Research output per year
Research output per year
Personal profile
Research interests
Congenital and acquired disorders of the thyroid and pituitary gland in children, with a focus on central congenital hypothyroidism.
specialisation
Ped. Endocrinologist, Head dept. of Ped. Endocrinology, Head Internship program Faculty of Medicine
Network
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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Just as Tall on Testosterone; a Neutral to Positive Effect on Adult Height of GnRHa and Testosterone in Trans Boys
Willemsen, L. A., Boogers, L. S., Wiepjes, C. M., Klink, D. T., van Trotsenburg, A. S. P., den Heijer, M. & Hannema, S. E., 17 Jan 2023, In: The Journal of clinical endocrinology and metabolism. 108, 2, p. 414-421 8 p.Research output: Contribution to journal › Article › Academic › peer-review
Open Access -
Machine learning to improve false-positive results in the Dutch newborn screening for congenital hypothyroidism
Stroek, K., Visser, A., van der Ploeg, C. P. B., Zwaveling-Soonawala, N., Heijboer, A. C., Bosch, A. M., van Trotsenburg, A. S. P., Boelen, A., Hoogendoorn, M. & de Jonge, R., 1 Jun 2023, In: Clinical Biochemistry. 116, p. 7-10 4 p.Research output: Contribution to journal › Article › Academic › peer-review
Open Access -
Meta-Analysis of DNA Methylation Datasets Shows Aberrant DNA Methylation of Thyroid Development or Function Genes in Down Syndrome
Lauffer, P., Zwaveling-Soonawala, N., Li, S., Bacalini, M. G., Naumova, O. Y., Wiemels, J., Boelen, A., Henneman, P., de Smith, A. J. & van Trotsenburg, A. S. P., 1 Jan 2023, In: Thyroid. 33, 1, p. 53-62 10 p.Research output: Contribution to journal › Article › Academic › peer-review
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2022 European Thyroid Association Guideline for the management of pediatric Graves’ disease
Mooij, C. F., Cheetham, T. D., Verburg, F. A., Eckstein, A., Pearce, S. H., Léger, J. & van Trotsenburg, A. S. P., 1 Jan 2022, In: European thyroid journal. 11, 1, e210073.Research output: Contribution to journal › Article › Academic › peer-review
Open Access20 Citations (Scopus) -
An animal model for Pierpont syndrome: a mouse bearing the Tbl1xr1Y446C/Y446C mutation
Hu, Y., Lauffer, P., Stewart, M., Codner, G., Mayerl, S., Heuer, H., Ng, L., Forrest, D., van Trotsenburg, P., Jongejan, A., Fliers, E., Hennekam, R. & Boelen, A., 25 Aug 2022, In: Human Molecular Genetics. 31, 17, p. 2951-2963 13 p.Research output: Contribution to journal › Article › Academic › peer-review
Open Access