Search Results

No Association Between a Common Single Nucleotide Polymorphism, rs4141463, in the MACROD2 Gene and Autism Spectrum Disorder

by Curran, S, Bolton, P, Rozsnyai, K, Chiocchetti, A, Klauck, SM, Duketis, E, Poustka, F, Schlitt, S, Freitag, CM, Lee, I, Muglia, P, Poot, M, Staal, W, de Jonge, MV, Ophoff, RA, Lewis, C, Skuse, D, Mandy, W, Vassos, E, Fossdal, R, Magnusson, P, Hreidarsson, S, Saemundsen, E, Stefansson, H, Stefansson, K, Collier, D, ITAN
Published 2011

No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder

by CURRAN S, BOLTON P, ROZSNYAI K, CHIOCCHETTI A, KLAUCK SM, DUKETIS E, POUSTKA F, SCHLITT S, FREITAG CM, LEE I, MUGLIA P, ITAN incl, ZUDDAS, ALESSANDRO, POOT M, STAAL W, DE JONGE MV, OPHOFF RA, LEWIS C, SKUSE D, MANDY W, VASSOS E, FOSSDAL R, MAGNUSSON P, HREIDARSSON S, SAEMUNDSEN E, STEFANSSON H, STEFANSSON K, COLLIER D.
Published in American Journal of Medical Genetics Part B: Neuropsychiatric Genetics (2011)

No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder.

by Curran, S., Bolton, P., Rozsnyai, K., Chiocchetti, A., Klauck, S.M., Duketis, E., Poustka, F., Schlitt, S., Freitag, C.M., Lee, I. van der, Muglia, P., Poot, M., Staal, W.G., Jonge, M.V. de, Ophoff, R.A., Lewis, C., Skuse, D., Mandy, W., Vassos, E., Fossdal, R., Magnusson, P., Hreidarsson, S., Saemundsen, E., Stefansson, H., Stefansson, K., Collier, D.
Published in American Journal of Medical Genetics Part B: Neuropsychiatric Genetics (2011)

No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder

by Curran, S, Bolton, P, Rozsnyai, K, Chiocchetti, A, Klauck, SM, Duketis, E, Poustka, F, Schlitt, S, Freitag, CM, Lee, I, Muglia, P, ITAN, Poot, M, Staal, W, de Jonge, MV, Ophoff, RA, Lewis, C, Skuse, D, Mandy, W, Vassos, E, Fossdal, R, Magnusson, P, Hreidarsson, S, Saemundsen, E, Stefansson, H, Stefansson, K, Collier, D, Bravaccio, C, Da Ros, L, Bernardina, BD, Elia, M, Grittani, S, Margari, L, Masi, G, Molteni, M, Pignatti, PF, Prandini, P, Tiberti, A, Trabetti, E, Zoccante, L, Zuddas, A., CURATOLO, PAOLO
Published in American Journal of Medical Genetics Part B: Neuropsychiatric Genetics (2011)

No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder.

by Curran S, Bolton P, Rozsnyai K, Chiocchetti A, Klauck SM, Duketis E, Poustka F, Schlitt S, Freitag CM, Lee I, Muglia P, ITAN, Poot M, Staal W, de Jonge MV, Ophoff RA, Lewis C, Skuse D, Mandy W, Vassos E, Fossdal R, Magnusson P, Hreidarsson S, Saemundsen E, Stefansson H, Stefansson K, Collier D. ITAN: Bravaccio C, Curatolo P, Da Ros L, Bernardina BD, Elia M, Grittani S, Masi G, Molteni M, Pignatti PF, Prandini P, Tiberti A, Trabetti E, Zoccante L, Zuddas A., MARGARI, Lucia
Published 2011

