<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Saklatvala JR</submitter><funding>UK Medical Research Council Integrative Epidemiology Unit</funding><funding>Estonian Research Council</funding><funding>Innovative Medicines Initiative 2 Joint Undertaking</funding><funding>National Institute for Health Research (NIHR)</funding><funding>NIHR Advanced Fellowship</funding><funding>Wellcome Trust</funding><pagination>14</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12857016</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Psoriasis is a common inflammatory skin disease with heterogeneous presentation. Up to 30% of individuals have severe disease with a greater surface area of skin involvement, co-morbidity burden and impact on quality of life. Prognostic biomarkers of psoriasis severity could improve allocation of clinical resources and enable earlier intervention to prevent disease progression, and a genetic biomarker would be cost-effective, stable over time, and unaffected by treatment or comorbidity.&lt;h4>Methods&lt;/h4>Psoriasis severity was studied in four European population-based biobanks (Estonian Biobank, HUNT, FinnGen, UK Biobank) and classified based on level of clinical intervention received, with criteria for severe disease including hospitalisation due to psoriasis, use of syste</pubmed_abstract><journal>Genome medicine</journal><pubmed_title>Genetic liability to psoriasis predicts severe disease outcomes.</pubmed_title><pmcid>PMC12857016</pmcid><funding_grant_id>PRG1911 and TK (TK214)</funding_grant_id><funding_grant_id>220875/Z/20/Z</funding_grant_id><funding_grant_id>MC_UU_00011/1, 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Up to 30% of individuals have severe disease with a greater surface area of skin involvement, co-morbidity burden and impact on quality of life. Prognostic biomarkers of psoriasis severity could improve allocation of clinical resources and enable earlier intervention to prevent disease progression, and a genetic biomarker would be cost-effective, stable over time, and unaffected by treatment or comorbidity.&lt;h4>Methods&lt;/h4>Psoriasis severity was studied in four European population-based biobanks (Estonian Biobank, HUNT, FinnGen, UK Biobank) and classified based on level of clinical intervention received, with criteria for severe disease including hospitalisation due to psoriasis, use of syste</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-14T06:09:11.86Z</modification><creation>2026-06-14T03:15:04.849Z</creation></dates><accession>S-EPMC12857016</accession><cross_references><pubmed>41408349</pubmed><doi>10.1186/s13073-025-01561-2</doi></cross_references></HashMap>