Genome-wide association for sarcoidosis identifies novel risk loci and genetic heritability in African and European ancestries: a meta-analysis from the Finngen, Million Veteran Program, UK Biobank, and Biobank Japan datasets.
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| Title: | Genome-wide association for sarcoidosis identifies novel risk loci and genetic heritability in African and European ancestries: a meta-analysis from the Finngen, Million Veteran Program, UK Biobank, and Biobank Japan datasets. |
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| Authors: | Ricci A; Centre for Genomic Medicine and Rare Diseases, Internal Medicine Unit, Department of Medical and Surgical Sciences, University Hospital of Modena - Policlinico, University of Modena and Reggio Emilia, Via del Pozzo 71,41121, Modena, Italy. andrea.ricci@unimore.it.; Internal Medicine Unit, University Hospital of Modena - Policlinico, University of Modena and Reggio Emilia, Modena, Italy. andrea.ricci@unimore.it., Andolfi F; Centre for Rare Lung Diseases, Pneumology Unit, Department of Medical and Surgical Sciences, University Hospital of Modena - Policlinico, ERN Lung, University of Modena and Reggio Emilia,Via del Pozzo 71, 41121, Modena, Italy., Sabbatini D; Department of Neurosciences Dns, University of Padova, Padova, Italy.; Unit of Biostatistics, Epidemiology and Public Health, Department of Cardiac, Thoracic, Vascular Sciences, and Public Health, University of Padova, Padova, Italy., Gozzi F; Centre for Rare Lung Diseases, Pneumology Unit, Department of Medical and Surgical Sciences, University Hospital of Modena - Policlinico, ERN Lung, University of Modena and Reggio Emilia,Via del Pozzo 71, 41121, Modena, Italy. filippo.gozzi@unimore.it., Betto GD; Centre for Genomic Medicine and Rare Diseases, Internal Medicine Unit, Department of Medical and Surgical Sciences, University Hospital of Modena - Policlinico, University of Modena and Reggio Emilia, Via del Pozzo 71,41121, Modena, Italy.; Internal Medicine Unit, University Hospital of Modena - Policlinico, University of Modena and Reggio Emilia, Modena, Italy., Ventura P; Centre for Genomic Medicine and Rare Diseases, Internal Medicine Unit, Department of Medical and Surgical Sciences, University Hospital of Modena - Policlinico, University of Modena and Reggio Emilia, Via del Pozzo 71,41121, Modena, Italy.; Internal Medicine Unit, University Hospital of Modena - Policlinico, University of Modena and Reggio Emilia, Modena, Italy., Buzzetti E; Centre for Genomic Medicine and Rare Diseases, Internal Medicine Unit, Department of Medical and Surgical Sciences, University Hospital of Modena - Policlinico, University of Modena and Reggio Emilia, Via del Pozzo 71,41121, Modena, Italy.; Internal Medicine Unit, University Hospital of Modena - Policlinico, University of Modena and Reggio Emilia, Modena, Italy., Pietrangelo A; Centre for Genomic Medicine and Rare Diseases, Internal Medicine Unit, Department of Medical and Surgical Sciences, University Hospital of Modena - Policlinico, University of Modena and Reggio Emilia, Via del Pozzo 71,41121, Modena, Italy.; Internal Medicine Unit, University Hospital of Modena - Policlinico, University of Modena and Reggio Emilia, Modena, Italy., Clini E; Centre for Rare Lung Diseases, Pneumology Unit, Department of Medical and Surgical Sciences, University Hospital of Modena - Policlinico, ERN Lung, University of Modena and Reggio Emilia,Via del Pozzo 71, 41121, Modena, Italy., Tonelli R; Centre for Rare Lung Diseases, Pneumology Unit, Department of Medical and Surgical Sciences, University Hospital of Modena - Policlinico, ERN Lung, University of Modena and Reggio Emilia,Via del Pozzo 71, 41121, Modena, Italy., Andrisani D; Centre for Rare Lung Diseases, Pneumology Unit, Department of Medical and Surgical Sciences, University Hospital of Modena - Policlinico, ERN Lung, University of Modena and Reggio Emilia,Via del Pozzo 71, 41121, Modena, Italy., de Guzman Marinduque BJ; School of Medicine and Surgery, University of Modena and Reggio Emilia, Modena, Italy., Bergamini E; Internal Medicine Unit, University Hospital of Modena - Policlinico, University of Modena and Reggio Emilia, Modena, Italy., Vecchi C; Internal Medicine Unit, University Hospital of Modena - Policlinico, University of Modena and Reggio Emilia, Modena, Italy., Pegoraro E; Department of Neurosciences Dns, University of Padova, Padova, Italy., Gregori D; Unit of Biostatistics, Epidemiology and Public Health, Department of Cardiac, Thoracic, Vascular Sciences, and Public Health, University of Padova, Padova, Italy., Corradini E; Centre for Genomic Medicine and Rare Diseases, Internal Medicine Unit, Department of Medical and Surgical Sciences, University Hospital of Modena - Policlinico, University of Modena and Reggio Emilia, Via del Pozzo 71,41121, Modena, Italy.; Internal Medicine Unit, University Hospital of Modena - Policlinico, University of Modena and Reggio Emilia, Modena, Italy., Cerri S; Centre for Rare Lung Diseases, Pneumology Unit, Department of Medical and Surgical Sciences, University Hospital of Modena - Policlinico, ERN Lung, University of Modena and Reggio Emilia,Via del Pozzo 71, 41121, Modena, Italy. |
| Source: | Orphanet journal of rare diseases [Orphanet J Rare Dis] 2025 Dec 29; Vol. 20 (1), pp. 638. Date of Electronic Publication: 2025 Dec 29. |
| Publication Type: | Journal Article; Meta-Analysis |
| Journal Info: | Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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