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

Tidskrift

Fler filtreringsmöjligheter
  1. 2019
  2. 2018
  3. Familial transmission of externalizing syndromes in extended Swedish families

    Kenneth S. Kendler, Ohlsson, H., Jan Sundquist & Kristina Sundquist, 2018 apr 1, I : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 177, 3, s. 308-318 11 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  4. The involvement of the canonical Wnt-signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism: Association study and meta-analysis

    Grünblatt, E., Nemoda, Z., Werling, A. M., Roth, A., Angyal, N., Tarnok, Z., Hauke Thomsen, Peters, T., Hinney, A., Hebebrand, J., Lesch, K. P., Romanos, M. & Walitza, S., 2018 jan 1, (Accepted/In press) I : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  5. 2017
  6. 2010
  7. Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: large-scale collaborative study

    Evangelou, E., Maraganore, D. M., Annesi, G., Brighina, L., Brice, A., Elbaz, A., Ferrarese, C., Hadjigeorgiou, G. M., Krueger, R., Lambert, J-C., Lesage, S., Markopoulou, K., Mellick, G. D., Meeus, B., Pedersen, N. L., Quattrone, A., Van Broeckhoven, C., Sharma, M., Silburn, P. A., Tan, E-K. & 3 andraWirdefeldt, K., Ioannidis, J. P. A. & Genetic Epidemiology of Parkinson's Disease (GEOPD) Consortium, 2010 jan 5, I : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 153B, 1, s. 220-8 9 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  8. 2008
  9. Analysis of X chromosome inactivation in autism spectrum disorders

    Gong, Z., Bacchelli, E., Blasi, F., Toma, C., Betancur, C., Chaste, P., Delorme, R., Durand, C. M., Fauchereau, F., Goubran Botros, H., Leboyer, M., Mouren-Simeoni, M-C., Nygren, G., Anckarsäter, H., Råstam, M., Gillberg, C., Gillberg, C., Moreno-De-Luca, D., Carone, S., Nummela, I. & 6 andraRossi, M., Battaglia, A., (MGSAC), T. I. M. G. S. O. A. C., Jarvela, I., Maestrini, E. & Bourgeron, T., 2008, I : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 147B, 6, s. 830-835

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  10. Association of complement factor HY402H gene polymorphism with Alzheimer's disease

    Zetterberg, M., Landgren, S., Andersson, M. E., Palmer, M. S., Gustafson, D. R., Skoog, I., Lennart Minthon, Thelle, D. S., Wallin, A., Bogdanovic, N., Andreasen, N., Blennow, K. & Zetterberg, H., 2008, I : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 147B, 6, s. 720-726

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  11. Autism spectrum conditons in myotonic dystrophy type 1: A study on 57 individuals with congenital and childhood forms

    Ekstrom, A-B., Hakenas-Plate, L., Samuelsson, L., Tulinius, M. & Wentz, E., 2008, I : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 147B, 6, s. 918-926

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  12. 2007
  13. Association of adenomatous polyposis coli (APC) gene polymorphisms with autism spectrum disorder (ASD)

    Zhou, X-L., Giacobini, M., Anderlid, B-M., Anckarsäter, H., Omrani, D., Gillberg, C., Nordenskjold, M. & Lindblom, A., 2007, I : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 144B, 3, s. 351-354

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  14. Mutation screening of the ARX gene in patients with autism

    Chaste, P., Nygren, G., Anckarsäter, H., Maria Råstam, Coleman, M., Leboyer, M., Gillberg, C. & Betancur, C., 2007, I : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 144, 2, s. 228-230

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  15. Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly

    Buxbaum, J. D., Cai, G., Chaste, P., Nygren, G., Goldsmith, J., Reichert, J., Anckarsäter, H., Maria Råstam, Smith, C. J., Silverman, J. M., Hollander, E., Leboyer, M., Gillberg, C., Verloes, A. & Betancur, C., 2007, I : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 144B, 4, s. 484-491

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  16. 2006
  17. Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders

    Durand, C. M., Kappeler, C., Betancur, C., Delorme, R., Quach, H., Goubran-Botros, H., Melke, J., Nygren, G., Chabane, N., Bellivier, F., Szoke, A., Schurhoff, F., Maria Råstam, Anckarsäter, H., Gillberg, C., Leboyer, M. & Bourgeron, T., 2006, I : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 141, 1, s. 67-70

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift