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 I., Cichon S., Pietiläinen Olli P. H., Barnes M. R., Toulopoulou T., Picchioni M., Vassos E., Bramon E., Murray R., 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., RUGGERI, Mirella, TOSATO, Sarah, BONETTO, Chiara
Published in Human Molecular Genetics (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

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 Van der Meer, D., Sønderby, I., Kaufmann, T., Walters, G., Abdellaoui, A., Ames, D., Amunts, K., Andersson, M., Armstrong, N., Bernard, M., Blackburn, N., Blangero, J., Boomsma, D., Brodaty, H., Brouwer, R., Bülow, R., Cahn, W., Calhoun, V., Caspers, S., Cavalleri, G., Ching, C., Cichon, S., Ciufolini, S., Corvin, A., Crespo-Facorro, B., Curran, J., Dalvie, S., Dazzan, P., De Geus, E., De Zubicaray, G., De Zwarte, S., Delanty, N., Den Braber, A., Desrivieres, S., Di Forti, M., Doherty, J., Donohoe, G., Ehrlich, S., Eising, E., Espeseth, T., Fisher, S., Fladby, T., Frei, O., Frouin, V., Fukunaga, M., Gareau, T., Glahn, D., Grabe, H., Groenewold, N., Gústafsson, Ó., Haavik, J., Haberg, A., Hashimoto, R., Hehir-Kwa, J., Hibar, D., Hillegers, M., Hoffmann, P., Holleran, L., Hottenga, J., Hulshoff Pol, H., Ikeda, M., Jacquemont, S., Jahanshad, N., Jockwitz, C., Johansson, S., Jönsson, E., Kikuchi, M., Knowles, E., Kwok, J., Le Hellard, S., Linden, D., Liu, J., Lundervold, A., Martin, N., Mather, K., Mathias, S., McMahon, K., McRae, A., Medland, S., Moberget, T., Moreau, C., Morris, D., Mühleisen, T., Murray, R., Nordvik, J., Nyberg, L., Olde Loohuis, L., Ophoff, R., Owen, M., Paus, T., Pausova, Z., Peralta, J., Pike, B., Prieto, C., Quinlan, E., Reinbold, C., Reis Marques, T., Rucker, J., Sachdev, P., Sando, S., Schofield, P., Schork, A., Schumann, G., Shin, J., Shumskaya, E., Silva, A., Sisodiya, S., Steen, V., Stein, D., Strike, L., Tamnes, C., Teumer, A., Thalamuthu, A., Tordesillas-Gutiérrez, D., Uhlmann, A., Úlfarsson, M., Van 't Ent, D., Van den Bree, M., Vassos, E., Wen, W., Wittfeld, K., Wright, M., Zayats, T., Dale, A., Djurovic, S., Agartz, I., Westlye, L., Stefánsson, H., Stefánsson, K., Thompson, P., Andreassen, O.
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