Publications

2025

C. M. van der Laan, Ip, H. F., Schipper, M., Hottenga, J. - J., St Pourcain, B., Zayats, T., Pool, R., Krapohl, E. M. L., Brikell, I., Artigas, M. Soler, Cabana-Domínguez, J., Llonga, N., Nolte, I. M., Bolhuis, K., Palviainen, T., Zafarmand, H., Gordon, S., Aliev, F., S. Burt, A., Wang, C. A., Saunders, G., Karhunen, V., Adkins, D. E., Border, R., Peterson, R. E., Prinz, J. A., Thiering, E., Vilor-Tejedor, N., Ahluwalia, T. S., Allegrini, A., Rimfeld, K., Chen, Q., Lu, Y., Martin, J., Bosch, R., Ramos-Quiroga, J. Antoni, Neumann, A., Ensink, J., Grasby, K. L., Morosoli, J. J., Tong, X., Marrington, S., Scott, J. G., Shabalin, A. A., Corley, R., Evans, L. M., Sugden, K., Alemany, S., Sass, L., Vinding, R., Ehli, E. A., Hagenbeek, F. A., Derks, E. M., Larsson, H., Snieder, H., Cecil, C., Whipp, A. M., Korhonen, T., Vuoksimaa, E., Rose, R. J., Uitterlinden, A. G., Haavik, J., Harris, J. R., Helgeland, Ø., Johansson, S., Knudsen, G. Peggy S., Njolstad, P. Rasmus, Lu, Q., Rodriguez, A., Henders, A. K., Mamun, A., Najman, J. M., Brown, S., Hopfer, C., Krauter, K., Reynolds, C. A., Smolen, A., Stallings, M., Wadsworth, S., Wall, T. L., Eaves, L., Silberg, J. L., Miller, A., Havdahl, A., Llop, S., Lopez-Espinosa, M. - J., Bønnelykke, K., Sunyer, J., Arseneault, L., Standl, M., Heinrich, J., Boden, J., Pearson, J., Horwood, J., Kennedy, M., Poulton, R., Maes, H. H., Hewitt, J., Copeland, W. E., Middeldorp, C. M., Williams, G. M., Wray, N., Jarvelin, M. - R., McGue, M., Iacono, W., Caspi, A., Moffitt, T. E., Whitehouse, A. J. O., Pennell, C. E., Klump, K. L., Jiang, C., Dick, D. M., Reichborn-Kjennerud, T., Martin, N. G., Medland, S. E., Vrijkotte, T., Kaprio, J., Tiemeier, H., Smith, G. Davey, Hartman, C. A., Oldehinkel, A. J., Casas, M., Ribasés, M., Lichtenstein, P., Lundström, S., Plomin, R., Bartels, M., Nivard, M. G., and Boomsma, D. I., “Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes”, 2025.

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

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.

