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Author Details
Full Name
Sandro J de Souza
Affiliation
Universidade Federal do Rio Grande do Norte
ORCID
Career Start Year
1992
Papers
130
H Index
33
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36966975
Epidemiological-molecular profile of variants associated with type 2 diabetes mellitus in indigenous populations from the Brazilian Amazon.
Diabetes Res Clin Pract
2023
35085295
Family-based whole-exome sequencing identifies rare variants potentially related to cutaneous melanoma predisposition in Brazilian melanoma-prone families.
PLoS One
2022
35671453
The past, present and future of genomics and bioinformatics: A survey of Brazilian scientists.
Genet Mol Biol
2022
35455670
The Genomic Profile Associated with Risk of Severe Forms of COVID-19 in Amazonian Native American Populations.
J Pers Med
2022
35743738
Pharmacogenomic Profile of Amazonian Amerindians.
J Pers Med
2022
36551612
Incidence of Hereditary Gastric Cancer May Be Much Higher than Reported.
Cancers (Basel)
2022
34616737
Chemical Inhibition of Apurinic-Apyrimidinic Endonuclease 1 Redox and DNA Repair Functions Affects the Inflammatory Response via Different but Overlapping Mechanisms.
Front Cell Dev Biol
2021
33613639
The Shared Use of Extended Phenotypes Increases the Fitness of Simulated Populations.
Front Genet
2021
33499154
Identification of Variants (rs11571707, rs144848, and rs11571769) in the <i>BRCA2</i> Gene Associated with Hereditary Breast Cancer in Indigenous Populations of the Brazilian Amazon.
Genes (Basel)
2021
34617951
An integrated approach to identify bimodal genes associated with prognosis in câncer.
Genet Mol Biol
2021
32294118
Identification of NUDT15 gene variants in Amazonian Amerindians and admixed individuals from northern Brazil.
PLoS One
2020
32087727
neoANT-HILL: an integrated tool for identification of potential neoantigens.
BMC Med Genomics
2020
31759986
Analysis of the microarray gene expression for breast cancer progression after the application modified logistic regression.
Gene
2020
33193622
Exome Sequencing of Native Populations From the Amazon Reveals Patterns on the Peopling of South America.
Front Genet
2020
32693352
XPA deficiency affects the ubiquitin-proteasome system function.
DNA Repair (Amst)
2020
32592321
Assessment of somatic mutations in urine and plasma of Wilms tumor patients.
Cancer Med
2020
32187157
Distribution and linkage disequilibrium of the enhancer SNP rs5758550 among Latin American populations: influence of continental ancestry.
Pharmacogenet Genomics
2020
30366059
Resveratrol decreases the expression of genes involved in inflammation through transcriptional regulation.
Free Radic Biol Med
2019
31409704
Essential <i>Saccharomyces cerevisiae</i> genome instability suppressing genes identify potential human tumor suppressors.
Proc Natl Acad Sci U S A
2019
31229581
A comprehensive analysis of core polyadenylation sequences and regulation by microRNAs in a set of cancer predisposition genes.
Gene
2019
31281302
On the Impact of the Pangenome and Annotation Discrepancies While Building Protein Sequence Databases for Bacteria Proteogenomics.
Front Microbiol
2019
31419696
Influence of BRCA1 Germline Mutations in the Somatic Mutational Burden of Triple-Negative Breast Cancer.
Transl Oncol
2019
30301969
Uncovering association networks through an eQTL analysis involving human miRNAs and lincRNAs.
Sci Rep
2018
30148116
Mutation Detection in Tumor-Derived Cell Free DNA Anticipates Progression in a Patient With Metastatic Colorectal Cancer.
Front Oncol
2018
29982381
Whole Genome Sequencing of the Pirarucu (Arapaima gigas) Supports Independent Emergence of Major Teleost Clades.
Genome Biol Evol
2018
29868112
Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer.
Front Genet
2018
30378298
Sex-biased gene expression in the frontal cortex of common marmosets (Callithrix jacchus) and potential behavioral correlates.
Brain Behav
2018
28582591
A tool for integrating genetic and mass spectrometry-based peptide data: Proteogenomics Viewer: PV: A genome browser-like tool, which includes MS data visualization and peptide identification parameters.
Bioessays
2017
29190970
Genome-wide identification of cancer/testis genes and their association with prognosis in a pan-cancer analysis.
Oncotarget
2017
27071721
A genetic network that suppresses genome rearrangements in Saccharomyces cerevisiae and contains defects in cancers.
Nat Commun
2016
28097125
Bioinformatics Analysis of the Human Surfaceome Reveals New Targets for a Variety of Tumor Types.
Int J Genomics
2016
27863505
A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease.
Hum Genomics
2016
27158220
A New Approach for Identification of Cancer-related Pathways using Protein Networks and Genomic Data.
Cancer Inform
2016
27399331
NFAT1 transcription factor regulates cell cycle progression and cyclin E expression in B lymphocytes.
Cell Cycle
2016
26194008
Populational landscape of INDELs affecting transcription factor-binding sites in humans.
BMC Genomics
2015
26618088
Splicing Express: a software suite for alternative splicing analysis using next-generation sequencing data.
PeerJ
2015
24710071
S-score: a scoring system for the identification and prioritization of predicted cancer genes.
PLoS One
2014
25405079
Identification of rare alternative splicing events in MS/MS data reveals a significant fraction of alternative translation initiation sites.
PeerJ
2014
23359205
Gene copy-number polymorphism caused by retrotransposition in humans.
PLoS Genet
2013
24386182
High-throughput sequencing of a South American Amerindian.
PLoS One
2013
24222238
"Extended Fitness" hypothesis: a link between individual and group selection.
Genet Mol Res
2013
24195083
The human cell surfaceome of breast tumors.
Biomed Res Int
2013
23420281
Modeling tumor evolutionary dynamics.
Front Physiol
2013
23529588
Testing for natural selection in human exonic splicing regulators associated with evolutionary rate shifts.
J Mol Evol
2013
22528879
Domain shuffling and the increasing complexity of biological networks.
Bioessays
2012
23390370
SurfaceomeDB: a cancer-orientated database for genes encoding cell surface proteins.
Cancer Immun
2012
22948334
Evolutionary history of exon shuffling.
Genetica
2012
23064119
SPLOOCE: a new portal for the analysis of human splicing variants.
RNA Biol
2012
20926528
PVALB, a new Hürthle adenoma diagnostic marker identified through gene expression.
J Clin Endocrinol Metab
2011
21326368
Analysis of allelic differential expression in the human genome using allele-specific serial analysis of gene expression tags.
Genome
2011
1 - 50 of 130
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Sirio-Libanes Hospital
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Robert L Strausberg
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9
Otavia L Caballero
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Co-authored papers
8
Andr?? M Ribeiro-Dos-Santos
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Co-authored papers
8
Emmanuel Dias-Neto
A.C. Camargo Cancer Center
Co-authored papers
7
Elisa Napolitano E Ferreira
A.C.Camargo Cancer Center
Co-authored papers
7
Marco A Zago
Center for Cell-Based Therapy (CTC)
Co-authored papers
7
Gregory J Riggins
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Beatriz Stransky
Metropole Digital Institute (IMD), Federal University of Rio Grande do Norte (UFRN)
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Lucila Ohno-Machado
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Lucila Ohno-Machado
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