D.H. (Dylan) de Vries, BSc

PhD student genetics department UMCG

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

Research

Publications
  1. 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

  2. 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

  3. 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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