Joeri van der Velde

Search results

• 2021

  Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

  Solve-RD-DITF-RND, The Solve-RD Consortium, Schüle, R., Timmann, D., Erasmus, C. E., Reichbauer, J., Wayand, M., van de Warrenburg, B., Schöls, L., Wilke, C., Bevot, A., Zuchner, S., Beltran, S., Laurie, S., Matalonga, L., Graessner, H. & Synofzik, M., Sept-2021, In: European Journal of Human Genetics. 29, 9, p. 1462-1465 4 p.

  Research output: Contribution to journal › Erratum

  Open Access

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  16 Downloads (Pure)

• Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2)

  Solve-RD SNV-indel working group, Solve-RD-DITF-ITHACA, de Boer, E., Ockeloen, C. W., Matalonga, L., Horvath, R., Rodenburg, R. J., Coenen, M. J. H., Janssen, M., Henssen, D., Gilissen, C., Steyaert, W., Paramonov, I., Trimouille, A., Kleefstra, T., Verloes, A. & Vissers, L. E. L. M., Sept-2021, In: European Journal of Human Genetics. 29, 9, p. 1470-1471 2 p.

  Research output: Contribution to journal › Erratum

  Open Access

  File
  1 Citation (Scopus)

  14 Downloads (Pure)
• 2019

  Correction to: The 1000IBD project: multi-omics data of 1000 inflammatory bowel disease patients; data release 1

  Imhann, F., Van der Velde, K. J., Barbieri, R., Alberts, R., Voskuil, M. D., Vila, A. V., Collij, V., Spekhorst, L. M., Van der Sloot, K. W. J., Peters, V., Van Dullemen, H. M., Visschedijk, M. C., Festen, E. A. M., Swertz, M. A., Dijkstra, G. & Weersma, R. K., 27-Mar-2019, In: Bmc gastroenterology. 19, 1, 1 p., 44.

  Research output: Contribution to journal › Erratum

  Open Access

  File
  7 Citations (Scopus)

  236 Downloads (Pure)