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Expression of adipokines and estrogen receptors in adipose tissue and placenta of patients with gestational diabetes mellitus

Molecular and cellular endocrinology, 2010-01, Vol.314 (1), p.150-156

2010

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Hereditary truncating mutations of DNA repair and other genes in BRCA1/BRCA2/PALB2-negatively tested breast cancer patients

Clinical genetics, 2016-10, Vol.90 (4), p.324-333

2016

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RE: frameshift variant FANCLc.1096_1099dupATTA is not associated with high breast cancer risk

Clinical genetics, 2016-10, Vol.90 (4), p.387-389

2016

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Functional evaluation of breast cancer case-associated non-coding variants in BRCA1/2

European journal of cancer (1990), 2016-07, Vol.61, p.S26-S26

2016

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Identification of pancreatic cancer susceptibility genes in the Czech Republic

European journal of cancer (1990), 2016-07, Vol.61, p.S26-S26

2016

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CHEK2 gene analysis in 1020 high-risk breast and ovarian cancer patients in the Czech Republic

European journal of cancer (1990), 2016-07, Vol.61, p.S27-S27

2016

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Classifying variants in the CHEK2 gene: the importance of collaboration

European journal of cancer (1990), 2017-02, Vol.72, p.S25-S25

2017

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Mutation analysis of the PALB2 gene in unselected pancreatic cancer patients in the Czech Republic

Cancer genetics, 2016-05, Vol.209 (5), p.199-204

2016

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1156 A High Prevalence of PALB2 Mutations Among Familial Breast Cancer Patients in the Czech Republic

European journal of cancer (1990), 2012-07, Vol.48, p.S278-S278

2012

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967: Hereditary variants of genes coding for TP53 and its regulators (CHK2 and WIP1) in high-risk breast cancer patients

European journal of cancer (1990), 2014-07, Vol.50, p.S236-S236

2014

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965: Characterization of breast cancer (BC) predisposition variants in high risk BRCA1- and BRCA2-negative BC patients using panel next-gen sequencing

European journal of cancer (1990), 2014-07, Vol.50, p.S235-S236

2014

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328: Identification and quantification of BRCA1 splicing variants

European journal of cancer (1990), 2014-07, Vol.50, p.S78-S78

2014

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959: Identification of pathogenic mutations in RAD51 paralogs in BRCA1/2-negative ovarian cancer patients in the Czech Republic

European journal of cancer (1990), 2014-07, Vol.50, p.S234-S234

2014

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419 USER-based Approach for Identification of BRCA1 Alternative Splicing Variants

European journal of cancer (1990), 2012-07, Vol.48, p.S102-S102

2012

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Influence of dihydropyrimidine dehydrogenase gene (DPYD) coding sequence variants on the development of fluoropyrimidine-related toxicity in patients with high-grade toxicity and patients with excellent tolerance of fluoropyrimidine-based chemotherapy

Neoplasma, 2009, Vol.56 (4), p.303-316

2009

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418 Alternative Splicing Variants BRCA1Δ14-15 and Δ17-19 Differentially Impair the DNA Double Strand Break Response of MCF-7 Cells

European journal of cancer (1990), 2012-07, Vol.48, p.S101-S102

2012

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Alterations of CHEK2 forkhead-associated domain increase the risk of Hodgkin lymphoma

Neoplasma, 2011, Vol.58 (5), p.392-395

2011

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Role of single nucleotide polymorphisms and haplotypes in BRCA1 in breast cancer : Czech case-control study

Breast cancer research and treatment, 2007-06, Vol.103 (2), p.219-224

2007

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Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers

Neoplasma, 2010, Vol.57 (3), p.280-285

2010

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85 Risk of non-Hodgkin lymphoma development in patients carrying mutations in CHEK2 gene or polymorphism R72P in P53 gene

European journal of cancer supplements, 2010, Vol.8 (5), p.22-22

2010

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Polygenic risk score (PRS) and its potential for breast cancer risk stratification

Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti, 2023, Vol.36 (3), p.198

2023

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Mutation analysis of the MYH gene in unrelated Czech APC mutation-negative polyposis patients

European journal of cancer (1990), 2007-07, Vol.43 (10), p.1617-1621

2007

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Long-term BRCA1 down-regulation by small hairpin RNAs targeting the 3' untranslated region

Neoplasma, 2008, Vol.55 (2), p.130

2008

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84 Genomic rearrangements in BRCA1/2 and CHEK2 genes in Czech high-risk breast/ovarian cancer patients

European journal of cancer supplements, 2010, Vol.8 (5), p.22-22

2010

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507 In vitro analysis of population specific BRCA1 splicing variants

European journal of cancer supplements, 2010, Vol.8 (5), p.130-130

2010

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Expression of adipokines and estrogen receptors in adipose tissue and placenta of patients with gestational diabetes mellitus

Hereditary truncating mutations of DNA repair and other genes in BRCA1/BRCA2/PALB2-negatively tested breast cancer patients

RE: frameshift variant FANCLc.1096_1099dupATTA is not associated with high breast cancer risk

Functional evaluation of breast cancer case-associated non-coding variants in BRCA1/2

Identification of pancreatic cancer susceptibility genes in the Czech Republic

CHEK2 gene analysis in 1020 high-risk breast and ovarian cancer patients in the Czech Republic

Classifying variants in the CHEK2 gene: the importance of collaboration

Mutation analysis of the PALB2 gene in unselected pancreatic cancer patients in the Czech Republic

1156 A High Prevalence of PALB2 Mutations Among Familial Breast Cancer Patients in the Czech Republic

967: Hereditary variants of genes coding for TP53 and its regulators (CHK2 and WIP1) in high-risk breast cancer patients

965: Characterization of breast cancer (BC) predisposition variants in high risk BRCA1- and BRCA2-negative BC patients using panel next-gen sequencing

328: Identification and quantification of BRCA1 splicing variants

959: Identification of pathogenic mutations in RAD51 paralogs in BRCA1/2-negative ovarian cancer patients in the Czech Republic

419 USER-based Approach for Identification of BRCA1 Alternative Splicing Variants

Influence of dihydropyrimidine dehydrogenase gene (DPYD) coding sequence variants on the development of fluoropyrimidine-related toxicity in patients with high-grade toxicity and patients with excellent tolerance of fluoropyrimidine-based chemotherapy

418 Alternative Splicing Variants BRCA1Δ14-15 and Δ17-19 Differentially Impair the DNA Double Strand Break Response of MCF-7 Cells

Alterations of CHEK2 forkhead-associated domain increase the risk of Hodgkin lymphoma

Role of single nucleotide polymorphisms and haplotypes in BRCA1 in breast cancer : Czech case-control study

Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers

85 Risk of non-Hodgkin lymphoma development in patients carrying mutations in CHEK2 gene or polymorphism R72P in P53 gene

Polygenic risk score (PRS) and its potential for breast cancer risk stratification

Mutation analysis of the MYH gene in unrelated Czech APC mutation-negative polyposis patients

Long-term BRCA1 down-regulation by small hairpin RNAs targeting the 3' untranslated region

84 Genomic rearrangements in BRCA1/2 and CHEK2 genes in Czech high-risk breast/ovarian cancer patients

507 In vitro analysis of population specific BRCA1 splicing variants

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