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Age-related shift in LTD is dependent on neuronal adenosine A(2A) receptors interplay with mGluR5 and NMDA receptors.
Temido-Ferreira, M. and Ferreira, D.G. and Batalha, V.L. and Marques-Morgado, I. and Coelho, J.E. and Pereira, P. and Gomes, R. and Pinto, A. and Carvalho, S. and Canas, P.M. and Cuvelier, L. and Buée-Scherrer, V. and Faivre, E. and Baqi, Y. and Müller, C.E. and Pimentel, J. and Schiffmann, S.N. and Buée, L. and Bader, M. and Outeiro, T.F. and Blum, D. and Cunha, R.A. and Marie, H. and Pousinha, P.A. and Lopes, L.V.
Molecular Psychiatry 27 June 2018 (In Press)

De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females.
Palmer, E.E. and Stuhlmann, T. and Weinert, S. and Haan, E. and Van Esch, H. and Holvoet, M. and Boyle, J. and Leffler, M. and Raynaud, M. and Moraine, C. and van Bokhoven, H. and Kleefstra, T. and Kahrizi, K. and Najmabadi, H. and Ropers, H.H. and Delgado, M.R. and Sirsi, D. and Golla, S. and Sommer, A. and Pietryga, M.P. and Chung, W.K. and Wynn, J. and Rohena, L. and Bernardo, E. and Hamlin, D. and Faux, B.M. and Grange, D.K. and Manwaring, L. and Tolmie, J. and Joss, S. and Cobben, J.M. and Duijkers, F.A.M. and Goehringer, J.M. and Challman, T.D. and Hennig, F. and Fischer, U. and Grimme, A. and Suckow, V. and Musante, L. and Nicholl, J. and Shaw, M. and Lodh, S.P. and Niu, Z. and Rosenfeld, J.A. and Stankiewicz, P. and Jentsch, T.J. and Gecz, J. and Field, M. and Kalscheuer, V.M.
Molecular Psychiatry 23 (2): 222-230. February 2018

Genetics of intellectual disability in consanguineous families.
Hu, H. and Kahrizi, K. and Musante, L. and Fattahi, Z. and Herwig, R. and Hosseini, M. and Oppitz, C. and Abedini, S.S. and Suckow, V. and Larti, F. and Beheshtian, M. and Lipkowitz, B. and Akhtarkhavari, T. and Mehvari, S. and Otto, S. and Mohseni, M. and Arzhangi, S. and Jamali, P. and Mojahedi, F. and Taghdiri, M. and Papari, E. and Soltani Banavandi, M.J. and Akbari, S. and Tonekaboni, S.H. and Dehghani, H. and Ebrahimpour, M.R. and Bader, I. and Davarnia, B. and Cohen, M. and Khodaei, H. and Albrecht, B. and Azimi, S. and Zirn, B. and Bastami, M. and Wieczorek, D. and Bahrami, G. and Keleman, K. and Vahid, L.N. and Tzschach, A. and Gärtner, J. and Gillessen-Kaesbach, G. and Varaghchi, J.R. and Timmermann, B. and Pourfatemi, F. and Jankhah, A. and Chen, W. and Nikuei, P. and Kalscheuer, V.M. and Oladnabi, M. and Wienker, T.F. and Ropers, H.H. and Najmabadi, H.
Molecular Psychiatry 4 January 2018 (In Press)


Structural brain changes are associated with response of negative symptoms to prefrontal repetitive transcranial magnetic stimulation in patients with schizophrenia.
Hasan, A. and Wobrock, T. and Guse, B. and Langguth, B. and Landgrebe, M. and Eichhammer, P. and Frank, E. and Cordes, J. and Woelwer, W. and Musso, F. and Winterer, G. and Gaebel, W. and Hajak, G. and Ohmann, C. and Verde, P.E. and Rietschel, M. and Ahmed, R. and Honer, W.G. and Dechent, P. and Malchow, B. and Castro, M.F.U. and Dwyer, D. and Cabral, C. and Kreuzer, P.M. and Poeppl, T.B. and Schneider-Axmann, T. and Falkai, P. and Koutsouleris, N.
Molecular Psychiatry 22 (6): 857-864. June 2017


SorCS2 is required for BDNF-dependent plasticity in the hippocampus.
Glerup, S. and Bolcho, U. and Molgaard, S. and Bøggild, S. and Vaegter, C.B. and Smith, A.H. and Nieto-Gonzalez, J.L. and Ovesen, P.L. and Pedersen, L.F. and Fjorback, A.N. and Kjolby, M. and Login, H. and Holm, M.M. and Andersen, O.M. and Nyengaard, J.R. and Willnow, T.E. and Jensen, K. and Nykjaer, A.
Molecular Psychiatry 21 (12): 1740-1751. December 2016

