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

Zurek B, Ellwanger K, Vissers LELM, Schüle R, Synofzik M, Töpf A, de Voer RM, Laurie S, Matalonga L, Gilissen C, Ossowski S, 't Hoen PAC, Vitobello A, Schulze-Hentrich JM, Riess O, Brunner HG, Brookes AJ, Rath A, Bonne G, Gumus G, Verloes A, Hoogerbrugge N, Evangelista T, Harmuth T, Swertz M, Spalding D, Hoischen A, Beltran S, Graessner H, Solve-RD consortium

Open source

DOI: 10.1038/s41431-021-00859-0
Published: 2021 Sep
Container: European journal of human genetics : EJHG
Publisher: Not recorded
Open access: yes

Credibility signals

limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.

Show all credibility signals

cautionDOI registered: No matching Crossref record was present in this response. Source: Crossref; license: CC0 metadata
cautionDOI resolves: No matching Crossref record was present in this response. Source: Crossref; license: CC0 metadata
not scoredDirectory of Open Access Journals: No matching DOAJ record was present in this response. No allow-list match; this is not evidence of low credibility. Source: DOAJ; license: CC0
not scoredMEDLINE indexed: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredOpenAlex core source: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredKnown publisher allow-list: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredROR affiliation: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
not scoredRetraction Watch expression of concern: No expression of concern notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
not scoredRetraction Watch correction: No correction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
supportingOpen access status: Normalized open-access status: open. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
not scoredPublication license: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredPublication version: A publication version was supplied but is not scored. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer

Cite this work

BibTeX

@article{allodium:10.1038/s41431-021-00859-0,
  title = {Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases.},
  author = {Zurek B and Ellwanger K and Vissers LELM and Schüle R and Synofzik M and Töpf A and de Voer RM and Laurie S and Matalonga L and Gilissen C and Ossowski S and 't Hoen PAC and Vitobello A and Schulze-Hentrich JM and Riess O and Brunner HG and Brookes AJ and Rath A and Bonne G and Gumus G and Verloes A and Hoogerbrugge N and Evangelista T and Harmuth T and Swertz M and Spalding D and Hoischen A and Beltran S and Graessner H and Solve-RD consortium},
  year = {2021},
  journal = {European journal of human genetics : EJHG},
  doi = {10.1038/s41431-021-00859-0},
  url = {https://doi.org/10.1038/s41431-021-00859-0}
}

RIS

TY  - JOUR
TI  - Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases.
AU  - Zurek B
AU  - Ellwanger K
AU  - Vissers LELM
AU  - Schüle R
AU  - Synofzik M
AU  - Töpf A
AU  - de Voer RM
AU  - Laurie S
AU  - Matalonga L
AU  - Gilissen C
AU  - Ossowski S
AU  - 't Hoen PAC
AU  - Vitobello A
AU  - Schulze-Hentrich JM
AU  - Riess O
AU  - Brunner HG
AU  - Brookes AJ
AU  - Rath A
AU  - Bonne G
AU  - Gumus G
AU  - Verloes A
AU  - Hoogerbrugge N
AU  - Evangelista T
AU  - Harmuth T
AU  - Swertz M
AU  - Spalding D
AU  - Hoischen A
AU  - Beltran S
AU  - Graessner H
AU  - Solve-RD consortium
PY  - 2021
JO  - European journal of human genetics : EJHG
DO  - 10.1038/s41431-021-00859-0
UR  - https://doi.org/10.1038/s41431-021-00859-0
ER  -

APA

B, Z., K, E., LELM, V., R, S., M, S., A, T., RM, D. V., S, L., L, M., C, G., S, O., PAC, '. H., A, V., JM, S., O, R., HG, B., AJ, B., A, R., G, B., G, G., A, V., N, H., T, E., T, H., M, S., D, S., A, H., S, B., H, G., & consortium, S. (2021). Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases.. European journal of human genetics : EJHG. https://doi.org/10.1038/s41431-021-00859-0

Source records

pubmed · retrieved 2026-09-26T01:48:01.641Z
europe-pmc · retrieved 2026-09-26T01:48:01.645Z
hal · retrieved 2026-09-26T01:48:01.686Z