Personal profile
Expertises
Neurogenetics; neuropsychiatry
Main research areas
Neuropsychiatry
Current research
Neurogenetics
Potential conflicts of interest
None
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Dive into the research topics where Trine Bjørg Hammer is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
Research output
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Biallelic variants in CELSR1 cause brain malformations, neurodevelopmental disorders and epilepsy in humans
Bonardi, C. M., Møller, R. S., Ruiz-Reig, N., Chai, G., Madsen, C. G., Bayat, A., Hammer, T. B., Fenger, C. D., Gardella, E., Gawlinski, P., Dawidziuk, M., Wiszniewski, W., Bekiesinska-Figatowska, M., Cabet, S., Rossi, M., Lesca, G., Gouy, E., Jepsen, B., Mieszczanek, T. S. & Sanchez Russo, R. & 8 others, , 13 Jan 2026, In: Nature Communications. 17, 1, p. 862 862.Research output: Contribution to journal › Journal article › Research › peer-review
2 Citations (Scopus) -
De novo variants in the splicing factor gene SF3B1 are associated with neurodevelopmental disorders
Uguen, K., Bergot, T., Scott-Boyer, M.-P., Chapalain, S., Desdouets, C., Commet, S., Zhu, C., Xu, Y., Wang, Y., Roscioli, T., Tran-Mau-Them, F., Faivre, L., Maraval, J., Delanne, J., Denommé-Pichon, A.-S., Vitobello, A., Jost, C., Planes, M., Hiatt, S. & Wheeler, P. & 47 others, , 23 Jan 2026, In: Nature Communications. 17, 1, 17 p., 1569.Research output: Contribution to journal › Journal article › Research › peer-review
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GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy
Lemke, J. R., Eoli, A., Krey, I., Popp, B., Strehlow, V., Wittekind, D. A., Vuorinen, A.-L., Aldhalaan, H. M., Baer, S., de Saint Martin, A., Hammer, T. B., Herman, I., Hornemann, F., Ingebrigtsen, T., Lederer, D., Lesca, G., Marafie, D., Mathot, M., Rosenfeld, J. A. & Møller, R. S. & 12 others, , Jan 2026, In: Molecular Psychiatry. 31, 1, p. 374-382 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
3 Citations (Scopus) -
Biallelic loss-of-function variants in ZNF142 are associated with a robust DNA methylation signature affecting a limited number of genomic loci
Hildonen, M., Ciolfi, A., Ferilli, M., Cappelletti, C., Al Alam, C., Amor, D. J., Barakat, T. S., Benoit, V., Birk, O. S., Callewaert, B., Cazurro-Gutiérrez, A., De Wachter, M., Doco-Fenzy, M., Gómez-Puertas, P., Hammer, T. B., Jamra, R. A., Kaiyrzhanov, R., Kameyama, S., Keren, B. & Kresge, C. & 21 others, , Jul 2025, In: European journal of human genetics : EJHG. 33, 7, p. 896-903 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
3 Citations (Scopus) -
Diagnostic yield of whole exome sequencing in a cohort of 825 patients
Andersen, P. F., Ek, J., Karstensen, H. G., Bak, M., Grønborg, S., Hove, H. B., Diness, B., Hjortshøj, T. D., Hammer, T. B., Høi-Hansen, C., Greulich, B. S., Bisgaard, A.-M., Duno, M. & Østergaard, E., Dec 2025, In: European Journal of Medical Genetics. 78, p. 105043 105043.Research output: Contribution to journal › Journal article › Research › peer-review