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Genetic investigation of syndromic forms of obesity.
Int J Obes (Lond). 2022 Sep;46(9):1582-1586. doi: 10.1038/s41366-022-01149-5. Epub 2022 May 21.
Int J Obes (Lond). 2022.
PMID: 35597848
Copy number variations in a Brazilian cohort with autism spectrum disorders highlight the contribution of cell adhesion genes.
Costa CIS, da Silva Montenegro EM, Zarrei M, de Sá Moreira E, Silva IMW, de Oliveira Scliar M, Wang JYT, Zachi EC, Branco EV, da Costa SS, Lourenço NCV, Vianna-Morgante AM, Rosenberg C, Krepischi ACV, Scherer SW, Passos-Bueno MR.
Costa CIS, et al. Among authors: de oliveira scliar m.
Clin Genet. 2022 Jan;101(1):134-141. doi: 10.1111/cge.14072. Epub 2021 Nov 15.
Clin Genet. 2022.
PMID: 34664255
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DNA methylation patterns suggest the involvement of DNMT3B and TET1 in osteosarcoma development.
Pires SF, de Barros JS, da Costa SS, de Oliveira Scliar M, Van Helvoort Lengert A, Boldrini É, da Silva SRM, Tasic L, Vidal DO, Krepischi ACV, Maschietto M.
Pires SF, et al. Among authors: de oliveira scliar m.
Mol Genet Genomics. 2023 May;298(3):721-733. doi: 10.1007/s00438-023-02010-8. Epub 2023 Apr 5.
Mol Genet Genomics. 2023.
PMID: 37020053
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SCAF4-related syndromic intellectual disability.
Carvalho LML, Pinto CF, de Oliveira Scliar M, Otto PA, Krepischi ACV, Rosenberg C.
Carvalho LML, et al. Among authors: de oliveira scliar m.
Am J Med Genet A. 2023 Feb;191(2):570-574. doi: 10.1002/ajmg.a.63032. Epub 2022 Nov 5.
Am J Med Genet A. 2023.
PMID: 36333968
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