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Items where Author is "Franke, B."

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Number of items: 16.

2017

Naaijen, J. and Bralten, J. and Poelmans, G. and Image Consortium, and Glennon, J. C. and Franke, B. and Buitelaar, J. K.. (2017) Glutamatergic and GABAergic gene sets in attention-deficit/hyperactivity disorder: association to overlapping traits in ADHD and autism. Translational Psychiatry, 7 (1). e999.

2016

Zayats, T. and Jacobsen, K. K. and Kleppe, R. and Jacob, C. P. and Kittel-Schneider, S. and Ribases, M. and Ramos-Quiroga, J. A. and Richarte, V. and Casas, M. and Mota, N. R. and Grevet, E. H. and Klein, M. and Corominas, J. and Bralten, J. and Galesloot, T. and Vasquez, A. A. and Herms, S. and Forstner, A. J. and Larsson, H. and Breen, G. and Asherson, P. and Gross-Lesch, S. and Lesch, K. P. and Cichon, S. and Gabrielsen, M. B. and Holmen, O. L. and Bau, C. H. and Buitelaar, J. and Kiemeney, L. and Faraone, S. V. and Cormand, B. and Franke, B. and Reif, A. and Haavik, J. and Johansson, S.. (2016) Exome chip analyses in adult attention deficit hyperactivity disorder. Translational Psychiatry, 6 (10). e923.

