E;Ebstein RP;Edenberg HJ;Elia J;Ennis S;Etain B;Fanous A;Farmer AE;Ferrier IN;Flickinger M;Fombonne E;Foroud T;Frank J;Franke B;Fraser C;Freedman R;Freimer NB;Freitag CM;Friedl M;Frisén L;Gallagher L;Gejman PV;Georgieva L;Gershon ES;Geschwind DH;Giegling I;Gill M;Gordon SD;Gordon-Smith K;Green EK;Greenwood TA;Grice DE;Gross M;Grozeva D;Guan W;Gurling H;De Haan L;Haines JL;Hakonarson H;Hallmayer J;Hamilton SP;Hamshere ML;Hansen TF;Hartmann AM;Hautzinger M;Heath AC;Henders AK;Herms S;Hickie IB;Hipolito M;Hoefels S;Holmans PA;Holsboer F;Hoogendijk WJ;Hottenga JJ;Hultman CM;Hus V;Ingason A;Ising M;Jamain S;Jones EG;Jones I;Jones L;Tzeng JY;Kähler AK;Kahn RS;Kandaswamy R;Keller MC;Kennedy JL;Kenny E;Kent L;Kim Y;Kirov GK;Klauck SM;Klei L;Knowles JA;Kohli MA;Koller DL;Konte B;Korszun A;Krabbendam L;Krasucki R;Kuntsi J;Kwan P;Landén M;Långström N;Lathrop M;Lawrence J;Lawson WB;Leboyer M;Ledbetter DH;Lee PH;Lencz T;Lesch KP;Levinson DF;Lewis CM;Li J;Lichtenstein P;Lieberman JA;Lin DY;Linszen DH;Liu C;Lohoff FW;Loo SK;Lord C;Lowe JK;Lucae S;MacIntyre DJ;Madden PA;Maestrini E;Magnusson PK;Mahon PB;Maier W;Malhotra AK;Mane SM;Martin CL;Martin NG;Mattheisen M;Matthews K;Mattingsdal M;McCarroll SA;McGhee KA;McGough JJ;McGrath PJ;McGuffin P;McInnis MG;McIntosh A;McKinney R;McLean AW;McMahon FJ;McMahon WM;McQuillin A;Medeiros H;Medland SE;Meier S;Melle I;Meng F;Meyer J;Middeldorp CM;Middleton L;Milanova V;Miranda A;Monaco AP;Montgomery GW;Moran JL;Moreno-De-Luca D;Morken G;Morris DW;Morrow EM;Moskvina V;Muglia P;Mühleisen TW;Muir WJ;Müller-Myhsok B;Murtha M;Myers RM;Myin-Germeys I;Neale MC;Nelson SF;Nievergelt CM;Nikolov I;Nimgaonkar V;Nolen WA;Nöthen MM;Nurnberger JI;Nwulia EA;Nyholt DR;O'Dushlaine C;Oades RD;Olincy A;Oliveira G;Olsen L;Ophoff RA;Osby U;Owen MJ;Palotie A;Parr JR;Paterson AD;Pato CN;Pato MT;Penninx BW;Pergadia ML;Pericak-Vance MA;Pickard BS;Pimm J;Piven J;Posthuma D;Potash JB;Poustka F;Propping P;Puri V;Quested DJ;Quinn EM;Ramos-Quiroga JA;Rasmussen HB;Raychaudhuri S;Rehnström K;Reif A;Ribasés M;Rice JP;Rietschel M;Roeder K;Roeyers H;Rossin L;Rothenberger A;Rouleau G;Ruderfer D;Rujescu D;Sanders AR;Sanders SJ;Santangelo SL;Sergeant JA;Schachar R;Schalling M;Schatzberg AF;Scheftner WA;Schellenberg GD;Scherer SW;Schork NJ;Schulze TG;Schumacher J;Schwarz M;Scolnick E;Scott LJ;Shi J;Shilling PD;Shyn SI;Silverman JM;Slager SL;Smalley SL;Smit JH;Smith EN;Sonuga-Barke EJ;St Clair D;State M;Steffens M;Steinhausen HC;Strauss JS;Strohmaier J;Stroup TS;Sutcliffe JS;Szatmari P;Szelinger S;Thirumalai S;Thompson RC;Todorov AA;Tozzi F;Treutlein J;Uhr M;van den Oord EJ;Van Grootheest G;Van Os J;Vicente AM;Vieland VJ;Vincent JB;Visscher PM;Walsh CA;Wassink TH;Watson SJ;Weissman MM;Werge T;Wienker TF;Wijsman EM;Willemsen