American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 1552-4841

Journal

  1. 2020
  2. Smit, D. J. A., Cath, D., Zilhao, N. R., Ip, H. F., Denys, D., den Braber, A., de Geus, E. J. C., Verweij, K. J. H., Hottenga, J-J., & Boomsma, D. I. (2020). Genetic meta-analysis of obsessive-compulsive disorder and self-report compulsive symptoms. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 183(4), 208-216. https://doi.org/10.1002/ajmg.b.32777
  3. 2019
  4. 2018
  5. Quarrell, O. W., Clarke, A. J., Compton, C., de Die-Smulders, C. E. M., Fryer, A., Jenkins, S., Lahiri, N., MacLeod, R., Miedzybrodzka, Z., Morrison, P. J., Musgrave, H., O'Driscoll, M., Strong, M., van Belzen, M. J., Vermeer, S., Verschuuren-Bemelmans, C. C., & Bijlsma, E. K. (2018). Predictive testing of minors for Huntington's disease: The UK and Netherlands experiences. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 177(1), 35-39. https://doi.org/10.1002/ajmg.b.32582
  6. 2017
  7. Lester, K. J., Coleman, J. R. I., Roberts, S., Keers, R., Breen, G., Bogels, S., Creswell, C., Hudson, J. L., McKinnon, A., Nauta, M., Rapee, R. M., Schneider, S., Silverman, W. K., Thastum, M., Waite, P., Wergeland, G. J. H., & Eley, T. C. (2017). Genetic variation in the endocannabinoid system and response to Cognitive Behavior Therapy for child anxiety disorders. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 174(2), 144-155. https://doi.org/10.1002/ajmg.b.32467
  8. 2016
  9. Malki, K., Du Rietz, E., Crusio, W. E., Pain, O., Paya-Cano, J., Karadaghi, R. L., Sluyter, F., Boer, de, S. F., Sandnabba, K., Schalkwyk, L. C., Asherson, P., & Tosto, M. G. (2016). Transcriptome analysis of genes and gene networks involved in aggressive behavior in mouse and zebrafish. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 171(6), 827-838. https://doi.org/10.1002/ajmg.b.32451
  10. Pappa, I., St Pourcain, B., Benke, K., Cavadino, A., Hakulinen, C., Nivard, M. G., Nolte, I. M., Tiesler, C. M. T., Bakermans-Kranenburg, M. J., Davies, G. E., Evans, D. M., Geoffroy, M-C., Grallert, H., Groen-Blokhuis, M. M., Hudziak, J. J., Kemp, J. P., Keltikangas-Jarvinen, L., McMahon, G., Mileva-Seitz, V. R., ... Tiemeier, H. (2016). A Genome-Wide Approach to Children's Aggressive Behavior: The EAGLE consortium. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 171(5), 562-572. https://doi.org/10.1002/ajmg.b.32333
  11. Malki, K., Tosto, M. G., Pain, O., Sluyter, F., Mineur, Y. S., Crusio, W. E., de Boer, S., Sandnabba, K. N., Kesserwani, J., Robinson, E., Schalkwyk, L. C., & Asherson, P. (2016). Comparative mRNA analysis of behavioral and genetic mouse models of aggression. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 171(3), 427-436. https://doi.org/10.1002/ajmg.b.32424
  12. 2015
  13. Thissen, A. J. A. M., Bralten, J., Rommelse, N. N. J., Arias-Vasquez, A., Greven, C. U., Heslenfeld, D., Luman, M., Oosterlaan, J., Hoekstra, P. J., Hartman, C., Franke, B., & Buitelaar, J. K. (2015). The role of age in association analyses of ADHD and related neurocognitive functioning: A proof of concept for dopaminergic and serotonergic genes. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 168(6), 471-479. https://doi.org/10.1002/ajmg.b.32290
  14. 2014
  15. Morris, J. K., Garne, E., Wellesley, D., Addor, M-C., Arriola, L., Barisic, I., Beres, J., Bianchi, F., Budd, J., Dias, C. M., Gatt, M., Klungsoyr, K., Khoshnood, B., Latos-Bielenska, A., Mullaney, C., Nelen, V., Neville, A. J., O'Mahony, M., Queisser-Luft, A., ... Dolk, H. (2014). Major Congenital Anomalies in Babies Born With Down Syndrome: A EUROCAT Population-Based Registry Study. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 164A(12), 2979-2986. https://doi.org/10.1002/ajmg.a.36780
  16. Rump, P., de Leeuw, N., van Essen, A. J., Verschuuren - Bemelmans, C. C., Veenstra-Knol, H. E., Swinkels, M. E. M., Oostdijk, W., Ruivenkamp, C., Reardon, W., de Munnik, S., Ruiter, M., Frumkin, A., Lev, D., Evers, C., Sikkema-Raddatz, B., Dijkhuizen, T., & van Ravenswaaij-Arts, C. M. (2014). Central 22q11.2 Deletions. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 164(11), 2707-2723. https://doi.org/10.1002/ajmg.a.36711
  17. de Zeeuw, E. L., van Beijsterveldt, C. E. M., Glasner, T. J., Bartels, M., Ehli, E. A., Davies, G. E., Hudziak, J. J., Rietveld, C. A., Groen-Blokhuis, M. M., Hottenga, J. J., de Geus, E. J. C., Boomsma, D. I., & Social Science Genetic Assotiation Consortium (2014). Polygenic scores associated with educational attainment in adults predict educational achievement and ADHD symptoms in children. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 165(6), 510-520. https://doi.org/10.1002/ajmg.b.32254
  18. 2013
