Multi-Omics Integration in Clinical Practice for the Identification of Genetic Variants in Rare Diseases
- DOI
- 10.1016/j.arcmed.2026.103506
- Published
- 2026-12
- Container
- Archives of Medical Research
- Publisher
- Elsevier BV
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.arcmed.2026.103506,
title = {Multi-Omics Integration in Clinical Practice for the Identification of Genetic Variants in Rare Diseases},
author = {Jonathan Olival and Jordi Pijuan and Natàlia Caelles-Gramunt and Nidia Barco-Armengol and Leila Maestro and Guerau Fernández and Janet Hoenicka and Francesc Palau},
year = {2026},
journal = {Archives of Medical Research},
doi = {10.1016/j.arcmed.2026.103506},
url = {https://doi.org/10.1016/j.arcmed.2026.103506}
}RIS
TY - JOUR TI - Multi-Omics Integration in Clinical Practice for the Identification of Genetic Variants in Rare Diseases AU - Jonathan Olival AU - Jordi Pijuan AU - Natàlia Caelles-Gramunt AU - Nidia Barco-Armengol AU - Leila Maestro AU - Guerau Fernández AU - Janet Hoenicka AU - Francesc Palau PY - 2026 JO - Archives of Medical Research DO - 10.1016/j.arcmed.2026.103506 UR - https://doi.org/10.1016/j.arcmed.2026.103506 ER -
APA
Olival, J., Pijuan, J., Caelles-Gramunt, N., Barco-Armengol, N., Maestro, L., Fernández, G., Hoenicka, J., & Palau, F. (2026). Multi-Omics Integration in Clinical Practice for the Identification of Genetic Variants in Rare Diseases. Archives of Medical Research. https://doi.org/10.1016/j.arcmed.2026.103506
Source records
- crossref · retrieved 2026-09-26T12:30:52.470Z