Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Zoltán Bochdanovits"'
Correction: Modulatory Effects of the Piccolo Genotype on Emotional Memory in Health and Depression.
Autor:
Saskia Woudstra, Marie-José van Tol, Zoltán Bochdanovits, Nic J. van der Wee, Frans G. Zitman, Mark A. van Buchem, Esther M. Opmeer, André Aleman, Brenda W. Penninx, Dick J. Veltman, Witte J. Hoogendijk
Publikováno v:
PLoS ONE, Vol 8, Iss 8 (2013)
Externí odkaz:
https://doaj.org/article/ecf6ff90856f4e1b86ccec1d814e0a98
Autor:
Eva C Verbeek, Marianna R Bevova, Zoltán Bochdanovits, Patrizia Rizzu, Ingrid M C Bakker, Tiny Uithuisje, Eco J De Geus, Johannes H Smit, Brenda W Penninx, Dorret I Boomsma, Witte J G Hoogendijk, Peter Heutink
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e79921 (2013)
Major depressive disorder (MDD) is a psychiatric disorder, characterized by periods of low mood of more than two weeks, loss of interest in normally enjoyable activities and behavioral changes. MDD is a complex disorder and does not have a single gen
Externí odkaz:
https://doaj.org/article/1f07d89530b04e40bf196189b9215346
Autor:
Saskia Woudstra, Marie-José van Tol, Zoltán Bochdanovits, Nic J van der Wee, Frans G Zitman, Mark A van Buchem, Esther M Opmeer, André Aleman, Brenda W Penninx, Dick J Veltman, Witte J Hoogendijk
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e61494 (2013)
Major depressive disorder (MDD) has been associated with biased memory formation for mood-congruent information, which may be related to altered monoamine levels. The piccolo (PCLO) gene, involved in monoaminergic neurotransmission, has previously be
Externí odkaz:
https://doaj.org/article/111afbf5b34d48719109a9c6349935da
Autor:
Eva C Verbeek, Ingrid M C Bakker, Marianna R Bevova, Zoltán Bochdanovits, Patrizia Rizzu, David Sondervan, Gonneke Willemsen, Eco J de Geus, Johannes H Smit, Brenda W Penninx, Dorret I Boomsma, Witte J G Hoogendijk, Peter Heutink
Publikováno v:
PLoS ONE, Vol 7, Iss 5, p e37384 (2012)
Major depressive disorder (MDD) is a psychiatric disorder that is characterized--amongst others--by persistent depressed mood, loss of interest and pleasure and psychomotor retardation. Environmental circumstances have proven to influence the aetiolo
Externí odkaz:
https://doaj.org/article/12e27116c15a470b9effc8a28fe5067f
Autor:
Iraad F Bronner, Zoltán Bochdanovits, Patrizia Rizzu, Wouter Kamphorst, Rivka Ravid, John C van Swieten, Peter Heutink
Publikováno v:
PLoS ONE, Vol 4, Iss 8, p e6826 (2009)
BACKGROUND:Understanding the aetiologies of neurodegenerative diseases such as Alzheimer's disease (AD), Pick's disease (PiD), Progressive Supranuclear Palsy (PSP) and Frontotemporal dementia (FTD) is often hampered by the considerable clinical and m
Externí odkaz:
https://doaj.org/article/785a746c503549a089e46a6558ad7e19
Autor:
Javier Simón-Sánchez, Harro Seelaar, Zoltán Bochdanovits, Dorly J H Deeg, John C van Swieten, Peter Heutink
Publikováno v:
PLoS ONE, Vol 4, Iss 10, p e7494 (2009)
A single nucleotide polymorphism (rs5848) located in the 3'- untranslated region of GRN has recently been associated with a risk of frontotemporal lobar degeneration (FTLD) in North American population particularly in pathologically confirmed cases w
Externí odkaz:
https://doaj.org/article/85471a47b7ca427c86a66cffbefab37a
Autor:
Zoltán Bochdanovits, David Sondervan, Sophie Perillous, Toos van Beijsterveldt, Dorret Boomsma, Peter Heutink
Publikováno v:
PLoS ONE, Vol 3, Iss 2, p e1593 (2008)
The human genome encodes a limited number of genes yet contributes to individual differences in a vast array of heritable traits. A possible explanation for the capacity our genome to generate this virtually unlimited range of phenotypic variation in
Externí odkaz:
https://doaj.org/article/305f4667863d448d8f2226169bbec76d
Autor:
