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Dive into the research topics where Inge Mathijssen 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
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Sproetjes, café-au-laitvlekken en cutane noduli
Translated title of the contribution :A man with axillary and inguinal freckling, café-au-lait spots, and cutaneous nodules Research output: Contribution to journal › Article › Professional
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Maternal–Foetal HLA-DQB1 Incompatibility Is Associated With Pregnancy-Induced Hypertensive Disorders in a Genetically Isolated Population
Hof, L. J. V., van der Hoorn, M.-L. P., Migdis, S., Haasnoot, G. W., Peereboom, E. T. M., Spierings, E., van der Linden, P. J. E., Anholts, J. D. H., de Vreede, H., Ottenhof, W., Roelen, D. L., Eikmans, M., Mathijssen, I. B. & Lashley, L. E. E. L. O., 1 Aug 2025, In: HLA. 106, 2, e70374.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile31 Downloads (Pure) -
Counseling couples at risk of having a child with homozygous familial hypercholesterolemia – Clinical experience and recommendations
Tromp, T. R., Reijman, M. D., Wiegman, A., Hovingh, G. K., Defesche, J. C., van Maarle, M. C. & Mathijssen, I. B., 1 Mar 2023, In: Journal of clinical lipidology. 17, 2, p. 291-296 6 p.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile22 Downloads (Pure) -
De novo variants in the PABP domain of PABPC1 lead to developmental delay
Wegler, M., Jia, X., Alders, M., Bouman, A., Chen, J., Duan, X., Lauzon, J. L., Mathijssen, I. B., Sticht, H., Syrbe, S., Tan, S., Guo, H. & Abou Jamra, R., Aug 2022, In: Genetics in medicine. 24, 8, p. 1761-1773 13 p.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile16 Downloads (Pure) -
Erratum: Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms(Genet Med (2021)23(103-110)(s41436020009394)(10.1038/s41436-020-00939-4))
van Walree, E. S., Dombrowsky, G., Jansen, I. E., Umićević Mirkov, M., Zwart, R., Ilgun, A., Guo, D., Clur, S.-A. B., Amin, A. S., Savage, J. E., van der Wal, A. C., Waisfisz, Q., Maugeri, A., Wilsdon, A., Bu'Lock, F. A., Hurles, M. E., Dittrich, S., Berger, F., Audain Martinez, E. & Christoffels, V. M. & 6 others, , 1 Apr 2022, In: Genetics in medicine. 24, 4, p. 965 1 p.Research output: Contribution to journal › Comment/Letter to the editor › Academic
Open AccessFile5 Downloads (Pure)
Press/Media
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Polikliniek erfelijke ziektes Volendam groot succes
30/12/2014
1 Media contribution
Press/Media: Press / Media
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Nieuw leven: De Volendamse ziekte. En toen had baby Kees het ook.
27/12/2014
1 Media contribution
Press/Media: Press / Media