Publications

Export 166 results:
Author Title Type [ Year(Asc)]
2025
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.
2024
E. Verhoef, Allegrini, A. G., Jansen, P. R., Lange, K., Wang, C. A., Morgan, A. T., Ahluwalia, T. S., Symeonides, C., Andreassen, O. A., Bartels, M., Boomsma, D., Dale, P. S., Ehli, E., Fernandez-Orth, D., Guxens, M., Hakulinen, C., Harris, K. Mullan, Haworth, S., de Hoyos, L., Jaddoe, V., Keltikangas-Järvinen, L., Lehtimäki, T., Middeldorp, C., Min, J. L., Mishra, P. P., Njølstad, P. Rasmus, Sunyer, J., Tate, A. E., Timpson, N., van der Laan, C., Vrijheid, M., Vuoksimaa, E., Whipp, A., Ystrom, E., Consortium, A. C. T. I. O. N., group, B. Infant Stu, Eising, E., Franken, M. - C., Hypponen, E., Mansell, T., Olislagers, M., Omerovic, E., Rimfeld, K., Schlag, F., Selzam, S., Shapland, C. Yang, Tiemeier, H., Whitehouse, A. J. O., Saffery, R., Bønnelykke, K., Reilly, S., Pennell, C. E., Wake, M., Cecil, C. A. M., Plomin, R., Fisher, S. E., and Pourcain, B. St., “Genome-Wide Analyses of Vocabulary Size in Infancy and Toddlerhood: Associations With Attention-Deficit/Hyperactivity Disorder, Literacy, and Cognition-Related Traits”, Biological Psychiatry, vol. 95, no. 9, pp. 859 - 869, 2024.
A. Niehues, de Visser, C., Hagenbeek, F. A., Kulkarni, P., Pool, R., Karu, N., Kindt, A. S. D., Singh, G., Vermeiren, R. R. J. M., Boomsma, D. I., van Dongen, J., Hoen, P. A. C. ’t, and van Gool, A. J., “A multi-omics data analysis workflow packaged as a FAIR Digital Object”, GigaScience, vol. 13, p. giad115, 2024.
2023
R. Boen, Kaufmann, T., van der Meer, D., Frei, O., Agartz, I., Ames, D., Andersson, M., Armstrong, N. J., Artiges, E., Atkins, J. R., Bauer, J., Benedetti, F., Boomsma, D. I., Brodaty, H., Brosch, K., Buckner, R. L., Cairns, M. J., Calhoun, V., Caspers, S., Cichon, S., Corvin, A. P., Facorro, B. Crespo, Dannlowski, U., David, F. S., de Geus, E. J. C., de Zubicaray, G. I., Desrivieres, S., Doherty, J. L., Donohoe, G., Ehrlich, S., Eising, E., Espeseth, T., Fisher, S. E., Forstner, A. J., Uyà, L. Fortaner, Frouin, V., Fukunaga, M., Ge, T., Glahn, D. C., Goltermann, J., Grabe, H. J., Green, M. J., Groenewold, N. A., Grotegerd, D., Hahn, T., Hashimoto, R., Hehir-Kwa, J. Y., Henskens, F. A., Holmes, A. J., Haberg, A. K., Haavik, J., Jacquemont, S., Jansen, A., Jockwitz, C., Jönsson, E. G., Kikuchi, M., Kircher, T., Kumar, K., Le Hellard, S., Leu, C., Linden, D. E., Liu, J., Loughnan, R., Mather, K. A., McMahon, K. L., McRae, A. F., Medland, S. E., Meinert, S., Moreau, C. A., Morris, D. W., Mowry, B. J., Mühleisen, T. W., Nenadić, I., Nöthen, M. M., Nyberg, L., Owen, M. J., Paolini, M., Paus, T., Pausova, Z., Persson, K., Quidé, Y., Marques, T. Reis, Sachdev, P. S., Sando, S. B., Schall, U., Scott, R. J., Selbæk, G., Shumskaya, E., Silva, A. I., Sisodiya, S. M., Stein, F., Stein, D. J., Straube, B., Streit, F., Strike, L. T., Teumer, A., Teutenberg, L., Thalamuthu, A., Tooney, P. A., Tordesillas-Gutiérrez, D., Trollor, J. N., Ent, Dvan 't, van den Bree, M. B. M., van Haren, N. E. M., Vazquez-Bourgon, J., Völzke, H., Wen, W., Wittfeld, K., Ching, C. R. K., Westlye, L. T., Thompson, P. M., Bearden, C. E., Selmer, K. K., Alnæs, D., Andreassen, O. A., and Sonderby, I. E., “Beyond the global brain differences: Intra-individual variability differences in 1q21.1 distal and 15q11.2 {BP1-BP2} deletion carriers”, Biological Psychiatry, 2023.
