Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Genomic disorders and inherited multi-system disorders Functional Neurogenomics [IGMD 3]"'
Autor:
Nitin Purandare, Radboud M. Marijnissen, J. de Graaf, Suzanne Holewijn, Boudewijn A.A. Bus, Barbara Franke, M. den Heijer, R.C. Oude Voshaar, Jan K. Buitelaar
Publikováno v:
Psychological Medicine, 41, 7, pp. 1419-28
Psychological Medicine, 41, 1419-28
Psychological Medicine, 41(7), 1419-1428. Cambridge University Press
Psychological Medicine, 41, 1419-28
Psychological Medicine, 41(7), 1419-1428. Cambridge University Press
BackgroundDepression increases the risk of subsequent vascular events in both cardiac and non-cardiac patients. Atherosclerosis, the underlying process leading to vascular events, has been associated with depression. This association, however, may be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9db9945212085cf84ee6a056d806efca
https://research.rug.nl/en/publications/36b60b0d-5e60-4570-a7bc-c72bc4382d20
https://research.rug.nl/en/publications/36b60b0d-5e60-4570-a7bc-c72bc4382d20
Autor:
Marieke E. van der Schaaf, Dirk E. M. Geurts, Roshan Cools, Robbert J. Verkes, Martine R. van Schouwenburg, Esther Aarts, Mieke van Holstein, Barbara Franke
Publikováno v:
Psychopharmacology, 218, 567-78
Psychopharmacology
Psychopharmacology, 218, 3, pp. 567-78
Psychopharmacology
Psychopharmacology, 218, 3, pp. 567-78
Rationale Accumulating evidence indicates that the cognitive effects of dopamine depend on the subtype of dopamine receptor that is activated. In particular, recent work with animals as well as current theorizing has suggested that cognitive flexibil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb14609f645ef2a9b3416794540f40e6
https://doi.org/10.1007/s00213-011-2340-2
https://doi.org/10.1007/s00213-011-2340-2
Autor:
Ingason, Andrés, Kirov, George, Giegling, Ina, Hansen, Thomas, Isles, Anthony R., Jakobsen, Klaus D., Kristinsson, Kari T., le Roux, Louise, Gustafsson, Omar, Craddock, Nick, Möller, Hans-Jürgen, McQuillin, Andrew, Muglia, Pierandrea, Cichon, Sven, Rietschel, Marcella, Ophoff, Roel A., Djurovic, Srdjan, Andreassen, Ole A., Pietiläinen, Olli P. H., Peltonen, Leena, Dempster, Emma, Collier, David A., St Clair, David, Rasmussen, Henrik B., Glenthøj, Birte Y., Kiemeney, Lambertus A., Franke, Barbara, Tosato, Sarah, Bonetto, Chiara, Saemundsen, Evald, Hreidarsson, Stefán J., Nöthen, Markus M., Gurling, Hugh, O'Donovan, Michael C., Owen, Michael J., Sigurdsson, Engilbert, Petursson, Hannes, Stefansson, Hreinn, Rujescu, Dan, Stefansson, Kari, Werge, Thomas, Linszen, Don
Publikováno v:
American journal of psychiatry, 168(4), 408-417. American Psychiatric Association
ResearcherID
American Journal of Psychiatry, 168(4), 408-417. American Psychiatric Publishing, Inc.
American Journal of Psychiatry, 168, 408-17
American Journal of Psychiatry; Vol 168
American Journal of Psychiatry
American Journal of Psychiatry, 168, 4, pp. 408-17
ResearcherID
American Journal of Psychiatry, 168(4), 408-417. American Psychiatric Publishing, Inc.
