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 |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 41466414 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: 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. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Ricci+A%22">Ricci A</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Andolfi+F%22">Andolfi F</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Sabbatini+D%22">Sabbatini D</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Gozzi+F%22">Gozzi F</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Betto+GD%22">Betto GD</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Ventura+P%22">Ventura P</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Buzzetti+E%22">Buzzetti E</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Pietrangelo+A%22">Pietrangelo A</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Clini+E%22">Clini E</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Tonelli+R%22">Tonelli R</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Andrisani+D%22">Andrisani D</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22de+Guzman+Marinduque+BJ%22">de Guzman Marinduque BJ</searchLink>; School of Medicine and Surgery, University of Modena and Reggio Emilia, Modena, Italy.<br /><searchLink fieldCode="AU" term="%22Bergamini+E%22">Bergamini E</searchLink>; Internal Medicine Unit, University Hospital of Modena - Policlinico, University of Modena and Reggio Emilia, Modena, Italy.<br /><searchLink fieldCode="AU" term="%22Vecchi+C%22">Vecchi C</searchLink>; Internal Medicine Unit, University Hospital of Modena - Policlinico, University of Modena and Reggio Emilia, Modena, Italy.<br /><searchLink fieldCode="AU" term="%22Pegoraro+E%22">Pegoraro E</searchLink>; Department of Neurosciences Dns, University of Padova, Padova, Italy.<br /><searchLink fieldCode="AU" term="%22Gregori+D%22">Gregori D</searchLink>; Unit of Biostatistics, Epidemiology and Public Health, Department of Cardiac, Thoracic, Vascular Sciences, and Public Health, University of Padova, Padova, Italy.<br /><searchLink fieldCode="AU" term="%22Corradini+E%22">Corradini E</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Cerri+S%22">Cerri S</searchLink>; 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. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101266602%22">Orphanet journal of rare diseases</searchLink> [Orphanet J Rare Dis] 2025 Dec 29; Vol. 20 (1), pp. 638. <i>Date of Electronic Publication: </i>2025 Dec 29. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Meta-Analysis – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101266602 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1750-1172 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217501172%22">17501172 </searchLink><i>NLM ISO Abbreviation: </i>Orphanet J Rare Dis <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=41466414 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-025-04097-1 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 638 Titles: – TitleFull: 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. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Ricci A – PersonEntity: Name: NameFull: Andolfi F – PersonEntity: Name: NameFull: Sabbatini D – PersonEntity: Name: NameFull: Gozzi F – PersonEntity: Name: NameFull: Betto GD – PersonEntity: Name: NameFull: Ventura P – PersonEntity: Name: NameFull: Buzzetti E – PersonEntity: Name: NameFull: Pietrangelo A – PersonEntity: Name: NameFull: Clini E – PersonEntity: Name: NameFull: Tonelli R – PersonEntity: Name: NameFull: Andrisani D – PersonEntity: Name: NameFull: de Guzman Marinduque BJ – PersonEntity: Name: NameFull: Bergamini E – PersonEntity: Name: NameFull: Vecchi C – PersonEntity: Name: NameFull: Pegoraro E – PersonEntity: Name: NameFull: Gregori D – PersonEntity: Name: NameFull: Corradini E – PersonEntity: Name: NameFull: Cerri S IsPartOfRelationships: – BibEntity: Dates: – D: 29 M: 12 Text: 2025 Dec 29 Type: published Y: 2025 Identifiers: – Type: issn-electronic Value: 1750-1172 Numbering: – Type: volume Value: 20 – Type: issue Value: 1 Titles: – TitleFull: Orphanet journal of rare diseases Type: main |
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