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Genomic architecture of autism from comprehensive whole-genome sequence annotation.
Cell. 2022 Nov 10;185(23):4409-4427.e18. doi: 10.1016/j.cell.2022.10.009.
Cell. 2022.
PMID: 36368308
Free PMC article.
Developmental implications of genetic testing for physical indications.
Baribeau DA, Hoang N, Selvanayagam T, Stavropoulos DJ, Costain G, Scherer SW, Vorstman J.
Baribeau DA, et al. Among authors: selvanayagam t.
Eur J Hum Genet. 2022 Nov;30(11):1297-1300. doi: 10.1038/s41431-022-01181-z. Epub 2022 Sep 6.
Eur J Hum Genet. 2022.
PMID: 36068265
Free PMC article.
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Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity.
Selvanayagam T, Walker S, Gazzellone MJ, Kellam B, Cytrynbaum C, Stavropoulos DJ, Li P, Birken CS, Hamilton J, Weksberg R, Scherer SW.
Selvanayagam T, et al.
Eur J Hum Genet. 2018 Nov;26(11):1588-1596. doi: 10.1038/s41431-018-0189-0. Epub 2018 Jul 5.
Eur J Hum Genet. 2018.
PMID: 29976977
Free PMC article.
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Copy number variation in Han Chinese individuals with autism spectrum disorder.
Gazzellone MJ, Zhou X, Lionel AC, Uddin M, Thiruvahindrapuram B, Liang S, Sun C, Wang J, Zou M, Tammimies K, Walker S, Selvanayagam T, Wei J, Wang Z, Wu L, Scherer SW.
Gazzellone MJ, et al. Among authors: selvanayagam t.
J Neurodev Disord. 2014;6(1):34. doi: 10.1186/1866-1955-6-34. Epub 2014 Aug 23.
J Neurodev Disord. 2014.
PMID: 25170348
Free PMC article.
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Evaluation of DNA/BSA Binding and Chemical Nuclease Activity of L-Tyrosine-Based Mn(III) and Fe(III) Metallo-Intercalators.
Rajaretnam BB, Chellappa J, Solomon DA, Subramanian IP, Selvanayagam TDM.
Rajaretnam BB, et al. Among authors: selvanayagam tdm.
Acta Chim Slov. 2019 Feb;66(1):196-207.
Acta Chim Slov. 2019.
PMID: 33855480
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