![]() | JACQUINET, A., Flasse, L., Dohet, M., Vanhaeren, R., Pendeville-Samain, H., Saunders, C., Lehman, A., Pienkowski, C., Morcel, K., Guerrier, D., Bours, V.* , & Peers, B.*. (2026). Variants in NR6A1 as a cause for congenital renal, vertebral and uterine anomalies. Human Genetics. doi:10.1007/s00439-025-02806-1 Peer Reviewed verified by ORBi* These authors have contributed equally to this work. |
![]() | Vanhaeren, R., Jacquinet, A., Dohet, M., Flasse, L., Kerff, F., & Peers, B. (12 September 2025). Investigating MRKH syndrome using nr6a1a/b mutant zebrafish models [Poster presentation]. GIGA DAY. |
![]() | Vanhaeren, R., Jacquinet, A., Dohet, M., Flasse, L., Kerff, F., & Peers, B. (11 July 2025). Modeling MRKH syndrome in zebrafish through deleterious nr6a1a/b mutations [Poster presentation]. 19th International Zebrafish Conference. |
![]() | Dohet, M., Flasse, L., GRISART, B., Dideberg, V., & Peers, B. (30 May 2024). GENETIC DIAGNOSIS OF INHERITED KIDNEY DISEASES BY MODELIZATION IN ZEBRAFISH [Poster presentation]. interuniversity PhD student day, Louvain-la-Neuve, Belgium. |
![]() | Vanhaeren, R., Dohet, M., Jacquinet, A., & Peers, B. (30 May 2024). Role and mechanism of action of the orphan nuclear receptor NR6A1 in vertebrate development [Poster presentation]. InterUniversity PhD Student Day 2024, Louvain-la-Neuve, Belgium. |
![]() | Jacquinet, A., Flasse, L., Dohet, M., Pendeville-Samain, H., Plougonven, E., Léonard, A., Guerrier, D., Peers, B., & Bours, V. (2023). Identification of NR6A1 as a new gene involved in congenital urogenital anomalies [Poster presentation]. 56th European Human Genetics Conference 2023. Editorial reviewed |