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A rigorous in silico genomic interrogation at 1p13.3 reveals 16 autosomal dominant candidate genes in syndromic neurodevelopmental disorders.
Ben-Mahmoud A, Jun KR, Gupta V, Shastri P, de la Fuente A, Park Y, Shin KC, Kim CA, da Cruz AD, Pinto IP, Minasi LB, Silva da Cruz A, Faivre L, Callier P, Racine C, Layman LC, Kong IK, Kim CH, Kim WY, Kim HG. Ben-Mahmoud A, et al. Among authors: minasi lb. Front Mol Neurosci. 2022 Oct 6;15:979061. doi: 10.3389/fnmol.2022.979061. eCollection 2022. Front Mol Neurosci. 2022. PMID: 36277487 Free PMC article.
Diagnostic yield of patients with undiagnosed intellectual disability, global developmental delay and multiples congenital anomalies using karyotype, microarray analysis, whole exome sequencing from Central Brazil.
Leite AJDC, Pinto IP, Leijsten N, Ruiterkamp-Versteeg M, Pfundt R, de Leeuw N, da Cruz AD, Minasi LB. Leite AJDC, et al. Among authors: minasi lb. PLoS One. 2022 Apr 7;17(4):e0266493. doi: 10.1371/journal.pone.0266493. eCollection 2022. PLoS One. 2022. PMID: 35390071 Free PMC article.
Single-Nucleotide Polymorphism Variations Associated With Specific Genes Putatively Identified Enhanced Genetic Predisposition for 305-Day Milk Yield in the Girolando Crossbreed.
da Cruz AS, Silva DC, Minasi LB, de Farias Teixeira LK, Rodrigues FM, da Silva CC, do Carmo AS, da Silva MVGB, Utsunomiya YT, Garcia JF, da Cruz AD. da Cruz AS, et al. Among authors: minasi lb. Front Genet. 2021 Jan 15;11:573344. doi: 10.3389/fgene.2020.573344. eCollection 2020. Front Genet. 2021. PMID: 33584786 Free PMC article.
30 results