  19. Bena, F., Bruno, D. L., Eriksson, M., van Ravenswaaij-Arts, C., Stark, Z., Dijkhuizen, T., Gerkes, E., Gimelli, S., Ganesamoorthy, D., Thuresson, A. C., Labalme, A., Till, M., Bilan, F., Pasquier, L., Kitzis, A., Dubourgm, C., Rossi, M., Bottani, A., Gagnebin, M., ... Schoumans, J. (2013). Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 162B(4), 388-403. https://doi.org/10.1002/ajmg.b.32148
  20. 2012
  21. Luciano, M., Lopez, L. M., de Moor, M. H. M., Harris, S. E., Davies, G., Nutile, T., Krueger, R. F., Esko, T., Schlessinger, D., Toshiko, T., Derringer, J. L., Realo, A., Hansell, N. K., Pergadia, M. L., Pesonen, A-K., Sanna, S., Terracciano, A., Madden, P. A. F., Penninx, B., ... Deary, I. J. (2012). Longevity candidate genes and their association with personality traits in the elderly. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 159B(2), 192-200. https://doi.org/10.1002/ajmg.b.32013
  22. 2011
  23. Tian, Y., Liao, I. H., Zhan, X., Gunther, J. R., Ander, B. P., Liu, D., Lit, L., Jickling, G. C., Corbett, B. A., Bos-Veneman, N. G. P., Hoekstra, P. J., & Sharp, F. R. (2011). Exon Expression and Alternatively Spliced Genes in Tourette Syndrome. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 156B(1), 72-78. https://doi.org/10.1002/ajmg.b.31140
  24. 2010
  25. van Munster, B. C., de Rooij, S. E. J. A., Yazdanpanah, M., Tienari, P. J., Pitkala, K. H., Osse, R. J., Adamis, D., Smit, O., van der Steen, M. S., van Houten, M., Rahkonen, T., Sulkava, R., Laurila, J. V., Strandberg, T. E., Tulen, J. H. M., Zwang, L., MacDonald, A. J. D., Treloar, A., Sijbrands, E. J. G., ... Korevaar, J. C. (2010). The Association of the Dopamine Transporter Gene and the Dopamine Receptor 2 Gene With Delirium, a Meta-Analysis. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 153B(2), 648-655. https://doi.org/10.1002/ajmg.b.31034
  26. Katerberg, H., Cath, D. C., Denys, D. A. J. P., Heutink, P., Polman, A., van Nieuwerburgh, F. C. W., Deforce, D. L. D., Bochdanovits, Z., van Balkom, A. J. L. M., & den Boer, J. A. (2010). The Role of the COMT Val(158)Met Polymorphism in the Phenotypic Expression of Obsessive-Compulsive Disorder. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 153B(1), 167-176. https://doi.org/10.1002/ajmg.b.30971
  27. 2009
  28. Katerberg, H., Lochner, C., Cath, D. C., de Jonge, P., Bochdanovits, Z., Moolman-Smook, J. C., Hemmings, S. M. J., Carey, P. D., Stein, D. J., Sondervan, D., den Boer, J. A., van Balkom, A. J. L. M., Polman, A., & Heutink, P. (2009). The role of the brain-derived neurotrophic factor (BDNF) val66met variant in the phenotypic expression of obsessive-compulsive disorder (OCD). American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 150B(8), 1050-1062. https://doi.org/10.1002/ajmg.b.30930
  29. 2008
  30. Meulenkamp, T. M., Tibben, A., Mollema, E. D., Van Langen, I. M., Wiegman, A., De Wert, G. M., De Beaufort, I. D., Wilde, A. A. M., & Smets, E. M. A. (2008). Predictive genetic testing for cardiovascular diseases: Impact on carrier children. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 146(24), 3136-3146. https://doi.org/10.1002/ajmg.a.32592
  31. Chen, W., Zhou, K., Sham, P., Franke, B., Kuntsi, J., Campbell, D., Fleischman, K., Knight, J., Andreou, P., Arnold, R., Altink, M., Boer, F., Boholst, M. J., Buschgens, C., Butler, L., Christiansen, H., Fliers, E., Howe-Forbes, R., Gabriels, I., ... Asherson, P. (2008). DSM-IV Combined Type ADHD Shows Familial Association With Sibling Trait Scores: A Sampling Strategy For QTL Linkage. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 147B(8), 1450-1460. https://doi.org/10.1002/ajmg.b.30672
  32. Zhou, K., Dempfle, A., Arcos-Burgos, M., Bakker, S. C., Banaschewski, T., Biederman, J., Buitelaar, J., Castellanos, F. X., Doyle, A., Ebstein, R. P., Ekholm, J., Forabosco, P., Franke, B., Freitag, C., Friedel, S., Gill, M., Hebebrand, J., Hinney, A., Jacob, C., ... Asherson, P. (2008). Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 147B(8), 1392-8. https://doi.org/10.1002/ajmg.b.30878
  33. Rosa, A., Picchioni, M. M., Kalidindi, S., Loat, C. S., Knight, J., Toulopoulou, T., Vonk, R., van der Schot, A. C., Nolen, W., Kahn, R. S., McGuffin, P., Murray, R. M., & Craig, I. W. (2008). Differential methylation of the X-chromosome is a possible source of discordance for bipolar disorder female monozygotic twins. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 147B(4), 459-462. https://doi.org/10.1002/ajmg.b.30616
  34. 2007
  35. 2005
  36. Hoogendoorn, M. L. C., Bakker, S. C., Schnack, H. G., Selten, J-P. C., Otten, H. G., Verduijn, W., van der Heijden, F. M. M. A., Pearson, P. L., Kahn, R. S., & Sinke, R. J. (2005). No association between 12 dopaminergic genes and schizophrenia in a large Dutch sample. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 134B(1), 6-9. https://doi.org/10.1002/ajmg.b.30147
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