Research output per year
Research output per year
Personal profile
Research interests
Congenital anomalies in the Dutch Caribbean
specialisation
Clinical Genetics
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
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DNA methylation episignature, extension of the clinical features, and comparative epigenomic profiling of Hao-Fountain syndrome caused by variants in USP7
van der Laan, L., Karimi, K., Rooney, K., Lauffer, P., McConkey, H., Caro, P., Relator, R., Levy, M. A., Bhai, P., Mignot, C., Keren, B., Briuglia, S., Sobering, A. K., Li, D., Vissers, L. E. L. M., Dingemans, A. J. M., Valenzuela, I., Verberne, E. A., Misra-Isrie, M., Zwijnenburg, P. J. G., & 8 others, 1 Mar 2024, In: Genetics in medicine. 26, 3, 101050.Research output: Contribution to journal › Article › Academic › peer-review
Open Access -
DNA methylation episignature, extension of the clinical features and comparative epigenomic profiling of Hao-Fountain syndrome caused by variants in USP7
van der Laan, L., Karimi, K., Rooney, K., Lauffer, P., McConkey, H., Caro, P., Relator, R., Levy, M. A., Bhai, P., Mignot, C., Keren, B., Briuglia, S., Sobering, A. K., Li, D., Vissers, L. E. L. M., Dingemans, A. J. M., Valenzuela, I., Verberne, E. A., Misra-Isrie, M., Zwijnenburg, P. J. G., & 8 others, 18 Dec 2023, (E-pub ahead of print) In: Genetics in medicine. p. 101050Research output: Contribution to journal › Article › Academic › peer-review
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Dutch Caribbean genetics: Diagnostics of congenital anomalies and genetic disorders in small island communities
Verberne, E. A., 2023, 210 p.Research output: PhD Thesis › Phd-Thesis - Research and graduation internal
Open Access -
Functional Insight into and Refinement of the Genomic Boundaries of the JARID2-Neurodevelopmental Disorder Episignature
van der Laan, L., Rooney, K., Haghshenas, S., Silva, A., McConkey, H., Relator, R., Levy, M. A., Valenzuela, I., Trujillano, L., Lasa-Aranzasti, A., Campos, B., Castells, N., Verberne, E. A., Maas, S., Alders, M., Mannens, M. M. A. M., van Haelst, M. M., Sadikovic, B. & Henneman, P., 1 Sept 2023, In: International journal of molecular sciences. 24, 18, 14240.Research output: Contribution to journal › Article › Academic › peer-review
Open Access1 Citation (Scopus) -
GMDS Intragenic Deletions Associate with Congenital Heart Disaese including Ebstein Anomaly
van Haelst, M. M., Lo-A-Njoe, S. M., Verberne, E. A., van der Veken, L. T., Arends, E., van Tintelen, JP. & Postma, A. V., 2023, In: Clinical Cardiogenetics: Third Edition. 13, 3, p. 106-112 7 p.Research output: Contribution to journal › Article › Academic › peer-review