American Journal of Psychiatry, 168, 408-17
American Journal of Psychiatry; Vol 168
American Journal of Psychiatry
American Journal of Psychiatry, 168, 4, pp. 408-17
To access publisher full text version of this article. Please click on the hyperlink in Additional Links field. OBJECTIVE: Rare copy number variants have been implicated in different neurodevelopmental disorders, with the same copy number variants of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f815f1a9a0441a65855fbd37275ec161
https://doi.org/10.1176/appi.ajp.2010.09111660
https://doi.org/10.1176/appi.ajp.2010.09111660
Autor:
Thorunn Rafnar, Lisa R. Yanek, Martin den Heijer, Bjarke Feenstra, Hilma Holm, Gyda Bjornsdottir, Inga Prokopenko, Frank Geller, Daniel F. Gudbjartsson, Patrick Sulem, Diane M. Becker, Sigurjon A. Gudjonsson, Barbara Franke, G. Bragi Walters, Kari Stefansson, Katja K.H. Aben, Augustine Kong, Lewis C. Becker, Lambertus A. Kiemeney, Michael Stumvoll, Simon N. Stacey, Gudmar Thorleifsson, Anke Tönjes, Peter Kovacs, Adalbjorg Jonasdottir, Unnur Thorsteinsdottir, Thorgeir E. Thorgeirsson, Mads Melbye, Heather A. Boyd, Reedik Mägi
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, 20, 2071-7
Human Molecular Genetics, 20, 10, pp. 2071-7
Human Molecular Genetics, 20, 2071-7
Human Molecular Genetics, 20, 10, pp. 2071-7
Contains fulltext : 96332.pdf (Publisher’s version ) (Closed access) Coffee is the most commonly used stimulant and caffeine is its main psychoactive ingredient. The heritability of coffee consumption has been estimated at around 50%. We performed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76c0957e178cea624a096b7abf1f49e7
https://doi.org/10.1093/hmg/ddr086
https://doi.org/10.1093/hmg/ddr086
Autor:
Barbara Franke, Rafaela Marco, Jessica Lasky-Su, Henrik Uebel, Isabel Gabriëls, Michael Gill, Hans-Christoph Steinhausen, Jan K. Buitelaar, Penny Andreou, Robert Kumsta, Robert D. Oades, Stephen V. Faraone, Richard P. Ebstein, Philip Asherson, Herbert Roeyers, Tobias Banaschewski, Fernando Mulas, Ueli Mueller, Edmund J.S. Sonuga-Barke, Jonna Kuntsi, Wolff Schlotz, Hanna Christiansen, Aribert Rothenberger, Richard Anney, Joseph Sergeant, Ana Miranda
Publikováno v:
Sonuga-Barke, E J S, Kumsta, R, Schlotz, W, Lasky-Su, J, Marco, R, Miranda, A, Mulas, F, Oades, R D, Banaschewski, T, Mueller, U, Andreou, P, Christiansen, H, Gabriels, I, Uebel, H, Kuntsi, J, Franke, B, Buitelaar, J, Ebstein, R, Gill, M, Anney, R, Roeyers, H, Rothenberger, A, Sergeant, J, Steinhausen, H C, Asherson, P & Faraone, S V 2011, ' A Functional Variant of the Serotonin Transporter Gene (SLC6A4) Moderates Impulsive Choice in Attention-Deficit/Hyperactivity Disorder Boys and Siblings ', Biological Psychiatry, vol. 70, no. 3, pp. 230-6 . https://doi.org/10.1016/j.biopsych.2011.01.040
BIOLOGICAL PSYCHIATRY
Biological Psychiatry, 70, 3, pp. 230-6
Biological Psychiatry, 70, 230-6
BIOLOGICAL PSYCHIATRY
Biological Psychiatry, 70, 3, pp. 230-6
Biological Psychiatry, 70, 230-6
Item does not contain fulltext BACKGROUND: Impulsive drive for immediate reward (IDIR) and delay aversion are dissociable elements of the preference for immediate over delayed rewards seen in attention-deficit/hyperactivity disorder (ADHD). We hypoth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54817db18a57bf5e45119337ec0a5a46
https://doi.org/10.1016/j.biopsych.2011.01.040
https://doi.org/10.1016/j.biopsych.2011.01.040
Autor:
Astri J. Lundervold, Josep Antoni Ramos-Quiroga, Stefan Johansson, Bru Cormand, Silke Gross-Lesch, Martine Hoogman, E.T. Landaas, Susanne Kreiker, Andreas Reif, Philip Asherson, Rosa Bosch, Stephen V. Faraone, Cristina Sánchez-Mora, Lambertus A. Kiemeney, Marta Ribasés, Jan K. Buitelaar, Mònica Bayés, Barbara Franke, Kaya K. Jacobsen, Lucas Brunso, Eric Mick, J. J. Sandra Kooij, Jan Haavik, Christian Jacob, Klaus-Peter Lesch, Miquel Casas, Noèlia Fernàndez-Castillo
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 156, 5, pp. 600-12
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 156, 600-12
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 156, 5, pp. 600-12
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 156, 600-12