J. J. Beck, Ahmed, T., Finnicum, C. T., Zwinderman, K., Ehli, E. A., Boomsma, D. I., and Hottenga, J. Jan, “Genetic ancestry estimates within dutch family units and across genotyping arrays: insights from empirical analysis using two estimation methods”, Genes (Basel), vol. 14, p. 1497, 2023.
V. V. Odintsova, Hagenbeek, F. A., Van der Laan, C. M., van de Weijer, S., and Boomsma, D. I., “Genetics and epigenetics of human aggression”, Handbook of Clinical Neurology, Brain and Crime, vol. 197, pp. 13–44, 2023.
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.
N. Hubers, Hagenbeek, F. A., Pool, R., Déjean, S., Harms, A. C., Roetman, P. J., van Beijsterveldt, C. E. M., Fanos, V., Ehli, E. A., Vermeiren, R. R. J. M., Bartels, M., Hottenga, J. Jan, Hankemeier, T., van Dongen, J., and Boomsma, D. I., “Integrative multi-omics analysis of genomic, epigenomic, and metabolomics data leads to new insights for Attention-Deficit/Hyperactivity Disorder”, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, p. e32955, 2023.
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.
2022
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.
A. G. Allegrini, van Beijsterveldt, T., Boomsma, D. I., Rimfeld, K., Pingault, J. - B., Plomin, R., Bartels, M., and Nivard, M. G., “Developmental co-occurrence of psychopathology dimensions in childhood”, JCPP Advances, vol. 2, p. e12100, 2022.
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.
V. V. Odintsova, Suderman, M., Hagenbeek, F. A., Caramaschi, D., Hottenga, J. - J., Pool, R., Consortium, B. I. O. S., Dolan, C. V., Ligthart, L., van Beijsterveldt, C. E. M., Willemsen, G., de Geus, E. J. C., Beck, J. J., Ehli, E. A., Cuellar-Partida, G., Evans, D. M., Medland, S. E., Relton, C. L., Boomsma, D. I., and van Dongen, J., “DNA methylation in peripheral tissues and left-handedness”, Scientific Reports, vol. 12, p. 5606, 2022.
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.