G;Williams N;Willsey AJ;Witt SH;Xu W;Young AH;Yu TW;Zammit S;Zandi PP;Zhang P;Zitman FG;Zöllner S;Devlin B;Kelsoe JR;Sklar P;Daly MJ;O'Donovan MC;Craddock N;Sullivan PF;Smoller JW;Kendler KS;Wray NR;Cross-Disorder Group of the Psychiatric Genomics Consortium;International Inflammatory Bowel Disease Genetics Consortium (IIBDGC), Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs., «NATURE GENETICS», 2013, 45, pp. 984 - 994 [Scientific article]
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., A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder., «HUMAN GENETICS», 2012, 131, pp. 565 - 579 [Scientific article]
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., Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders., «PLOS GENETICS», 2012, 8, Article number: e1002521 , pp. 1 - 17 [Scientific article]
Anney R; Klei L; Pinto D; Almeida J; Bacchelli E; Baird G; Bolshakova N; Bölte S; Bolton PF; Bourgeron T; Brennan S; Brian J; Casey J; Conroy J; Correia C; Corsello C; Crawford EL; de Jonge M; Delorme R; Duketis E; Duque F; Estes A; Farrar P; Fernandez BA; Folstein SE; Fombonne E; Gilbert J; Gillberg C; Glessner JT; Green A; Green J; Guter SJ; Heron EA; Holt R; Howe JL; Hughes G; Hus V; Igliozzi R; Jacob S; Kenny GP; Kim C; Kolevzon A; Kustanovich V; Lajonchere CM; Lamb JA; Law-Smith M; Leboyer M; Le Couteur A; Leventhal BL; Liu XQ; Lombard F; Lord C; Lotspeich L; Lund SC; Magalhaes TR; Mantoulan C; McDougle CJ; Melhem NM; Merikangas A; Minshew NJ; Mirza GK; Munson J; Noakes C; Nygren G; Papanikolaou K; Pagnamenta AT; Parrini B; Paton T; Pickles A; Posey DJ; Poustka F; Ragoussis J; Regan R; Roberts W; Roeder K; Roge B; Rutter ML; Schlitt S; Shah N; Sheffield VC; Soorya L; Sousa I; Stoppioni V; Sykes N; Tancredi R; Thompson AP; Thomson S; Tryfon A; Tsiantis J; Van Engeland H; Vincent JB; Volkmar F; Vorstman J; Wallace S; Wing K; Wittemeyer K; Wood S; Zurawiecki D; Zwaigenbaum L; Bailey AJ; Battaglia A; Cantor RM; Coon H; Cuccaro ML; Dawson G; Ennis S; Freitag CM; Geschwind DH; Haines JL; Klauck SM; McMahon WM; Maestrini E; Miller J; Monaco AP; Nelson SF; Nurnberger JI Jr; Oliveira G; Parr JR; Pericak-Vance MA; Piven J; Schellenberg GD; Scherer SW; Vicente AM; Wassink TH; Wijsman EM; Betancur C; Buxbaum JD; Cook EH; Gallagher L; Gill M; Hallmayer J; Paterson AD; Sutcliffe JS; Szatmari P; Vieland VJ; Hakonarson H; Devlin B, Individual common variants exert weak effects on the risk for autism spectrum disorders., «HUMAN MOLECULAR GENETICS», 2012, 21, pp. 4781 - 4792 [Scientific article]
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., A genome-wide scan for common alleles affecting risk for autism., «HUMAN MOLECULAR GENETICS», 2010, 19(20), pp. 4072 - 4082 [Scientific article]
