Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Angelien Heister"'
Autor:
Amaia Carrion-Castillo, Barbara Franke, Simon E. Fisher, Clyde Francks, Ben Maassen, Aryan van der Leij, Marlies Naber, Angelien Heister
Publikováno v:
European Journal of Human Genetics, 25(4), 452-460. Nature Publishing Group
European Journal of Human Genetics
European Journal of Human Genetics, 25, 4, pp. 452-460
European Journal of Human Genetics, 25, 452-460
European Journal of Human Genetics
European Journal of Human Genetics, 25, 4, pp. 452-460
European Journal of Human Genetics, 25, 452-460
Contains fulltext : 169900.pdf (Publisher’s version ) (Closed access) Dyslexia is a common specific learning disability with a substantive genetic component. Several candidate genes have been proposed to be implicated in dyslexia susceptibility, su
Autor:
Angelien Heister, Stefanie Berger, Marieke Klein, Josep Antoni Ramos-Quiroga, Sarah Kittel-Schneider, Marta Ribasés, Tetyana Zayats, Stefan Johansson, Claiton H.D. Bau, Klaus-Peter Lesch, Jan Haavik, Heike Weber, Eugenio H. Grevet, Bru Cormand, Alejandro Arias-Vasquez, Nina Roth Mota, Alysa E. Doyle, Remco R. R. Makkinje, Tessel E. Galesloot, Andreas Reif, Lambertus A. Kiemeney, Kaya K. Jacobsen, Martine Hoogman, Barbara Franke, Janneke Dammers, Tor-Arne Hegvik, Stephen V. Faraone
Publikováno v:
European Neuropsychopharmacology, 26, 9, pp. 1527-1532
European Neuropsychopharmacology, 26, 1527-1532
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
EUROPEAN NEUROPSYCHOPHARMACOLOGY
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
ResearcherID
European Neuropsychopharmacology, 26, 1527-1532
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
EUROPEAN NEUROPSYCHOPHARMACOLOGY
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
ResearcherID
Contains fulltext : 167943pub.pdf (Publisher’s version ) (Closed access) Attention-Deficit/Hyperactivity Disorder (ADHD) is a common neuropsychiatric disorder with a complex genetic background. DRD5, the gene encoding the dopamine receptor D5, was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::925acc19118f95182926333966a2a2bb
https://hdl.handle.net/2066/167943
https://hdl.handle.net/2066/167943
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
Autor:
Cyril Goizet, Mirna Assoum, Rowdy Meijer, Erik-Jan Kamsteeg, Berry Kremer, Mascha M.V.A.P. Schijvenaars, Bart P.C. van de Warrenburg, Joris A. Veltman, Arjan P.M. de Brouwer, Nine V A M Knoers, Nathalie Drouot, Jenny van der Wijst, S. Todorovic, Mathieu Anheim, Peer Arts, Alexis Brice, Angelien Heister, Giovanni Stevanin, Nienke Wieskamp, Albert David, Hans Scheffer, Christian Gilissen, Vedrana Milic-Rasic, Alexander Hoischen, Michel Koenig, Sascha Vermeer, Alexandra Durr, Michael Kwint, Kornelia Neveling, Hanns Lochmüller
Publikováno v:
The American Journal of Human Genetics; Vol 87
American Journal of Human Genetics, 87(6), 813-819. CELL PRESS
American Journal of Human Genetics, 87, 6, pp. 813-9
American Journal of Human Genetics, 87, 813-9
American Journal of Human Genetics, 87(6), 813-819. CELL PRESS
American Journal of Human Genetics, 87, 6, pp. 813-9
American Journal of Human Genetics, 87, 813-9
Contains fulltext : 89067.pdf (Publisher’s version ) (Closed access) Autosomal-recessive cerebellar ataxias comprise a clinically and genetically heterogeneous group of neurodegenerative disorders. In contrast to their dominant counterparts, unrave
Autor:
Josep Antoni Ramos-Quiroga, Christian Jacob, Andrea Boreatti-Hümmer, Noèlia Fernàndez-Castillo, Mònica Bayés, C.C. Kan, Miguel Casas, Philip Asherson, Klaus-Peter Lesch, Cristina Sánchez-Mora, Monika Heine, Bru Cormand, Nuria Gómez-Barros, Helene Barone Halleland, Lambertus A. Kiemeney, Jan Haavik, Ole Bernt Fasmer, E.T. Landaas, Marta Ribasés, Martine Hoogman, Andreas Reif, Angelien Heister, Anne Halmøy, Per M. Knappskog, Rosa Bosch, Stephen V. Faraone, Alejandro Arias Vasquez, Jan K. Buitelaar, Barbara Franke, Jasmin Romanos, A. Marije Boonstra, Stefan Johansson, J. J. Sandra Kooij
Publikováno v:
Neuropsychopharmacology, 35, 656-664. Nature Publishing Group
Neuropsychopharmacology, 35, 656-64
Neuropsychopharmacology
Neuropsychopharmacology, 35, 3, pp. 656-64
Boonstra, A M, Franke, B, Vasquez, A A, Johansson, S, Hoogman, M, Romanos, J & Boreatti-Hümmer, A 2010, ' Multicenter Analysis of the SLC6A3/DAT1 VNTR Haplotype in Persistent ADHD Suggests Differential Involvement of the Gene in Childhood and Persistent ADHD ', Neuropsychopharmacology, vol. 35, pp. 656-664 . https://doi.org/10.1038/npp.2009.170
Neuropsychopharmacology, 35, 656-64
Neuropsychopharmacology
Neuropsychopharmacology, 35, 3, pp. 656-64
Boonstra, A M, Franke, B, Vasquez, A A, Johansson, S, Hoogman, M, Romanos, J & Boreatti-Hümmer, A 2010, ' Multicenter Analysis of the SLC6A3/DAT1 VNTR Haplotype in Persistent ADHD Suggests Differential Involvement of the Gene in Childhood and Persistent ADHD ', Neuropsychopharmacology, vol. 35, pp. 656-664 . https://doi.org/10.1038/npp.2009.170
Contains fulltext : 89288.pdf (Publisher’s version ) (Closed access) Attention deficit/hyperactivity disorder (ADHD) is one of the most common neuropsychiatric disorders with a worldwide prevalence around 4-5% in children and 1-4% in adults. Althou
Autor:
Jan K. Buitelaar, Barbara Franke, Huibert Burger, A. Marije Boonstra, Sita H. Vermeulen, Angelien Heister, J. J. Sandra Kooij
Publikováno v:
American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 147(2), 201-208. Wiley-Liss Inc.