2021

I. E. Sønderby, van der Meer, D., Moreau, C., Kaufmann, T., G Walters, 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., Bøen, R., Cahn, W., Calhoun, V. D., Caspers, S., Ching, C. R. K., Cichon, S., Ciufolini, S., Crespo-Facorro, B., Curran, J. E., Dale, A. M., Dalvie, S., Dazzan, P., de Geus, E. J. C., de Zubicaray, G. I., de Zwarte, S. M. C., Desrivieres, S., Doherty, J. L., Donohoe, G., Draganski, B., Ehrlich, S., Eising, E., Espeseth, T., Fejgin, K., Fisher, S. E., Fladby, T., Frei, O., Frouin, V., Fukunaga, M., Gareau, T., Ge, T., Glahn, D. C., Grabe, H. J., Groenewold, N. A., Gústafsson, Ó., Haavik, J., Haberg, A. K., Hall, J., Hashimoto, R., Hehir-Kwa, J. Y., Hibar, D. P., Hillegers, M. H. J., Hoffmann, P., Holleran, L., Holmes, A. J., Homuth, G., Hottenga, J. - J., Pol, H. E. Hulshoff, Ikeda, M., Jahanshad, N., Jockwitz, C., Johansson, S., Jönsson, E. G., Jørgensen, N. R., Kikuchi, M., Knowles, E. E. M., Kumar, K., Le Hellard, S., Leu, C., Linden, D. E. J., Liu, J., Lundervold, A., Lundervold, A. Johansen, Maillard, A. M., Martin, N. G., Martin-Brevet, S., Mather, K. A., Mathias, S. R., McMahon, K. L., McRae, A. F., Medland, S. E., Meyer-Lindenberg, A., Moberget, T., Modenato, C., Sánchez, J. Monereo, Morris, D. W., Mühleisen, T. W., Murray, R. M., Nielsen, J., Nordvik, J. E., Nyberg, L., Loohuis, L. M. Olde, Ophoff, R. A., Owen, M. J., Paus, T., Pausova, Z., Peralta, J. M., G Pike, B., Prieto, C., Quinlan, E. B., Reinbold, C. S., Marques, T. Reis, Rucker, J. J. H., Sachdev, P. S., Sando, S. B., Schofield, P. R., Schork, A. J., Schumann, G., Shin, J., Shumskaya, E., Silva, A. I., Sisodiya, S. M., Steen, V. M., Stein, D. J., Strike, L. T., Suzuki, I. K., Tamnes, C. K., Teumer, A., Thalamuthu, A., Tordesillas-Gutiérrez, D., Uhlmann, A., Ulfarsson, M. O., Ent, Dvan 't, van den Bree, M. B. M., Vanderhaeghen, P., Vassos, E., Wen, W., Wittfeld, K., Wright, M. J., Agartz, I., Djurovic, S., Westlye, L. T., Stefansson, H., Stefansson, K., Jacquemont, S., Thompson, P. M., Andreassen, O. A., and group, E. N. I. G. M. A. - C. N. Vworking, “1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans”, Translational Psychiatry, vol. 11, p. 182, 2021.

H. F. Ip, Van der Laan, C. M., Krapohl, E. M. L., Brikell, I., Sánchez-Mora, C., Nolte, I. M., St Pourcain, B., Bolhuis, K., Palviainen, T., Zafarmand, H., Colodro-Conde, L., Gordon, S., Zayats, T., Aliev, F., Jiang, C., Wang, C. A., Saunders, G., Karhunen, V., Hammerschlag, A. R., Adkins, D. E., Border, R., Peterson, R. E., Prinz, J. A., Thiering, E., Seppälä, I., Vilor-Tejedor, N., Ahluwalia, T. S., Day, F. R., Hottenga, J. - J., Allegrini, A. G., Rimfeld, K., Chen, Q., Lu, Y., Martin, J., Artigas, M. Soler, Rovira, P., Bosch, R., Español, G., Quiroga, J. Antoni Ram, Neumann, A., Ensink, J., Grasby, K., Morosoli, J. J., Tong, X., Marrington, S., Middeldorp, C., Scott, J. G., Vinkhuyzen, A., Shabalin, A. A., Corley, R., Evans, L. M., Sugden, K., Alemany, S., Sass, L., Vinding, R., Ruth, K., Tyrrell, J., Davies, G. E., Ehli, E. A., Hagenbeek, F. A., de Zeeuw, E., van Beijsterveldt, T. C. E. M., Larsson, H., Snieder, H., Verhulst, F. C., Amin, N., Whipp, A. M., Korhonen, T., Vuoksimaa, E., Rose, R. J., Uitterlinden, A. G., Heath, A. C., Madden, P., Haavik, J., Harris, J. R., Helgeland, Ø., Johansson, S., Knudsen, G. Peggy S., Njolstad, P. Rasmus, Lu, Q., Rodriguez, A., Henders, A. K., Mamun, A., Najman, J. M., Brown, S., Hopfer, C., Krauter, K., Reynolds, C., Smolen, A., Stallings, M., Wadsworth, S., Wall, T. L., Silberg, J. L., Miller, A., Keltikangas-Järvinen, L., Hakulinen, C., Pulkki-R\aaback, L., Havdahl, A., Magnus, P., Raitakari, O. T., Perry, J. R. B., Llop, S., Lopez-Espinosa, M. - J., Bønnelykke, K., Bisgaard, H., Sunyer, J., Lehtimäki, T., Arseneault, L., Standl, M., Heinrich, J., Boden, J., Pearson, J., L Horwood, J., Kennedy, M., Poulton, R., Eaves, L. J., Maes, H. H., Hewitt, J., Copeland, W. E., Costello, E. J., Williams, G. M., Wray, N., Jarvelin, M. - R., McGue, M., Iacono, W., Caspi, A., Moffitt, T. E., Whitehouse, A., Pennell, C. E., Klump, K. L., S Burt, A., Dick, D. M., Reichborn-Kjennerud, T., Martin, N. G., Medland, S. E., Vrijkotte, T., Kaprio, J., Tiemeier, H., Smith, G. Davey, Hartman, C. A., Oldehinkel, A. J., Casas, M., Ribasés, M., Lichtenstein, P., Lundström, S., Plomin, R., Bartels, M., Nivard, M. G., and Boomsma, D. I., “Genetic association study of childhood aggression across raters, instruments, and age”, Translational Psychiatry, vol. 11, p. 413, 2021.

