Publication
2023
- Chawner, S. J. et al. 2023. Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions. JCPP Advances 3 (2) e12162. (10.1002/jcv2.12162)
- Chawner, S. J. R. A. et al. 2023. Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions. Translational Psychiatry 13 7. (10.1038/s41398-022-02296-z)
2022
- Maihofer, A. X. et al., 2022. Rare copy number variation in posttraumatic stress disorder. Molecular Psychiatry 27 , pp.5062-5069. (10.1038/s41380-022-01776-4)
- Maihofer, A. X. et al., 2022. Enhancing discovery of genetic variants for PTSD through integration of quantitative phenotypes and trauma exposure information. Biological Psychiatry 91 (7), pp.626-636. (10.1016/j.biopsych.2021.09.020)
- Warne, N. et al. 2022. Collecting genetic samples and linked mental health data from adolescents in schools: protocol co-production and a mixed-methods pilot of feasibility and acceptability. BMJ Open 12 (2) e049283. (10.1136/bmjopen-2021-049283)
2020
- Wong, H. et al., 2020. Contribution of de novo and inherited rare copy number variants to very preterm birth. Journal of Medical Genetics 57 (8), pp.552-557. (10.1136/jmedgenet-2019-106619)
2019
- Nievergelt, C. M. et al., 2019. International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci. Nature Communications 10 4558. (10.1038/s41467-019-12576-w)
Articles
- Chawner, S. J. et al. 2023. Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions. JCPP Advances 3 (2) e12162. (10.1002/jcv2.12162)
- Chawner, S. J. R. A. et al. 2023. Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions. Translational Psychiatry 13 7. (10.1038/s41398-022-02296-z)
- Maihofer, A. X. et al., 2022. Rare copy number variation in posttraumatic stress disorder. Molecular Psychiatry 27 , pp.5062-5069. (10.1038/s41380-022-01776-4)
- Maihofer, A. X. et al., 2022. Enhancing discovery of genetic variants for PTSD through integration of quantitative phenotypes and trauma exposure information. Biological Psychiatry 91 (7), pp.626-636. (10.1016/j.biopsych.2021.09.020)
- Warne, N. et al. 2022. Collecting genetic samples and linked mental health data from adolescents in schools: protocol co-production and a mixed-methods pilot of feasibility and acceptability. BMJ Open 12 (2) e049283. (10.1136/bmjopen-2021-049283)
- Wong, H. et al., 2020. Contribution of de novo and inherited rare copy number variants to very preterm birth. Journal of Medical Genetics 57 (8), pp.552-557. (10.1136/jmedgenet-2019-106619)
- Nievergelt, C. M. et al., 2019. International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci. Nature Communications 10 4558. (10.1038/s41467-019-12576-w)