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List of works by Edenir Inêz Palmero

A snapshot of current genetic testing practice in Lynch syndrome: The results of a representative survey of 33 Latin American existing centres/registries

scientific article published on 20 August 2019

A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America.

scientific article published on 5 September 2017

Association of polymorphisms with a family history of cancer and the presence of germline mutations in the BRCA1/BRCA2 genes

scientific article

BRCA1 and BRCA2 Pathogenic Sequence Variants in Women of African Origin or Ancestry

scientific article published on 03 July 2019

BRCA1 and BRCA2 rearrangements in Brazilian individuals with Hereditary Breast and Ovarian Cancer Syndrome.

scientific article published on April 2016

Cancer Genetic Counseling in Public Health Care Hospitals: The Experience of Three Brazilian Services

article

Cancer-related worry and risk perception in Brazilian individuals seeking genetic counseling for hereditary breast cancer

scientific article published on 22 April 2020

Clinical Characterization and Risk Profile of Individuals Seeking Genetic Counseling for Hereditary Breast Cancer in Brazil

article

Clinical and Molecular Assessment of Patients with Lynch Syndrome and Sarcomas Underpinning the Association with MSH2 Germline Pathogenic Variants

scientific article published on 09 July 2020

Clinical and Molecular Characterization of Surgically Treated Oropharynx Squamous Cell Carcinoma Samples

scientific article published on 11 August 2018

Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer.

scientific article published on 7 May 2018

Consistency of self-reported first-degree family history of cancer in a population-based study

scientific article published on 20 January 2009

Detailed haplotype analysis at the TP53 locus in p.R337H mutation carriers in the population of Southern Brazil: evidence for a founder effect.

scientific article published on February 2010

Detection of R337H, a germline TP53 mutation predisposing to multiple cancers, in asymptomatic women participating in a breast cancer screening program in Southern Brazil

article

Differential Profile of BRCA1 vs. BRCA2 Mutated Families: A Characterization of the Main Differences and Similarities in Patients

scientific article published on 01 June 2019

Enhanced magnetocrystalline anisotropy of Fe30Co70 nanowires by Cu additives and annealing.

scientific article

Evaluation of MLH1 variants of unclear significance

scientific article published on 30 April 2018

From colorectal cancer pattern to the characterization of individuals at risk: picture for genetic research in Latin America

article

Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1/2 Breast (and Breast/Ovarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) C

scientific article published on 26 October 2018

Genetic alterations detected by comparative genomic hybridization in BRCAX breast and ovarian cancers of Brazilian population.

scientific article

Genetic and epigenetic characterization of the BRCA1 gene in Brazilian women at-risk for hereditary breast cancer.

scientific article published on December 2016

Genetic cancer risk assessment: A screenshot of the psychosocial profile of women at risk for hereditary breast and ovarian cancer syndrome

scientific article published on 26 January 2020

Genomic rearrangements in BRCA1 and BRCA2: A literature review. ⬇️

scientific article

Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study

scientific article published on 01 March 2019

Genotype-phenotype correlation in 99 familial adenomatous polyposis patients: A prospective prevention protocol

scientific article published on 21 March 2019

Germline MLH1, MSH2 and MSH6 variants in Brazilian patients with colorectal cancer and clinical features suggestive of Lynch Syndrome.

scientific article published on 25 March 2018

Haplotypic characterization of BRCA1 c.5266dupC, the prevailing mutation in Brazilian hereditary breast/ovarian cancer

scientific article published on 01 January 2020

Identification of hereditary cancer in the general population: development and validation of a screening questionnaire for obtaining the family history of cancer

scientific article

Knowledge about hereditary cancer of women with family histories of breast, colorectal, or both types of cancer.

scientific article published in March 2015

Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

scientific article published on 01 September 2019

Magnetic interactions in compositionally modulated nanowire arrays.

scientific article published on 23 September 2016

Mechanisms and role of microRNA deregulation in cancer onset and progression

scientific article (publication date: 2011)

Mutation spectrum in South American Lynch syndrome families

scientific article published on 18 December 2013

Oncogenetics service and the Brazilian public health system: the experience of a reference Cancer Hospital

scientific article published on 13 May 2016

Optimization of a pentaplex panel for MSI analysis without control DNA in a Brazilian population: correlation with ancestry markers.

scientific article

Prevalence of BRCA1/BRCA2 mutations in a Brazilian population sample at-risk for hereditary breast cancer and characterization of its genetic ancestry

scientific article published on 12 October 2016

Prevalence of ERα-397 PvuII C/T, ERα-351 XbaI A/G and PGR PROGINS polymorphisms in Brazilian breast cancer-unaffected women.

scientific article published on 17 May 2012

Prevalence of the STK15 F31I polymorphism and its relationship with mammographic density.

scientific article published on 11 March 2011

Prevalence of the TP53 p.R337H mutation in breast cancer patients in Brazil

scientific article

Reproductive Risk Factors Related to Socioeconomic Status in Pregnant Women in Southern Brazil

article

Screening and characterization of BRCA2 c.156_157insAlu in Brazil: Results from 1380 individuals from the South and Southeast

scientific article published on 06 October 2018

Screening for germline BRCA1, BRCA2, TP53 and CHEK2 mutations in families at-risk for hereditary breast cancer identified in a population-based study from Southern Brazil

scientific article published on 24 May 2016

TP53 PIN3 and MDM2 SNP309 polymorphisms as genetic modifiers in the Li-Fraumeni syndrome: impact on age at first diagnosis.

scientific article published on 18 June 2009

TP53 variants of uncertain significance: increasing challenges in variant interpretation and genetic counseling

scientific article published on 01 October 2019

The Brazilian Founder MutationTP53p.R337H is Uncommon in Portuguese Women Diagnosed with Breast Cancer

scientific article published on 23 July 2014

The Brazilian TP53 mutation (R337H) and sarcomas

scientific article published on 24 January 2020

The TP53 mutation, R337H, is associated with Li-Fraumeni and Li-Fraumeni-like syndromes in Brazilian families.

scientific article published on 21 February 2006

The breast cancer immunophenotype of TP53-p.R337H carriers is different from that observed among other pathogenic TP53 mutation carriers

scientific article

The germline mutational landscape of BRCA1 and BRCA2 in Brazil.

scientific article

The interference of cold ischemia time in the quality of total RNA from frozen tumor samples ⬇️

scientific article published on May 5, 2012

Tumor protein 53 mutations and inherited cancer: beyond Li-Fraumeni syndrome.

scientific article published on January 2010

Whole-exome sequencing of non-BRCA1/BRCA2 mutation carrier cases at high-risk for hereditary breast/ovarian cancer

scientific article published on 16 December 2020

p53 signaling pathway polymorphisms, cancer risk and tumor phenotype in TP53 R337H mutation carriers.

scientific article published on 29 July 2017

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