Adams, H. H. and Hibar, D. P. and Chouraki, V. and Stein, J. L. and Nyquist, P. A. and Renteria, M. E. and Trompet, S. and Arias-Vasquez, A. and Seshadri, S. and Desrivieres, S. and Beecham, A. H. and Jahanshad, N. and Wittfeld, K. and Van der Lee, S. J. and Abramovic, L. and Alhusaini, S. and Amin, N. and Andersson, M. and Arfanakis, K. and Aribisala, B. S. and Armstrong, N. J. and Athanasiu, L. and Axelsson, T. and Beiser, A. and Bernard, M. and Bis, J. C. and Blanken, L. M. and Blanton, S. H. and Bohlken, M. M. and Boks, M. P. and Bralten, J. and Brickman, A. M. and Carmichael, O. and Chakravarty, M. M. and Chauhan, G. and Chen, Q. and Ching, C. R. and Cuellar-Partida, G. and Braber, A. D. and Doan, N. T. and Ehrlich, S. and Filippi, I. and Ge, T. and Giddaluru, S. and Goldman, A. L. and Gottesman, R. F. and Greven, C. U. and Grimm, O. and Griswold, M. E. and Guadalupe, T. and Hass, J. and Haukvik, U. K. and Hilal, S. and Hofer, E. and Hoehn, D. and Holmes, A. J. and Hoogman, M. and Janowitz, D. and Jia, T. and Kasperaviciute, D. and Kim, S. and Klein, M. and Kraemer, B. and Lee, P. H. and Liao, J. and Liewald, D. C. and Lopez, L. M. and Luciano, M. and Macare, C. and Marquand, A. and Matarin, M. and Mather, K. A. and Mattheisen, M. and Mazoyer, B. and McKay, D. R. and McWhirter, R. and Milaneschi, Y. and Mirza-Schreiber, N. and Muetzel, R. L. and Maniega, S. M. and Nho, K. and Nugent, A. C. and Loohuis, L. M. and Oosterlaan, J. and Papmeyer, M. and Pappa, I. and Pirpamer, L. and Pudas, S. and Putz, B. and Rajan, K. B. and Ramasamy, A. and Richards, J. S. and Risacher, S. L. and Roiz-Santianez, R. and Rommelse, N. and Rose, E. J. and Royle, N. A. and Rundek, T. and Samann, P. G. and Satizabal, C. L. and Schmaal, L. and Schork, A. J. and Shen, L. and Shin, J. and Shumskaya, E. and Smith, A. V. and Sprooten, E. and Strike, L. T. and Teumer, A. and Thomson, R. and Tordesillas-Gutierrez, D. and Toro, R. and Trabzuni, D. and Vaidya, D. and Van der Grond, J. and Van der Meer, D. and Van Donkelaar, M. M. and Van Eijk, K. R. and Van Erp, T. G. and Van Rooij, D. and Walton, E. and Westlye, L. T. and Whelan, C. D. and Windham, B. G. and Winkler, A. M. and Woldehawariat, G. and Wolf, C. and Wolfers, T. and Xu, B. and Yanek, L. R. and Yang, J. and Zijdenbos, A. and Zwiers, M. P. and Agartz, I. and Aggarwal, N. T. and Almasy, L. and Ames, D. and Amouyel, P. and Andreassen, O. A. and Arepalli, S. and Assareh, A. A. and Barral, S. and Bastin, M. E. and Becker, D. M. and Becker, J. T. and Bennett, D. A. and Blangero, J. and van Bokhoven, H. and Boomsma, D. I. and Brodaty, H. and Brouwer, R. M. and Brunner, H. G. and Buckner, R. L. and Buitelaar, J. K. and Bulayeva, K. B. and Cahn, W. and Calhoun, V. D. and Cannon, D. M. and Cavalleri, G. L. and Chen, C. and Cheng, C. Y. and Cichon, S. and Cookson, M. R. and Corvin, A. and Crespo-Facorro, B. and Curran, J. E. and Czisch, M. and Dale, A. M. and Davies, G. E. and De Geus, E. J. and De Jager, P. L. and de Zubicaray, G. I. and Delanty, N. and Depondt, C. and DeStefano, A. L. and Dillman, A. and Djurovic, S. and Donohoe, G. and Drevets, W. C. and Duggirala, R. and Dyer, T. D. and Erk, S. and Espeseth, T. and Evans, D. A. and Fedko, I. O. and Fernandez, G. and Ferrucci, L. and Fisher, S. E. and Fleischman, D. A. and Ford, I. and Foroud, T. M. and Fox, P. T. and Francks, C. and Fukunaga, M. and Gibbs, J. R. and Glahn, D. C. and Gollub, R. L. and Goring, H. H. and Grabe, H. J. and Green, R. C. and Gruber, O. and Gudnason, V. and Guelfi, S. and Hansell, N. K. and Hardy, J. and Hartman, C. A. and Hashimoto, R. and Hegenscheid, K. and Heinz, A. and Le Hellard, S. and Hernandez, D. G. and Heslenfeld, D. J. and Ho, B. C. and Hoekstra, P. J. and Hoffmann, W. and Hofman, A. and Holsboer, F. and Homuth, G. and Hosten, N. and Hottenga, J. J. and Pol, H. E. and Ikeda, M. and Ikram, M. K. and Jack, C. R. and Jr., and Jenkinson, M. and Johnson, R. and Jonsson, E. G. and Jukema, J. W. and Kahn, R. S. and Kanai, R. and Kloszewska, I. and Knopman, D. S. and Kochunov, P. and Kwok, J. B. and Lawrie, S. M. and Lemaitre, H. and Liu, X. and Longo, D. L. and Longstreth, W. T. and Jr., and Lopez, O. L. and Lovestone, S. and Martinez, O. and Martinot, J. L. and Mattay, V. S. and McDonald, C. and McIntosh, A. M. and McMahon, K. L. and McMahon, F. J. and Mecocci, P. and Melle, I. and Meyer-Lindenberg, A. and Mohnke, S. and Montgomery, G. W. and Morris, D. W. and Mosley, T. H. and Muhleisen, T. W. and Muller-Myhsok, B. and Nalls, M. A. and Nauck, M. and Nichols, T. E. and Niessen, W. J. and Nothen, M. M. and Nyberg, L. and Ohi, K. and Olvera, R. L. and Ophoff, R. A. and Pandolfo, M. and Paus, T. and Pausova, Z. and Penninx, B. W. and Pike, G. B. and Potkin, S. G. and Psaty, B. M. and Reppermund, S. and Rietschel, M. and Roffman, J. L. and Romanczuk-Seiferth, N. and Rotter, J. I. and Ryten, M. and Sacco, R. L. and Sachdev, P. S. and Saykin, A. J. and Schmidt, R. and Schofield, P. R. and Sigurdsson, S. and Simmons, A. and Singleton, A. and Sisodiya, S. M. and Smith, C. and Smoller, J. W. and Soininen, H. and Srikanth, V. and Steen, V. M. and Stott, D. J. and Sussmann, J. E. and Thalamuthu, A. and Tiemeier, H. and Toga, A. W. and Traynor, B. J. and Troncoso, J. and Turner, J. A. and Tzourio, C. and Uitterlinden, A. G. and Hernandez, M. C. and Van der Brug, M. and Van der Lugt, A. and Van der Wee, N. J. and Van Duijn, C. M. and Van Haren, N. E. and Van, T. Ent D. and Van Tol, M. J. and Vardarajan, B. N. and Veltman, D. J. and Vernooij, M. W. and Volzke, H. and Walter, H. and Wardlaw, J. M. and Wassink, T. H. and Weale, M. E. and Weinberger, D. R. and Weiner, M. W. and Wen, W. and Westman, E. and White, T. and Wong, T. Y. and Wright, C. B. and Zielke, H. R. and Zonderman, A. B. and Deary, I. J. and DeCarli, C. and Schmidt, H. and Martin, N. G. and De Craen, A. J. and Wright, M. J. and Launer, L. J. and Schumann, G. and Fornage, M. and Franke, B. and Debette, S. and Medland, S. E. and Ikram, M. A. and Thompson, P. M.. (2016) Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature Neuroscience, 19 (12). pp. 1569-1582.

