Diagnostic Uptake of Targeted Sequencing in Adults With Steatotic Liver Disease and a Suspected Genetic Contribution
The diagnostic uptake of TS was 22% for Mendelian disorder and 59% for possible contribution to clinical phenotype in selected adult patients with SLD. Evaluation of common variants, as captured by SLD-PRS, yields complementary information increasing the overall utility of the genetic examination.
Authors
- Oveis Jamialahmadi (ORCID: https://orcid.org/0000-0001-7139-4738)
- Stefano Romeo (ORCID: https://orcid.org/0000-0001-9168-4898)
- Jessica Rondena
- Luca Valenti (ORCID: https://orcid.org/0000-0001-8909-0345)
- Daniele Prati (ORCID: https://orcid.org/0000-0002-2281-7498)
- Vittoria Moretti (ORCID: https://orcid.org/0000-0003-1150-5568)
- Cristiana Bianco (ORCID: https://orcid.org/0000-0003-4611-6781)
- Luisa Ronzoni (ORCID: https://orcid.org/0000-0001-7820-6533)
- Maria Rosaria De Filippo (ORCID: https://orcid.org/0000-0001-8350-2599)
- Giulia Periti (ORCID: https://orcid.org/0009-0005-1265-4583)
- Francesco Malvestiti (ORCID: https://orcid.org/0000-0002-2430-5883)
- Hadi Eidgah Torghabehei
- Serena Pelusi
Institutions
- University of Milan (IT)
- Sahlgrenska University Hospital (SE)
- Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico (IT)
- Magna Graecia University (IT)
- University of Gothenburg (SE)
Publication Details
- Journal
- Liver International
- Published
- 2025-02-13
- DOI
- https://doi.org/10.1111/liv.70010
- Citations
- 3
- Primary Topic
- Liver Disease Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 4.06
Funders
- Gilead Sciences
- European Federation of Pharmaceutical Industries and Associations
- European Commission
- Ministero della Salute
- Ministero dell'Università e della Ricerca
- Horizon 2020 Framework Programme