Search Results - "Rodrigo Secolin"
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A review of ancestrality and admixture in Latin America and the caribbean focusing on native American and African descendant populations
Published in Frontiers in genetics (19-01-2023)“…Genomics can reveal essential features about the demographic evolution of a population that may not be apparent from historical elements. In recent years,…”
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2
Genetic variability in COVID-19-related genes in the Brazilian population
Published in Human genome variation (02-04-2021)“…SARS-CoV-2 utilizes the angiotensin-converting enzyme 2 (ACE2) receptor and transmembrane serine protease (TMPRSS2) to infect human lung cells. Previous…”
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3
MicroRNA hsa-miR-134 is a circulating biomarker for mesial temporal lobe epilepsy
Published in PloS one (06-04-2017)“…Epilepsy is misdiagnosed in up to 25% of patients, leading to serious and long-lasting consequences. Recently, circulating microRNAs have emerged as potential…”
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4
The Brazilian Initiative on Precision Medicine (BIPMed): fostering genomic data-sharing of underrepresented populations
Published in Npj genomic medicine (02-10-2020)“…The development of precision medicine strategies requires prior knowledge of the genetic background of the target population. However, despite the availability…”
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5
Dysregulation of NEUROG2 plays a key role in focal cortical dysplasia
Published in Annals of neurology (01-03-2018)“…Objective Focal cortical dysplasias (FCDs) are an important cause of drug‐resistant epilepsy. In this work, we aimed to investigate whether abnormal gene…”
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6
A Prediction Algorithm for Drug Response in Patients with Mesial Temporal Lobe Epilepsy Based on Clinical and Genetic Information
Published in PloS one (04-01-2017)“…Mesial temporal lobe epilepsy is the most common form of adult epilepsy in surgical series. Currently, the only characteristic used to predict poor response to…”
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7
Neurocysticercotic Calcifications and Hippocampal Sclerosis: A Case-Control Study
Published in PloS one (01-07-2015)“…The exact role of calcified neurocysticercotic lesions (CNLs) in epilepsy is yet unknown and controversial. Although the relationship between CNLs, epilepsy…”
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8
Exploring a Region on Chromosome 8p23.1 Displaying Positive Selection Signals in Brazilian Admixed Populations: Additional Insights Into Predisposition to Obesity and Related Disorders
Published in Frontiers in genetics (25-03-2021)“…We recently reported a deviation of local ancestry on the chromosome (ch) 8p23.1, which led to positive selection signals in a Brazilian population sample. The…”
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Gene Variants Associated With Venous Thrombosis: A Replication Study in a Brazilian Multicentre Study
Published in Clinical and applied thrombosis/hemostasis (2020)“…Single nucleotide polymorphisms (SNP) associated with Venous Thromboembolism (VTE) risk have been identified in European and American populations. Replicate…”
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10
Increased runs of homozygosity in the autosomal genome of Brazilian individuals with neurodevelopmental delay/intellectual disability and/or multiple congenital anomalies investigated by chromosomal microarray analysis
Published in Genetics and molecular biology (01-01-2022)“…Runs of homozygosity (ROH) in the human genome may be clinically relevant. The aim of this study was to report the frequency of increased ROH of the autosomal…”
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11
Inheritance pattern of molar-incisor hypomineralization
Published in Brazilian oral research (2021)“…The aim of this study was to investigate the segregation patterns of molar incisor hypomineralization (MIH) in families, given the evidence that its etiology…”
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12
A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population
Published in Journal of cranio-maxillo-facial surgery (01-01-2016)“…Abstract Purpose The aim of this study was to use the TaqMan OpenArray system to evaluate associations between 39 genes and the etiology of nonsyndromic cleft…”
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13
Association Analysis of Candidate Variants in Admixed Brazilian Patients With Genetic Generalized Epilepsies
Published in Frontiers in genetics (08-07-2021)“…Genetic generalized epilepsies (GGEs) include well-established epilepsy syndromes with generalized onset seizures: childhood absence epilepsy, juvenile…”
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14
Demographic history differences between Hispanics and Brazilians imprint haplotype features
Published in G3 : genes - genomes - genetics (06-07-2022)“…Admixture is known to greatly impact the genetic landscape of a population and, while genetic variation underlying human phenotypes has been shown to differ…”
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15
Multidimensional Approach Assessing the Role of Interleukin 1 Beta in Mesial Temporal Lobe Epilepsy
Published in Frontiers in neurology (05-08-2021)“…We aimed to investigate the role of interleukin-1 beta (IL-1β) in the mechanisms underlying mesial temporal lobe epilepsy with hippocampal sclerosis (MTLE+HS)…”
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16
Inducible Nitric Oxide Synthase Polymorphisms and Nitric Oxide Levels in Individuals with Chronic Periodontitis
Published in International journal of molecular sciences (15-06-2017)“…This study aimed to investigate whether the -1026(A>C)(rs2779249) and +2087(A>G)(2297518) polymorphisms in the gene were associated with chronic periodontitis…”
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p.Q192R SNP of PON1 seems not to be Associated with Carotid Atherosclerosis Risk Factors in an Asymptomatic and Normolipidemic Brazilian Population Sample
Published in Arquivos brasileiros de cardiologia (01-07-2015)“…Evidences suggest that paraoxonase 1 (PON1) confers important antioxidant and anti-inflammatory properties when associated with high-density lipoprotein (HDL)…”
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18
Assessing treatment response to prophylactic lithium use in patients with bipolar disorder
Published in Jornal Brasileiro de Psiquiatria (01-03-2016)“…ABSTRACT Objetive To identify potential clinical and epidemiological predictors of long-term response to lithium treatment. Methods A total of 40 adult…”
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Lack of association between the prothrombin rs1799963 polymorphism and juvenile myoclonic epilepsy
Published in Arquivos de neuro-psiquiatria (01-04-2015)“…Juvenile myoclonic epilepsy (JME) accounts for 26% of generalized idiopathic epileptic syndromes. The highest levels of thrombin activity are closely involved…”
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20
Analysis of energetically biased transcripts of viruses and transposable elements
Published in Genetics and molecular biology (2012)“…RNA interference (RNAi) is a natural endogenous process by which double-stranded RNA molecules trigger potent and specific gene silencing in eukaryotic cells…”
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