Morris Swertz

Search results

• 2021

  Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

  SOLVE-RD Consortium, Zurek, B., Ellwanger, K., Vissers, L. E. L. M., Schuele, R., Synofzik, M., Topf, A., de Voer, R. M., Laurie, S., Matalonga, L., Gilissen, C., Ossowski, S., 't Hoen, P. A. C., Vitobello, A., Schulze-Hentrich, J. M., Riess, O., Brunner, H. G., Brookes, A. J., Rath, A. & Bonne, G. & 10 others, Gumus, G., Verloes, A., Hoogerbrugge, N., Evangelista, T., Harmuth, T., Swertz, M., Spalding, D., Hoischen, A., Beltran, S. & Graessner, H., Sept-2021, In: European Journal of Human Genetics. 29, 9, p. 1325-1331 7 p.

  Research output: Contribution to journal › Editorial › Academic › peer-review

  Open Access

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  • Rare Disease 100%
  • Data Reanalysis 33%
  • Exome 25%
  • Case Forms 16%
  • Disease 12%
  60 Citations (Scopus)

  62 Downloads (Pure)