Bresser, T., Blanken, T. F., de Lange, S. C., Leerssen, J., Foster-Dingley, J. C., Lakbila-Kamal, O., Wassing, R., Ramautar, J. R., Stoffers, D., van den Heuvel, M. P., & Van Someren, E. J. W. (2024). Insomnia Subtypes Have Differentiating Deviations in Brain Structural Connectivity. Biological psychiatry, S0006-3223(24)01418-5. Advance online publication. https://doi.org/10.1016/j.biopsych.2024.06.014

Claeys, L., Zhytnik, L., Ventura, L., Wisse, L. E., Eekhoff, E. M. W., Pals, G., Bravenboer, N., Heine, V. M., & Micha, D. (2024). In Vitro Modelling of Osteogenesis Imperfecta with Patient-Derived Induced Mesenchymal Stem Cells. International journal of molecular sciences, 25(6), 3417. https://doi.org/10.3390/ijms25063417

Frei, O., Hindley, G., Shadrin, A. A., van der Meer, D., Akdeniz, B. C., Hagen, E., Cheng, W., O’Connell, K. S., Bahrami, S., Parker, N., Smeland, O. B., Holland, D., Schizophrenia Working Group of the Psychiatric Genomics Consortium, de Leeuw, C., Posthuma, D., Andreassen, O. A., & Dale, A. M. (2024). Improved functional mapping of complex trait heritability with GSA-MiXeR implicates biologically specific gene sets. Nature genetics, 56(6), 1310–1318. https://doi.org/10.1038/s41588-024-01771-1

Ge, R., Yu, Y., Qi, Y. X., Fan, Y. N., Chen, S., Gao, C., Haas, S. S., New, F., Boomsma, D. I., Brodaty, H., Brouwer, R. M., Buckner, R., Caseras, X., Crivello, F., Crone, E. A., Erk, S., Fisher, S. E., Franke, B., Glahn, D. C., Dannlowski, U., … ENIGMA Lifespan Working Group (2024). Normative modelling of brain morphometry across the lifespan with CentileBrain: algorithm benchmarking and model optimisation. The Lancet. Digital health, 6(3), e211–e221. https://doi.org/10.1016/S2589-7500(23)00250-9

González-Peñas, J., Alloza, C., Brouwer, R., Díaz-Caneja, C. M., Costas, J., González-Lois, N., Gallego, A. G., de Hoyos, L., Gurriarán, X., Andreu-Bernabeu, Á., Romero-García, R., Fañanas, L., Bobes, J., Pinto, A. G., Crespo-Facorro, B., Martorell, L., Arrojo, M., Vilella, E., Guitiérrez-Zotes, A., Perez-Rando, M., … Schnack, H. (2024). Accelerated Cortical Thinning in Schizophrenia is Associated With Rare and Common Predisposing Variation to Schizophrenia and Neurodevelopmental Disorders. Biological psychiatry, S0006-3223(24)01170-3. Advance online publication. https://doi.org/10.1016/j.biopsych.2024.03.011

Hanlon, K. S., Cheng, M., Ferrer, R. M., Ryu, J. R., Lee, B., De La Cruz, D., Patel, N., Espinoza, P., Santoscoy, M. C., Gong, Y., Ng, C., Nguyen, D. M., Nammour, J., Clark, S. W., Heine, V. M., Sun, W., Kozarsky, K., & Maguire, C. A. (2024). In vivo selection in non-human primates identifies AAV capsids for on-target CSF delivery to spinal cord. Molecular therapy : the journal of the American Society of Gene Therapy, 32(8), 2584–2603. https://doi.org/10.1016/j.ymthe.2024.05.040

Kipkemoi, P., Savage, J. E., Gona, J., Rimba, K., Kombe, M., Mwangi, P., Kipkoech, C., Posthuma, D., Newton, C. R. J. C., & Abubakar, A. (2024). Evaluation of the Psychometric Properties of the Social Communication Questionnaire in Rural Kenya. Journal of autism and developmental disorders, 10.1007/s10803-024-06380-9. Advance online publication. https://doi.org/10.1007/s10803-024-06380-9

Kipkemoi, P., Kariuki, S. M., Gona, J., Mwangi, F. W., Kombe, M., Kipkoech, C., Murimi, P., Mandy, W., Warrington, R., Skuse, D., Newton, C. R. J. C., & Abubakar, A. (2024). Utility of the 3Di short version in the identification and diagnosis of autism in children at the Kenyan coast. Frontiers in psychiatry, 15, 1234929. https://doi.org/10.3389/fpsyt.2024.1234929

Kipkemoi P, Mufford MS, Akena D, Alemayehu M, Atwoli L, Chibnik LB, Gelaye B, Gichuru S, Kariuki SM, Koenen KC, Kwobah E, Kyebuzibwa J, Mwema RM, Newton CRJC, Pretorius A, Stein DJ, Stevenson A, Stroud RE 2nd, Teferra S, Zingela Z, Post K, Korte KJ. Evaluation of the psychometric properties of the UBACC questionnaire in a multi-country psychiatric study in Africa. Compr Psychiatry. 2024 Aug 26;135:152526. doi: 10.1016/j.comppsych.2024.152526. Epub ahead of print. PMID: 39208558.