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.
Hu, H. and Haas, S.A. and Chelly, J. and Van Esch, H. and Raynaud, M. and de Brouwer, A.P.M. and Weinert, S. and Froyen, G. and Frints, S.G.M. and Laumonnier, F. and Zemojtel, T. and Love, M.I. and Richard, H. and Emde, A.K. and Bienek, M. and Jensen, C. and Hambrock, M. and Fischer, U. and Langnick, C. and Feldkamp, M. and Wissink-Lindhout, W. and Lebrun, N. and Castelnau, L. and Rucci, J. and Montjean, R. and Dorseuil, O. and Billuart, P. and Stuhlmann, T. and Shaw, M. and Corbett, M.A. and Gardner, A. and Willis-Owen, S. and Tan, C. and Friend, K.L. and Belet, S. and van Roozendaal, K.E.P. and Jimenez-Pocquet, M. and Moizard, M.P. and Ronce, N. and Sun, R. and O'Keeffe, S. and Chenna, R. and van Bömmel, A. and Goeke, J. and Hackett, A. and Field, M. and Christie, L. and Boyle, J. and Haan, E. and Nelson, J. and Turner, G. and Baynam, G. and Gillessen-Kaesbach, G. and Mueller, U. and Steinberger, D. and Budny, B. and Badura-Stronka, M. and Latos-Bieleńska, A. and Ousager, L.B. and Wieacker, P. and Rodríguez Criado, G. and Bondeson, M.L. and Annerén, G. and Dufke, A. and Cohen, M. and Van Maldergem, L. and Vincent-Delorme, C. and Echenne, B. and Simon-Bouy, B. and Kleefstra, T. and Willemsen, M. and Fryns, J.P. and Devriendt, K. and Ullmann, R. and Vingron, M. and Wrogemann, K. and Wienker, T.F. and Tzschach, A. and van Bokhoven, H. and Gecz, J. and Jentsch, T.J. and Chen, W. and Ropers, H.H. and Kalscheuer, V.M.
Molecular Psychiatry 21 (1): 133-148. January 2016


In utero gene therapy rescues microcephaly caused by Pqbp1-hypofunction in neural stem progenitor cells.
Ito, H. and Shiwaku, H. and Yoshida, C. and Homma, H. and Luo, H. and Chen, X. and Fujita, K. and Musante, L. and Fischer, U. and Frints, S.G.M. and Romano, C. and Ikeuchi, Y. and Shimamura, T. and Imoto, S. and Miyano, S. and Muramatsu, S.I. and Kawauchi, T. and Hoshino, M. and Sudol, M. and Arumughan, A. and Wanker, E.E. and Rich, T. and Schwartz, C. and Matsuzaki, F. and Bonni, A. and Kalscheuer, V.M. and Okazawa, H.
Molecular Psychiatry 20 (4): 459-471. April 2015


Soluble amyloid precursor proteins in the cerebrospinal fluid as novel potential biomarkers of Alzheimer's disease: a multicenter study.
Lewczuk, P. and Kamrowski-Kruck, H. and Peters, O. and Heuser, I. and Jessen, F. and Popp, J. and Buerger, K. and Hampel, H. and Froelich, L. and Wolf, S. and Prinz, B. and Jahn, H. and Luckhaus, C. and Perneczky, R. and Huell, M. and Schroeder, J. and Kessler, H. and Pantel, J. and Gertz, H.J. and Klafki, H.W. and Koelsch, H. and Reulbach, U. and Esselmann, H. and Maler, J.M. and Bibl, M. and Kornhuber, J. and Wiltfang, J.
Molecular Psychiatry 15 (2): 138-145. February 2010


The Met allele of the BDNF Val66Met polymorphism is associated with increased BDNF serum concentrations.
Lang, U.E. and Hellweg, R. and Sander, T. and Gallinat, J.
Molecular Psychiatry 14 (2): 120-122. February 2009


Association and linkage of allelic variants of the dopamine transporter gene in ADHD.
Friedel, S. and Saar, K. and Sauer, S. and Dempfle, A. and Walitza, S. and Renner, T. and Romanos, M. and Freitag, C. and Seitz, C. and Palmason, H. and Scherag, A. and Windemuth-Kieselbach, C. and Schimmelmann, B.G. and Wewetzer, C. and Meyer, J. and Warnke, A. and Lesch, K.P. and Reinhardt, R. and Herpertz-Dahlmann, B. and Linder, M. and Hinney, A. and Remschmidt, H. and Schaefer, H. and Konrad, K. and Huebner, N. and Hebebrand, J.
Molecular Psychiatry 12 (10): 923-933. October 2007


A genome-wide scan for attention-deficit/hyperactivity disorder in 155 german sib-pairs.
Hebebrand, J. and Dempfle, A. and Saar, K. and Thiele, H. and Herpertz-Dahlmann, B. and Linder, M. and Kiefl, H. and Remschmidt, H. and Hemminger, U. and Warnke, A. and Knoelker, U. and Heiser, P. and Friedel, S. and Hinney, A. and Schaefer, H. and Nuernberg, P. and Konrad, K.
Molecular Psychiatry 11 (2): 196-205. February 2006


Support for the involvement of TPH2 gene in affective disorders.
Harvey, M. and Shink, E. and Tremblay, M. and Gagne, B. and Raymond, C. and Labbe, M. and Walther, D.J. and Bader, M. and Barden, N.
Molecular Psychiatry 9 (11): 980-981. 20 July 2004


A second large family with catatonic schizophrenia supports the region distally of CHRNA7 on chromosome 15q14-15.
Meyer, J. and Rueschendorf, F. and Lesch, K.P.
Molecular Psychiatry 8 : 259-260. 1 March 2003


Exclusion of the neuronal nicotinic acetylcholine receptor alpha 7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the chromosome 15q13-22 locus.
Meyer, J. and Ortega, G. and Schraut, K. and Nuernberg, G. and Rueschendorf, F. and Saar, K. and Moessner, R. and Wienker, T.F. and Reis, A. and Stoeber, G. and Lesch, K.P.
Molecular Psychiatry 7 : 220-223. 1 January 2002


DRD4 exon III VNTR polymorphism-susceptibility factor for heroin dependence? Results of a case-control and a family-based association approach.
Franke, P. and Noethen, M.M. and Wang, T. and Knapp, M. and Lichtermann, D. and Neidt, H. and Sander, T. and Propping, P. and Maier, W.
Molecular Psychiatry 5, 1 : 101-104. 1 January 2000

This list was generated on Tue Oct 23 02:37:50 2018 CEST.
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