Genetic Heterogeneity of Autism Spectrum Disorder: Identification of Five Novel Mutations (RIMS2, FOXG1, AUTS2, ZCCHC17, and SPTBN5) in Iranian Families via Whole-Exome and Whole-Genome Sequencing.
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| Title: | Genetic Heterogeneity of Autism Spectrum Disorder: Identification of Five Novel Mutations (RIMS2, FOXG1, AUTS2, ZCCHC17, and SPTBN5) in Iranian Families via Whole-Exome and Whole-Genome Sequencing. |
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| Authors: | Mirahmadi M; Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran., Kahani SM; Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.; Department of Exomine, PardisGene Company, Tehran, Iran., Sharifi-Zarchi A; Department of Exomine, PardisGene Company, Tehran, Iran.; Department of Computer Engineering, Sharif University of Technology, Tehran, Iran., Firouzabadi SG; Genetics Research Centre, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Behjati F; Genetics Research Centre, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Garshasbi M; Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran. masoud.garshasbi@modares.ac.ir.; DeNA Laboratory, Department of Medical Genetics, Tehran, Iran. masoud.garshasbi@modares.ac.ir. |
| Source: | Biochemical genetics [Biochem Genet] 2026 Jun; Vol. 64 (3), pp. 3867-3895. Date of Electronic Publication: 2025 Aug 16. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Kluwer Academic/Plenum Publishers Country of Publication: United States NLM ID: 0126611 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-4927 (Electronic) Linking ISSN: 00062928 NLM ISO Abbreviation: Biochem Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 40819013 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Genetic Heterogeneity of Autism Spectrum Disorder: Identification of Five Novel Mutations (RIMS2, FOXG1, AUTS2, ZCCHC17, and SPTBN5) in Iranian Families via Whole-Exome and Whole-Genome Sequencing. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Mirahmadi+M%22">Mirahmadi M</searchLink>; Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Kahani+SM%22">Kahani SM</searchLink>; Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.; Department of Exomine, PardisGene Company, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Sharifi-Zarchi+A%22">Sharifi-Zarchi A</searchLink>; Department of Exomine, PardisGene Company, Tehran, Iran.; Department of Computer Engineering, Sharif University of Technology, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Firouzabadi+SG%22">Firouzabadi SG</searchLink>; Genetics Research Centre, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Behjati+F%22">Behjati F</searchLink>; Genetics Research Centre, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Garshasbi+M%22">Garshasbi M</searchLink>; Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran. masoud.garshasbi@modares.ac.ir.; DeNA Laboratory, Department of Medical Genetics, Tehran, Iran. masoud.garshasbi@modares.ac.ir. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220126611%22">Biochemical genetics</searchLink> [Biochem Genet] 2026 Jun; Vol. 64 (3), pp. 3867-3895. <i>Date of Electronic Publication: </i>2025 Aug 16. – 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="%22Kluwer+Academic%2FPlenum+Publishers%22">Kluwer Academic/Plenum Publishers </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>0126611 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1573-4927 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200062928%22">00062928 </searchLink><i>NLM ISO Abbreviation: </i>Biochem Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=40819013 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s10528-025-11226-9 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 3867 Titles: – TitleFull: Genetic Heterogeneity of Autism Spectrum Disorder: Identification of Five Novel Mutations (RIMS2, FOXG1, AUTS2, ZCCHC17, and SPTBN5) in Iranian Families via Whole-Exome and Whole-Genome Sequencing. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Mirahmadi M – PersonEntity: Name: NameFull: Kahani SM – PersonEntity: Name: NameFull: Sharifi-Zarchi A – PersonEntity: Name: NameFull: Firouzabadi SG – PersonEntity: Name: NameFull: Behjati F – PersonEntity: Name: NameFull: Garshasbi M IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: 2026 Jun Type: published Y: 2026 Identifiers: – Type: issn-electronic Value: 1573-4927 Numbering: – Type: volume Value: 64 – Type: issue Value: 3 Titles: – TitleFull: Biochemical genetics Type: main |
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