Publications

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H
F. Hagenbeek, Kluft, C., Hankemeier, T., Bartels, M., Draisma, H. H. M., Middeldorp, C., Berger, R., Noto, A., Lussu, M., Pool, R., Faa, G., and Boomsma, D. I., “Discovery of biochemical biomarkers for aggression: A role for metabolomics in psychiatry.”, Am J Med Genet B Neuropsychiatr Genet, 2016.
F. Hagenbeek, van Dongen, J., Kluft, C., and Ligthart, L., “Selected Lectures of the 13th International Workshop on Neonatology. LECT 39, Self-reported aggressive behavior in humans and biomarkers: a focus on lipids and methylation”, Journal of Pediatric and Neonatal Individualized Medicine (JPNIM), vol. 6, no. 2, pp. 52-55, 2017.
F. A. Hagenbeek, van Dongen, J., Pool, R., Roetman, P. J., Harms, A. C., Hottenga, J. Jan, Kluft, C., Colins, O. F., van Beijsterveldt, C. E. M., Fanos, V., Ehli, E. A., Hankemeier, T., Vermeiren, R. R. J. M., Bartels, M., Déjean, S., and Boomsma, D. I., “Integrative multi-omics analysis of childhood aggressive behavior”, Behavior Genetics, vol. 53, pp. 101–117, 2023.
F. A. Hagenbeek, Pool, R., van Dongen, J., Draisma, H. H. M., Hottenga, J. Jan, Willemsen, G., Abdellaoui, A., Fedko, I. O., Braber, Aden, Visser, P. Jelle, de Geus, E. J. C. N., van Dijk, K. Willems, Verhoeven, A., H Suchiman, E., Beekman, M., P Slagboom, E., van Duijn, C. M., Consortium, B. B. M. R. I. Metabolomi, Harms, A. C., Hankemeier, T., Bartels, M., Nivard, M. G., and Boomsma, D. I., “Heritability estimates for 361 blood metabolites across 40 genome-wide association studies”, Nature Communications, vol. 11, p. 39, 2020.
F. A. Hagenbeek, Pool, R., Van Asselt, A. J., Ehli, E. A., Smit, A. B., Bartels, M., Hottenga, J. Jan, Dolan, C. V., van Dongen, J., and Boomsma, D. I., “Intergenerational transmission of complex traits and the offspring methylome”, 2025.
F. Hagenbeek, van Dongen, J., Kluft, C., Hankemeier, T., Ligthart, L., Willemsen, G., de Geus, E. J. C., Vink, J. M., Bartels, M., and Boomsma, D. I., “Adult aggressive behavior in humans and biomarkers: a focus on lipids and methylation”, Journal of Pediatric and Neonatal Individualized Medicine (JPNIM), vol. 7, no. 2, 2018.
F. A. Hagenbeek, Roetman, P. J., Pool, R., Kluft, C., Harms, A. C., van Dongen, J., Colins, O. F., Talens, S., van Beijsterveldt, C. E. M., Vandenbosch, M. M. L. J. Z., de Zeeuw, E. L., Déjean, S., Fanos, V., Ehli, E. A., Davies, G. E., Hottenga, J. Jan, Hankemeier, T., Bartels, M., Vermeiren, R. R. J. M., and Boomsma, D. I., “Urinary Amine and organic acid metabolites evaluated as markers for childhood aggression: The ACTION biomarker study”, Frontiers in Psychiatry, vol. 11, p. 165, 2020.
F. A. Hagenbeek, van Dongen, J., Pool, R., and Boomsma, D. I., “Chapter 32 - Twins and omics: the role of twin studies in multi-omics”, in Twin Research for Everyone, A. Tarnoki, Tarnoki, D., Harris, J., and Segal, N. Academic Press, 2022, pp. 547-584.
G
A. D. Grotzinger, Rhemtulla, M., de Vlaming, R., Ritchie, S. J., Mallard, T. T., W. Hill, D., Ip, H. F., McIntosh, A. M., Deary, I. J., Koellinger, P. D., K. Harden, P., Nivard, M. G., and Tucker-Drob, E. M., “Genomic SEM Provides Insights into the Multivariate Genetic Architecture of Complex Traits”, bioRxiv, 2018.
C. U. Greven, Buitelaar, J. K., and Salum, G. A., “From positive psychology to psychopathology: the continuum of attention-deficit hyperactivity disorder”, Journal of Child Psychology and Psychiatry, vol. 59, pp. 203-212, 2018.
K. L. Grasby, Jahanshad, N., Painter, J. N., Colodro-Conde, L., Bralten, J., Hibar, D. P., Lind, P. A., Pizzagalli, F., Ching, C. R. K., and 357Authors, +, “The genetic architecture of the human cerebral cortex”, Science, vol. 367, p. eaay6690, 2020.
A. - R. Gatej, Lamers, A., van Domburgh, L., Crone, M., Ogden, T., Rijo, D., Aronen, E., Barroso, R., Boomsma, D. I., and Vermeiren, R., “Awareness and perceptions of clinical guidelines for the diagnostics and treatment of severe behavioural problems in children across Europe: A qualitative survey with academic experts”, European PsychiatryEuropean Psychiatry, vol. 57, pp. 1 - 9, 2019.
F
C. M. Freitag, Boomsma, D. I., Glennon, J. C., Franke, B., and Holtel, A., “Focused issue on conduct disorder and aggressive behaviour”, European Child {&} Adolescent Psychiatry, vol. 27, pp. 1231–1234, 2018.
