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Page 1
Mechanisms of structural chromosomal rearrangement formation.
Burssed B, Zamariolli M, Bellucco FT, Melaragno MI. Burssed B, et al. Among authors: zamariolli m. Mol Cytogenet. 2022 Jun 14;15(1):23. doi: 10.1186/s13039-022-00600-6. Mol Cytogenet. 2022. PMID: 35701783 Free PMC article. Review.
Response to Bassett et al.
Zamariolli M, Auwerx C, Sadler MC, van der Graaf A, Lepik K, Schoeler T, Moysés-Oliveira M, Dantas AG, Melaragno MI, Kutalik Z. Zamariolli M, et al. Am J Hum Genet. 2023 Jul 6;110(7):1219-1220. doi: 10.1016/j.ajhg.2023.05.017. Am J Hum Genet. 2023. PMID: 37419093 Free PMC article. No abstract available.
Variants in Candidate Genes for Phenotype Heterogeneity in Patients with the 22q11.2 Deletion Syndrome.
Nunes N, Carvalho Nunes B, Zamariolli M, Cordeiro de Queiroz Soares D, Caires Dos Santos L, Gollo Dantas A, Ayres Meloni V, Iole Belangero S, Gil-Da-Silva-Lopes VL, Ae Kim C, Melaragno MI. Nunes N, et al. Among authors: zamariolli m. Genet Res (Camb). 2024 Mar 30;2024:5549592. doi: 10.1155/2024/5549592. eCollection 2024. Genet Res (Camb). 2024. PMID: 38586596 Free PMC article.
Rare single-nucleotide variants in oculo-auriculo-vertebral spectrum (OAVS).
Zamariolli M, Colovati M, Moysés-Oliveira M, Nunes N, Caires Dos Santos L, Alvarez Perez AB, Bragagnolo S, Melaragno MI. Zamariolli M, et al. Mol Genet Genomic Med. 2019 Oct;7(10):e00959. doi: 10.1002/mgg3.959. Epub 2019 Aug 30. Mol Genet Genomic Med. 2019. PMID: 31469246 Free PMC article.
Sleep complaints in individuals with SYNGAP1-associated syndrome.
Mosini AC, Moysés-Oliveira M, Goes de Araujo JN, Guerreiro P, Cunha L, Zamariolli M, Xavier SD, Balbueno B, Berlim de Mello C, Moreira GA, Andersen ML, Tufik S. Mosini AC, et al. Among authors: zamariolli m. Sleep Med. 2025 Feb;126:282-289. doi: 10.1016/j.sleep.2024.12.026. Epub 2024 Dec 19. Sleep Med. 2025. PMID: 39733667
18 results