Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Tracey Petryshen"'
Autor:
Milou Straathof, Erwin L.A. Blezer, Caroline van Heijningen, Christel E. Smeele, Annette van der Toorn, Jan K. Buitelaar, Jeffrey C. Glennon, Willem M. Otte, Rick M. Dijkhuizen, Jan Buitelaar, Saskia de Ruiter, Jilly Naaijen, Sophie Akkermans, Maarten Mennes, Marcel Zwiers, Shahrzad Ilbegi, Leonie Hennissen, Jeffrey Glennon, Ilse van de Vondervoort, Katarzyna Kapusta, NaAAtalia Bielczyk, Houshang Amiri, Martha Havenith, Barbara Franke, Geert Poelmans, Janita Bralten, Tom Heskes, Elena Sokolova, Perry Groot, Steven Williams, DeAAclan Murphy, David Lythgoe, Muriel Bruchhage, Iulia Dud, Bogdan Voinescu, Ralf Dittmann, Tobias Banaschewski, Daniel Brandeis, Konstantin Mechler, Ruth Berg, Isabella Wolf, Alexander Häge, Michael Landauer, Sarah Hohmann, Regina Boecker Schlier, Matthias Ruff, René Mandl, Rick Dijkhuizen, Erwin Blezer, Kajo van der Marel, Pim Pullens, Wouter Mol, Willem Otte, Sarah Durston, VinAAcent Mensen, Bob Oranje, Daphna Joel, John Cryan, Tracey Petryshen, David Pauls, Mai Saito, Angelique Heckman, Sabine Bahn, Ameli Schwalber, Ioana Florea
Publikováno v:
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 33, 58-70
European Neuropsychopharmacology, 33, 58-70
European Neuropsychopharmacology, 33, pp. 58-70
European Neuropsychopharmacology, 33, 58-70
European Neuropsychopharmacology, 33, pp. 58-70
Obsessive-compulsive disorder (OCD) is increasingly considered to be a neurodevelopmental disorder. However, despite insights in neural substrates of OCD in adults, less is known about mechanisms underlying compulsivity during brain development in ch
Autor:
Declan Murphy, Maarten Mennes, Tobias Banaschewski, Tom Heskes, David Lythgoe, Rick Dijkhuizen, Tracey Petryshen, John Cryan, Jeffrey Glennon, Houshang Amiri, Muriel Bruchhage, Daphna Joel, Steve Williams
Publikováno v:
Zeitschrift für Kinder-und Jugendpsychiatrie und Psychotherapie, 46, 246-263
Zeitschrift fur Kinder-und Jugendpsychiatrie und Psychotherapie, 46(3), 246. Verlag Hans Huber
Zeitschrift für Kinder-und Jugendpsychiatrie und Psychotherapie, 46, 3, pp. 246-263
Zeitschrift fur Kinder-und Jugendpsychiatrie und Psychotherapie, 46(3), 246. Verlag Hans Huber
Zeitschrift für Kinder-und Jugendpsychiatrie und Psychotherapie, 46, 3, pp. 246-263
Contains fulltext : 193222.pdf (Publisher’s version ) (Closed access) OBJECTIVE: Research has implicated glutamatergic projections between the various frontal subregions in the pathogenesis of compulsivity and impulsivity. Reducing striatal glutama
Autor:
Eleni Giannoulatou, Nancy Buccola, Tune Pers, Sarah TOSATO, Christos Pantelis, James Walters, Hon-Cheong So, Igor Nenadić, Joseph Buxbaum, Lili Milani, Miloš Milovančević, Naomi Wray, Joanne Knight, Nicholas Wood, Srihari Gopal, Silviu-Alin Bacanu, Colin Palmer, Inez Myin-Germeys, Francis Anthony O'Neill, Matthew A Brown, Sang Hong Lee, Robert Plomin, Peter Visscher, Tracey Petryshen, Preben Bo Mortensen, Thomas Folkmann Hansen, Esben Agerbo, Digby Quested, Jianjun Liu, Engilbert Sigurdsson, Sara Marsal, Céline Bellenguez, Robert Freedman, Panos Deloukas, Ditte Demontis, Donald Black, David Collier, Fritz Zimprich, Clement C Zai, Nakao IWATA, Elvira Bramon, Masashi Ikeda, Andrew McIntosh, Bryan Mowry, Patrik Magnusson, Janis Klovins, Srdjan Djurovic, Jim Van Os, Ulrich Schall, Jan Lubinski, Milica Pejovic Milovancevic, Kang Sim, Rodney Scott, Anders Børglum, Jennifer Moran, Denise Harold, Sergi Papiol, Bradley Webb, Elisabeth Stögmann
Publikováno v:
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics, 180(3), 223. Wiley-Liss Inc.
