Pietra Graebin

Porto Alegre, RS, Brazil

Last Updated: 09/26/2026

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Found 11 publications

Uniparental disomy of chromosome 21: A statistical approach and application in paternity tests.

Uniparental disomy of chromosome 21: A statistical approach and application in paternity tests.

Journal: Forensic science international. Genetics

Published: February 05, 2020

Brazilian forensic casework analysis through MPS applications: Statistical weight-of-evidence and biological nature of criminal samples as an influence factor in quality metrics.

Brazilian forensic casework analysis through MPS applications: Statistical weight-of-evidence and biological nature of criminal samples as an influence factor in quality metrics.

Journal: Forensic science international

Published: July 23, 2019

Full mtDNA genome sequencing of Brazilian admixed populations: A forensic-focused evaluation of a MPS application as an alternative to Sanger sequencing methods.

Full mtDNA genome sequencing of Brazilian admixed populations: A forensic-focused evaluation of a MPS application as an alternative to Sanger sequencing methods.

Journal: Forensic science international. Genetics

Published: March 29, 2019

KIR gene haplotype A is associated with hospital mortality in patients with sepsis.

KIR gene haplotype A is associated with hospital mortality in patients with sepsis.

Journal: Clinical immunology (Orlando, Fla.)

Published: January 28, 2019

Forensic characterization of Brazilian regional populations through massive parallel sequencing of 124 SNPs included in HID ion Ampliseq Identity Panel.

Forensic characterization of Brazilian regional populations through massive parallel sequencing of 124 SNPs included in HID ion Ampliseq Identity Panel.

Journal: Forensic science international. Genetics

Published: October 01, 2018

Reduced frequency of two activating KIR genes in patients with sepsis.

Reduced frequency of two activating KIR genes in patients with sepsis.

Journal: Human immunology

Published: October 01, 2016

Effect of 593C>T GPx1 SNP alone and in synergy with 47C>T SOD2 SNP on the outcome of critically ill patients.

Effect of 593C>T GPx1 SNP alone and in synergy with 47C>T SOD2 SNP on the outcome of critically ill patients.

Journal: Cytokine

Published: June 11, 2014

Higher frequency of septic shock in septic patients with the 47C allele (rs4880) of the SOD2 gene.

Higher frequency of septic shock in septic patients with the 47C allele (rs4880) of the SOD2 gene.

Journal: Gene

Published: May 24, 2012

Ewing's sarcoma: analysis of single nucleotide polymorphism in the EWS gene.

Ewing's sarcoma: analysis of single nucleotide polymorphism in the EWS gene.

Journal: Gene

Published: May 22, 2012

The synergy of -260T T CD14 and -308GG TNF-α genotypes in survival of critically ill patients.

The synergy of -260T T CD14 and -308GG TNF-α genotypes in survival of critically ill patients.

Journal: Scandinavian journal of immunology

Published: May 08, 2012

Polymorphic variants in exon 8 at the 3' UTR of the HLA-G gene are associated with septic shock in critically ill patients.

Polymorphic variants in exon 8 at the 3' UTR of the HLA-G gene are associated with septic shock in critically ill patients.

Journal: Critical care (London, England)

Published: May 07, 2012

Showing 1-11 of 11

Last Updated: 09/26/2026