Projects per year
Personal profile
Research interests
To identify novel genes in families in which a strong autosomal dominant trait for extreme lipid disorders or premature atherosclerosis of unknown aetiology is observed.
specialisation
DNA, NGS, Sequencing, HDL, LDL
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
Projects
- 1 Active
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Meijers J.C.M.: Biochemistry of hemostasis and thrombosis
Cunha, M., Plug, T., de Ronde, M., Meijers, J., Levels, J. & Peter, J.
1/01/2007 → …
Project: Research
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Diacylglycerols and Lysophosphatidic Acid, Enriched on Lipoprotein(a), Contribute to Monocyte Inflammation
Dzobo, K. E., Cupido, A. J., Mol, B. M., Stiekema, L. C. A., Versloot, M., Winkelmeijer, M., Peter, J., Pennekamp, A-M., Havik, S. R., Vaz, F. M., van Weeghel, M., Prange, K. H. M., Levels, J. H. M., de Winther, M. P. J., Tsimikas, S., Groen, A. K., Stroes, E. S. G., de Kleijn, D. P. V. & Kroon, J., 1 Mar 2024, In: Arteriosclerosis, Thrombosis, and Vascular Biology. 44, 3, p. 720-740 21 p.Research output: Contribution to journal › Article › Academic › peer-review
Open Access -
Low-Cost High-Throughput Genotyping for Diagnosing Familial Hypercholesterolemia
Ibrahim, S., van Rooij, J., Verkerk, A. J. M. H., de Vries, J., Zuurbier, L., Defesche, J., Peter, J., Schonck, W. A. M., Sedaghati-Khayat, B., Kees Hovingh, G., Uitterlinden, A. G., Stroes, E. S. G. & Reeskamp, L. F., 1 Oct 2023, In: Circulation. Genomic and precision medicine. 16, 5, p. 462-469 8 p.Research output: Contribution to journal › Article › Academic › peer-review
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Use of Lipoprotein(a) to improve diagnosis and management in clinical familial hypercholesterolemia
Tromp, T. R., Ibrahim, S., Nurmohamed, N. S., Peter, J., Zuurbier, L., Defesche, J. C., Reeskamp, L. F., Hovingh, G. K. & Stroes, E. S. G., Jan 2023, In: Atherosclerosis. 365, p. 27-33 7 p.Research output: Contribution to journal › Article › Academic › peer-review
Open Access9 Citations (Scopus) -
Intronic variant screening with targeted next-generation sequencing reveals first pseudoexon in LDLR in familial hypercholesterolemia
Reeskamp, L. F., Balvers, M., Peter, J., van de Kerkhof, L., Klaaijsen, L. N., Motazacker, M. M., Grefhorst, A., van Riel, N. A. W., Hovingh, G. K., Defesche, J. C. & Zuurbier, L., 1 Mar 2021, In: Atherosclerosis. 321, p. 14-20 7 p.Research output: Contribution to journal › Article › Academic › peer-review
Open Access9 Citations (Scopus) -
Genetic variants in SUSD2 are associated with the risk of ischemic heart disease
Bruikman, C. S., Dalila, N., van Capelleveen, J. C., Kroon, J., Peter, J., Havik, S. R., Willems, M., Huisman, L. C., de Boer, O. J., Hovingh, G. K., Tybjaerg-Hansen, A. & Dallinga-Thie, G. M., 1 Jul 2020, In: Journal of clinical lipidology. 14, 4, p. 470-481 12 p.Research output: Contribution to journal › Article › Academic › peer-review
2 Citations (Scopus)