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Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.
Nat Genet. 2022 Sep;54(9):1320-1331. doi: 10.1038/s41588-022-01104-0. Epub 2022 Aug 18.
Nat Genet. 2022.
PMID: 35982160
Free PMC article.
Developing a tool to monitor knowledge translation in the health system: results from an international Delphi study.
Delnord M, Abboud LA, Costa C, Van Oyen H.
Delnord M, et al.
Eur J Public Health. 2021 Oct 11;31(4):695-702. doi: 10.1093/eurpub/ckab117.
Eur J Public Health. 2021.
PMID: 34333628
Free PMC article.
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Three generation families: Analysis of de novo variants in autism.
Costa CIS, da Silva Campos G, da Silva Montenegro EM, Wang JYT, Scliar M, Monfardini F, Zachi EC, Lourenço NCV, Chan AJS, Pereira SL, Engchuan W, Thiruvahindrapuram B, Zarrei M, Scherer SW, Passos-Bueno MR.
Costa CIS, et al.
Eur J Hum Genet. 2023 Sep;31(9):1017-1022. doi: 10.1038/s41431-023-01398-6. Epub 2023 Jun 6.
Eur J Hum Genet. 2023.
PMID: 37280359
Free PMC article.
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Dystrophin genetic variants and autism.
Passos-Bueno MR, Costa CIS, Zatz M.
Passos-Bueno MR, et al. Among authors: costa cis.
Discov Ment Health. 2022 Mar 24;2(1):4. doi: 10.1007/s44192-022-00008-z.
Discov Ment Health. 2022.
PMID: 37861890
Free PMC article.
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FMR1 premutation in children with autism spectrum disorders: Should additional diagnostic tests be performed?
Girardi ACS, van Opstal Takahashi VN, Vadasz E, Costa CIS, Zachi EC, Vianna-Morgante AM, Passos-Bueno MR.
Girardi ACS, et al. Among authors: costa cis.
Am J Med Genet A. 2022 Apr;188(4):1334-1337. doi: 10.1002/ajmg.a.62624. Epub 2022 Jan 3.
Am J Med Genet A. 2022.
PMID: 34981645
No abstract available.
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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.
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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