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Long read whole genome sequencing-based discovery of structural variants and their role in aetiology of non-syndromic autism spectrum disorder in India.

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Title: Long read whole genome sequencing-based discovery of structural variants and their role in aetiology of non-syndromic autism spectrum disorder in India.
Authors: Shah, Jhanvi1 (AUTHOR), Mondal, Debasrija2 (AUTHOR), Jain, Deepika3 (AUTHOR), Mhatre, Priti4 (AUTHOR), Patel, Ketan5 (AUTHOR), Iyer, Anand6 (AUTHOR), Pandya, Manoj7 (AUTHOR), Menghani, Bhargavi8 (AUTHOR), Dave, Gayatri9 (AUTHOR), Sheth, Jayesh1 (AUTHOR), Sheth, Frenny1 (AUTHOR), Ramdas, Shweta2 (AUTHOR) shwetaramdas@iisc.ac.in, Sheth, Harsh1 (AUTHOR) harsh.sheth@frige.co.in
Source: BMC Medical Genomics. 8/20/2025, Vol. 18 Issue 1, p1-12. 12p.
Database: Academic Search Ultimate
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  Data: <searchLink fieldCode="JN" term="%22BMC+Medical+Genomics%22">BMC Medical Genomics</searchLink>. 8/20/2025, Vol. 18 Issue 1, p1-12. 12p.
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        Value: 10.1186/s12920-025-02204-6
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              Text: 8/20/2025
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              Y: 2025
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