Response to methylphenidate in adults with ADHD is associated with a polymorphism in SLC6A3 (DAT1)
Kooij, J. Sandra, Boonstra, A. Marije, Vermeulen, Sita H., Heister, Angelien G., Burger, Huibert, Buitelaar, Jan K., Franke, Barbara
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.03.2008)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.03.2008)
Get full text
Journal Article
Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHD
Franke, Barbara, Vasquez, Alejandro Arias, Johansson, Stefan, Hoogman, Martine, Romanos, Jasmin, Boreatti-Hümmer, Andrea, Heine, Monika, Jacob, Christian P, Lesch, Klaus-Peter, Casas, Miguel, Ribasés, Marta, Bosch, Rosa, Sánchez-Mora, Cristina, Gómez-Barros, Núria, Fernàndez-Castillo, Noèlia, Bayés, Mònica, Halmøy, Anne, Halleland, Helene, Landaas, Elisabeth T, Fasmer, Ole B, Knappskog, Per M, Heister, Angelien J G A M, Kiemeney, Lambertus A, Kooij, J J Sandra, Boonstra, A Marije, Kan, Cees C, Asherson, Philip, Faraone, Stephen V, Buitelaar, Jan K, Haavik, Jan, Cormand, Bru, Ramos-Quiroga, Josep Antoni, Reif, Andreas
Published in Neuropsychopharmacology (New York, N.Y.) (01.02.2010)
Published in Neuropsychopharmacology (New York, N.Y.) (01.02.2010)
Get full text
Journal Article
An exploratory study of the relationship between four candidate genes and neurocognitive performance in adult ADHD
Boonstra, A. Marije, Kooij, J.J. Sandra, Buitelaar, Jan K., Oosterlaan, Jaap, Sergeant, Joseph A., Heister, J.G.A.M. Angelien, Franke, Barbara
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.04.2008)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.04.2008)
Get full text
Journal Article
Meta-analysis of the DRD5 VNTR in persistent ADHD
Klein, Marieke, Berger, Stefanie, Hoogman, Martine, Dammers, Janneke, Makkinje, Remco, Heister, Angelien J.G.A.M, Galesloot, Tessel E, Kiemeney, Lambertus A.L.M, Weber, Heike, Kittel-Schneider, Sarah, Lesch, Klaus-Peter, Reif, Andreas, Ribasés, Marta, Ramos-Quiroga, Josep Antoni, Cormand, Bru, Zayats, Tetyana, Hegvik, Tor-Arne, Jacobsen, Kaya K, Johansson, Stefan, Haavik, Jan, Mota, Nina R, Bau, Claiton H.D, Grevet, Eugenio H, Doyle, Alysa, Faraone, Stephen V, Arias-Vásquez, Alejandro, Franke, Barbara
Published in European neuropsychopharmacology (01.09.2016)
Published in European neuropsychopharmacology (01.09.2016)
Get full text
Journal Article
MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation
Kalay, Ersan, Uzumcu, Abdullah, Krieger, Elmar, Çaylan, Refik, Uyguner, Oya, Ulubil-Emiroglu, Melike, Erdol, Hidayet, Kayserili, Hülya, Hafiz, Gunter, Başerer, Nermin, Heister, Angelien J.G.M., Hennies, Hans C., Nürnberg, Peter, Başaran, Seher, Brunner, Han G., Cremers, Cor W.R.J., Karaguzel, Ahmet, Wollnik, Bernd, Kremer, Hannie
Published in American journal of medical genetics. Part A (15.10.2007)
Published in American journal of medical genetics. Part A (15.10.2007)
Get full text
Journal Article
No evidence for involvement of IL-4R and CD11B from the IBD1 region and STAT6 in the IBD2 region in Crohn's disease
DE JONG, Dirk J, FRANKE, Barbara, NABER, Anton H. J, WILLEMEN, Judith J. H. T, HEISTER, Angelien J. G. A. M, BRUNNER, Han G, DE KOVEL, Carolien G. F, HOL, Frans A
Published in European journal of human genetics : EJHG (01.11.2003)
Published in European journal of human genetics : EJHG (01.11.2003)
Get full text
Journal Article
Multicenter Analysis of the SLC6A3/DATI VNTR Haplotype in Persistent ADHD Suggests Differential Involvement of the Gene in Childhood and Persistent ADHD
FRANKE, Barbara, ARIAS VASQUEZ, Alejandro, RIBASES, Marta, BOSCH, Rosa, SANCHEZ-MORA, Cristina, GOMEZ-BARROS, Núria, FERNANDEZ-CASTILLO, Noèlia, BAYES, Monica, HALMØY, Anne, HALLELAND, Helene, LANDAAS, Elisabeth T, FASMER, Ole B, JOHANSSON, Stefan, KNAPPSKOG, Per M, HEISTER, Angelien J. G. A. M, KIEMENEY, Lambertus A, SANDRA KOOIJ, J. J, BOONSTRA, A. Marije, KAN, Cees C, ASHERSON, Philip, FARAONE, Stephen V, BUITELAAR, Jan K, HAAVIK, Jan, HOOGMAN, Martine, CORMAND, Bru, RAMOS-QUIROGA, Josep Antoni, REIF, Andreas, ROMANOS, Jasmin, BOREATTI-HÜMMER, Andrea, HEINE, Monika, JACOB, Christian P, LESCH, Klaus-Peter, CASAS, Miguel
Published in Neuropsychopharmacology (New York, N.Y.) (2010)
Get full text
Published in Neuropsychopharmacology (New York, N.Y.) (2010)
Journal Article
Mutant Mitochondrial Elongation Factor G1 and Combined Oxidative Phosphorylation Deficiency
Coenen, Marieke J.H, Antonicka, Hana, Ugalde, Cristina, Sasarman, Florin, Rossi, Rainer, Heister, J.G.A.M. Angelien, Newbold, Robert F, Trijbels, Frans J.M.F, van den Heuvel, Lambert P, Shoubridge, Eric A, Smeitink, Jan A.M
Published in The New England journal of medicine (11.11.2004)
Published in The New England journal of medicine (11.11.2004)
Get full text
Journal Article
α-Thalassemia in The Netherlands : a heterogeneous spectrum of both deletions and point mutations
HARTEVELD, K. L, LOSEKOOT, M, HEISTER, A. J. G. A. M, VAN DER WIELEN, M, GIORDANO, P. C, BERNINI, L. F
Published in Human genetics (01.09.1997)
Published in Human genetics (01.09.1997)
Get full text
Journal Article