2014

Li, M. and Luo, X.-J. and Rietschel, M. and Lewis, C. M. and Mattheisen, M. and Müller-Myhsok, B. and Jamain, S. and Leboyer, M. and Landén, M. and Thompson, P. M. and Cichon, S. and Nöthen, M. M. and Schulze, T. G. and Sullivan, P. F. and Bergen, S. E. and Donohoe, G. and Morris, D. W. and Hargreaves, A. and Gill, M. and Corvin, A. and Hultman, C. and Toga, A. W. and Shi, L. and Lin, Q. and Shi, H. and Gan, L. and Meyer-Lindenberg, A. and Czamara, D. and Henry, C. and Etain, B. and Bis, J. C. and Ikram, M. A. and Fornage, M. and Debette, S. and Launer, L. J. and Seshadri, S. and Erk, S. and Walter, H. and Heinz, A. and Bellivier, F. and Stein, J. L. and Medland, S. E. and Arias Vasquez, A. and Hibar, D. P. and Franke, B. and Martin, N. G. and Wright, M. J. and MooDS Bipolar Consortium, and Swedish Bipolar Study Group, and Alzheimer's Disease Neuroimaging Initiative, and Enigma Consortium, and Charge Consortium, and Su, B.. (2014) Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility. Molecular Psychiatry, 19 (4). pp. 452-461.

Steinberg, S. and de Jong, S. and Mattheisen, M. and Costas, J. and Demontis, D. and Jamain, S. and Pietiläinen, O. P. H. and Lin, K. and Papiol, S. and Huttenlocher, J. and Sigurdsson, E. and Vassos, E. and Giegling, I. and Breuer, R. and Fraser, G. and Walker, N. and Melle, I. and Djurovic, S. and Agartz, I. and Tuulio-Henriksson, A. and Suvisaari, J. and Lönnqvist, J. and Paunio, T. and Olsen, L. and Hansen, T. and Ingason, A. and Pirinen, M. and Strengman, E. and Group, and Hougaard, D. M. and Ørntoft, T. and Didriksen, M. and Hollegaard, M. V. and Nordentoft, M. and Abramova, L. and Kaleda, V. and Arrojo, M. and Sanjuán, J. and Arango, C. and Etain, B. and Bellivier, F. and Méary, A. and Schürhoff, F. and Szoke, A. and Ribolsi, M. and Magni, V. and Siracusano, A. and Sperling, S. and Rossner, M. and Christiansen, C. and Kiemeney, L. A. and Franke, B. and van den Berg, L. H. and Veldink, J. and Curran, S. and Bolton, P. and Poot, M. and Staal, W. and Rehnstrom, K. and Kilpinen, H. and Freitag, C. M. and Meyer, J. and Magnusson, P. and Saemundsen, E. and Martsenkovsky, I. and Bikshaieva, I. and Martsenkovska, I. and Vashchenko, O. and Raleva, M. and Paketchieva, K. and Stefanovski, B. and Durmishi, N. and Pejovic Milovancevic, M. and Lecic Tosevski, D. and Silagadze, T. and Naneishvili, N. and Mikeladze, N. and Surguladze, S. and Vincent, J. B. and Farmer, A. and Mitchell, P. B. and Wright, A. and Schofield, P. R. and Fullerton, J. M. and Montgomery, G. W. and Martin, N. G. and Rubino, I. A. and van Winkel, R. and Kenis, G. and De Hert, M. and Réthelyi, J. M. and Bitter, I. and Terenius, L. and Jönsson, E. G. and Bakker, S. and van Os, J. and Jablensky, A. and Leboyer, M. and Bramon, E. and Powell, J. and Murray, R. and Corvin, A. and Gill, M. and Morris, D. and O'Neill, F. A. and Kendler, K. and Riley, B. and Wellcome Trust Case Control Consortium, and Craddock, N. and Owen, M. J. and O'Donovan, M. C. and Thorsteinsdottir, U. and Kong, A. and Ehrenreich, H. and Carracedo, A. and Golimbet, V. and Andreassen, O. A. and Børglum, A. D. and Mors, O. and Mortensen, P. B. and Werge, T. and Ophoff, R. A. and Nöthen, M. M. and Rietschel, M. and Cichon, S. and Ruggeri, M. and Tosato, S. and Palotie, A. and St Clair, D. and Rujescu, D. and Collier, D. A. and Stefansson, H. and Stefansson, K.. (2014) Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry, 19 (1). pp. 108-114.

