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Author Details

Sandro J de Souza
Universidade Federal do Rio Grande do Norte
1992
130
33
PMIDPaper TitleJournal TitlePublished Year
36966975Epidemiological-molecular profile of variants associated with type 2 diabetes mellitus in indigenous populations from the Brazilian Amazon.Diabetes Res Clin Pract2023
35085295Family-based whole-exome sequencing identifies rare variants potentially related to cutaneous melanoma predisposition in Brazilian melanoma-prone families.PLoS One2022
35671453The past, present and future of genomics and bioinformatics: A survey of Brazilian scientists.Genet Mol Biol2022
35455670The Genomic Profile Associated with Risk of Severe Forms of COVID-19 in Amazonian Native American Populations.J Pers Med2022
35743738Pharmacogenomic Profile of Amazonian Amerindians.J Pers Med2022
36551612Incidence of Hereditary Gastric Cancer May Be Much Higher than Reported.Cancers (Basel)2022
34616737Chemical Inhibition of Apurinic-Apyrimidinic Endonuclease 1 Redox and DNA Repair Functions Affects the Inflammatory Response via Different but Overlapping Mechanisms.Front Cell Dev Biol2021
33613639The Shared Use of Extended Phenotypes Increases the Fitness of Simulated Populations.Front Genet2021
33499154Identification 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
34617951An integrated approach to identify bimodal genes associated with prognosis in câncer.Genet Mol Biol2021
32294118Identification of NUDT15 gene variants in Amazonian Amerindians and admixed individuals from northern Brazil.PLoS One2020
32087727neoANT-HILL: an integrated tool for identification of potential neoantigens.BMC Med Genomics2020
31759986Analysis of the microarray gene expression for breast cancer progression after the application modified logistic regression.Gene2020
33193622Exome Sequencing of Native Populations From the Amazon Reveals Patterns on the Peopling of South America.Front Genet2020
32693352XPA deficiency affects the ubiquitin-proteasome system function.DNA Repair (Amst)2020
32592321Assessment of somatic mutations in urine and plasma of Wilms tumor patients.Cancer Med2020
32187157Distribution and linkage disequilibrium of the enhancer SNP rs5758550 among Latin American populations: influence of continental ancestry.Pharmacogenet Genomics2020
30366059Resveratrol decreases the expression of genes involved in inflammation through transcriptional regulation.Free Radic Biol Med2019
31409704Essential <i>Saccharomyces cerevisiae</i> genome instability suppressing genes identify potential human tumor suppressors.Proc Natl Acad Sci U S A2019
31229581A comprehensive analysis of core polyadenylation sequences and regulation by microRNAs in a set of cancer predisposition genes.Gene2019
31281302On the Impact of the Pangenome and Annotation Discrepancies While Building Protein Sequence Databases for Bacteria Proteogenomics.Front Microbiol2019
31419696Influence of BRCA1 Germline Mutations in the Somatic Mutational Burden of Triple-Negative Breast Cancer.Transl Oncol2019
30301969Uncovering association networks through an eQTL analysis involving human miRNAs and lincRNAs.Sci Rep2018
30148116Mutation Detection in Tumor-Derived Cell Free DNA Anticipates Progression in a Patient With Metastatic Colorectal Cancer.Front Oncol2018
29982381Whole Genome Sequencing of the Pirarucu (Arapaima gigas) Supports Independent Emergence of Major Teleost Clades.Genome Biol Evol2018
29868112Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer.Front Genet2018
30378298Sex-biased gene expression in the frontal cortex of common marmosets (Callithrix jacchus) and potential behavioral correlates.Brain Behav2018
28582591A 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.Bioessays2017
29190970Genome-wide identification of cancer/testis genes and their association with prognosis in a pan-cancer analysis.Oncotarget2017
27071721A genetic network that suppresses genome rearrangements in Saccharomyces cerevisiae and contains defects in cancers.Nat Commun2016
28097125Bioinformatics Analysis of the Human Surfaceome Reveals New Targets for a Variety of Tumor Types.Int J Genomics2016
27863505A 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 Genomics2016
27158220A New Approach for Identification of Cancer-related Pathways using Protein Networks and Genomic Data.Cancer Inform2016
27399331NFAT1 transcription factor regulates cell cycle progression and cyclin E expression in B lymphocytes.Cell Cycle2016
26194008Populational landscape of INDELs affecting transcription factor-binding sites in humans.BMC Genomics2015
26618088Splicing Express: a software suite for alternative splicing analysis using next-generation sequencing data.PeerJ2015
24710071S-score: a scoring system for the identification and prioritization of predicted cancer genes.PLoS One2014
25405079Identification of rare alternative splicing events in MS/MS data reveals a significant fraction of alternative translation initiation sites.PeerJ2014
23359205Gene copy-number polymorphism caused by retrotransposition in humans.PLoS Genet2013
24386182High-throughput sequencing of a South American Amerindian.PLoS One2013
24222238"Extended Fitness" hypothesis: a link between individual and group selection.Genet Mol Res2013
24195083The human cell surfaceome of breast tumors.Biomed Res Int2013
23420281Modeling tumor evolutionary dynamics.Front Physiol2013
23529588Testing for natural selection in human exonic splicing regulators associated with evolutionary rate shifts.J Mol Evol2013
22528879Domain shuffling and the increasing complexity of biological networks.Bioessays2012
23390370SurfaceomeDB: a cancer-orientated database for genes encoding cell surface proteins.Cancer Immun2012
22948334Evolutionary history of exon shuffling.Genetica2012
23064119SPLOOCE: a new portal for the analysis of human splicing variants.RNA Biol2012
20926528PVALB, a new Hürthle adenoma diagnostic marker identified through gene expression.J Clin Endocrinol Metab2011
21326368Analysis of allelic differential expression in the human genome using allele-specific serial analysis of gene expression tags.Genome2011
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Collaborators

Instituto Metropole Digital, Universidade Federal do Rio Grande do Norte
Co-authored papers 28
University of Hull
Co-authored papers 25
Hospital Sirio Libanes
Co-authored papers 24
Hospital Sirio-Libanes
Co-authored papers 22
AC Camargo Cancer Center
Co-authored papers 15
Ribeirao Preto Medical School - University of Sao Paulo
Co-authored papers 12
Instituto do Cerebro, Universidade Federal do Rio Grande do Norte
Co-authored papers 10
Sirio-Libanes Hospital
Co-authored papers 9
Ludwig Institute for Cancer Research
Co-authored papers 9
Ludwig Institute for Cancer Research Ltd.
Co-authored papers 8
Institute for Systems Genetics, NYU School of Medicine
Co-authored papers 8
A.C. Camargo Cancer Center
Co-authored papers 7
A.C.Camargo Cancer Center
Co-authored papers 7
Center for Cell-Based Therapy (CTC)
Co-authored papers 7
Co-authored papers 7
Metropole Digital Institute (IMD), Federal University of Rio Grande do Norte (UFRN)
Co-authored papers 7
Co-authored papers 6
Escola de Administracao de Empresas - FGV, Stanford University, University of California San Diego, University of Sao Paulo, Yale School of Medicine
Co-authored papers 6
Faculdade de Ciencias Agrarias e Veterinarias, Universidade Estadual Paulista (UNESP)
Co-authored papers 6
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Harvard Medical School
Co-authored papers 4
Universidade Federal de Santa Maria
Co-authored papers 4
International Research Center, A.C. Camargo Cancer Center
Co-authored papers 4
Instituto Rene Rachou
Co-authored papers 4
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Instituto Butantan
Co-authored papers 4
Ludwig Institute for Cancer Research
Co-authored papers 3
Instituto de Matematica e Estatistica, Universidade de Sao Paulo
Co-authored papers 3
Ludwig Institute for Cancer Research San Diego Branch
Co-authored papers 3
Bluestar Genomics Inc.
Co-authored papers 3