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, 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

Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease

by Helgadottir, A, Thorleifsson, G, Alexandersson, KF, Tragante, V, Thorsteinsdottir, M, Eiriksson, FF, Gretarsdottir, S, Björnsson, E, Magnusson, O, Sveinbjornsson, G, Jonsdottir, I, Steinthorsdottir, V, Ferkingstad, E, Jensson, BÖ, Stefansson, H, Olafsson, I, Christensen, AH, Torp-Pedersen, C, Køber, L, Pedersen, OB, Erikstrup, C, Sørensen, E, Brunak, S, Banasik, K, Hansen, TF, Nyegaard, M, Eyjolfssson, GI, Sigurdardottir, O, Thorarinsson, BL, Matthiasson, SE, Steingrimsdottir, T, Bjornsson, ES, Danielsen, R, Asselbergs, FW, Arnar, DO, Ullum, H, Bundgaard, H, Sulem, P, Thorsteinsdottir, U, Thorgeirsson, G, Holm, H, Gudbjartsson, DF, Stefansson, K
Published 2020

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

by Thorleifsson, G, Walters, GB, Hewitt, AW, Masson, G, Helgason, A, DeWan, A, Sigurdsson, A, Jonasdottir, A, Gudjonsson, SA, Magnusson, KP, Stefansson, H, Lam, DSC, Tam, POS, Gudmundsdottir, GJ, Southgate, L, Burdon, KP, Gottfredsdottir, MS, Aldred, MA, Mitchell, P, St Clair, D, Collier, DA, Tang, N, Sveinsson, O, Macgregor, S, Martin, NG, Cree, AJ, Gibson, J, MacLeod, A, Jacob, A, Ennis, S, Young, TL, Chan, JCN, Karwatowski, WSS, Hammond, CJ, Thordarson, K, Zhang, M, Wadelius, C, Lotery, AJ, Trembath, RC, Pang, CP, Hoh, J, Craig, JE, Kong, A, Mackey, DA, Jonasson, F, Thorsteinsdottir, U, Stefansson, K
Published in Nature Genetics (2010)

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)

Identification of common genetic variants influencing spontaneous dizygotic twinning and female fertility

by Mbarek, H., Steinberg, S., Nyholt, D.R., Gordon, S.D., Miller, M.B., McRae, A.F., Hottenga, J.J., Day, F.R., Willemsen, G., Geus, E.J.C. de, Davies, G.E., Martin, H.C., Penninx, B.W.J.H., Jansen, R., McAloney, K., Vink, J.M., Kaprio, J., Plomin, R., Spector, T.D., Magnusson, P.K.E., Reversade, B., Harris, R.A., Aagaard, K., Kristjansson, R.P., Olafsson, I., Eyjolfsson, G.I., Sigurdardottir, O., Iacono, W.G., Lambalk, C.B., Montgomery, G.W., McGue, M.K., Ong, K.K., Perry, J.R.B., Martin, N.G., Stefánsson, H., Stefánsson, K., Boomsma, D.I.
Published in The American Journal of Human Genetics (2016)

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

GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study

by Rongve, A. (Arvid), Witoelar, A. (Aree), Ruiz, A. (Agustín), Athanasiu, L. (Lavinia), Abdelnour, C. (Carla), Clarimon, J. (Jordi), Heilmann-Heimbach, S. (Stefanie), Hernández, I. (Isabel), Moreno-Grau, S. (Sonia), de Rojas, I. (Itziar), Morenas-Rodríguez, E. (Estrella), Fladby, T. (Tormod), Sando, Sigrid B., Bråthen, G. (Geir), Blanc, F. (Frederic), Bousiges, O. (Olivier), Lemstra, Afina W., van Steenoven, I. (Inger), Londos, E. (Elisabet), Almdahl, Ina S., Pålhaugen, L. (Lene), Eriksen, Jon A., Djurovic, S. (Srdjan), Stordal, E. (Eystein), Saltvedt, I. (Ingvild), Ulstein, Ingun D., Bettella, F. (Francesco), Desikan, Rahul S., Idland, A. (Ane-Victoria), Toft, M. (Mathias), Pihlstrøm, L. (Lasse), Snaedal, J. (Jon), Tárraga, L. (Lluís), Boada, M. (Mercè), Lleó, A. (Alberto), Stefánsson, H. (Hreinn), Stefánsson, K. (Kári), Ramírez, A. (Alfredo), Aarsland, D. (Dag), Andreassen, Ole A.
Published in Scientific Reports (2019)

Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression

by Forstner, A., Awasthi, S., Wolf, C., Maron, E., Erhardt, A., Czamara, D., Eriksson, E., Lavebratt, C., Allgulander, C., Friedrich, N., Becker, J., Hecker, J., Rambau, S., Conrad, R., Geiser, F., McMahon, F., Moebus, S., Hess, T., Buerfent, B., Hoffmann, P., Herms, S., Heilmann-Heimbach, S., Kockum, I., Olsson, T., Alfredsson, L., Weber, H., Alpers, G., Arolt, V., Fehm, L., Fydrich, T., Gerlach, A., Hamm, A., Kircher, T., Pane-Farre, C., Pauli, P., Rief, W., Strohle, A., Plag, J., Lang, T., Wittchen, H., Mattheisen, M., Meier, S., Metspalu, A., Domschke, K., Reif, A., Hovatta, I., Lindefors, N., Andersson, E., Schalling, M., Mbarek, H., Milaneschi, Y., de Geus, E., Boomsma I, D., Penninx, B., Thorgeirsson, T., Steinberg, S., Stefansson, K., Stefansson, H., Muller-Myhsok, B., Hansen, T., Borglum, A., Werge, T., Mortensen, P., Nordentoft, M., Hougaard, D., Hultman, C., Sullivan, P., Nothen, M., Woldbye, D., Mors, O., Binder, E., Rueck, C., Ripke, S., Deckert, J., Schumacher, J.
Published in Molecular Psychiatry (2021)

Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression

by Forstner, AJ, Awasthi, S, Wolf, C, Maron, E, Erhardt, A, Czamara, D, Eriksson, E, Lavebratt, C, Allgulander, C, Friedrich, N, Becker, J, Hecker, J, Rambau, S, Conrad, R, Geiser, F, McMahon, FJ, Moebus, S, Hess, T, Buerfent, BC, Hoffmann, P, Herms, S, Heilmann-Heimbach, S, Kockum, I, Olsson, T, Alfredsson, L, Weber, H, Alpers, GW, Arolt, V, Fehm, L, Fydrich, T, Gerlach, AL, Hamm, A, Kircher, T, Pané-Farré, CA, Pauli, P, Rief, W, Ströhle, A, Plag, J, Lang, T, Wittchen, H-U, Mattheisen, M, Meier, S, Metspalu, A, Domschke, K, Reif, A, Hovatta, I, Lindefors, N, Andersson, E, Schalling, M, Mbarek, H, Milaneschi, Y, de Geus, EJC, Boomsma, DI, Penninx, BWJH, Thorgeirsson, TE, Steinberg, S, Stefansson, K, Stefansson, H, Müller-Myhsok, B, Hansen, TF, Børglum, AD, Werge, T, Mortensen, PB, Nordentoft, M, Hougaard, DM, Hultman, CM, Sullivan, PF, Nöthen, MM, Woldbye, DPD, Mors, O, Binder, EB, Rück, C, Ripke, S, Deckert, J, Schumacher, J
Published 2019

Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression

by Forstner A.J, Awasthi S, Wolf C, Maron E, Erhardt A, Czamara D, Eriksson E, Lavebratt C, Allgulander C, Friedrich N, Becker J, Hecker J, Rambau S, Conrad R, Geiser F, McMahon F.J, Moebus S, Hess T, Buerfent B.C, Hoffmann P, Herms S, Heilmann-Heimbach S, Kockum I, Olsson T, Alfredsson L, Weber H, Alpers G.W, Arolt V, Fehm L, Fydrich T, Gerlach A.L, Hamm A, Kircher T, Pané-Farré C.A, Pauli P, Rief W, Ströhle A, Plag J, Lang T, Wittchen H.-U, Mattheisen M, Meier S, Metspalu A, Domschke K, Reif A, Hovatta I, Lindefors N, Andersson E, Schalling M, Mbarek H, Milaneschi Y, de Geus E.J.C, Boomsma D.I, Penninx B.W.J.H, Thorgeirsson T.E, Steinberg S, Stefansson K, Stefansson H, Müller-Myhsok B, Hansen T.F, Børglum A.D, Werge T, Mortensen P.B, Nordentoft M., Hougaard D.M., Hultman C.M., Sullivan P.F., Nöthen M.M., Woldbye D.P.D., Mors O., Binder E.B., Rück C., Ripke S., Deckert J., Schumacher J.
Published 2021