2013

Mota, N. R. and Bau, C. H. and Banaschewski, T. and Buitelaar, J. K. and Ebstein, R. P. and Franke, B. and Gill, M. and Kuntsi, J. and Manor, I. and Miranda, A. and Mulas, F. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. A. and Sonuga-Barke, E. J. and Steinhausen, H. -C. and Faraone, S. V. and Asherson, P.. (2013) Association between DRD2/DRD4 interaction and conduct disorder : A potential developmental pathway to alcohol dependence. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 162, H. 6. pp. 546-549.

Bralten, J. and Franke, B. and Waldman, ID. and Rommelse, N. and Hartman, C. and Asherson, P. and Banaschewski, T. and Ebstein, RP. and Gill, M. and Miranda, A. and Oades, RD. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Osterlaan, J. and Sonuga-Barke, EJ. and Steinhausen, H. -C. and Faraone, SV. and Buitelaar, J. and Arias-Vásquez, A.. (2013) Candidate genetic pathways for attention-deficit/hyperactivity disorder (ADHD) show association to hyperactive/impulsive symptoms in children with ADHD. Journal of the American Academy of Child and Adolescent Psychiatry, 52 (11). pp. 1204-1212.

Hamshere, M. L. and Langley, K. and Martin, J. and Agha, S. S. and Stergiakouli, E. and Anney, R. J. and Buitelaar, J. and Faraone, S. V. and Lesch, K. P. and Neale, B. M. and Franke, B. and Sonuga-Barke, E. and Asherson, P. and Merwood, A. and Kuntsi, J. and Medland, S. E. and Ripke, S. and Steinhausen, H. -C. and Freitag, C. and Reif, A. and Renner, T. J. and Romanos, M. and Romanos, J. and Warnke, A. and Meyer, J. and Palmason, H. and Vasquez, A. A. and Lambregts-Rommelse, N. and Roeyers, H. and Biederman, J. and Doyle, A. E. and Hakonarson, H. and Rothenberger, A. and Banaschewski, T. and Oades, R. D. and McGough, J. J. and Kent, L. and Williams, N. and Owen, M. J. and Holmans, P. and O'Donovan, M. C. and Thapar, A.. (2013) High loading of polygenic risk for ADHD in children comorbid for aggression. American Journal of Psychiatry, Vol. 170, H. 8. pp. 909-916.

2009

Hawi, Z. and Kent, L. and Hill, M. and Anney, R. J. L. and Brookes, K. J. and Barry, E. and Franke, B. and Banaschewski, T. and Buitelaar, J. and Ebstein, R. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Sonuga-Barke, E. and Steinhausen, H.-C. and Faraone, S. V. and Asherson, P. and Gill, M.. (2009) ADHD and DAT1: further evidence of paternal over-transmission of risk alleles and haplotype. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 150B, H. 1. pp. 97-102.

2008

Asherson, P. and Zhou, K. and Anney, R. J. L. and Franke, B. and Buitelaar, J. and Ebstein, R. and Gill, M. and Altink, M. and Arnold, R. and Boer, F. and Brookes, K. and Buschgens, C. and Butler, L. and Cambell, D. and Chen, W. and Christiansen, H. and Feldman, L. and Fleischman, K. and Fliers, E. and Howe-Forbes, R. and Goldfarb, A. and Heise, A. and Gabriëls, I. and Johansson, L. and Lubetzki, I. and Marco, R. and Medad, S. and Minderaa, R. and Mulas, F. and Müller, U. and Mulligan, A. and Neale, B. and Rijsdijk, F. and Rabin, K. and Rommelse, N. and Sethna, V. and Sorohan, J. and Uebel, H. and Psychogiou, L. and Weeks, A. and Barrett, R. and Xu, X. and Banaschewski, T. and Sonuga-Barke, E. and Eisenberg, J. and Manor, I. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Steinhausen, H.-C. and Taylor, E. and Thompson, M. and Faraone, S. V.. (2008) A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16. Molecular Psychiatry, 13 (5). pp. 514-521.