Koch, E., Pardiñas, A. F., O’Connell, K. S., Selvaggi, P., Collados, J. C., Babic, A., Marshall, S. E., Van der Eycken, E., Angulo, C., Lu, Y., Sullivan, P. F., Dale, A. M., Molden, E., Posthuma, D., White, N., Schubert, A., Djurovic, S., Heimer, H., Stefánsson, H., Stefánsson, K., … Andreassen, O. A. (2024). How real-world data can facilitate the development of precision medicine treatment in psychiatry. Biological psychiatry, S0006-3223(24)00003-9. Advance online publication. https://doi.org/10.1016/j.biopsych.2024.01.001

Leerssen, J., Aghajani, M., Bresser, T., Rösler, L., Winkler, A. M., Foster-Dingley, J. C., & Van Someren, E. J. W. (2024). Cognitive, Behavioral, and Circadian Rhythm Interventions for Insomnia Alter Emotional Brain Responses. Biological psychiatry. Cognitive neuroscience and neuroimaging, 9(1), 60–69. https://doi.org/10.1016/j.bpsc.2023.03.007

Mallio, C. A., Buoso, A., Stiffi, M., Cea, L., Vertulli, D., Bernetti, C., Di Gennaro, G., van den Heuvel, M. P., & Beomonte Zobel, B. (2024). Mapping the Neural Basis of Neuroeconomics with Functional Magnetic Resonance Imaging: A Narrative Literature Review. Brain sciences, 14(5), 511. https://doi.org/10.3390/brainsci14050511

Mannens, C. C. A., Hu, L., Lönnerberg, P., Schipper, M., Reagor, C. C., Li, X., He, X., Barker, R. A., Sundström, E., Posthuma, D., & Linnarsson, S. (2024). Chromatin accessibility during human first-trimester neurodevelopment. Nature, 10.1038/s41586-024-07234-1. Advance online publication. https://doi.org/10.1038/s41586-024-07234-1

Poortman S.R.,  Barendse M.E.A., Setiaman N.,  van den Heuvel M.P.,  de Lange S.C., Hillegers M.H.J,  van Haren, N.E.M. (2024). Age Trajectories of the Structural Connectome in Child and Adolescent Offspring of Individuals With Bipolar Disorder or Schizophrenia, Biological Psychiatry Global Open Science, 4 (5), https://doi.org/10.1016/j.bpsgos.2024.100336.

Savage, J. E., & Thijssen, A. B. (2024). Insights from genetically stratified analyses comparing subtypes of alcohol misuse. Science progress, 107(2), 368504241260375. https://doi.org/10.1177/00368504241260375

Tesli, N., Jaholkowski, P., Haukvik, U. K., Jangmo, A., Haram, M., Rokicki, J., Friestad, C., Tielbeek, J. J., Næss, Ø., Skardhamar, T., Gustavson, K., Ask, H., Fazel, S., Tesli, M., & Andreassen, O. A. (2024). Conduct disorder – a comprehensive exploration of comorbidity patterns, genetic and environmental risk factors. Psychiatry research, 331, 115628. https://doi.org/10.1016/j.psychres.2023.115628

Tissink, E. P., Shadrin, A. A., van der Meer, D., Parker, N., Hindley, G., Roelfs, D., Frei, O., Fan, C. C., Nagel, M., Nærland, T., Budisteanu, M., Djurovic, S., Westlye, L. T., van den Heuvel, M. P., Posthuma, D., Kaufmann, T., Dale, A. M., & Andreassen, O. A. (2024). Abundant pleiotropy across neuroimaging modalities identified through a multivariate genome-wide association study. Nature communications, 15(1), 2655. https://doi.org/10.1038/s41467-024-46817-4

Tchoukalova, Y. D., Phung, T. N., Kennedy, M. M., Miranda-Grandjean, D., Becquer, E., Chen, L., Zhang, N., Dinu, V., Wilson, M. A., & Lott, D. G. (2024). Idiopathic Subglottic Stenosis Is Associated With More Frequent and Abnormal Squamous Metaplasia. The Annals of otology, rhinology, and laryngology, 133(2), 214–223. https://doi.org/10.1177/00034894231201016

van Berkel, A. A., Lammertse, H. C. A., Öttl, M., Koopmans, F., Misra-Isrie, M., Meijer, M., Dilena, R., van Hasselt, P. M., Engelen, M., van Haelst, M., Smit, A. B., van der Sluis, S., Toonen, R. F., & Verhage, M. (2023). Reduced MUNC18-1 Levels, Synaptic Proteome Changes, and Altered Network Activity in STXBP1-Related Disorder Patient Neurons. Biological psychiatry global open science, 4(1), 284–298. https://doi.org/10.1016/j.bpsgos.2023.05.004

— Consortium papers —

Epi25 Collaborative. Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes. Nat Neurosci. 2024 Oct;27(10):1864-1879. doi: 10.1038/s41593-024-01747-8. Epub 2024 Oct 3. PMID: 39363051.

Qu, K., Li, M. X., Yu, P., International Headache Genetics Consortium, Wu, B. H., Shi, M., & Dong, M. (2024). HMG-CoA reductase is a potential therapeutic target for migraine: a mendelian randomization study. Scientific reports, 14(1), 12094. https://doi.org/10.1038/s41598-024-61628-9

Trastulla L, Dolgalev G, Moser S, Jiménez-Barrón LT, Andlauer TFM, von Scheidt M; Schizophrenia Working Group of the Psychiatric Genomics Consortium; Budde M, Heilbronner U, Papiol S, Teumer A, Homuth G, Völzke H, Dörr M, Falkai P, Schulze TG, Gagneur J, Iorio F, Müller-Myhsok B, Schunkert H, Ziller MJ. Distinct genetic liability profiles define clinically relevant patient strata across common diseases. Nat Commun. 2024 Jul 1;15(1):5534. doi: 10.1038/s41467-024-49338-2. PMID: 38951512; PMCID: PMC11217418.

— Book chapters —

de Maciel BAPC, van den Heuvel M, Brouwer RM Genetics of Neuroanatomy, Encyclopedia of the Human Brain, p 148-155. Elsevier, 2025.