Lista de obras -

AMPD1 gene mutations are associated with obesity and diabetes in Polish patients with cardiovascular diseases

artículo científico publicado en 2011

Age of diagnosis of colorectal cancer in HNPCC patients is more complex than that predicted by R72P polymorphism in TP53.

artículo científico publicado en 2006

Analysis of Human CD36 Gene Sequence Alterations in the Oxidized Low-Density Lipoprotein-Binding Region Using Denaturing High-Performance Liquid Chromatography

artículo científico publicado en 2010

Aurora-A and Cyclin D1 polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer.

artículo científico publicado en 2008

BRCA1 mutations and colorectal cancer in Poland.

artículo científico publicado en 2010

CDKN2A common variant and multi-organ cancer risk--a population-based study

artículo científico publicado en 2006

CHEK2 mutations and HNPCC-related colorectal cancer.

artículo científico publicado en 2010

Chromosome 8q23.3, 10p14 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome – a combined analysis of the Australian, Dutch and Polish Lynch syndrome cohorts

article

Clinical characteristics of tumors derived from colorectal cancer patients who harbor the tumor necrosis factor alpha-1031T/T and NOD2 3020insC polymorphism.

artículo científico publicado en 2009

Clinical, molecular and geographical features of hereditary breast/ovarian cancer in latvia

artículo científico publicado en 2005

Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in Lynch syndrome

artículo científico publicado en 2010

Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers

artículo científico publicado en 2012

Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients

artículo científico publicado en 2009

DNA repair gene polymorphisms and risk of early onset colorectal cancer in Lynch syndrome

artículo científico publicado en 2012

DNA testing for variants conferring low or moderate increase in the risk of cancer

artículo científico publicado en 2008

Frequency of mutations related to hereditary haemochromatosis in northwestern Poland

artículo científico publicado en 2008

Genetic Polymorphisms in Xenobiotic Clearance Genes and Their Influence on Disease Expression in Hereditary Nonpolyposis Colorectal Cancer Patients

artículo científico publicado en 2006

HFE gene mutations in patients with alcoholic liver disease. A prospective study from northwestern Poland.

artículo científico publicado en 2010

Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age.

artículo científico publicado en 2009

Hereditary Colorectal Cancer (CRC) Program in Latvia

IGF1 is a modifier of disease risk in hereditary non-polyposis colorectal cancer

artículo científico publicado en 2008

Inflammatory response gene polymorphisms and their relationship with colorectal cancer risk

artículo científico publicado en 2008

Lack of association between genetic polymorphisms in cytokine genes and disease expression in patients with hereditary non-polyposis colorectal cancer

artículo científico publicado en 2007

Low-risk Genes and Multi-organ Cancer Risk in the Polish Population

artículo científico publicado en 2006

MDM2 SNP309 T>G alone or in combination with theTP53 R72P polymorphism does not appear to influence disease expression and age of diagnosis of colorectal cancer in HNPCC patients

artículo científico publicado en 2006

MSH2 and MLH1 testing

artículo científico publicado en 2008

MSH6 syndrome

artículo científico publicado en 2008

MTHFR 677 C>T and 1298 A>C polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2009

Molecular basis of inherited predispositions for tumors.

artículo científico publicado en 2002

Mutation analysis of MLH1 and MSH2 genes performed by denaturing high-performance liquid chromatography

artículo científico publicado en 2002

NCAN Cross-Disorder Risk Variant Is Associated With Limbic Gray Matter Deficits in Healthy Subjects and Major Depression

artículo científico publicado en 2015

Nationwide study of clinical and molecular features of hereditary non-polyposis colorectal cancer (HNPCC) in Latvia.

artículo científico publicado en 2007

Ovarian cancer of endometrioid type as part of the MSH6 gene mutation phenotype

artículo científico publicado en 2002

Pilot study on low penetrance breast and colorectal cancer predisposition markers in latvia

artículo científico publicado en 2006

Polymorphism in the P-glycoprotein drug transporter MDR1 gene in colon cancer patients.

