D.H. (Dylan) de Vries, BSc

PhD student genetics department UMCG

E-mail:
d.h.de.vries umcg.nl

Research

Publications
  1. The single-cell eQTLGen consortium

    Van Der Wijst, M. G. P., De Vries, D. H., Groot, H. E., Trynka, G., Hon, C. C., Bonder, M. J., Stegle, O., Nawijn, M. C., Idaghdour, Y., Van Der Harst, P., Ye, C. J., Powell, J., Theis, F. J., Mahfouz, A., Heing, M. & Franke, L., 9-Mar-2020, In : eLife. 9, 21 p., 52155.

    Research output: Contribution to journalArticleAcademicpeer-review

  2. CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018)

    DDD Study, 2-May-2019, In : Nature Communications. 10, 4 p., 2079.

    Research output: Contribution to journalArticleAcademicpeer-review

  3. An integrative approach for building personalized gene regulatory networks for precision medicine

    van der Wijst, M. G. P., de Vries, D. H., Brugge, H., Westra, H-J. & Franke, L., 19-Dec-2018, In : Genome medicine. 10, 15 p., 96.

    Research output: Contribution to journalArticleAcademicpeer-review

  4. Single-cell RNA sequencing identifies celltype-specific cis-eQTLs and co-expression QTLs

    Lifelines Cohort Study & BIOS Consortium, 2-Apr-2018, In : Nature Genetics. 50, 4, p. 493-497 5 p.

    Research output: Contribution to journalArticleAcademicpeer-review

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