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di Stefano, M., Ciceri, T., Leemans, A., de Zwarte, S. M. C., De Luca, A., & Peruzzo, D. (2025). Diffusion MRI of the prenatal fetal brain: a methodological scoping review. NeuroImage, 320, Article 121453. [DOI] [Portal]

de Zwarte, S. M. C., Teeuw, J., He, J., Bekker, M. N., van Sloun, R. J. G., & Hulshoff Pol, H. E. (2024). Automated Segmentation of Fetal Intracranial Volume in Three-Dimensional Ultrasound Using Deep Learning: Identifying Sex Differences in Prenatal Brain Development. Human Brain Mapping, 45(17), Article e70058. [DOI] [Portal]

Schijven, D., Postema, M. C., Fukunaga, M., Matsumoto, J., Miura, K., de Zwarte, S. M. C., ENIGMA-Schizophrenia Working Group, & Francks, C. (2023). Large-scale analysis of structural brain asymmetries in schizophrenia via the ENIGMA consortium. Proceedings of the National Academy of Sciences of the United States of America, 120(14), Article e2213880120. [DOI]

Schick, A., van Winkel, R., Lin, B. D., Luykx, J. J., de Zwarte, S. M. C., van Eijk, K. R., GROUP investigators, Myin-Germeys, I., & Reininghaus, U. (2023). Polygenic risk, familial liability and stress reactivity in psychosis: an experience sampling study. Psychological Medicine, 53(7), 2798-2807. [DOI]

Ching, C. R. K., & ENIGMA Bipolar Disorder Working Group (2022). What we learn about bipolar disorder from large-scale neuroimaging: Findings and future directions from the ENIGMA Bipolar Disorder Working Group. Human Brain Mapping, 43(1), 56-82. [DOI]

de Zwarte, S. M. C., Brouwer, R. M., ENIGMA Relatives Working Group, Kahn, R. S., & van Haren, N. (2022). Intelligence, educational attainment, and brain structure in those at familial high-risk for schizophrenia or bipolar disorder. Human Brain Mapping, 43(1), 414-430. [DOI]

de Zwarte, S. M. C., Brouwer, R. M., Kahn, R. S., & van Haren, N. E. M. (2022). Schizophrenia and Bipolar Polygenic Risk Scores in Relation to Intracranial Volume. Genes, 13(4), Article 695. [DOI]

Caspi, Y., de Zwarte, S. M. C., Iemenschot, I. J., Lumbreras, R., de Heus, R., Bekker, M. N., & Hulshoff Pol, H. (2022). Automatic measurements of fetal intracranial volume from 3D ultrasound scans. Frontiers in Neuroimaging, 1, 996702. [DOI]

Brouwer, R. M., Klein, M., Grasby, K., Schnack, H. G., Jahanshad, N., Teeuw, J., ENIGMA-Plasticity Working Group, & Hulshoff Pol, H. E. (2022). Genetic variants associated with longitudinal changes in brain structure across the lifespan. Nature Neuroscience, 25, 421-432. [DOI] [Portal]

Teeuw, J., Ori, A. P. S., Brouwer, R. M., de Zwarte, S. M. C., Schnack, H. G., Hulshoff Pol, H., & Ophoff, R. A. (2021). Accelerated aging in the brain, epigenetic aging in blood, and polygenic risk for schizophrenia. Schizophrenia Research, 231, 189-197. [DOI]

Thygesen, J. H., Presman, A., Harju-Seppänen, J., Irizar, H., Jones, R., Kuchenbaecker, K. B., Lin, K., Alizadeh, B. Z., Austin-Zimmerman, I., Bartels-Velthuis, A., Bhat, A., Bruggeman, R., Cahn, W., Calafato, S., Crespo-Facorro, B., de Haan, L., de Zwarte, S. M. C., Di Forti, M., Díez-Revuelta , Á., ... Bramon, E. (2021). Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study. Molecular Psychiatry, 26(9), 5307-5319. [DOI]

Pazoki, R., Lin, B. D., van Eijk, K. R., Schijven, D., de Zwarte, S., GROUP investigators, Guloksuz, S., & Luykx, J. J. (2021). Phenome-wide and genome-wide analyses of quality of life in schizophrenia. BJPsych Open, 7(1), Article e13. [DOI]

ENIGMA-CNV working group, Sønderby, I. E., van der Meer, D., Moreau, C., Kaufmann, T., Walters, G. B., Ellegaard, M., Abdellaoui, A., Ames, D., Amunts, K., Andersson, M., Armstrong, N. J., Bernard, M., Blackburn, N. B., Blangero, J., Boomsma, D. I., Brodaty, H., Brouwer, R. M., Bülow, R., ... Wright, M. J. (2021). 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans. Translational Psychiatry, 11(1), Article 182. [DOI]

Habtewold, T. D., Liemburg, E. J., Islam, M. A., de Zwarte, S., Boezen, H. M., GROUP investigators, Bruggeman, R., & Alizadeh, B. Z. (2020). Association of schizophrenia polygenic risk score with data-driven cognitive subtypes: A six-year longitudinal study in patients, siblings and controls. Schizophrenia Research, 223, 135-147. [DOI]