artículo científico publicado en 2005

Polymorphism of the CD36 Gene and Cardiovascular Risk Factors in Patients with Coronary Artery Disease Manifested at a Young Age

artículo científico publicado en 2011

Prevalence of the NOD2 3020insC mutation in aggregations of breast and lung cancer

artículo científico publicado en 2005

The 3020insC Allele of NOD2 Predisposes to Cancers of Multiple Organs

artículo científico publicado en 2005

The 3020insC allele of NOD2 predisposes to early-onset breast cancer

artículo científico publicado en 2005

The Association of the COMT V158M Polymorphism with Endometrial/Ovarian Cancer in HNPCC Families Adhering to the Amsterdam Criteria

artículo científico publicado en 2006

The NOD2 3020insC mutation and the risk of colorectal cancer

artículo científico publicado en 2004

Variant alleles of the CYP1B1 gene are associated with colorectal cancer susceptibility

artículo científico publicado en 2010

Lista de obras de

AMPD1 gene mutations are associated with obesity and diabetes in Polish patients with cardiovascular diseases

Age of diagnosis of colorectal cancer in HNPCC patients is more complex than that predicted by R72P polymorphism in TP53.

Analysis of Human CD36 Gene Sequence Alterations in the Oxidized Low-Density Lipoprotein-Binding Region Using Denaturing High-Performance Liquid Chromatography

Aurora-A and Cyclin D1 polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer.

BRCA1 mutations and colorectal cancer in Poland.

CDKN2A common variant and multi-organ cancer risk--a population-based study

CHEK2 mutations and HNPCC-related colorectal cancer.

Chromosome 8q23.3, 10p14 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome – a combined analysis of the Australian, Dutch and Polish Lynch syndrome cohorts

Clinical characteristics of tumors derived from colorectal cancer patients who harbor the tumor necrosis factor alpha-1031T/T and NOD2 3020insC polymorphism.

Clinical, molecular and geographical features of hereditary breast/ovarian cancer in latvia

Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in Lynch syndrome

Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers

Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients

DNA repair gene polymorphisms and risk of early onset colorectal cancer in Lynch syndrome

DNA testing for variants conferring low or moderate increase in the risk of cancer

Frequency of mutations related to hereditary haemochromatosis in northwestern Poland

Genetic Polymorphisms in Xenobiotic Clearance Genes and Their Influence on Disease Expression in Hereditary Nonpolyposis Colorectal Cancer Patients

HFE gene mutations in patients with alcoholic liver disease. A prospective study from northwestern Poland.

Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age.

Hereditary Colorectal Cancer (CRC) Program in Latvia

IGF1 is a modifier of disease risk in hereditary non-polyposis colorectal cancer

Inflammatory response gene polymorphisms and their relationship with colorectal cancer risk

Lack of association between genetic polymorphisms in cytokine genes and disease expression in patients with hereditary non-polyposis colorectal cancer

Low-risk Genes and Multi-organ Cancer Risk in the Polish Population

MDM2 SNP309 T>G alone or in combination with theTP53 R72P polymorphism does not appear to influence disease expression and age of diagnosis of colorectal cancer in HNPCC patients

MSH2 and MLH1 testing

MSH6 syndrome

MTHFR 677 C>T and 1298 A>C polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer

Molecular basis of inherited predispositions for tumors.

Mutation analysis of MLH1 and MSH2 genes performed by denaturing high-performance liquid chromatography

NCAN Cross-Disorder Risk Variant Is Associated With Limbic Gray Matter Deficits in Healthy Subjects and Major Depression

Nationwide study of clinical and molecular features of hereditary non-polyposis colorectal cancer (HNPCC) in Latvia.

Ovarian cancer of endometrioid type as part of the MSH6 gene mutation phenotype

Pilot study on low penetrance breast and colorectal cancer predisposition markers in latvia

Polymorphism in the P-glycoprotein drug transporter MDR1 gene in colon cancer patients.

Polymorphism of the CD36 Gene and Cardiovascular Risk Factors in Patients with Coronary Artery Disease Manifested at a Young Age

Prevalence of the NOD2 3020insC mutation in aggregations of breast and lung cancer

The 3020insC Allele of NOD2 Predisposes to Cancers of Multiple Organs

The 3020insC allele of NOD2 predisposes to early-onset breast cancer

The Association of the COMT V158M Polymorphism with Endometrial/Ovarian Cancer in HNPCC Families Adhering to the Amsterdam Criteria

The NOD2 3020insC mutation and the risk of colorectal cancer

Variant alleles of the CYP1B1 gene are associated with colorectal cancer susceptibility