Disruption of the neurexin 1 gene is associated with schizophrenia

by Toulopoulou, T, Wiersma, D, Murray, R, Ruggeri, M, Tosato, S, Bonetto, C, Steinberg, S, Sigurdsson, E, Sigmundsson, T, Petursson, H, Gylfason, A, Olason, PI, Hardarsson, G, Jonsdottir, GA, Cahn, W, de Haan, L, Krabbendam, L, MyinGermeys, I, Werge, T, Kiemeney, LA, Franke, B, Pietiläinen, OPH, Picchioni, M, Vassos, E, Ettinger, U, Rietschel, M, Gustafsson, O, BuizerVoskamp, JE, Fossdal, R, Giegling, I, Sabatti, C, Ophoff, RA, Möller, HJ, Hartmann, AM, Hoffmann, P, Crombie, C, Rujescu, D, Veltman, J, Fraser, G, St Clair, D, Peltonen, L, Stefansson, K, Barnes, MR, Ingason, A, Stefansson, H, Nöthen, MM, Walker, N, Lonnqvist, J, Suvisaari, J, TuulioHenriksson, A
Published in Human Molecular Genetics (2009)

Disruption of the neurexin 1 gene is associated with schizophrenia

by RUJESCU D., INGASON I., CICHON S., PIETILÄINEN OLLI P.H., BARNES M.R., TOULOPOULOU T., PICCHIONI M., VASSOS E., BRAMON E., MURRAY R., RUGGERI, Mirella, TOSATO, Sarah, BONETTO, Chiara, STEINBERG S., SIGURDSSON E., SIGMUNDSSON T., PETURSSON H., GYLFASON A., OLASON P.I., HARDARSSON G., JONSDOTTIR G.A., GUSTAFSSON O., FOSSDAL R., GIEGLING I., MÖLLER H.-J., HARTMANN A., HOFFMANN P., CROMBIE C., FRASER G., WALKER N., LONNQVIST J., SUVISAARI J., TUULIO-HENRIKSSON A., ANDREASSEN O.A., DJUROVIC S., HANSEN T., WERGE T., MELLE I., KIEMENEY L.A., FRANKE B., BUIZER-VOSKAMP J.E., OPHOFF R.A., GROUP INVESTIGATORS, RIETSCHEL M., NÖTHEN M.M., STEFANSSON K., PELTONEN L., ST CLAIR D., STEFANSSON H., COLLIER D.A.
Published 2009

Disruption of the neurexin 1 gene is associated with schizophrenia.

by Rujescu, D., Ingason, A., Cichon, S., Pietilainen, O.P.H., Barnes, M.R., Toulopoulou, T., Picchioni, M., Vassos, E., Ettinger, U., Bramon, E., Murray, R., Ruggeri, M., Tosato, S., Bonetto, C., Steinberg, S., Sigurdsson, E., Sigmundsson, T., Petursson, H., Gylfason, A, Olason, P., Hardarsson, G., Jonsdottir, G.A., Gustafsson, O., Fossdal, R., Giegling, I., Moller, H.J., Hartmann, A.M., Hoffmann, P., Crombie, C., Fraser, G., Walker, N., Lonnqvist, J., Suvisaari, J., Tuulio-Henriksson, A., Djurovic, S., Melle, I., Andreassen, O.A., Hansen, T., Werge, T., Kiemeney, L.A.L.M., Franke, B., Veltman, J.A., Buizer-Voskamp, J.E., Sabatti, C., Ophoff, R.A., Rietschel, M., Nothen, Markus, Stefansson, K., Peltonen, L., St Clair, D., Stefansson, H., Collier, D.A.
Published in Human Molecular Genetics (2009)

Disruption of the neurexin 1 gene is associated with schizophrenia

by Rujescu, D, Giegling, I, Möller, H-J, Hartmann, AM, Stefansson, K, Ingason, A, Steinberg, S, Gylfason, A, Olason, PI, Hardarsson, G, Jonsdottir, GA, Gustafsson, O, Fossdal, R, Stefansson, H, Hansen, T, Werge, T, Cichon, S, Hoffmann, P, Nöthen, MM, Pietiläinen, OPH, Peltonen, L, Barnes, MR, Toulopoulou, T, Picchioni, M, Vassos, E, Ettinger, U, Bramon, E, Murray, R, Ruggeri, M, Tosato, S, Bonetto, C, Sigurdsson, E, Sigmundsson, T, Petursson, H, Crombie, C, Fraser, G, St Clair, D, Walker, N, Lonnqvist, J, Suvisaari, J, Tuulio-Henriksson, A, Djurovic, S, Melle, I, Andreassen, OA, Kiemeney, LA, Franke, B, Veltman, J, Buizer-Voskamp, JE, Ophoff, RA, Sabatti, C, Rietschel, M, Collier, DA, Kahn, RS, Cahn, W, Linszen, D, de Haan, L, von Os, J, Krabbendam, L, Myin-Germeys, I, Wiersma, D, Bruggeman, R
Published 2009

