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Lysa Bernardes Minasi

Observed names: L.B. Minasi, Lysa B. Minasi, Lysa Bernandes Minasi, Lysa Minasi, MINASI, LYSA BERNADES, Minasi, Lysa, Minasi, Lysa Bernardes
ORCID: 0000-0003-2734-4797
Observed ORCID: 0000-0003-2734-4797
OpenAlex ID: A5078253544
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
2022 · Ana Julia da Cunha Leite, Irene Plaza Pinto, et al. · PLoS ONE · 38
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Reward Deficiency Syndrome in Children: Obesity and Metabolic Disorders are Associated with the SNP TaqIA C32806T of the DRD2 Gene
2015 · Renata M. Pinto, Daniela M. e Silva, et al. · Obesity Research - Open Journal · 26
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Single-Nucleotide Polymorphism Variations Associated With Specific Genes Putatively Identified Enhanced Genetic Predisposition for 305-Day Milk Yield in the Girolando Crossbreed
2021 · Alex Silva da Cruz, Danilo Conrado Silva, et al. · Frontiers in Genetics · 22
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Genetic markers for improving farm animals
2019 · Rajib Deb, Chandra Sekhar Mukhopadhyay, et al. · Elsevier eBooks · 16
Screening for Intellectual Disability Using High-Resolution CMA Technology in a Retrospective Cohort from Central Brazil
2014 · Rodrigo Roncato Pereira, Irene Plaza Pinto, et al. · PLoS ONE · 15
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Mosaic Tetrasomy of 9p24.3q21.11 postnatally identified in an infant born with multiple congenital malformations: a case report
2018 · Irene Plaza Pinto, Lysa Bernardes Minasi, et al. · BMC Pediatrics · 13
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Identification of trends in scientific publications related to genetic polymorphisms in gestational diabetes mellitus
2016 · J.S. Gomes, L.B. Minasi, et al. · Genetics and Molecular Research · 11
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Lack of association between IL-10 -1082G/A polymorphism and chronic periodontal disease in adults
2015 · R. Hannum, F.R. Godoy, et al. · Genetics and Molecular Research · 11
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Do GSTT1 and GSTM1 polymorphisms influence intoxication events in individuals occupationally exposed to pesticides?
2013 · Fernanda Ribeiro Godoy, Emília Oliveira Alves Costa, et al. · Environmental Science and Pollution Research · 11
Mutation rates in 21 autosomal short tandem repeat loci in a population from Goiás, Brazil
2017 · Thaís Cidália Vieira, Marc Alexandre Duarte Gigonzac, et al. · Electrophoresis · 9
Molecular Characterization of Koolen De Vries Syndrome in Two Girls with Idiopathic Intellectual Disability from Central Brazil
2017 · Gustavo R. Nascimento, Irene P. Pinto, et al. · Molecular Syndromology · 9
CASE-REPORT Association between an ACAN gene variable number tandem repeat polymorphism and lumbar disc herniation: a case control study
2016 · N.L.L. Casa, A.J. Casa Junior, et al. · Genetics and Molecular Research · 9
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A non-syndromic intellectual disability associated with a de novo microdeletion at 7q and 18p, microduplication at Xp, and 18q partial trisomy detected using chromosomal microarray analysis approach
2014 · Irene Plaza Pinto, Lysa Bernardes Minasi, et al. · Molecular Cytogenetics · 9
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A rigorous in silico genomic interrogation at 1p13.3 reveals 16 autosomal dominant candidate genes in syndromic neurodevelopmental disorders
2022 · Afif Ben-Mahmoud, Kyung Ran Jun, et al. · Frontiers in Molecular Neuroscience · 8
Short Communication Cytogenetic damage in the buccal epithelium of Brazilian aviators occupationally exposed to agrochemicals
2011 · L.B. Minasi, E.O.A. Costa, et al. · Genetics and Molecular Research · 7
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c.1103T>C (p.Ile368Th) de novo Variant in Synaptotagmin 1 (SYT1) Gene is Pathogenic, Leading to an Ultra-Rare Neurodevelopmental Disorder: The Baker-Gordon Syndrome
2024 · Milena Porto, Geovanna Castro, et al. · International Medical Case Reports Journal · 6
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Frequency of Esophageal Eosinophilia in a Pediatric Population from Central Brazil
2018 · Daniel Strozzi, Marco Aurélio Silveira Botacin, et al. · Scientific Reports · 5
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Standardization of capillary electrophoresis for diagnosis of fragile X syndrome in the Brazilian public health system
2016 · Marc Alexandre Duarte Gigonzac, Lilian Souza Teodoro, et al. · Electrophoresis · 5
The Identification of Microdeletion and Reciprocal Microduplication in 22q11.2 Using High-Resolution CMA Technology
2016 · Ana Julia Cunha Leite, Irene Plaza Pinto, et al. · BioMed Research International · 4
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Postnatal diagnosis of constitutive ring chromosome 13 using both conventional and molecular cytogenetic approaches
2015 · L.B. Minasi, I.P. Pinto, et al. · Genetics and Molecular Research · 4
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Molecular analysis of patients suspected of Fragile X Syndrome
2015 · A.P. Amancio, C.A. de O. Melo, et al. · Genetics and Molecular Research · 4
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Household survey on prevalence and risk factors for obesity in owned cats from Central Brazil
2026 · Danilo Conrado Silva, Mariana Yukari Hayasaki Porsani, et al. · PLoS ONE · 3
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Genomic variations in patients with myelodysplastic syndrome and karyotypes without numerical or structural changes
2021 · Cristiano Luiz Ribeiro, Irene P. Pinto, et al. · Scientific Reports · 3
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The influence of six polymorphisms of uncoupling protein 3 (UCP3) gene and childhood obesity: a case–control study
2023 · Jakeline S. Fortes, Renata M. Pinto, et al. · BMC Pediatrics · 2
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A rare case of a boy with de novo microduplication at 5q35.2q35.3 from central Brazil
2017 · F.G. Reis, I.P. Pinto, et al. · Genetics and Molecular Research · 2
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Works count: 61
Citation count: 260
H-index: 9
I10-index: 9
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