Gene-Based Burden Testing of Rare Variants in Hemiplegic Migraine: A Computational Approach to Uncover the Genetic Architecture of a Rare Brain Disorder.
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| Title: | Gene-Based Burden Testing of Rare Variants in Hemiplegic Migraine: A Computational Approach to Uncover the Genetic Architecture of a Rare Brain Disorder. |
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| Authors: | Alfayyadh MM; Centre for Genomics and Personalised Health, Genomics Research Centre, School of Biomedical Sciences, Queensland University of Technology (QUT), Brisbane, QLD 4059, Australia., Maksemous N; Centre for Genomics and Personalised Health, Genomics Research Centre, School of Biomedical Sciences, Queensland University of Technology (QUT), Brisbane, QLD 4059, Australia.; Central Analytical Research Facility (CARF), Faculty of Sciences, Queensland University of Technology (QUT), Brisbane, QLD 4059, Australia., Sutherland HG; Centre for Genomics and Personalised Health, Genomics Research Centre, School of Biomedical Sciences, Queensland University of Technology (QUT), Brisbane, QLD 4059, Australia., Lea RA; Centre for Genomics and Personalised Health, Genomics Research Centre, School of Biomedical Sciences, Queensland University of Technology (QUT), Brisbane, QLD 4059, Australia.; Central Analytical Research Facility (CARF), Faculty of Sciences, Queensland University of Technology (QUT), Brisbane, QLD 4059, Australia., Griffiths LR; Centre for Genomics and Personalised Health, Genomics Research Centre, School of Biomedical Sciences, Queensland University of Technology (QUT), Brisbane, QLD 4059, Australia. |
| Source: | Genes [Genes (Basel)] 2025 Jul 09; Vol. 16 (7). Date of Electronic Publication: 2025 Jul 09. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 40725463 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Gene-Based Burden Testing of Rare Variants in Hemiplegic Migraine: A Computational Approach to Uncover the Genetic Architecture of a Rare Brain Disorder. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Alfayyadh+MM%22">Alfayyadh MM</searchLink>; Centre for Genomics and Personalised Health, Genomics Research Centre, School of Biomedical Sciences, Queensland University of Technology (QUT), Brisbane, QLD 4059, Australia.<br /><searchLink fieldCode="AU" term="%22Maksemous+N%22">Maksemous N</searchLink>; Centre for Genomics and Personalised Health, Genomics Research Centre, School of Biomedical Sciences, Queensland University of Technology (QUT), Brisbane, QLD 4059, Australia.; Central Analytical Research Facility (CARF), Faculty of Sciences, Queensland University of Technology (QUT), Brisbane, QLD 4059, Australia.<br /><searchLink fieldCode="AU" term="%22Sutherland+HG%22">Sutherland HG</searchLink>; Centre for Genomics and Personalised Health, Genomics Research Centre, School of Biomedical Sciences, Queensland University of Technology (QUT), Brisbane, QLD 4059, Australia.<br /><searchLink fieldCode="AU" term="%22Lea+RA%22">Lea RA</searchLink>; Centre for Genomics and Personalised Health, Genomics Research Centre, School of Biomedical Sciences, Queensland University of Technology (QUT), Brisbane, QLD 4059, Australia.; Central Analytical Research Facility (CARF), Faculty of Sciences, Queensland University of Technology (QUT), Brisbane, QLD 4059, Australia.<br /><searchLink fieldCode="AU" term="%22Griffiths+LR%22">Griffiths LR</searchLink>; Centre for Genomics and Personalised Health, Genomics Research Centre, School of Biomedical Sciences, Queensland University of Technology (QUT), Brisbane, QLD 4059, Australia. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101551097%22">Genes</searchLink> [Genes (Basel)] 2025 Jul 09; Vol. 16 (7). <i>Date of Electronic Publication: </i>2025 Jul 09. – 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="%22MDPI%22">MDPI </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101551097 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2073-4425 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2220734425%22">20734425 </searchLink><i>NLM ISO Abbreviation: </i>Genes (Basel) <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=40725463 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.3390/genes16070807 Languages: – Code: eng Text: English Titles: – TitleFull: Gene-Based Burden Testing of Rare Variants in Hemiplegic Migraine: A Computational Approach to Uncover the Genetic Architecture of a Rare Brain Disorder. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Alfayyadh MM – PersonEntity: Name: NameFull: Maksemous N – PersonEntity: Name: NameFull: Sutherland HG – PersonEntity: Name: NameFull: Lea RA – PersonEntity: Name: NameFull: Griffiths LR IsPartOfRelationships: – BibEntity: Dates: – D: 09 M: 07 Text: 2025 Jul 09 Type: published Y: 2025 Identifiers: – Type: issn-electronic Value: 2073-4425 Numbering: – Type: volume Value: 16 – Type: issue Value: 7 Titles: – TitleFull: Genes Type: main |
| ResultId | 1 |