European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene.

by Rafnar T, Vermeulen SH, Sulem P, Thorleifsson G, Aben KK, Witjes JA, Grotenhuis AJ, Verhaegh GW, Hulsbergen van de Kaa CA, Besenbacher S, Gudbjartsson D, Stacey SN, Gudmundsson J, Johannsdottir H, Bjarnason H, Zanon C, Helgadottir H, Jonasson JG, Tryggvadottir L, Jonsson E, Geirsson G, Nikulasson S, Petursdottir V, Bishop DT, Chung Sak S, Choudhury A, Elliott F, Barrett JH, Knowles MA, de Verdier PJ, Ryk C, Lindblom A, Rudnai P, Gurzau E, Koppova K, Panadero A, Sanz Velez JI, Sanchez M, Valdivia G, Garcia Prats MD, Hengstler JG, Selinski S, Gerullis H, Ovsiannikov D, Khezri A, Aminsharifi A, Malekzadeh M, van den Berg LH, Ophoff RA, Veldink JH, Zeegers MP, Kellen E, Fostinelli J, Andreoli D, Arici C, Porru S, Buntinx F, Ghaderi A, Golka K, Mayordomo JI, Kumar R, Steineck G, Kiltie AE, Kong A, Thorsteinsdottir U, Stefansson K, Kiemeney LA, VINEIS, Paolo, POLIDORO, Silvia, GUARRERA, Simonetta, SACERDOTE, Carlotta, MATULLO, Giuseppe
Published in Human Molecular Genetics (2011)

European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene.

by Rafnar, T., Vermeulen, S.H., Sulem, P., Thorleifsson, G., Aben, K.K., Witjes, J.A., Grotenhuis, A.J., Verhaegh, G.W., Hulsbergen van Kaa, C.A., Besenbacher, S., Gudbjartsson, D., Stacey, S.N., Gudmundsson, J., Johannsdottir, H., Bjarnason, H., Zanon, C., Helgadottir, H., Jonasson, J. G., Tryggvadottir, L., Jonsson, E., Geirsson, G., Nikulasson, S., Petursdottir, V., Bishop, D.T., Chung Sak, S., Choudhury, A., Elliott, F., Barrett, J.H., Knowles, M.A., de Verdier, P.J., Ryk, C., Lindblom, A., Rudnai, P., Gurzau, E., Koppova, K., Vineis, P., Polidoro, S., Guarrera, S., Sacerdote, C., Panadero, A., Sanz Velez, J.I., Sanchez, M., Valdivia, G., Garcia Prats, M.D., Hengstler, J.G., Selinski, S., Gerullis, H., Ovsiannikov, D., Khezri, A., Aminsharifi, A., Malekzadeh, M., van den Berg, L.H., Ophoff, R.A., Veldink, J H., Zeegers, M.P.A., Kellen, E., Fostinelli, J., Andreoli, D., Arici, C., Porru, S., Buntinx, F.J.V.M., Ghaderi, A., Golka, K., Mayordomo, J.I., Matullo, G., Kumar, R., Steineck, G., Kiltie, A.E., Kong, A., Thorsteinsdottir, U., Stefansson, K., Kiemeney, L.A.
Published in Human Molecular Genetics (2011)

Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition

by van der Meer, D, Sonderby, IE, Kaufmann, T, Walters, GB, Abdellaoui, A, Ames, D, Amunts, K, Andersson, M, Armstrong, NJ, Bernard, M, Blackburn, NB, Blangero, J, Boomsma, DI, Brodaty, H, Brouwer, RM, Bulow, R, Cahn, W, Calhoun, VD, Caspers, S, Cavalleri, GL, Ching, CRK, Cichon, S, Ciufolini, S, Corvin, A, Crespo-Facorro, B, Curran, JE, Dalvie, S, Dazzan, P, de Geus, EJC, de Zubicaray, GI, de Zwarte, SMC, Delanty, N, den Braber, A, Desrivieres, S, Di Forti, M, Doherty, JL, Donohoe, G, Ehrlich, S, Eising, E, Espeseth, T, Fisher, SE, Fladby, T, Frei, O, Frouin, V, Fukunaga, M, Gareau, T, Glahn, DC, Grabe, HJ, Groenewold, NA, Gustafsson, O, Haavik, J, Haberg, AK, Hashimoto, R, Hehir-Kwa, JY, Hibar, DP, Hillegers, MHJ, Hoffmann, P, Holleran, L, Hottenga, J-J, Hulshoff Pol, HE, Ikeda, M, Jacquemont, S, Jahanshad, N, Jockwitz, C, Johansson, S, Jonsson, EG, Kikuchi, M, Knowles, EEM, Kwok, JB, Le Hellard, S, Linden, DEJ, Liu, J, Lundervold, A, Lundervold, AJ, Martin, NG, Mather, KA, Mathias, SR, McMahon, KL, McRae, AF, Medland, SE, Moberget, T, Moreau, C, Morris, DW, Muhleisen, TW, Murray, RM, Nordvik, JE, Nyberg, L, Loohuis, LMO, Ophoff, RA, Owen, MJ, Paus, T, Pausova, Z, Peralta, JM, Pike, B, Prieto, C, Burke Quinlan, E, Reinbold, CS, Marques, TR, Rucker, JJH, Sachdev, PS, Sando, SB, Schofield, PR, Silva, AI, Sisodiya, SM, Steen, VM, Stein, DJ, Strike, LT, Tamnes, CK, Teumer, A, Thalamuthu, A, Tordesillas-Gutierrez, D, Uhlmann, A, Ulfarsson, MO, van 't Ent, D, van den Bree, MBM, Vassos, E, Wen, W, Wittfeld, K, Wright, MJ, Zayats, T, Dale, AM, Djurovic, S, Agartz, I, Westlye, LT, Stefansson, H, Stefansson, K, Thompson, PM, Andreassen, OA
Published in JAMA Psychiatry (2020)

Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition

by van der Meer, D, Sonderby, IE, Kaufmann, T, Walters, GB, Abdellaoui, A, Ames, D, Amunts, K, Andersson, M, Armstrong, NJ, Bernard, M, Blackburn, NB, Blangero, J, Boomsma, DI, Brodaty, H, Brouwer, RM, Bulow, R, Cahn, W, Calhoun, VD, Caspers, S, Cavalleri, GL, Ching, CRK, Cichon, S, Ciufolini, S, Corvin, A, Crespo-Facorro, B, Curran, JE, Dalvie, S, Dazzan, P, de Geus, EJC, de Zubicaray, GI, de Zwarte, SMC, Delanty, N, den Braber, A, Desrivieres, S, Di Forti, M, Doherty, JL, Donohoe, G, Ehrlich, S, Eising, E, Espeseth, T, Fisher, SE, Fladby, T, Frei, O, Frouin, V, Fukunaga, M, Gareau, T, Glahn, DC, Grabe, HJ, Groenewold, NA, Gustafsson, O, Haavik, J, Haberg, AK, Hashimoto, R, Hehir-Kwa, JY, Hibar, DP, Hillegers, MHJ, Hoffmann, P, Holleran, L, Hottenga, J-J, Hulshoff Pol, HE, Ikeda, M, Jacquemont, S, Jahanshad, N, Jockwitz, C, Johansson, S, Jonsson, EG, Kikuchi, M, Knowles, EEM, Kwok, JB, Le Hellard, S, Linden, DEJ, Liu, J, Lundervold, A, Lundervold, AJ, Martin, NG, Mather, KA, Mathias, SR, McMahon, KL, McRae, AF, Medland, SE, Moberget, T, Moreau, C, Morris, DW, Muhleisen, TW, Murray, RM, Nordvik, JE, Nyberg, L, Loohuis, LMO, Ophoff, RA, Owen, MJ, Paus, T, Pausova, Z, Peralta, JM, Pike, B, Prieto, C, Burke Quinlan, E, Reinbold, CS, Marques, TR, Rucker, JJH, Sachdev, PS, Sando, SB, Schofield, PR, Silva, AI, Sisodiya, SM, Steen, VM, Stein, DJ, Strike, LT, Tamnes, CK, Teumer, A, Thalamuthu, A, Tordesillas-Gutierrez, D, Uhlmann, A, Ulfarsson, MO, van 't Ent, D, van den Bree, MBM, Vassos, E, Wen, W, Wittfeld, K, Wright, MJ, Zayats, T, Dale, AM, Djurovic, S, Agartz, I, Westlye, LT, Stefansson, H, Stefansson, K, Thompson, PM, Andreassen, OA
Published in JAMA Psychiatry (2020)

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

by Writing Committee for the ENIGMA-CNV Working Group, van der Meer, D, Sønderby, IE, Kaufmann, T, Walters, GB, Abdellaoui, A, Ames, D, Amunts, K, Andersson, M, Armstrong, NJ, Bernard, M, Blackburn, NB, Blangero, J, Boomsma, DI, Brodaty, H, Brouwer, RM, Bülow, R, Cahn, W, Calhoun, VD, Caspers, S, Cavalleri, GL, Ching, CRK, Cichon, S, Ciufolini, S, Corvin, A, Crespo-Facorro, B, Curran, JE, Dalvie, S, Dazzan, P, de Geus, EJC, de Zubicaray, GI, de Zwarte, SMC, Delanty, N, den Braber, A, Desrivieres, S, Di Forti, M, Doherty, JL, Donohoe, G, Ehrlich, S, Eising, E, Espeseth, T, Fisher, SE, Fladby, T, Frei, O, Frouin, V, Fukunaga, M, Gareau, T, Glahn, DC, Grabe, HJ, Groenewold, NA, Gústafsson, Ó, Haavik, J, Haberg, AK, Hashimoto, R, Hehir-Kwa, JY, Hibar, DP, Hillegers, MHJ, Hoffmann, P, Holleran, L, Hottenga, J-J, Hulshoff Pol, HE, Ikeda, M, Jacquemont, S, Jahanshad, N, Jockwitz, C, Johansson, S, Jönsson, EG, Kikuchi, M, Knowles, EEM, Kwok, JB, Le Hellard, S, Linden, DEJ, Liu, J, Lundervold, A, Lundervold, AJ, Martin, NG, Mather, KA, Mathias, SR, McMahon, KL, McRae, AF, Medland, SE, Moberget, T, Moreau, C, Morris, DW, Mühleisen, TW, Murray, RM, Nordvik, JE, Nyberg, L, Olde Loohuis, LM, Ophoff, RA, Owen, MJ, Paus, T, Pausova, Z, Peralta, JM, Pike, B, Prieto, C, Quinlan, EB, Reinbold, CS, Reis Marques, T, Rucker, JJH, Sachdev, PS, Sando, SB, Schofield, PR, Schork, AJ, Schumann, G, Shin, J, Shumskaya, E, Silva, AI, Sisodiya, SM, Steen, VM, Stein, DJ, Strike, LT, Tamnes, CK, Teumer, A, Thalamuthu, A, Tordesillas-Gutiérrez, D, Uhlmann, A, Úlfarsson, MÖ, van 't Ent, D, van den Bree, MBM, Vassos, E, Wen, W, Wittfeld, K, Wright, MJ, Zayats, T, Dale, AM, Djurovic, S, Agartz, I, Westlye, LT, Stefánsson, H, Stefánsson, K, Thompson, PM, Andreassen, OA
Published 2019