Zobrazeno 1 - 7
of 7
pro vyhledávání: '"59"'
Autor:
Graham K. Murray, Hisham Ziauddeen, H.J. Taverne, J. Haarsma, Ian M. Goodyer, Teresa Katthagen, J.D. Griffin, Thomas J. Spencer, Kelly M. J. Diederen, C Miller, Paul C. Fletcher
Publikováno v:
Molecular Psychiatry
Haarsma, J, Fletcher, P, Griffin, J, Taverne, H, Ziauddeen, H, Spencer, T, Miller, C, Katthagen, T, Goodyear, I, Diederen, K & Murray, G 2020, ' Precision-weighting of cortical unsigned prediction error signals benefits learning, is mediated by dopamine, and is impaired in psychosis ', Molecular Psychiatry, vol. 0, no. 0, pp. 1-14 . https://doi.org/10.1038/s41380-020-0803-8
Haarsma, J, Fletcher, P, Griffin, J, Taverne, H, Ziauddeen, H, Spencer, T, Miller, C, Katthagen, T, Goodyear, I, Diederen, K & Murray, G 2020, ' Precision-weighting of cortical unsigned prediction error signals benefits learning, is mediated by dopamine, and is impaired in psychosis ', Molecular Psychiatry, vol. 0, no. 0, pp. 1-14 . https://doi.org/10.1038/s41380-020-0803-8
Recent theories of cortical function construe the brain as performing hierarchical Bayesian inference. According to these theories, the precision of prediction errors plays a key role in learning and decision-making, is controlled by dopamine and con
Autor:
Karen L. Jones, Judith A Van de Water
Publikováno v:
Molecular Psychiatry. 24:252-265
It has been estimated that autism spectrum disorder (ASD) now affects 1 in 59 children in the United States. Although the cause(s) of ASD remain largely unknown, it is becoming increasingly apparent that ASD can no longer be defined simply as a behav
Autor:
Danyllo Oliveira, Fred H. Gage, Ernesto Goulart, Maria C. Marchetto, Thalita Figueiredo, Mayana Zatz, Gerson Shigeru Kobayashi, Shani Stern, Renata Santos, Ana P.D. Mendes, Fernando Kok, Danielle de Paula Moreira
Publikováno v:
Molecular Psychiatry
Molecular Psychiatry, Nature Publishing Group, 2020, Online ahead of print. ⟨10.1038/s41380-020-00862-9⟩
Molecular Psychiatry, Nature Publishing Group, 2020, Online ahead of print. ⟨10.1038/s41380-020-00862-9⟩
International audience; A homozygous mutation in the inositol monophosphatase 1 (IMPA1) gene was recently identified in nine individuals with severe intellectual disability (ID) and disruptive behavior. These individuals belong to the same family fro
Autor:
Igor Rudan, Daniel I. Chasman, Helena Schmidt, Stefan Herms, Sharon L.R. Kardia, Oliver Stegle, Alison Pattie, Jenna Price, Gerardo Heiss, Karen A. Mather, L. J. Launer, Johan G. Eriksson, Christopher Oldmeadow, Ian Ford, Saira Saeed Mirza, Alan F. Wright, Ozren Polasek, Joshua M. Shulman, Maria K. Jonsdottir, André G. Uitterlinden, Rodney J. Scott, Kurt Lohman, Anita L. DeStefano, Peter W. Schofield, Perminder S. Sachdev, Stefania Bandinelli, Johan Wouter Jukema, John M. Starr, Rudolf S N Fehrmann, Y. C. Hsieh, William M. Meeks, Paul M. Ridker, R.G.J. Westendorp, Le Yu, J. C. van Swieten, Vilmundur Gudnason, Myriam Fornage, Melissa Garcia, Carla A. Ibrahim-Verbaas, James F. Wilson, Jean-Charles Lambert, Qiong Yang, Laura H. Coker, Stella Trompet, Lina Zgaga, Jennifer A. Smith, David J. Llewellyn, Nicole A. Kochan, Ben A. Oostra, Katja Petrovic, Peter Hoffmann, Qi Sun, James T. Becker, Najaf Amin, Vincent Chouraki, Brendan M. Buckley, D C Liewald, Jun Ding, Christiane Wolf, P. L. DeJager, Reinhold Schmidt, Chloe Fawns-Ritchie, Stéphanie Debette, Jing Wang, J. C. Bis, Nicola J. Armstrong, David J. Stott, Albert Hofman, Nazanin