Lista de obras -

A preliminary evaluation of next-generation sequencing as a screening tool for targeted genotyping of erythrocyte and platelet antigens in blood donors.

artículo científico publicado en 2017

Age at onset of bilateral breast cancer, the presence of hereditary BRCA1, BRCA2, CHEK2 gene mutations and positive family history of cancer.

artículo científico publicado en 2009

Association of the BRCA1 promoter polymorphism rs11655505 with the risk of familial breast and/or ovarian cancer

artículo científico publicado en 2013

Clinical importance of FANCD2, BRIP1, BRCA1, BRCA2 and FANCF expression in ovarian carcinomas.

artículo científico publicado en 2019

Combination Testing Using a Single MSH5 Variant alongside HLA Haplotypes Improves the Sensitivity of Predicting Coeliac Disease Risk in the Polish Population.

artículo científico publicado en 2015

Common functional alterations identified in blood transcriptome of autoimmune cholestatic liver and inflammatory bowel diseases

scientific article published on 10 May 2019

GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma

artículo científico publicado en 2017

Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population.

artículo científico publicado en 2016

High frequency of BRCA1 founder mutations in Polish women with nonfamilial breast cancer

scientific article published on 01 December 2012

IDH1/2 Mutations Predict Shorter Survival in Chondrosarcoma.

artículo científico publicado en 2018

Limited Practical Utility of Liquid Biopsy in the Treated Patients with Advanced Breast Cancer

scientific article published on 28 July 2020

Limited significance of family history for presence of BRCA1 gene mutation in Polish breast and ovarian cancer cases

artículo científico publicado en 2012

New recurrent BRCA1/2 mutations in Polish patients with familial breast/ovarian cancer detected by next generation sequencing

artículo científico publicado en 2015

Novel germline mutations in BRCA2 gene among breast and breast-ovarian cancer families from Poland.

artículo científico publicado en 2010

PALB2 mutations in BRCA1/2-mutation negative breast and ovarian cancer patients from Poland

artículo científico publicado en 2017

Prediction of fetal blood group and platelet antigens from maternal plasma using next-generation sequencing

scientific article published on 08 January 2019

Preliminary studies on DNA retardation by MutS applied to the detection of point mutations in clinical samples

artículo científico publicado en 2005

Prevalence of the most frequent BRCA1 mutations in Polish population

artículo científico publicado en 2011

Redefining the Practical Utility of Blood Transcriptome Biomarkers in Inflammatory Bowel Diseases

scientific article published on 01 April 2019

Signatures of circulating microRNA in four sarcoma subtypes

scientific article published on 01 January 2020

Somatic aberrations of BRCA1 gene are associated with ALDH1, EGFR and tumor progression in prostate cancer

article

Whole-exome sequencing identifies novel pathogenic variants across the ATP7B gene and some modifiers of Wilson's disease phenotype

scientific article published on 08 October 2018

Lista de obras de

A preliminary evaluation of next-generation sequencing as a screening tool for targeted genotyping of erythrocyte and platelet antigens in blood donors.

Age at onset of bilateral breast cancer, the presence of hereditary BRCA1, BRCA2, CHEK2 gene mutations and positive family history of cancer.

Association of the BRCA1 promoter polymorphism rs11655505 with the risk of familial breast and/or ovarian cancer

Clinical importance of FANCD2, BRIP1, BRCA1, BRCA2 and FANCF expression in ovarian carcinomas.

Combination Testing Using a Single MSH5 Variant alongside HLA Haplotypes Improves the Sensitivity of Predicting Coeliac Disease Risk in the Polish Population.

Common functional alterations identified in blood transcriptome of autoimmune cholestatic liver and inflammatory bowel diseases

GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma

Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population.

High frequency of BRCA1 founder mutations in Polish women with nonfamilial breast cancer

IDH1/2 Mutations Predict Shorter Survival in Chondrosarcoma.

Limited Practical Utility of Liquid Biopsy in the Treated Patients with Advanced Breast Cancer

Limited significance of family history for presence of BRCA1 gene mutation in Polish breast and ovarian cancer cases

New recurrent BRCA1/2 mutations in Polish patients with familial breast/ovarian cancer detected by next generation sequencing

Novel germline mutations in BRCA2 gene among breast and breast-ovarian cancer families from Poland.

PALB2 mutations in BRCA1/2-mutation negative breast and ovarian cancer patients from Poland

Prediction of fetal blood group and platelet antigens from maternal plasma using next-generation sequencing

Preliminary studies on DNA retardation by MutS applied to the detection of point mutations in clinical samples

Prevalence of the most frequent BRCA1 mutations in Polish population

Redefining the Practical Utility of Blood Transcriptome Biomarkers in Inflammatory Bowel Diseases

Signatures of circulating microRNA in four sarcoma subtypes

Somatic aberrations of BRCA1 gene are associated with ALDH1, EGFR and tumor progression in prostate cancer

Whole-exome sequencing identifies novel pathogenic variants across the ATP7B gene and some modifiers of Wilson's disease phenotype