Harold, D, Connolly, S, Riley, B P, Kendler, K S, McCarthy, S E, McCombie, W R, Richards, A, Owen, M J, O'Donovan, M C, Walters, J, Wellcome Trust Case Control Consortium 2, The Schizophrenia Working Group of the Psychiatric Genomics Consortium, Donohoe, G, Gill, M, Corvin, A & Morris, D W 2019, ' Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia ', American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, vol. 180, no. 3, pp. 223-231 . https://doi.org/10.1002/ajmg.b.32716
American journal of medical genetics. Part B, Neuropsychiatric genetics, 180(3), 223-231. Wiley-Liss Inc.
Am J Med Genet B Neuropsychiatr Genet
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, vol 180, iss 3
Harold, D, Connolly, S, Riley, B P, Kendler, K S, McCarthy, S E, McCombie, W R, Richards, A, Owen, M J, O'Donovan, M C, Walters, J, Wellcome Trust Case Control Consortium 2, The Schizophrenia Working Group of the Psychiatric Genomics Consortium, Donohoe, G, Gill, M, Corvin, A & Morris, D W 2019, ' Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia ', American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, vol. 180, no. 3, pp. 223-231 . https://doi.org/10.1002/ajmg.b.32716
American journal of medical genetics. Part B, Neuropsychiatric genetics, 180(3), 223-231. Wiley-Liss Inc.
Am J Med Genet B Neuropsychiatr Genet
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, vol 180, iss 3
Genome‐wide association studies (GWASs) are highly effective at identifying common risk variants for schizophrenia. Rare risk variants are also important contributors to schizophrenia etiology but, with the exception of large copy number variants,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6b27234803db5d60315706f8029d6c6
https://lirias.kuleuven.be/handle/123456789/649473
https://lirias.kuleuven.be/handle/123456789/649473
Autor:
Nicholas Schork, Peter Schofield, Nancy Buccola, Paola Giusti-Rodríguez, Verena Zuber, Sarah TOSATO, Detelina Grozeva, Christos Pantelis, James Walters, Joseph Buxbaum, Miloš Milovančević, Niklas Långström, Gunnar Morken, Julia Newton-Bishop, Pamela Mahon, Inez Myin-Germeys, Sang Hong Lee, Peter Visscher, Lisa Jones, Michael O'Donovan, Bettina Kulle Andreassen, Francis McMahon, Tracey Petryshen, Thomas Folkmann Hansen, Esben Agerbo, Benedicto Crespo-Facorro, Jianjun Liu, Engilbert Sigurdsson, William Coryell, Arnoldo Frigessi, Robert Freedman, Soumya Raychaudhuri, Donald Black, Allan Young, Fritz Zimprich, Clement C Zai, Stéphane Jamain, Nakao IWATA, Pierandrea Muglia, Elvira Bramon, Masashi Ikeda, Andrew McIntosh, Bryan Mowry, Janis Klovins, Paul Tooney, Ulrich Schall, Jan Lubinski, Milica Pejovic Milovancevic, Kang Sim, Rodney Scott, Jennifer Moran, Bradley Webb, Elisabeth Stögmann
Publikováno v:
BMC genomics
BMC genomics, vol 19, iss 1
BMC Genomics, Vol 19, Iss 1, Pp 1-15 (2018)
BMC Genomics
BMC Genomics, 19(1). BioMed Central
BMC genomics, 19(1):494. BioMed Central
BMC Genomics. 2018 Jun 25;19(1):494
