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Autism spectrum disorder throughout history: Paleogenetic analysis.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Autism spectrum disorder throughout history: Paleogenetic analysis.
Συγγραφείς: Zamfirov, Milen, Kenanov, Dimitar
Πηγή: International Journal of Innovative Research & Scientific Studies; 2026, Vol. 9 Issue 1, p91-97, 7p
Θεματικοί όροι: Autism spectrum disorders, Genetic mutation, Gene libraries, Nucleotide sequencing, Etiology of diseases, Genetic techniques, Fossil DNA, Missense mutation
Περίληψη: This article provides a brief historical overview of the earliest publications on autism spectrum disorder and the subsequent scientific discussions. The main focus is on the analysis of data on genes that have been confirmed to be associated with this condition. The aim of the study is to demonstrate, by processing data from sequenced human genomes obtained from various databases. Methods used in the analysis: Data on missense SNPs for 1230 genes from SFARI GENE were extracted. Then a search was performed for matches in David Reich's Lab (provides genotypes and single nucleotide polymorphisms (SNPs). The matches found were compiled into a table using a custom Perl script. In the article we show that analysis of gene mutations through the paleogenetic approach is a method that can also be employed for other disorders with unknown etiology. [ABSTRACT FROM AUTHOR]
Copyright of International Journal of Innovative Research & Scientific Studies is the property of International Journal of Innovative Research & Scientific Studies and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: Autism spectrum disorder throughout history: Paleogenetic analysis.
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  Data: International Journal of Innovative Research & Scientific Studies; 2026, Vol. 9 Issue 1, p91-97, 7p
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  Data: <searchLink fieldCode="DE" term="%22Autism+spectrum+disorders%22">Autism spectrum disorders</searchLink><br /><searchLink fieldCode="DE" term="%22Genetic+mutation%22">Genetic mutation</searchLink><br /><searchLink fieldCode="DE" term="%22Gene+libraries%22">Gene libraries</searchLink><br /><searchLink fieldCode="DE" term="%22Nucleotide+sequencing%22">Nucleotide sequencing</searchLink><br /><searchLink fieldCode="DE" term="%22Etiology+of+diseases%22">Etiology of diseases</searchLink><br /><searchLink fieldCode="DE" term="%22Genetic+techniques%22">Genetic techniques</searchLink><br /><searchLink fieldCode="DE" term="%22Fossil+DNA%22">Fossil DNA</searchLink><br /><searchLink fieldCode="DE" term="%22Missense+mutation%22">Missense mutation</searchLink>
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  Data: This article provides a brief historical overview of the earliest publications on autism spectrum disorder and the subsequent scientific discussions. The main focus is on the analysis of data on genes that have been confirmed to be associated with this condition. The aim of the study is to demonstrate, by processing data from sequenced human genomes obtained from various databases. Methods used in the analysis: Data on missense SNPs for 1230 genes from SFARI GENE were extracted. Then a search was performed for matches in David Reich's Lab (provides genotypes and single nucleotide polymorphisms (SNPs). The matches found were compiled into a table using a custom Perl script. In the article we show that analysis of gene mutations through the paleogenetic approach is a method that can also be employed for other disorders with unknown etiology. [ABSTRACT FROM AUTHOR]
– Name: Abstract
  Label:
  Group: Ab
  Data: <i>Copyright of International Journal of Innovative Research & Scientific Studies is the property of International Journal of Innovative Research & Scientific Studies and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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RecordInfo BibRecord:
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      – Type: doi
        Value: 10.53894/ijirss.v9i1.11173
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      – Code: eng
        Text: English
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        PageCount: 7
        StartPage: 91
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      – SubjectFull: Autism spectrum disorders
        Type: general
      – SubjectFull: Genetic mutation
        Type: general
      – SubjectFull: Gene libraries
        Type: general
      – SubjectFull: Nucleotide sequencing
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      – SubjectFull: Etiology of diseases
        Type: general
      – SubjectFull: Genetic techniques
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      – SubjectFull: Fossil DNA
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      – SubjectFull: Missense mutation
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            – D: 01
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              Text: 2026
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              Y: 2026
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