Common genetic modifiers influence cardiomyopathy susceptibility among the carriers of rare pathogenic variants.
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| Title: | Common genetic modifiers influence cardiomyopathy susceptibility among the carriers of rare pathogenic variants. |
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| Authors: | Klasfeld SJ; Internal Medicine Research Unit, Pfizer Research and Development, Cambridge, MA 02139, USA; Rare Disease Research Unit, Pfizer Research and Development, Cambridge, MA 02139, USA., Knutson KA; Clinical Omics and Biomarker Statistics, Pfizer Research and Development, Cambridge, MA 02139, USA., Miller MR; Internal Medicine Research Unit, Pfizer Research and Development, Cambridge, MA 02139, USA., Fauman EB; Internal Medicine Research Unit, Pfizer Research and Development, Cambridge, MA 02139, USA., Berghout J; Rare Disease Research Unit, Pfizer Research and Development, Cambridge, MA 02139, USA., Moccia R; Rare Disease Research Unit, Pfizer Research and Development, Cambridge, MA 02139, USA; Machine Learning and Computational Sciences, Pfizer Research and Development, Cambridge, MA 02139, USA. Electronic address: robert.moccia@pfizer.com., Kim HI; Internal Medicine Research Unit, Pfizer Research and Development, Cambridge, MA 02139, USA. Electronic address: hyein.kim@pfizer.com. |
| Source: | HGG advances [HGG Adv] 2025 Jul 10; Vol. 6 (3), pp. 100460. Date of Electronic Publication: 2025 May 22. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Elsevier Inc Country of Publication: United States NLM ID: 101772885 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2666-2477 (Electronic) Linking ISSN: 26662477 NLM ISO Abbreviation: HGG Adv Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 40411145 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Common genetic modifiers influence cardiomyopathy susceptibility among the carriers of rare pathogenic variants. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Klasfeld+SJ%22">Klasfeld SJ</searchLink>; Internal Medicine Research Unit, Pfizer Research and Development, Cambridge, MA 02139, USA; Rare Disease Research Unit, Pfizer Research and Development, Cambridge, MA 02139, USA.<br /><searchLink fieldCode="AU" term="%22Knutson+KA%22">Knutson KA</searchLink>; Clinical Omics and Biomarker Statistics, Pfizer Research and Development, Cambridge, MA 02139, USA.<br /><searchLink fieldCode="AU" term="%22Miller+MR%22">Miller MR</searchLink>; Internal Medicine Research Unit, Pfizer Research and Development, Cambridge, MA 02139, USA.<br /><searchLink fieldCode="AU" term="%22Fauman+EB%22">Fauman EB</searchLink>; Internal Medicine Research Unit, Pfizer Research and Development, Cambridge, MA 02139, USA.<br /><searchLink fieldCode="AU" term="%22Berghout+J%22">Berghout J</searchLink>; Rare Disease Research Unit, Pfizer Research and Development, Cambridge, MA 02139, USA.<br /><searchLink fieldCode="AU" term="%22Moccia+R%22">Moccia R</searchLink>; Rare Disease Research Unit, Pfizer Research and Development, Cambridge, MA 02139, USA; Machine Learning and Computational Sciences, Pfizer Research and Development, Cambridge, MA 02139, USA. Electronic address: robert.moccia@pfizer.com.<br /><searchLink fieldCode="AU" term="%22Kim+HI%22">Kim HI</searchLink>; Internal Medicine Research Unit, Pfizer Research and Development, Cambridge, MA 02139, USA. Electronic address: hyein.kim@pfizer.com. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101772885%22">HGG advances</searchLink> [HGG Adv] 2025 Jul 10; Vol. 6 (3), pp. 100460. <i>Date of Electronic Publication: </i>2025 May 22. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier+Inc%22">Elsevier Inc </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101772885 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2666-2477 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2226662477%22">26662477 </searchLink><i>NLM ISO Abbreviation: </i>HGG Adv <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=40411145 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.xhgg.2025.100460 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 100460 Titles: – TitleFull: Common genetic modifiers influence cardiomyopathy susceptibility among the carriers of rare pathogenic variants. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Klasfeld SJ – PersonEntity: Name: NameFull: Knutson KA – PersonEntity: Name: NameFull: Miller MR – PersonEntity: Name: NameFull: Fauman EB – PersonEntity: Name: NameFull: Berghout J – PersonEntity: Name: NameFull: Moccia R – PersonEntity: Name: NameFull: Kim HI IsPartOfRelationships: – BibEntity: Dates: – D: 10 M: 07 Text: 2025 Jul 10 Type: published Y: 2025 Identifiers: – Type: issn-electronic Value: 2666-2477 Numbering: – Type: volume Value: 6 – Type: issue Value: 3 Titles: – TitleFull: HGG advances Type: main |
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