Mina Ryten, Daniah Trabzuni, J. Ding, Bart Post, Albert Hofman, Jean-Charles Lambert, Olaf Riess, Michele T.M. Hu, Andrew B. Singleton, Stephen Sawcer, X. Huang, Caroline H. Williams-Gray, H. R. Zielke, C Smith, Peter Lichtner, B.P.C. van de Warrenburg, Bernard Ravina, F. Durif, Ellen Sidransky, Mike A. Nalls, Karen E. Morrison, J. R. Gibbs, Robert L. Johnson, Peter Heutink, David J. Burn, Michael Bonin, Sarah Edkins, T. Gasser, Luigi Ferrucci, H. Chau, Sampath Arepalli, Chris C. A. Spencer, Yoav Ben-Shlomo, Honglei Chen, Caroline M. Tanner, Zoltán Bochdanovits, Ruth Chia, Heiko Huber, Kari Stefansson, Dena G. Hernandez, Jean-Marc Taymans, Veerle Baekelandt, Iakov N. Rudenko, Evy Lobbestael, Huw R. Morris, A. Goate, C. Moorby, Lois E. Greene, Manu Sharma, Emma Gray, Ira Shoulson, Janet Brooks, Juan C. Troncoso, K. Shaw, Laura Civiero, Alessandra Biffi, Hans Scheffer, Matthew Moore, Alan B. Zonderman, S. Sveinbjornsdottir, Avazeh Tashakkori-Ghanbaria, Jean-Christophe Corvol, Vincent Plagnol, H. Petursson, Alice Kaganovich, M M Wickremaratchi, Nigel Williams, Thomas Foltynie, Henk W. Berendse, P. Damier, A. Strange, J. M. Cooper, Simon C. Potter, Patricia Limousin, Jiali Gao, Sophie Winder-Rhodes, M. Van Der Brug, Marie Vidailhet, Elisa Greggio, Nicholas W. Wood, Kevin Talbot, M. R. Cookson, Johanna Huttenlocher, J.J. van Hilten, Dan L. Longo, Alisdair McNeill, François Tison, K.D. van Dijk, David N. Hauser, Allissa Dillman, Suneil K. Kalia, Lorraine V. Kalia, Patrick F. Chinnery, Alexis Brice, Kelechi Ndukwe, J. F. Dartigues, M. Gardner, Mohamad Saad, Palmi V. Jonsson, Kailash P. Bhatia, Roger A. Barker, André G. Uitterlinden, Maria Martinez, R. Walker, Elisa Majounie, Fernando Rivadeneira, Joel S. Perlmutter, Panagiotis Deloukas, Bryan J. Traynor, Ese E. Mudanohwo, Grisel Lopez, UM Sheerin, Joanne D. Stockton, Thomas Illig, Andres M. Lozano, Rita Guerreiro, David T. Dexter, Andrew J. Lees, Sean Chong, Gavin Hudson, Cordelia Langford, Günther Deuschl, Ravindran Kumaran, Janice L. Holton, Tamas Revesz, B.R. Bloem, Alexandra Beilina, Clare Elizabeth Harris, Daniela Berg, Anthony H.V. Schapira, Suzanne Lesage, Sean S. O'Sullivan, Albert R. Hollenbeck, James A. Pearson, R. M. A. de Bie, Delia Lorenz, Sarah E. Hunt, Richard O'Brien, Gavin Charlesworth, Maciej B. Olszewski, Stacy Steinberg, Kathrin Brockmann, Carl E Clarke, Patrizia Rizzu, Claudia Schulte, Hreinn Stefansson, Daan C. Velseboer, Omar Gustafsson, Jonathan R. Evans, Alexandra Durr, Javier Simón-Sánchez, Pierre Pollak, H. Z. Munchen, Jose Bras, Carl Counsell, John Hardy
Publikováno v:
Proceedings of the National Academy of Sciences, 111(7), 2626-2631
Proceedings of the National Academy of Sciences USA, 111, 2626-31
Proceedings of the National Academy of Sciences of the United States of America, 111(7), 2626-2631. National Academy of Sciences
Proc. Natl. Acad. Sci. U.S.A. 111, 2626-2631 (2014)
Proceedings of the National Academy of Sciences USA, 111, 7, pp. 2626-31
Proceedings of the National Academy of Sciences USA, 111, 2626-31
Proceedings of the National Academy of Sciences of the United States of America, 111(7), 2626-2631. National Academy of Sciences
Proc. Natl. Acad. Sci. U.S.A. 111, 2626-2631 (2014)
Proceedings of the National Academy of Sciences USA, 111, 7, pp. 2626-31
Item does not contain fulltext Mutations in leucine-rich repeat kinase 2 (LRRK2) cause inherited Parkinson disease (PD), and common variants around LRRK2 are a risk factor for sporadic PD. Using protein-protein interaction arrays, we identified BCL2-
Autor:
Zoltán Bochdanovits, Peter Heutink, Aad van der Vaart, Witte J.G. Hoogendijk, Javier Simón-Sánchez, Marianne A. Jonker
Publikováno v:
European Journal of Human Genetics, 22(2), 238-242. Nature Publishing Group
Bochdanovits, Z, Simon Sanchez, J, Jonker, M A, Hoogendijk, W J G, van der Vaart, A W & Heutink, P 2014, ' Accurate prediction of a minimal region around a genetic association signal that contains the causal variant ', European Journal of Human Genetics, vol. 22, no. 2, pp. 238-242 . https://doi.org/10.1038/ejhg.2013.115
Bochdanovits, Z, Simon Sanchez, J, Jonker, M A, Hoogendijk, W J G, van der Vaart, A W & Heutink, P 2014, ' Accurate prediction of a minimal region around a genetic association signal that contains the causal variant ', European Journal of Human Genetics, vol. 22, no. 2, pp. 238-242 . https://doi.org/10.1038/ejhg.2013.115
In recent years, genome-wide association studies have been very successful in identifying loci for complex traits. However, typically these findings involve noncoding and/or intergenic SNPs without a clear functional effect that do not directly point
Publikováno v:
Statistica Neerlandica. 65:239-258
We consider estimation and testing of linkage equilibrium from genotypic data on a random sample of sibs, such as monozygotic and dizygotic twins. We compute the maximum likelihood estimator with an EM-algorithm and a likelihood ratio statistic that