Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects
- DOI
- 10.1097/md.0000000000000925
- Published
- 2015-06
- Container
- Medicine
- Publisher
- Ovid Technologies (Wolters Kluwer Health)
- 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.
- supportingDOI resolves: A matching record was returned by Crossref.
- 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.
- not scoredMEDLINE indexed: Not checked or no result supplied; no credibility inference made.
- not scoredOpenAlex core source: Not checked or no result supplied; no credibility inference made.
- not scoredKnown publisher allow-list: Not checked or no result supplied; no credibility inference made.
- not scoredROR affiliation: Not checked or no result supplied; no credibility inference made.
- not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- 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.
- not scoredRetraction Watch correction: No correction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredOpen access status: Not checked or no result supplied; no credibility inference made.
- not scoredPublication license: Not checked or no result supplied; no credibility inference made.
- not scoredPublication version: A publication version was supplied but is not scored.
- supportingMetadata completeness: All 6 scored descriptive metadata groups are present.
Cite this work
BibTeX
@article{allodium:10.1097/md.0000000000000925,
title = {Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects},
author = {Abderrahim Oussalah and Paolo Bosco and Guido Anello and Rosario Spada and Rosa-Maria Guéant-Rodriguez and Céline Chery and Pierre Rouyer and Thomas Josse and Antonino Romano and Maurizzio Elia and Jean-Pierre Bronowicki and Jean-Louis Guéant},
year = {2015},
journal = {Medicine},
doi = {10.1097/md.0000000000000925},
url = {https://doi.org/10.1097/md.0000000000000925}
}RIS
TY - JOUR TI - Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects AU - Abderrahim Oussalah AU - Paolo Bosco AU - Guido Anello AU - Rosario Spada AU - Rosa-Maria Guéant-Rodriguez AU - Céline Chery AU - Pierre Rouyer AU - Thomas Josse AU - Antonino Romano AU - Maurizzio Elia AU - Jean-Pierre Bronowicki AU - Jean-Louis Guéant PY - 2015 JO - Medicine DO - 10.1097/md.0000000000000925 UR - https://doi.org/10.1097/md.0000000000000925 ER -
APA
Oussalah, A., Bosco, P., Anello, G., Spada, R., Guéant-Rodriguez, R., Chery, C., Rouyer, P., Josse, T., Romano, A., Elia, M., Bronowicki, J., & Guéant, J. (2015). Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects. Medicine. https://doi.org/10.1097/md.0000000000000925
Source records
- crossref · retrieved 2026-11-08T16:50:29.626Z