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm.

by Gretarsdottir, S, Baas, AF, Thorleifsson, G, Holm, H, den Heijer, M, de Vries, JP, Kranendonk, SE, Zeebregts, CJ, van Sterkenburg, SM, Geelkerken, RH, van Rij, AM, Williams, MJ, Boll, AP, Kostic, JP, Jonasdottir, A, Walters, GB, Masson, G, Sulem, P, Saemundsdottir, J, Mouy, M, Magnusson, KP, Tromp, G, Elmore, JR, Sakalihasan, N, Limet, R, Defraigne, JO, Ferrell, RE, Ronkainen, A, Ruigrok, YM, Wijmenga, C, Grobbee, DE, Shah, SH, Granger, CB, Quyyumi, AA, Vaccarino, V, Patel, RS, Zafari, AM, Levey, AI, Austin, H, Girelli, D, Pignatti, PF, Olivieri, O, Martinelli, N, Malerba, G, Trabetti, E, Becker, LC, Becker, DM, Reilly, MP, Rader, DJ, Mueller, T, Dieplinger, B, Haltmayer, M, Urbonavicius, S, Lindblad, B, Gottsäter, A, Gaetani, E, Pola, R, Wells, P, Rodger, M, Forgie, M, Langlois, N, Corral, J, Vicente, V, Fontcuberta, J, España, F, Grarup, N, Jørgensen, T, Witte, DR, Hansen, T, Pedersen, O, Aben, KK, de Graaf, J, Holewijn, S, Folkersen, L, Franco-Cereceda, A, Eriksson, P, Collier, DA, Stefansson, H, Steinthorsdottir, V, Rafnar, T, Valdimarsson, EM, Magnadottir, HB, Sveinbjornsdottir, S, Olafsson, I, Magnusson, MK, Palmason, R, Haraldsdottir, V, Andersen, K, Onundarson, PT, Thorgeirsson, G, Kiemeney, LA, Powell, JT, Carey, DJ, Kuivaniemi, H, Lindholt, JS, Jones, GT, Kong, A, Blankensteijn, JD, Matthiasson, SE, Thorsteinsdottir, U, Stefansson, K
Published 2010

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

by Gretarsdottir S, Baas AF, Thorleifsson G, Holm H, den Heijer M, de Vries JP, Kranendonk SE, Zeebregts CJ, van Sterkenburg SM, Geelkerken RH, van Rij AM, Williams MJ, Boll AP, Kostic JP, Jonasdottir A, Walters GB, Masson G, Sulem P, Saemundsdottir J, Mouy M, Magnusson KP, Tromp G, Elmore JR, Sakalihasan N, Limet R, Defraigne JO, Ferrell RE, Ronkainen A, Ruigrok YM, Wijmenga C, Grobbee DE, Shah SH, Granger CB, Quyyumi AA, Vaccarino V, Patel RS, Zafari AM, Levey AI, Austin H, Becker LC, Becker DM, Reilly MP, Rader DJ, Mueller T, Dieplinger B, Haltmayer M, Urbonavicius S, Lindblad B, Gottsäter A, Gaetani E, Pola R, Wells P, Rodger M, Forgie M, Langlois N, Corral J, Vicente V, Fontcuberta J, España F, Grarup N, Jørgensen T, Witte DR, Hansen T, Pedersen O, Aben KK, de Graaf J, Holewijn S, Folkersen L, Franco Cereceda A, Eriksson P, Collier DA, Stefansson H, Steinthorsdottir V, Rafnar T, Valdimarsson EM, Magnadottir HB, Sveinbjornsdottir S, Olafsson I, Magnusson MK, Palmason R, Haraldsdottir V, Andersen K, Onundarson PT, Thorgeirsson G, Kiemeney LA, Powell JT, Carey DJ, Kuivaniemi H, Lindholt JS, Jones GT, Kong A, Blankensteijn JD, Matthiasson SE, Thorsteinsdottir U, Stefansson K., GIRELLI, Domenico, PIGNATTI, Pierfranco, OLIVIERI, Oliviero, MARTINELLI, Nicola, MALERBA, Giovanni, TRABETTI, Elisabetta
Published in Nature Genetics (2010)

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