C. Finkenauer, Buyukcan-Tetik, A., Baumeister, R. F., Schoemaker, K., Bartels, M., and Vohs, K. D., “Out of Control Identifying the Role of Self-Control Strength in Family Violence”, Current Directions in Psychological Science, vol. 24, pp. 261–266, 2015.
I. O. Fedko, Hottenga, J. - J., Helmer, Q., Mbarek, H., Huider, F., Amin, N., Beulens, J. W., Bremmer, M. A., Elders, P. J., Galesloot, T. E., Kiemeney, L. A., van Loo, H. M., H Picavet, S. J., Rutters, F., van der Spek, A., van de Wiel, A. M., van Duijn, C., de Geus, E. J. C., Feskens, E. J. M., Hartman, C. A., Oldehinkel, A. J., Smit, J. H., Verschuren, W. M. Monique, Penninx, B. W. J. H., Boomsma, D. I., and Bot, M., “Measurement and genetic architecture of lifetime depression in the Netherlands as assessed by LIDAS (Lifetime Depression Assessment Self-report)”, Psychological Medicine, vol. 51, pp. 1–10, 2020.
I. O. Fedko, Wesseldijk, L. W., Nivard, M. G., Hottenga, J. - J., van Beijsterveldt, C. E. M., Middeldorp, C., Bartels, M., and Boomsma, D. I., “Heritability of Behavioral Problems in 7-Year Olds Based on Shared and Unique Aspects of Parental Views”, Behavior Genetics, vol. 47, pp. 152–163, 2017.
G. Faa, Manchia, M., Pintus, R., Gerosa, C., Marcialis, M. Antonietta, and Fanos, V., “Fetal programming of neuropsychiatric disorders.”, Birth Defects Res C Embryo Today, vol. 108, no. 3, pp. 207-223, 2016.
E
E. Eising, Mirza-Schreiber, N., de Zeeuw, E. L., Wang, C. A., Truong, D. T., Allegrini, A. G., Shapland, C. Yang, Zhu, G., Wigg, K. G., Gerritse, M. L., Molz, B., Alagöz, G., Gialluisi, A., Abbondanza, F., Rimfeld, K., van Donkelaar, M., Liao, Z., Jansen, P. R., Andlauer, T. F. M., Bates, T. C., Bernard, M., Blokland, K., Bonte, M., Børglum, A. D., Bourgeron, T., Brandeis, D., Ceroni, F., Csépe, V., Dale, P. S., de Jong, P. F., DeFries, J. C., Démonet, J. - F. \ccois, Demontis, D., Feng, Y., Gordon, S. D., Guger, S. L., Hayiou-Thomas, M. E., Hernández-Cabrera, J. A., Hottenga, J. - J., Hulme, C., Kere, J., Kerr, E. N., Koomar, T., Landerl, K., Leonard, G. T., Lovett, M. W., Lyytinen, H., Martin, N. G., Martinelli, A., Maurer, U., Michaelson, J. J., Moll, K., Monaco, A. P., Morgan, A. T., Nöthen, M. M., Pausova, Z., Pennell, C. E., Pennington, B. F., Price, K. M., Rajagopal, V. M., Ramus, F., Richer, L., Simpson, N. H., Smith, S. D., Snowling, M. J., Stein, J., Strug, L. J., Talcott, J. B., Tiemeier, H., van der Schroeff, M. P., Verhoef, E., Watkins, K. E., Wilkinson, M., Wright, M. J., Barr, C. L., Boomsma, D. I., Carreiras, M., Franken, M. - C. J., Gruen, J. R., Luciano, M., Müller-Myhsok, B., Newbury, D. F., Olson, R. K., Paracchini, S., Paus, T. \vs, Plomin, R., Reilly, S., Schulte-Körne, G., J Tomblin, B., van Bergen, E., Whitehouse, A. J. O., Willcutt, E. G., St Pourcain, B., Francks, C., and Fisher, S. E., “Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people”, Proceedings of the National Academy of Sciences (PNAS), vol. 119, p. e2202764119, 2022.
D
G. Drouard, Hagenbeek, F. A., Whipp, A., Pool, R., Hottenga, J. - J., Jansen, R., Hubers, N., Afonin, A., Willemsen, G., de Geus, E. J. C., Ripatti, S., Pirinen, M., Kanninen, K. M., Boomsma, D. I., van Dongen, J., Kaprio, J., Consortium, B. I. O. S., and Consortium, B. B. M. R. I. - N. L. Metabolomi, “Longitudinal multi-omics study reveals common etiology underlying association between plasma proteome and BMI trajectories in adolescent and young adult twins”, medRxiv. 2023.
C. Doust, Fontanillas, P., Eising, E., Gordon, S. D., Wang, Z., Alagöz, G., Molz, B., Team, 23andM. Research, Consortium, Q. Trait Work, St Pourcain, B., Francks, C., Marioni, R. E., Zhao, J., Paracchini, S., Talcott, J. B., Monaco, A. P., Stein, J. F., Gruen, J. R., Olson, R. K., Willcutt, E. G., DeFries, J. C., Pennington, B. F., Smith, S. D., Wright, M. J., Martin, N. G., Auton, A., Bates, T. C., Fisher, S. E., and Luciano, M., “Discovery of 42 genome-wide significant loci associated with dyslexia”, Nature Genetics, vol. 54, pp. 1621–1629, 2022.

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