Schizophrenia and Bipolar Disorder Working Groups of the Psychiatric Genomics Consortium 2018, ' A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework ', BMC Genomics, vol. 19, no. 1, 494, pp. 494 . https://doi.org/10.1186/s12864-018-4859-7
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
BMC genomics, vol 19, iss 1
BMC Genomics, Vol 19, Iss 1, Pp 1-15 (2018)
BMC Genomics
BMC Genomics, 19(1). BioMed Central
BMC genomics, 19(1):494. BioMed Central
BMC Genomics. 2018 Jun 25;19(1):494
Schizophrenia and Bipolar Disorder Working Groups of the Psychiatric Genomics Consortium 2018, ' A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework ', BMC Genomics, vol. 19, no. 1, 494, pp. 494 . https://doi.org/10.1186/s12864-018-4859-7
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
BACKGROUND: There is considerable evidence that many complex traits have a partially shared genetic basis, termed pleiotropy. It is therefore useful to consider integrating genome-wide association study (GWAS) data across several traits, usually at t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb02259fa7c54f6a523dc071d6309fa2
Autor:
Nancy Buccola, Jonas Bybjerg-Grauholm, Sarah TOSATO, Christos Pantelis, James Walters, Igor Nenadić, Joseph Buxbaum, Thanneer Malai Perumal, Miloš Milovančević, Naomi Wray, Silviu-Alin Bacanu, Danielle Posthuma, Inez Myin-Germeys, Francis Anthony O'Neill, Sang Hong Lee, Kristen Dang, Peter Visscher, Tracey Petryshen, Esben Agerbo, Jianjun Liu, Engilbert Sigurdsson, Sara Marsal, Robert Freedman, Donald Black, Fritz Zimprich, Clement C Zai, Nakao IWATA, Elvira Bramon, Masashi Ikeda, Andrew McIntosh, Bryan Mowry, Patrik Magnusson, Janis Klovins, Thomas D. Als, Ulrich Schall, Milica Pejovic Milovancevic, Kang Sim, Rodney Scott, Anders Børglum, Jennifer Moran, Merete Nordentoft, Jakob Grove, Sergi Papiol, Bradley Webb, Elisabeth Stögmann
Publikováno v:
Nature Genetics, 51(6), 1068-1068. Nature Publishing Group
iPSYCH-GEMS Schizophrenia Working Group, CommonMind Consortium & The Schizophrenia Working Group of the Psychiatric Genomics Consortium 2019, ' Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk ', Nature Genetics, vol. 51, no. 6, pp. 1068-1068 . https://doi.org/10.1038/s41588-019-0435-6
iPSYCH-GEMS Schizophrenia Working Group, CommonMind Consortium & The Schizophrenia Working Group of the Psychiatric Genomics Consortium 2019, ' Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk ', Nature Genetics, vol. 51, no. 6, pp. 1068-1068 . https://doi.org/10.1038/s41588-019-0435-6
In the HTML version of the article originally published, the author group ‘The Schizophrenia Working Group of the Psychiatric Genomics Consortium’ was displayed incorrectly. The error has been corrected in the HTML version of the article.
Publikováno v:
European Neuropsychopharmacology. 29:S730
The Genetics of Endophenotypes of Neurofunction to Understand Schizophrenia (GENUS) Consortium aims to understand the genetic mechanisms of impaired brain function underlying schizophrenia. The consortium is examining the influence of genetic variati
Publikováno v:
Biological Psychiatry. 81:S284