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lysa minasi
lysa minasi
Pontifícia Universidade Católica de Goias
E-mail confirmado em pucgoias.edu.br - Página inicial
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Ano
Screening for intellectual disability using high-resolution CMA technology in a retrospective cohort from Central Brazil
RR Pereira, IP Pinto, LB Minasi, AV de Melo, DM da Cruz e Cunha, ...
PloS one 9 (7), e103117, 2014
192014
Identification of trends in scientific publications related to genetic polymorphisms in gestational diabetes mellitus
JS Gomes, LB Minasi, AD da Cruz, FM Rodrigues
Genet Mol Res 15 (2), gmr. 15027672, 2016
172016
Diagnostic yield of patients with undiagnosed intellectual disability, global developmental delay and multiples congenital anomalies using karyotype, microarray analysis, whole …
AJC Leite, IP Pinto, N Leijsten, M Ruiterkamp-Versteeg, R Pfundt, ...
PLoS One 17 (4), e0266493, 2022
142022
Single-Nucleotide Polymorphism variations associated with specific genes putatively identified enhanced genetic predisposition for 305-day milk yield in the Girolando crossbreed
AS Da Cruz, DC Silva, LB Minasi, LK de Farias Teixeira, FM Rodrigues, ...
Frontiers in Genetics 11, 573344, 2021
142021
Lack of association between IL-10-1082G/A polymorphism and chronic periodontal disease in adults
R Hannum, FR Godoy, AS da Cruz, TC Vieira, LB Minasi, D de Silva, ...
Genet Mol Res 14 (4), 17828-17833, 2015
132015
Cytogenetic damage in the buccal epithelium of Brazilian aviators occupationally exposed to agrochemicals
LB Minasi, EO Costa, DM Silva, CO Melo, JG de Almeida, TC Vieira, ...
Genet Mol Res 10 (4), 3924-9, 2011
132011
Do GSTT1 and GSTM1 polymorphisms influence intoxication events in individuals occupationally exposed to pesticides?
FR Godoy, EOA Costa, AA da Silva Reis, MP Batista, AV de Melo, ...
Environmental Science and Pollution Research 21, 3706-3712, 2014
112014
A non-syndromic intellectual disability associated with a de novo microdeletion at 7q and 18p, microduplication at Xp, and 18q partial trisomy detected using …
IP Pinto, LB Minasi, AS da Cruz, AV de Melo, DM da Cruz e Cunha, ...
Molecular Cytogenetics 7, 1-7, 2014
102014
Mosaic Tetrasomy of 9p24. 3q21. 11 postnatally identified in an infant born with multiple congenital malformations: a case report
IP Pinto, LB Minasi, R Steckelberg, CC da Silva, AD da Cruz
BMC pediatrics 18, 1-4, 2018
92018
Molecular characterization of koolen de vries syndrome in two girls with idiopathic intellectual disability from Central Brazil
GR Nascimento, IP Pinto, AV de Melo, DM da Cruz, CL Ribeiro, ...
Molecular Syndromology 8 (3), 155-160, 2017
92017
CASE-REPORT Association between an ACAN gene variable number tandem repeat polymorphism and lumbar disc herniation: a case control study.
NL Casa, CJ AJ, AV Melo, LS Teodoro, GR Nascimento, AF Sousa, ...
Genetics and Molecular Research: GMR 15 (4), 2016
82016
Mutation rates in 21 autosomal short tandem repeat loci in a population from Goiás, Brazil
TC Vieira, MA Duarte Gigonzac, R Goulart Rodovalho, ...
Electrophoresis 38 (21), 2791-2794, 2017
72017
Genetic markers for improving farm animals
R Deb, CS Mukhopadhyay, GS Sengar, AS da Cruz, DC Silva, IP Pinto, ...
Genomics and Biotechnological Advances in Veterinary, Poultry, and Fisheries …, 2020
62020
A rigorous in silico genomic interrogation at 1p13.3 reveals 16 autosomal dominant candidate genes in syndromic neurodevelopmental disorders
A Ben-Mahmoud, KR Jun, V Gupta, P Shastri, A de la Fuente, Y Park, ...
Frontiers in Molecular Neuroscience 15, 979061, 2022
52022
The Identification of Microdeletion and Reciprocal Microduplication in 22q11. 2 Using High‐Resolution CMA Technology
AJC Leite, IP Pinto, DMC Cunha, CL Ribeiro, CC da Silva, AD da Cruz, ...
BioMed research international 2016 (1), 7415438, 2016
52016
Molecular analysis of patients suspected of Fragile X Syndrome
AP Amancio, CAO de Melo, AM de Vieira, LB Minasi, DME de Silva, ...
Genetics and Molecular Research 14 (4), 14660-14669, 2015
52015
Postnatal diagnosis of constitutive ring chromosome 13 using both conventional and molecular cytogenetic approaches
LB Minasi, IP Pinto, JG de Almeida, AV de Melo, DMC Cunha, CL Ribeiro, ...
Genetics and Molecular Research 14 (1), 11692-11699, 2015
52015
Genomic variations in patients with myelodysplastic syndrome and karyotypes without numerical or structural changes
CL Ribeiro, IP Pinto, SSS Pereira, LB Minasi, F de SM Kluthcouski, ...
Scientific Reports 11 (1), 2783, 2021
42021
Standardization of capillary electrophoresis for diagnosis of fragile X syndrome in the Brazilian public health system
MAD Gigonzac, LS Teodoro, LB Minasi, TC Vieira, AD da Cruz
Electrophoresis 37 (23-24), 3076-3078, 2016
42016
Longos trechos contíguos em homozigose identificados por análise cromossômica por microarranjos em uma população com deficiência intelectual e transtorno do espectro autista do …
AR de Carvalho Neta, IP Pinto, AS da Cruz, AD da Cruz, LB Minasi
Conjecturas 24 (1), 355-367, 2024
32024
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Artigos 1–20