Marcel Reinders

DR.

20082019
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Research Output 2008 2019

A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer Disease European DNA biobank), EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementia), Netherlands Brain Bank (NBB) & The GIFT (Genetic Investigation in Frontotemporal Dementia and Alzheimer’s Disease) Study Group, 2019, In : Acta Neuropathologica.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access

Early steroid withdrawal compared with standard immunosuppression in kidney transplantation - Interim analysis of the Amsterdam-Leiden-Groningen randomized controlled trial

van Sandwijk, M. S., de Vries, A. P. J., Bakker, S. J. L., ten Berge, I. J. M., Berger, S. P., Bouatou, Y. R., de Fijter, J. W., Florquin, S., Homan van der Heide, J. J., Idu, M. M., Krikke, C., van der Pant, K. A. M. I., Reinders, M. E., Ringers, J., van der Weerd, N. C., Bemelman, F. J. & Sanders, J-S. S., 2018, In : Transplantation Direct. 4, 6, e354.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access

Characterization of pathogenic SORL1 genetic variants for association with Alzheimer's disease: A clinical interpretation strategy

Holstege, H., Van Der Lee, S. J., Hulsman, M., Wong, T. H., Van Rooij, J. G. J., Weiss, M., Louwersheimer, E., Wolters, F. J., Amin, N., Uitterlinden, A. G., Hofman, A., Ikram, M. A., Van Swieten, J. C., Meijers-Heijboer, H., Van Der Flier, W. M., Reinders, M. J. T., Van Duijn, C. M. & Scheltens, P., 1 Aug 2017, In : European Journal of Human Genetics. 25, 8, p. 973-981 9 p.

Research output: Contribution to journalArticleAcademicpeer-review

WISExome: A within-sample comparison approach to detect copy number variations in whole exome sequencing data

Straver, R., Weiss, M. M., Waisfisz, Q., Sistermans, E. A. & Reinders, M. J. T., 1 Dec 2017, In : European Journal of Human Genetics. 25, 12, p. 1354-1363 10 p.

Research output: Contribution to journalArticleAcademicpeer-review