Specialization
Focus of research
Genetic obesity, Epigenetics
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DNA methylation analysis of NOTCH1 variants reveals the first episignature for non-syndromic congenital heart defects
Dombrowsky, G., van der Laan, L., Silva, A., Breckpot, J., Audain, E., Wilsdon, A., Levy, M. A., Vos, N., Mannens, M., Wang, J., Jain, A., Lesurf, R., Winlaw, D., Bezzina, C. R., Thomas, M. A., Caliebe, A., Klaassen, S., Berger, F., Dittrich, S. & Stiller, B. & 15 others, , 1 Dec 2026, In: Genome Medicine. 18, 1, 2.Research output: Contribution to journal › Article › Academic › peer-review
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Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options
Vos, N., Kleinendorst, L., van der Laan, L., van Uhm, J., Jansen, P. R., van Eeghen, A. M., Maas, S. M., Mannens, M. M. A. M. & van Haelst, M. M., Nov 2024, In: European journal of human genetics. 32, 11, p. 1387-1401 15 p.Research output: Contribution to journal › Article › Academic › peer-review
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The utility of obesity polygenic risk scores from research to clinical practice: A review
Jansen, P. R., Vos, N., van Uhm, J., Dekkers, I. A., van der Meer, R., Mannens, M. M. A. M. & van Haelst, M. M., Nov 2024, In: Obesity Reviews. 25, 11, p. 1-14 14 p., e13810.Research output: Contribution to journal › Review article › Academic › peer-review
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