Consensus recommendations for next-generation sequencing-based genetic testing in Rare Neurological diseases.

Maver A, Lohmann K, Urbanczyk LM, Arnesen A, Barić I, Bauer P, Bhatia KP, Boesch S, Borovečki F, Brüggemann N, Fang ZH, Gabriel H, Haack TB, Houlden H, Janković M, Kamsteeg EJ, Mancuso M, Mascalzoni D, Molnar MJ, Münchau A, Neveling K, Novaković I, Peterlin B, Schols L, Schuermans N, Shiels K, Sturm M, Taylor R, Tijssen MAJ, Vissers LELM, Williams V, Graessner H, European Reference Network for Rare Neurological Disorders (ERN-RND)

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DOI: 10.1038/s41431-026-02198-4
Published: 2026 Jul 28
Container: European journal of human genetics : EJHG
Publisher: Not recorded
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1038/s41431-026-02198-4,
  title = {Consensus recommendations for next-generation sequencing-based genetic testing in Rare Neurological diseases.},
  author = {Maver A and Lohmann K and Urbanczyk LM and Arnesen A and Barić I and Bauer P and Bhatia KP and Boesch S and Borovečki F and Brüggemann N and Fang ZH and Gabriel H and Haack TB and Houlden H and Janković M and Kamsteeg EJ and Mancuso M and Mascalzoni D and Molnar MJ and Münchau A and Neveling K and Novaković I and Peterlin B and Schols L and Schuermans N and Shiels K and Sturm M and Taylor R and Tijssen MAJ and Vissers LELM and Williams V and Graessner H and European Reference Network for Rare Neurological Disorders (ERN-RND)},
  year = {2026},
  journal = {European journal of human genetics : EJHG},
  doi = {10.1038/s41431-026-02198-4},
  url = {https://doi.org/10.1038/s41431-026-02198-4}
}

RIS

TY  - JOUR
TI  - Consensus recommendations for next-generation sequencing-based genetic testing in Rare Neurological diseases.
AU  - Maver A
AU  - Lohmann K
AU  - Urbanczyk LM
AU  - Arnesen A
AU  - Barić I
AU  - Bauer P
AU  - Bhatia KP
AU  - Boesch S
AU  - Borovečki F
AU  - Brüggemann N
AU  - Fang ZH
AU  - Gabriel H
AU  - Haack TB
AU  - Houlden H
AU  - Janković M
AU  - Kamsteeg EJ
AU  - Mancuso M
AU  - Mascalzoni D
AU  - Molnar MJ
AU  - Münchau A
AU  - Neveling K
AU  - Novaković I
AU  - Peterlin B
AU  - Schols L
AU  - Schuermans N
AU  - Shiels K
AU  - Sturm M
AU  - Taylor R
AU  - Tijssen MAJ
AU  - Vissers LELM
AU  - Williams V
AU  - Graessner H
AU  - European Reference Network for Rare Neurological Disorders (ERN-RND)
PY  - 2026
JO  - European journal of human genetics : EJHG
DO  - 10.1038/s41431-026-02198-4
UR  - https://doi.org/10.1038/s41431-026-02198-4
ER  -

APA

A, M., K, L., LM, U., A, A., I, B., P, B., KP, B., S, B., F, B., N, B., ZH, F., H, G., TB, H., H, H., M, J., EJ, K., M, M., D, M., MJ, M., A, M., K, N., I, N., B, P., L, S., N, S., K, S., M, S., R, T., MAJ, T., LELM, V., V, W., H, G., & (ERN-RND), E. R. N. F. R. N. D. (2026). Consensus recommendations for next-generation sequencing-based genetic testing in Rare Neurological diseases.. European journal of human genetics : EJHG. https://doi.org/10.1038/s41431-026-02198-4

Source records

pubmed · retrieved 2026-09-26T09:23:53.143Z