Z. Wang, Emmerich, A., Pillon, N. J., Moore, T., Hemerich, D., Cornelis, M. C., Mazzaferro, E., Broos, S., Ahluwalia, T. S., Bartz, T. M., Bentley, A. R., Bielak, L. F., Chong, M., Chu, A. Y., Berry, D., Dorajoo, R., Dueker, N. D., Kasbohm, E., Feenstra, B., Feitosa, M. F., Gieger, C., Graff, M., Hall, L. M., Haller, T., Hartwig, F. P., Hillis, D. A., Huikari, V., Heard-Costa, N., Holzapfel, C., Jackson, A. U., Johansson, \A. A., Jørgensen, A. Moltke, Kaakinen, M. A., Karlsson, R., Kerr, K. F., Kim, B., Koolhaas, C. M., Kutalik, Z., Lagou, V., Lind, P. A., Lorentzon, M., Lyytikäinen, L. - P., Mangino, M., Metzendorf, C., Monroe, K. R., Pacolet, A., Pérusse, L., Pool, R., Richmond, R. C., Rivera, N. V., Robiou-du-Pont, S., Schraut, K. E., Schulz, C. - A., Stringham, H. M., Tanaka, T., Teumer, A., Turman, C., van der Most, P. J., Vanmunster, M., van Rooij, F. J. A., van Vliet-Ostaptchouk, J. V., Zhang, X., Zhao, J. - H., Zhao, W., Balkhiyarova, Z., Balslev-Harder, M. N., Baumeister, S. E., Beilby, J., Blangero, J., Boomsma, D. I., Brage, S., Braund, P. S., Brody, J. A., Bruinenberg, M., Ekelund, U., Liu, C. - T., Cole, J. W., Collins, F. S., L Cupples, A., Esko, T., Enroth, S., Faul, J. D., Fernandez-Rhodes, L., Fohner, A. E., Franco, O. H., Galesloot, T. E., Gordon, S. D., Grarup, N., Hartman, C. A., Heiss, G., Hui, J., Illig, T., Jago, R., James, A., Joshi, P. K., Jung, T., Kähönen, M., Kilpeläinen, T. O., Koh, W. - P., Kolcic, I., Kraft, P. P., Kuusisto, J., Launer, L. J., Li, A., Linneberg, A., Luan, J. 'an, Vidal, P. Marques, Medland, S. E., Milaneschi, Y., Moscati, A., Musk, B., Nelson, C. P., Nolte, I. M., Pedersen, N. L., Peters, A., Peyser, P. A., Power, C., Raitakari, O. T., Reedik, M., Reiner, A. P., Ridker, P. M., Rudan, I., Ryan, K., Sarzynski, M. A., Scott, L. J., Scott, R. A., Sidney, S., Siggeirsdottir, K., Smith, A. V., Smith, J. A., Sonestedt, E., Strøm, M., E Tai, S., Teo, K. K., Thorand, B., Tönjes, A., Tremblay, A., Uitterlinden, A. G., Vangipurapu, J., van Schoor, N., Völker, U., Willemsen, G., Williams, K., Wong, Q., Xu, H., Young, K. L., Yuan, J. Min, M Zillikens, C., Zonderman, A. B., Ameur, A., Bandinelli, S., Bis, J. C., Boehnke, M., Bouchard, C., Chasman, D. I., Smith, G. Davey, de Geus, E. J. C., Deldicque, L., Dörr, M., Evans, M. K., Ferrucci, L., Fornage, M., Fox, C., ,, Gudnason, V., Gyllensten, U., Hansen, T., Hayward, C., Horta, B. L., Hypponen, E., Jarvelin, M. - R., W Johnson, C., Kardia, S. L. R., Kiemeney, L. A., Laakso, M., Langenberg, C., Lehtimäki, T., Le Marchand, L., Study, L. Cohort, Magnusson, P. K. E., Martin, N. G., Melbye, M., Metspalu, A., Meyre, D., North, K. E., Ohlsson, C., Oldehinkel, A. J., Orho-Melander, M., Pare, G., Park, T., Pedersen, O., Penninx, B. W. J. H., Pers, T. H., Polasek, O., Prokopenko, I., Rotimi, C. N., Samani, N. J., Sim, X., Snieder, H., Sørensen, T. I. A., Spector, T. D., Timpson, N. J., van Dam, R. M., van der Velde, N., van Duijn, C. M., Vollenweider, P., Völzke, H., Voortman, T., Waeber, G., Wareham, N. J., Weir, D. R., Wichmann, H. - E., Wilson, J. F., Hevener, A. L., Krook, A., Zierath, J. R., Thomis, M. A. I., Loos, R. J. F., and Hoed, Mden, “Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention”, Nature Genetics, vol. 54, pp. 1332–1344, 2022.
B. L. Mitchell, Saklatvala, J. R., Dand, N., Hagenbeek, F. A., Li, X., Min, J. L., Thomas, L., Bartels, M., Hottenga, J. Jan, Lupton, M. K., Boomsma, D. I., Dong, X., Hveem, K., Løset, M., Martin, N. G., Barker, J. N., Han, J., Smith, C. H., Rentería, M. E., and Simpson, M. A., “Genome-wide association meta-analysis identifies 29 new acne susceptibility loci”, Nature Communications, vol. 13, p. 702, 2022.