Contains fulltext : 97904.pdf (Publisher’s version ) (Closed access) Attention-deficit hyperactivity disorder (ADHD) is a common behavioral disorder affecting about 4-8% of children. ADHD persists into adulthood in around 65% of cases, either as th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d962b274953fa4e99e851c28e0b166c7
https://doi.org/10.1002/ajmg.b.31202
https://doi.org/10.1002/ajmg.b.31202
Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34.3 microdeletions
Autor:
N Morrison, Marjolein H. Willemsen, Helger G. Yntema, John Tolmie, N. de Leeuw, Willy M. Nillesen, Gea Beunders, Tjitske Kleefstra, Han G. Brunner, M Callaghan, S T M Keijzers-Vloet, A W M Nieuwint, Alexander Hoischen, J M van Hagen
Publikováno v:
Willemsen, M H, Beunders, G, Callaghan, M, de Leeuw, N, Nillesen, W M, Yntema, H G, van Hagen, J M, Nieuwint, A W M, Morrison, N, Keijzers-Vloet, S T M, Hoischen, A, Brunner, H G, Tolmie, J & Kleefstra, T 2011, ' Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34.3 microdeletions ', Clinical Genetics, vol. 80, no. 1, pp. 31-38 . https://doi.org/10.1111/j.1399-0004.2010.01607.x
Clinical Genetics, 80(1), 31-38. Wiley-Blackwell
Clinical Genetics, 80, 1, pp. 31-8
Clinical Genetics, 80, 31-8
Clinical Genetics, 80(1), 31-38. Wiley-Blackwell
Clinical Genetics, 80, 1, pp. 31-8
Clinical Genetics, 80, 31-8
Contains fulltext : 97912.pdf (Publisher’s version ) (Closed access) The Kleefstra syndrome (Online Mendelian Inheritance in Man 607001) is caused by a submicroscopic 9q34.3 deletion or by intragenic euchromatin histone methyl transferase 1 (EHMT1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f209a7a2d604877a0d5b2e8087df48ff
https://hdl.handle.net/2066/97912
https://hdl.handle.net/2066/97912
Autor:
Linda Reus, Leo A. van Vlimmeren, Maria W.G. Nijhuis-van der Sanden, Machiel J. Zwarts, Barto J. Otten, Michèl A.A.P. Willemsen
Publikováno v:
Neuroscience and Biobehavioral Reviews, 35, 3, pp. 956-69
Neuroscience and Biobehavioral Reviews, 35, 956-69
Neuroscience and Biobehavioral Reviews, 35, 956-69
Contains fulltext : 98113.pdf (Publisher’s version ) (Closed access) Motor problems in Prader-Willi syndrome (PWS) are presumably related to abnormal body composition and certain neuromuscular abnormalities. The authors reviewed the literature to e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fae0a60bd232db0e025e460186cd12d9
https://doi.org/10.1016/j.neubiorev.2010.10.015
https://doi.org/10.1016/j.neubiorev.2010.10.015
Autor:
Nicolien Hanemaaijer, William Reardon, Ernie M.H.F. Bongers, Joke B. G. M. Verheij, Trijnie Dijkhuizen, Roel Hordijk, Birgit Sikkema-Raddatz, Nicole de Leeuw, Conny M. A. van Ravenswaaij-Arts, Andrew Green, Helger G. Yntema, Dorien Lugtenberg, Han G. Brunner, Ilse Feenstra, Bert B.A. de Vries
Publikováno v:
European Journal of Human Genetics, 19, 11, pp. 1152-60
European Journal of Human Genetics, 19, 1152-60
European Journal of Human Genetics, 19(11), 1152-1160. Nature Publishing Group
European Journal of Human Genetics, 19, 1152-60
European Journal of Human Genetics, 19(11), 1152-1160. Nature Publishing Group
High-resolution genome-wide array analysis enables detailed screening for cryptic and submicroscopic imbalances of microscopically balanced de novo rearrangements in patients with developmental delay and/or congenital abnormalities. In this report, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::635c660f3da3f549be0f884edf26f5f1
https://hdl.handle.net/2066/96666
https://hdl.handle.net/2066/96666
Autor:
Petra van Setten, Amanda Branten, Dirk Lefeber, Uwe Kornak, Eva Morava, Sascha Vermeer, Jefte M. Drijvers, Charles W. O'Neill, Alphons de Jong, Ron A. Wevers, Cor W. R. J. Cremers, Joris H. Robben, Angelien Heister, Jirko Kühnisch, Hedi L Claahsen-van der Grinten, Michèl A.A.P. Willemsen, Peter M.T. Deen, Hannie Kremer, Krysta Voesenek, Sabine Stumpp
Publikováno v:
Journal of Clinical Endocrinology and Metabolism, 96, 1, pp. E189-98
Journal of Clinical Endocrinology and Metabolism, 96, E189-98
Journal of Clinical Endocrinology and Metabolism, 96, E189-98
Contains fulltext : 96664.pdf (Publisher’s version ) (Closed access) CONTEXT: Mutations in ANKH cause the highly divergent conditions familial chondrocalcinosis and craniometaphyseal dysplasia. The gene product ANK is supposed to regulate tissue mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfb7e6daf9bb96897e8f3e93f0c3cae6
https://doi.org/10.1210/jc.2010-1539
https://doi.org/10.1210/jc.2010-1539