Karbalai, G. Eiriksdottir, Luke C. Pilling, D. S. Knopman, Maaike Schuur, Alexa S. Beiser, Annette L. Fitzpatrick, David A. Bennett, Aarno Palotie, Lude Franke, Sven Cichon, Mirna Kirin, Markus M. Nöthen, Thomas H. Mosley, Lynda M. Rose, Alan J. Gow, Caroline Hayward, Lori B. Chibnik, Ian J. Deary, Albert V. Smith, Jan Bressler, T.B. Harris, Stephen T. Turner, David J. Porteous, C M van Duijn, M. A. Ikram, Elizabeth G. Holliday, Mike A. Nalls, Luigi Ferrucci, Sudha Seshadri, Francine Grodstein, Marlene C. W. Stewart, Philip A. Wolf, Alexander Teumer, P.E. Slagboom, Jerome I. Rotter, Blair H. Smith, Juha Karjalainen, Susan M. Resnick, A.J.M. de Craen, Toshiko Tanaka, Alan D. Penman, Hans-Jörgen Grabe, Gary Davies, Oscar L. Lopez, Yongmei Liu, Kristine Yaffe, Veronique Vitart, Stela McLachlan, Katri Räikkönen, Rebecca F. Gottesman, Rhoda Au, Lynne J. Hocking, Carsten Oliver Schmidt, John Attia, Bruce M. Psaty, Wei Zhao, Jari Lahti
Publikováno v:
Molecular Psychiatry, 21(2), 189-197. Nature Publishing Group
Molecular Psychiatry, 21(2), 189-197
Ibrahim-Verbaas, C A, Bressler, J, Debette, S, Schuur, M, Smith, A V, Bis, J C, Davies, G, Trompet, S, Smith, J A, Wolf, C, Chibnik, L B, Liu, Y, Vitart, V, Kirin, M, Petrovic, K, Polasek, O, Zgaga, L, Fawns-Ritchie, C, Hoffmann, P, Karjalainen, J, Lahti, J, Llewellyn, D J, Schmidt, C O, Mather, K A, Chouraki, V, Sun, Q, Resnick, S M, Rose, L M, Oldmeadow, C, Stewart, M, Smith, B H, Gudnason, V, Yang, Q, Mirza, S S, Jukema, J W, deJager, P L, Harris, T B, Liewald, D, Amin, N, Gow, A J, Pattie, A, Starr, J M, McLachlan, S, Porteous, D J, Price, J F, Rudan, I, Hayward, C, Wright, A F & Wilson, J F & Deary, I 2016, ' GWAS for executive function and processing speed suggests involvement of the CADM2 gene ', Molecular Psychiatry, vol. 21, pp. 189-197 . https://doi.org/10.1038/mp.2015.37
Ibrahim-Verbaas, CA; Bressler, J; Debette, S; Schuur, M; Smith, AV; Bis, JC; et al.(2016). GWAS for executive function and processing speed suggests involvement of the CADM2 gene. MOLECULAR PSYCHIATRY, 21(2), 189-197. doi: 10.1038/mp.2015.37. UCLA: Retrieved from: http://www.escholarship.org/uc/item/7d8152n1
Molecular psychiatry 21(2), 189-197 (2015). doi:10.1038/mp.2015.37
Neurology Working Group of the CHARGE Consortium 2016, ' GWAS for executive function and processing speed suggests involvement of the CADM2 gene ', Molecular Psychiatry, vol. 21, no. 2, pp. 189-197 . https://doi.org/10.1038/mp.2015.37
Molecular psychiatry 21, 189–197 (2016). doi:10.1038/mp.2015.37
Molecular Psychiatry, 21(2), 189-197
Ibrahim-Verbaas, C A, Bressler, J, Debette, S, Schuur, M, Smith, A V, Bis, J C, Davies, G, Trompet, S, Smith, J A, Wolf, C, Chibnik, L B, Liu, Y, Vitart, V, Kirin, M, Petrovic, K, Polasek, O, Zgaga, L, Fawns-Ritchie, C, Hoffmann, P, Karjalainen, J, Lahti, J, Llewellyn, D J, Schmidt, C O, Mather, K A, Chouraki, V, Sun, Q, Resnick, S M, Rose, L M, Oldmeadow, C, Stewart, M, Smith, B H, Gudnason, V, Yang, Q, Mirza, S S, Jukema, J W, deJager, P L, Harris, T B, Liewald, D, Amin, N, Gow, A J, Pattie, A, Starr, J M, McLachlan, S, Porteous, D J, Price, J F, Rudan, I, Hayward, C, Wright, A F & Wilson, J F & Deary, I 2016, ' GWAS for executive function and processing speed suggests involvement of the CADM2 gene ', Molecular Psychiatry, vol. 21, pp. 189-197 . https://doi.org/10.1038/mp.2015.37
Ibrahim-Verbaas, CA; Bressler, J; Debette, S; Schuur, M; Smith, AV; Bis, JC; et al.(2016). GWAS for executive function and processing speed suggests involvement of the CADM2 gene. MOLECULAR PSYCHIATRY, 21(2), 189-197. doi: 10.1038/mp.2015.37. UCLA: Retrieved from: http://www.escholarship.org/uc/item/7d8152n1
Molecular psychiatry 21(2), 189-197 (2015). doi:10.1038/mp.2015.37
Neurology Working Group of the CHARGE Consortium 2016, ' GWAS for executive function and processing speed suggests involvement of the CADM2 gene ', Molecular Psychiatry, vol. 21, no. 2, pp. 189-197 . https://doi.org/10.1038/mp.2015.37
Molecular psychiatry 21, 189–197 (2016). doi:10.1038/mp.2015.37
To access publisher's full text version of this article, please click on the hyperlink in Additional Links field or click on the hyperlink at the top of the page marked Files. This article is open access. To identify common variants contributing to n
Autor:
Paul C Guest, Patricia Ohrmann, Lan Wang, F E Torrey, Sabine Bahn, Laura W. Harris, Hassan Rahmoune, Robert H. Yolken, B. Bogerts, Anna Barnes, George McAllister, N. J. M. van Beveren, Matthias Rothermundt, Simon Baron-Cohen, Johann Steiner, Michael Spain, Emanuel Schwarz, Laura Kranaster, Thomas Suslow, Dagmar Koethe, F M Leweke
Publikováno v:
Molecular Psychiatry, 17(5), 494-502. Nature Publishing Group
Molecular Psychiatry; Vol 17
Molecular Psychiatry
Molecular Psychiatry; Vol 17
Molecular Psychiatry
Biomarkers are now used in many areas of medicine but are still lacking for psychiatric conditions such as schizophrenia (SCZ). We have used a multiplex molecular profiling approach to measure serum concentrations of 181 proteins and small molecules
Autor:
Cichon, S., Craddock, N., Daly, M.J., Faraone, S.V., Gejman, P.V., Kelsoe, J., Lehner, T., Levinson, D.F., Moran, A.P., Sklar, P., Sullivan, P.F., Boomsma, D.I., de Geus, E.J.C., Posthuma, D., Willemsen, G.
Publikováno v:
Molecular Psychiatry, 14(1), 10-17. Nature Publishing Group
Molecular Psychiatry, 14, 1, pp. 10-17
Molecular Psychiatry, 14, 10-17
Cichon, S, Craddock, N, Daly, M J, Faraone, S V, Gejman, P V, Kelsoe, J, Lehner, T, Levinson, D F, Moran, A P, Sklar, P, Sullivan, P F, Boomsma, D I, de Geus, E J C, Posthuma, D & Willemsen, G 2009, ' A framework for interpreting genome-wide association studies of psychiatric disorders ', Molecular Psychiatry, vol. 14, no. 1, pp. 10-17 . https://doi.org/10.1038/mp.2008.126
Molecular Psychiatry, 14, 1, pp. 10-17
Molecular Psychiatry, 14, 10-17
Cichon, S, Craddock, N, Daly, M J, Faraone, S V, Gejman, P V, Kelsoe, J, Lehner, T, Levinson, D F, Moran, A P, Sklar, P, Sullivan, P F, Boomsma, D I, de Geus, E J C, Posthuma, D & Willemsen, G 2009, ' A framework for interpreting genome-wide association studies of psychiatric disorders ', Molecular Psychiatry, vol. 14, no. 1, pp. 10-17 . https://doi.org/10.1038/mp.2008.126
Genome-wide association studies (GWAS) have yielded a plethora of new findings in the past 3 years. By early 2009, GWAS on 47 samples of subjects with attention-deficit hyperactivity disorder, autism, bipolar disorder, major depressive disorder and s
Autor:
Anthony O. Ahmed, Jason M. Bruggemann, Katherine M. Allen, Rhoshel K. Lenroot, Danielle Weinberg, Thomas W. Weickert, Kristy R. Howell, Cherrie Galletly, Dennis T Liu, Anilkumar Pillai, Cynthia Shannon Weickert
Publikováno v:
Molecular psychiatry. 21(5)
A large body of evidence indicates alterations in brain regional cellular energy metabolism and blood flow in schizophrenia. Among the different molecules regulating blood flow, vascular endothelial growth factor (VEGF) is generally accepted as the m