E. S. Jami, Hammerschlag, A. R., Ip, H. F., Allegrini, A. G., Benyamin, B., Border, R., Diemer, E. W., Jiang, C., Karhunen, V., Lu, Y., Lu, Q., Mallard, T. T., Mishra, P. P., Nolte, I. M., Palviainen, T., Peterson, R. E., Sallis, H. M., Shabalin, A. A., Tate, A. E., Thiering, E., Vilor-Tejedor, N., Wang, C., Zhou, A., Adkins, D. E., Alemany, S., Ask, H., Chen, Q., Corley, R. P., Ehli, E. A., Evans, L. M., Havdahl, A., Hagenbeek, F. A., Hakulinen, C., Henders, A. K., Hottenga, J. Jan, Korhonen, T., Mamun, A., Marrington, S., Neumann, A., Rimfeld, K., Rivadeneira, F., Silberg, J. L., van Beijsterveldt, C. E., Vuoksimaa, E., Whipp, A. M., Tong, X., Andreassen, O. A., Boomsma, D. I., Brown, S. A., S Burt, A., Copeland, W., Dick, D. M., K Harden, P., Harris, K. Mullan, Hartman, C. A., Heinrich, J., Hewitt, J. K., Hopfer, C., Hypponen, E., Jarvelin, M. - R., Kaprio, J., Keltikangas-Järvinen, L., Klump, K. L., Krauter, K., Kuja-Halkola, R., Larsson, H., Lehtimäki, T., Lichtenstein, P., Lundström, S., Maes, H. H., Magnus, P., Munafò, M. R., Najman, J. M., Njølstad, P. \aalR., Oldehinkel, A. J., Pennell, C. E., Plomin, R., Reichborn-Kjennerud, T., Reynolds, C., Rose, R. J., Smolen, A., Snieder, H., Stallings, M., Standl, M., Sunyer, J., Tiemeier, H., Wadsworth, S. J., Wall, T. L., Whitehouse, A. J. O., Williams, G. M., Ystrøm, E., Nivard, M. G., Bartels, M., and Middeldorp, C. M., “Genome-wide association meta-analysis of childhood and adolescent internalizing symptoms”, Journal of the American Academy of Child & Adolescent Psychiatry, vol. 61, pp. 934–945, 2022.
F. A. Hagenbeek, van Dongen, J., Pool, R., Harms, A. C., Roetman, P. J., Fanos, V., van Keulen, B. J., Walker, B. R., Karu, N., Pol, H. E. Hulshoff, Rotteveel, J., Finken, M. J. J., Vermeiren, R. R. J. M., Kluft, C., Bartels, M., Hankemeier, T., and Boomsma, D. I., “Heritability of urinary amines, organic acids, and steroid hormones in children”, Metabolites, vol. 12, p. 474, 2022.
K. M. Price, Wigg, K. G., Eising, E., Feng, Y., Blokland, K., Wilkinson, M., Kerr, E. N., Guger, S. L., Consortium, Q. Trait Work, Fisher, S. E., Lovett, M. W., Strug, L. J., and Barr, C. L., “Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities”, Translational Psychiatry, vol. 12, p. 495, 2022.
T. T. Mallard, Savage, J. E., Johnson, E. C., Huang, Y., Edwards, A. C., Hottenga, J. J., Grotzinger, A. D., Gustavson, D. E., Jennings, M. V., Anokhin, A., Dick, D. M., Edenberg, H. J., Kramer, J. R., Lai, D., Meyers, J. L., Pandey, A. K., Harden, K. Paige, Nivard, M. G., de Geus, E. J. C., Boomsma, D. I., Agrawal, A., Davis, L. K., Clarke, T. - K., Palmer, A. A., and Sanchez-Roige, S., “Item-level genome-wide association study of the Alcohol Use Disorders Identification Test in three population-based cohorts”, The American Journal of Psychiatry, vol. 179, pp. 58–70, 2022.

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