ImprintCap, a powerful NGS-based technology to investigate the molecular background of imprinting disorders

Frédéric Brioude, Martin A. Haagmans, Marcel Mannens, Irene Netchine, Marielle Alders, Peter Henneman, Jet Bliek

Open source

DOI: 10.1186/s13148-025-01916-x
Published: 2025-07-07
Container: Clinical Epigenetics
Publisher: Springer Science and Business Media LLC
Open access: unknown

Credibility signals

uncertain Score 64/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.

Show all credibility signals

supportingDOI registered: A matching record was returned by Crossref. Source: Crossref; license: CC0 metadata
supportingDOI resolves: A matching record was returned by Crossref. 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
not scoredOpen access status: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
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
supportingMetadata completeness: All 6 scored descriptive metadata groups are present. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer

Cite this work

BibTeX

@article{allodium:10.1186/s13148-025-01916-x,
  title = {ImprintCap, a powerful NGS-based technology to investigate the molecular background of imprinting disorders},
  author = {Frédéric Brioude and Martin A. Haagmans and Marcel Mannens and Irene Netchine and Marielle Alders and Peter Henneman and Jet Bliek},
  year = {2025},
  journal = {Clinical Epigenetics},
  doi = {10.1186/s13148-025-01916-x},
  url = {https://doi.org/10.1186/s13148-025-01916-x}
}

RIS

TY  - JOUR
TI  - ImprintCap, a powerful NGS-based technology to investigate the molecular background of imprinting disorders
AU  - Frédéric Brioude
AU  - Martin A. Haagmans
AU  - Marcel Mannens
AU  - Irene Netchine
AU  - Marielle Alders
AU  - Peter Henneman
AU  - Jet Bliek
PY  - 2025
JO  - Clinical Epigenetics
DO  - 10.1186/s13148-025-01916-x
UR  - https://doi.org/10.1186/s13148-025-01916-x
ER  -

APA

Brioude, F., Haagmans, M. A., Mannens, M., Netchine, I., Alders, M., Henneman, P., & Bliek, J. (2025). ImprintCap, a powerful NGS-based technology to investigate the molecular background of imprinting disorders. Clinical Epigenetics. https://doi.org/10.1186/s13148-025-01916-x

Source records

crossref · retrieved 2026-09-25T22:08:17.824Z