Researcher

van Amelsvoort, T.A.M.J.

Persoonlijk hoogleraar, H/MS

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  1. 2019
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    GROUP investigators, Genetic Risk Outcome Psychosis , van Rooijen, G., van Rooijen, M., Maat, A., Vermeulen, J. M., ... van Winkel, R. (2019). Longitudinal evidence for a relation between depressive symptoms and quality of life in schizophrenia using structural equation modeling. Schizophrenia Research, 208, 82-89. https://doi.org/10.1016/j.schres.2019.04.011
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    Swets, M., van Dijk, F. A., Schirmbeck, F., Peen, J., de Haan, L., Alizadeh, B. Z., ... van Winkel, R. (2019). Patterns of obsessive-compulsive symptoms and social functioning in schizophrenia; a replication study. Psychiatry Research, 271, 421-427. https://doi.org/10.1016/j.psychres.2018.11.071
  12. 2018
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    Int Brain Behavior Consortium, Zhao, Y., Guo, T., Fiksinski, A., Breetvelt, E., McDonald-McGinn, D. M., ... Morrow, B. E. (2018). Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects. American Journal of Medical Genetics Part A, 176(10), 2172-2181. https://doi.org/10.1002/ajmg.a.40359
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  24. 2017
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    Boot, E., Hollak, C. E. M., Huijbregts, S. C. J., Jahja, R., van Vliet, D., Nederveen, A. J., ... Booij, J. (2017). Cerebral dopamine deficiency, plasma monoamine alterations and neurocognitive deficits in adults with phenylketonuria. Psychological Medicine, 47(16), 2854-2865. https://doi.org/10.1017/S0033291717001398
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    Bassett, A. S., Lowther, C., Merico, D., Costain, G., Chow, E. W. C., van Amelsvoort, T., ... Int 22q11 2DS Brain Behav Conso (2017). Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome. American Journal of Psychiatry, 174(11), 1054-1063. https://doi.org/10.1176/appi.ajp.2017.16121417
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    Demaerel, W., Hestand, M. S., Vergaelen, E., Swillen, A., Lopez-Sanchez, M., Perez-Jurado, L. A., ... Vermeesch, J. R. (2017). Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements. American Journal of Human Genetics, 101(4), 616-622. https://doi.org/10.1016/j.ajhg.2017.09.002
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    Johnston, H. R., Chopra, P., Wingo, T. S., Patel, V., Epstein, M. P., Mulle, J. G., ... Cutler, D. J. (2017). PEMapper and PECaller provide a simplified approach to whole-genome sequencing. Proceedings of the National Academy of Sciences of the United States of America, 114(10), E1923-E1932. https://doi.org/10.1073/pnas.1618065114
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    Wang, Y., Zhang, Y., Liu, L., Cui, J., Wang, J., Shum, D. H. K., ... Chan, R. C. K. (2017). A Meta-Analysis of Working Memory Impairments in Autism Spectrum Disorders. Neuropsychology Review, 27(1), 46-61. https://doi.org/10.1007/s11065-016-9336-y
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  39. 2016
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    Nieman, D. H., Dragt, S., van Duin, E. D. A., Denneman, N., Overbeek, J. M., de Haan, L., ... Linszen, D. H. (2016). COMT Val(158)Met genotype and cannabis use in people with an At Risk Mental State for psychosis: Exploring Gene x Environment interactions. Schizophrenia Research, 174(1-3), 24-28. https://doi.org/10.1016/j.schres.2016.03.015
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    Verschure, D. O., Boot, E., van Amelsvoort, T. A., Booij, J., van Eck-Smit, B. L. F., Somsen, G. A., & Verberne, H. J. (2016). Cardiac sympathetic activity in 22q11.2 deletion syndrome. International Journal of Cardiology, 212, 346-351. https://doi.org/10.1016/j.ijcard.2016.03.185
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  53. 2015
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