Brookes, K. J. and Xu, X. and Anney, R. and Franke, B. and Zhou, K. and Chen, Wai and Banaschewski, T. and Buitelaar, J. and Ebstein, R. and Eisenberg, J. and Gill, M. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Sonuga-Barke, E. and Steinhausen, H.-C. and Taylor, E. and Faraone, S. V. and Asherson, P.. (2008) Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: evidence for allelic heterogeneity. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 147B, H. 8. pp. 1519-1523.

Christiansen, H. and Chen, W. and Oades, R. D. and Asherson, P. and Taylor, E. A. and Lasky-Su, J. and Zhou, K. and Banaschewski, T. and Buschgens, C. and Franke, B. and Gabriels, I. and Manor, I. and Marco, R. and Müller, U. C. and Mulligan, A. and Psychogiou, L. and Rommelse, N. N. J. and Uebel, H. and Buitelaar, J. and Ebstein, R. P. and Eisenberg, J. and Gill, M. and Miranda, A. and Mulas, F. and Roeyers, H. and Rothenberger, A. and Sergeant, J. A. and Sonuga-Barke, E. J. S. and Steinhausen, H.-C. and Thompson, M. and Faraone, S. V.. (2008) Co-transmission of conduct problems with attention-deficit/hyperactivity disorder : familial evidence for a distinct disorder. Journal of neural transmission, Vol. 115, No. 2. pp. 163-175.

Brookes, K. J. and Neale, B. and Xu, X. and Thapar, A. and Gill, M. and Langley, K. and Hawi, Z. and Mill, J. and Taylor, E. and Franke, B. and Chen, W. and Ebstein, R. and Buitelaar, J. and Banaschewski, T. and Sonuga-Barke, E. and Eisenberg, J. and Manor, I. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Steinhausen, H. C. and Faraone, S. V. and Asherson, P.. (2008) Differential dopamine receptor D4 allele association with ADHD dependent of proband season of birth. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 147B (1). pp. 94-99.

Xu, X. and Duman, E. A. and Aysimi, E. and Anney, R. and Brookes, K. and Franke, B. and Zhou, K. and Buschgens, C. and Chen, W. and Christiansen, H. and Eisenberg, J. and Gabriëls, I. and Manor, I. and Marco, R. and Müller, U. C. and Mulligan, A. and Rommelse, N. and Thompson, M. and Uebel, H. and Banaschewski, T. and Buitelaar, J. and Ebstein, R. and Gill, M. and Miranda, A. and Mulas, F. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Sonuga-Barke, E. and Steinhausen, H.-C. and Taylor, E. and Faraone, S. V. and Asherson, P.. (2008) No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 147B, H. 7. pp. 1306-1309.

Xu, X. and Hawi, Z. and Brookes, K. J. and Anney, R. and Bellgrove, M. and Franke, B. and Barry, E. and Chen, W. and Kuntsi, J. and Banaschewski, T. and Buitelaar, J. and Ebstein, R. and Fitzgerald, M. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Sonuga-Barke, E. and Steinhausen, H.-C. and Faraone, S. V. and Gill, M. and Asherson, P.. (2008) Replication of a rare protective allele in the noradrenaline transporter gene and ADHD. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 147B, H. 8. pp. 1564-1567.

2006

Brookes, K. and Xu, X. and Chen, W. and Zhou, K. and Neale, B. and Lowe, N. and Anney, R. and Aneey, R. and Franke, B. and Gill, M. and Ebstein, R. and Buitelaar, J. and Sham, P. and Campbell, D. and Knight, J. and Andreou, P. and Altink, M. and Arnold, R. and Boer, F. and Buschgens, C. and Butler, L. and Christiansen, H. and Feldman, L. and Fleischman, K. and Fliers, E. and Howe-Forbes, R. and Goldfarb, A. and Heise, A. and Gabriëls, I. and Korn-Lubetzki, I. and Johansson, L. and Marco, R. and Medad, S. and Minderaa, R. and Mulas, F. and Müller, U. and Mulligan, A. and Rabin, K. and Rommelse, N. and Sethna, V. and Sorohan, J. and Uebel, H. and Psychogiou, L. and Weeks, A. and Barrett, R. and Craig, I. and Banaschewski, T. and Sonuga-Barke, E. and Eisenberg, J. and Kuntsi, J. and Manor, I. and McGuffin, P. and Miranda, A. and Oades, R. D. and Plomin, R. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Steinhausen, H.-C. and Taylor, E. and Thompson, M. and Faraone, S. V. and Asherson, P.. (2006) The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes. Molecular Psychiatry, 11 (10). pp. 934-953.

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