ENIGMA-CNV working group (2020). Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition. JAMA Psychiatry, 77(4), 420-430. [DOI]

Thompson, P. M., Jahanshad, N., Ching, C. R. K., & ENIGMA Consortium (2020). ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries. Translational Psychiatry, 10(1), Article 100. [DOI]

Sønderby, I. E., & ENIGMA-CNV working group (2020). Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia. Molecular Psychiatry, 25(3), 584-602. [DOI]

ENIGMA Genetics Working Group (2020). The genetic architecture of the human cerebral cortex. Science, 367(6484), Article eaay6690. [DOI]

van den Heuvel, M. P., Scholtens, L. H., van der Burgh , H. K., Agosta, F., Alloza , C., Arango, C., Auyeung, B., Baron-Cohen, S., Basaia, S., Benders, M. N. J. L., Beyer, F., Booij, L., Braun, K. P. J., Busatto Filho, G., Cahn, W., Cannon, D. M., Chaim-Avancini, T. M., Chan, S. S. M., Chen , E. Y. H., ... de Lange, S. C. (2019). 10Kin1day: a bottom-up neuroimaging initiative. Frontiers in Neurology, 10, Article 425. [DOI]

de Zwarte, S. M. C., Brouwer, R. M., Tsouli, A., Cahn, W., Hillegers, M. H. J., Hulshoff Pol, H., Kahn, R. S., & van Haren, N. E. M. (2019). Running in the Family? Structural Brain Abnormalities and IQ in Offspring, Siblings, Parents, and Co-twins of Patients with Schizophrenia. Schizophrenia Bulletin, 45(6), 1209-1217. [DOI]

de Zwarte, S. M. C., Brouwer, R. M., ENIGMA Relatives Working Group, Kahn, R. S., & van Haren, N. E. M. (2019). The Association Between Familial Risk and Brain Abnormalities Is Disease Specific: An ENIGMA-Relatives Study of Schizophrenia and Bipolar Disorder. Biological Psychiatry, 86(7), 545-556. [DOI]

Blokland, G. A. M., Del Re, E. C., Mesholam-Gately, R. I., Jovicich, J., Trampush, J. W., Keshavan, M. S., DeLisi, L. E., Walters, J. T. R., Turner, J. A., Malhotra, A. K., Lencz, T., Shenton, M. E., Voineskos, A. N., Rujescu, D., Giegling, I., Kahn, R. S., Roffman, J. L., Holt, D. J., Ehrlich, S., ... Petryshen, T. L. (2018). Understand Schizophrenia (GENUS) consortium: A collaborative cognitive and neuroimaging genetics project. Schizophrenia Research, 195, 306-317. [DOI]

Ranlund, S., Calafato, S., Thygesen, J. H., Lin, K., Cahn, W., Crespo-Facorro, B., de Zwarte, S. M. C., Díez, Á., Di Forti, M., GROUP, Iyegbe, C., Jablensky, A., Jones, R., Hall, M.-H., Kahn, R. S., Kalaydjieva, L., Kravariti, E., McDonald, C., McIntosh, A. M., ... Bramon, E. (2018). A polygenic risk score analysis of psychosis endophenotypes across brain functional, structural, and cognitive domains. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 177(1), 21-34. [DOI]

van Erp, T. G. M., Walton, E., Hibar, D. P., Schmaal, L., Jiang, W., Glahn, D. C., Pearlson, G. D., Yao, N., Fukunaga, M., Hashimoto, R., Okada, N., Yamamori, H., Bustillo, J. R., Clark, V. P., Agartz, I., Mueller, B. A., Cahn, W., de Zwarte, S. M. C., Hulshoff Pol, H. E., ... Turner, J. A. (2018). Cortical Brain Abnormalities in 4474 Individuals With Schizophrenia and 5098 Control Subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) Consortium. Biological Psychiatry, 84(9), 644-654. [DOI]

Guadalupe, T., Mathias, S. R., van Erp, T. G. M., ENIGMA Lateralization Working Group , Fisher, S. E., & Francks, C. (2017). Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex. Brain Imaging and Behavior, 11(5), 1497-1514. [DOI]

Walton, E., Hibar, D. P., van Erp, T. G. M., ENIGMA-Schizophrenia Working Group, Turner, J. A., & Ehrlich, S. (2017). Prefrontal cortical thinning links to negative symptoms in schizophrenia via the ENIGMA consortium. Psychological Medicine, 48(1), 82-94. [DOI]

Walton, E., Hibar, D. P., van Erp, T. G. M., ENIGMA-Schizophrenia Working Group, Turner, J. A., & Ehrlich, S. (2017). Positive symptoms associate with cortical thinning in the superior temporal gyrus via the ENIGMA Schizophrenia consortium. Acta Psychiatrica Scandinavica, 135(5), 439-447. [DOI]

de Zwarte, S. M. C., Johnston, J. A. Y., Cox Lippard, E. T., & Blumberg, H. P. (2014). Frontotemporal White Matter in Adolescents with, and at-Risk for, Bipolar Disorder. Journal of Clinical Medicine, 3(1), 233-254. [DOI]