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 201-8
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 2, pp. 201-8
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147(2), 201-208. Wiley-Liss Inc.
Kooij, J J S, Boonstra, A M, Vermeulen, S H, Heister, J G A M, Burger, H, Buitelaar, J K & Franke, B 2008, ' Response to methylphenidate in adults with ADHD is associated with a polymorphism in SLC6A3 (DAT1). ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 147, no. 2, pp. 201-208 . https://doi.org/10.1002/ajmg.b.30586
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 147B(2), 201-208. Wiley
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 201-8
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 2, pp. 201-8
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147(2), 201-208. Wiley-Liss Inc.
Kooij, J J S, Boonstra, A M, Vermeulen, S H, Heister, J G A M, Burger, H, Buitelaar, J K & Franke, B 2008, ' Response to methylphenidate in adults with ADHD is associated with a polymorphism in SLC6A3 (DAT1). ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 147, no. 2, pp. 201-208 . https://doi.org/10.1002/ajmg.b.30586
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 147B(2), 201-208. Wiley
Contains fulltext : 71149.pdf (Publisher’s version ) (Closed access) In this pharmacogenetic study in adults with ADHD (n = 42), a stratified analysis was performed of the association between response to methylphenidate (MPH), assessed under double
Autor:
Barbara Franke, Jan K. Buitelaar, A. Marije Boonstra, J. J. Sandra Kooij, Joseph A. Sergeant, Jaap Oosterlaan, J.G.A.M. Angelien Heister
Publikováno v:
American journal of medical genetics. Part B, Neuropsychiatric genetics, 147B(3), 397-402. Wiley-Liss Inc.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B(3), 397-402. Wiley-Liss Inc.
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147, 3, pp. 397-402
Boonstra, A M, Kooij, S J J, Buitelaar, J, Oosterlaan, J, Sergeant, J A, Heister, J G A M & Franke, B 2008, ' An exploratory study of the relationship between four candidate genes and neurocognitive performance in adult ADHD ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 147B, no. 3, pp. 397-402 . https://doi.org/10.1002/ajmg.b.30595
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147, 397-402
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B(3), 397-402. Wiley-Liss Inc.
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147, 3, pp. 397-402
Boonstra, A M, Kooij, S J J, Buitelaar, J, Oosterlaan, J, Sergeant, J A, Heister, J G A M & Franke, B 2008, ' An exploratory study of the relationship between four candidate genes and neurocognitive performance in adult ADHD ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 147B, no. 3, pp. 397-402 . https://doi.org/10.1002/ajmg.b.30595
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147, 397-402
Contains fulltext : 69754.pdf (Publisher’s version ) (Closed access) Since neurocognitive performance is a possible endophenotype for Attention Deficit Hyperactivity Disorder (ADHD) we explored the relationship between four genetic polymorphisms an
Autor:
Carolien G.F. de Kovel, Frans A. Hol, Han G. Brunner, Anton H. Naber, Judith J H T Willemen, Angelien Heister, Dirk J. de Jong, Barbara Franke
Publikováno v:
European Journal of Human Genetics, 11, 884-7
European Journal of Human Genetics, 11, 11, pp. 884-7
European Journal of Human Genetics, 11, 11, pp. 884-7
Item does not contain fulltext Linkage studies have identified the inflammatory bowel disease (IBD)1 locus on chromosome 16 and the IBD2 locus on chromosome 12 to be involved in Crohn's disease. NOD2/CARD15 was identified as the gene of interest with
Autor:
Susanne T. de Bot, Bart P.C. van de Warrenburg, Angelien Heister, Erik-Jan Kamsteeg, Hubertus P. H. Kremer, Marsha Voorendt, Aad Verrips, Hans Scheffer, Wendy Buijsman, Sascha Vermeer
Publikováno v:
Journal of Neurology, 260, 7, pp. 1765-9
Journal of Neurology, 260, 1765-9
Journal of Neurology; Vol 260
Journal of Neurology, 260(7), 1765-1769. SPRINGER HEIDELBERG
Journal of Neurology, 260, 1765-9
Journal of Neurology; Vol 260
Journal of Neurology, 260(7), 1765-1769. SPRINGER HEIDELBERG
Item does not contain fulltext SPG8 is a rare autosomal dominant hereditary spastic paraplegia (AD-HSP), with only six SPG8 families described so far. Our purpose was to screen for KIAA0196 (SPG8) mutations in AD-HSP patients and to investigate their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::539b5c5a6baba478d5a76c54957aad03
https://hdl.handle.net/2066/144002
https://hdl.handle.net/2066/144002
Publikováno v:
Journal of General Virology. 77:2515-2521
Human aminopeptidase N (hAPN or CD13) and porcine aminopeptidase N (pAPN) are functional receptors for human coronavirus (HCV) 229E and porcine transmissible gastroenteritis virus (TGEV), respectively. However, hAPN cannot function as a receptor for