1. 2017
  2. Whole exome sequencing in thrombophilic pedigrees to identify genetic risk factors for venous thromboembolism

    Cunha, M. L. R., Meijers, J. C. M., Rosendaal, F. R., Vlieg, A. V. H., Reitsma, P. H. & Middeldorp, S., 2017, In: PLoS ONE. 12, 11, e0187699.

    Research output: Contribution to journalArticleAcademicpeer-review

  3. 2016
  4. Circulating nucleosomes and elastase α1-antitrypsin complexes and the novel thrombosis susceptibility locus SLC44A2

    Heestermans, M., Cunha, M. L. R., Reitsma, P. H., Zeerleder, S. S., Middeldorp, S. & van Vlijmen, B. J. M., 2016, In: Thrombosis research. 142, p. 8-10

    Research output: Contribution to journalComment/Letter to the editorAcademic

  5. 2015
  6. A novel mutation in the F5 gene (factor V Amsterdam) associated with bleeding independent of factor V procoagulant function

    Cunha, M. L. R., Bakhtiari, K., Peter, J., Marquart, J. A., Meijers, J. C. M. & Middeldorp, S., 2015, In: Blood. 125, 11, p. 1822-1825

    Research output: Contribution to journalArticleAcademicpeer-review

  7. Introduction to the analysis of next generation sequencing data and its application to venous thromboembolism

    Cunha, M. L. R., Meijers, J. C. M. & Middeldorp, S., 2015, In: Thrombosis and haemostasis. 114, 5, p. 920-932

    Research output: Contribution to journalArticleAcademicpeer-review

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