J. J. Beck, Pool, R., van de Weijer, M., Chen, X., Krapohl, E., Gordon, S. D., Nygaard, M., Debrabant, B., Palviainen, T., van der Zee, M. D., Baselmans, B., Finnicum, C. T., Yi, L., Lundström, S., van Beijsterveldt, T., Christiansen, L., Heikkilä, K., Kittelsrud, J., Loukola, A., Ollikainen, M., Christensen, K., Martin, N. G., Plomin, R., Nivard, M., Bartels, M., Dolan, C., Willemsen, G., de Geus, E., Almqvist, C., Magnusson, P. K. E., Mbarek, H., Ehli, E. A., Boomsma, D. I., and Hottenga, J. - J., “Genetic meta-analysis of twin birth weight shows high genetic correlation with singleton birth weight”, Human Molecular Genetics, vol. 30, pp. 1894–1905, 2021.

V. V. Odintsova, Rebattu, V., Hagenbeek, F. A., Pool, R., Beck, J. J., Ehli, E. A., van Beijsterveldt, C. E. M., Ligthart, L., Willemsen, G., de Geus, E. J. C., Hottenga, J. - J., Boomsma, D. I., and van Dongen, J., “Predicting complex traits and exposures from polygenic scores and blood and buccal DNA methylation profiles”, Frontiers in Psychiatry, vol. 12, p. 688464, 2021.

2020

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.

2019

L. Ligthart, van Beijsterveldt, C. E. M., Kevenaar, S. T., de Zeeuw, E., van Bergen, E., Bruins, S., Pool, R., Helmer, Q., van Dongen, J., Hottenga, J. - J., Ent, D. Van't, Dolan, C. V., Davies, G. E., Ehli, E. A., Bartels, M., Willemsen, G., de Geus, E. J. C., and Boomsma, D. I., “The Netherlands Twin Register: Longitudinal research based on twin and twin-family designs”, Twin Research and Human Genetics, vol. 22, pp. 623–636, 2019.

2017

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.

2016

J. van Dongen, Nivard, M. G., Willemsen, G., Hottenga, J. - J., Helmer, Q., Dolan, C. V., Ehli, E. A., Davies, G. E., van Iterson, M., Breeze, C. E., Beck, S., Consortium, B. I. O. S., H. Suchiman, E., Jansen, R., Van Meurs, J. B. J., Heijmans, B. T., P. Slagboom, E., and Boomsma, D. I., “Genetic and environmental influences interact with age and sex in shaping the human methylome”, Nat Commun, vol. 7, 2016.

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