| 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 | 19 | 2014 |
| 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 | 17 | 2016 |
| 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 | 14 | 2022 |
| 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 | 14 | 2021 |
| 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 | 13 | 2015 |
| 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 | 13 | 2011 |
| 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 | 11 | 2014 |
| 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 | 10 | 2014 |
| 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 | 9 | 2018 |
| 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 | 9 | 2017 |
| 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 | 8 | 2016 |
| 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 | 7 | 2017 |
| 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 | 6 | 2020 |
| 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 | 5 | 2022 |
| 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 | 5 | 2016 |
| 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 | 5 | 2015 |
| 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 | 5 | 2015 |
| 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 | 4 | 2021 |
| 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 | 4 | 2016 |
| 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 | 3 | 2024 |
Aparecido Divino da CruzProfessor Titular, Potntifícia Universidade Católica de GoiásVerified email at pucgoias.edu.br
