Lista de obras -

A Range of Cancers Is Associated with the rs6983267 Marker on Chromosome 8

A common variant of CDKN2A (p16) predisposes to breast cancer

artículo científico publicado en 2005

A large germline deletion in the Chek2 kinase gene is associated with an increased risk of prostate cancer

artículo científico publicado en 2006

A personalised approach to prostate cancer screening based on genotyping of risk founder alleles

artículo científico publicado en 2013

A protein truncating BRCA1 allele with a low penetrance of breast cancer

artículo científico publicado en 2004

An inherited NBN mutation is associated with poor prognosis prostate cancer

artículo científico publicado en 2012

Attitudes toward preventive oophorectomy among BRCA1 mutation carriers in Poland

artículo científico publicado en 2004

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies

artículo científico publicado en 2003

BRCA1 mutation, leptin and estrogen levels in breast cancer patients

artículo científico publicado en 2005

BRCA1-positive breast cancers in young women from Poland.

artículo científico publicado en 2006

Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies

artículo científico publicado en 2005

Breast cancer predisposing alleles in Poland

artículo científico publicado en 2005

CHEK2 is a multiorgan cancer susceptibility gene

artículo científico publicado en 2004

CHEK2 variants predispose to benign, borderline and low-grade invasive ovarian tumors

artículo científico publicado en 2006

Cancer risks in first-degree relatives of CHEK2 mutation carriers: effects of mutation type and cancer site in proband

artículo científico publicado en 2009

Clinical characteristics of breast cancer in patients with an NBS1 mutation

artículo científico publicado en 2013

Clinical characteristics of laryngeal cancer in BRCA-1 mutation carriers

artículo científico publicado en 2009

Clinical features of familial ovarian cancer lacking mutations in BRCA1 or BRCA2

artículo científico publicado en 2004

Common variants of DNA repair genes and malignant melanoma

artículo científico publicado en 2007

Comparison of Alu-PCR, microsatellite instability, and immunohistochemical analyses in finding features characteristic for hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2001

Detection of germline mutations in the BRCA1 gene by RNA-based sequencing

artículo científico publicado en 2001

Effect of CHEK2 missense variant I157T on the risk of breast cancer in carriers of other CHEK2 or BRCA1 mutations

artículo científico publicado en 2008

Electroretinographic Changes in Eyes of Patients with BRCA1 Gene Mutation ⬇️

artículo científico publicado el 1 de mayo de 2003

Estrogen receptor status in CHEK2-positive breast cancers: implications for chemoprevention

artículo científico publicado en 2008

Founder mutations in the BRCA1 gene in Polish families with breast-ovarian cancer

artículo científico publicado en 2000

Founder mutations in the BRCA1 gene in west Belarusian breast-ovarian cancer families

artículo científico publicado en 2001

Frequency and nature of germline Rb-1 gene mutations in a series of patients with sporadic unilateral retinoblastoma

artículo científico publicado en 1999

Frequency of three BRCA1 gene founder mutations in breast/ovarian cancer families from the Pomerania-Kujawy region of Poland

artículo científico publicado en 2003

Germline mutations in the von Hippel-Lindau (VHL) gene in patients from Poland: disease presentation in patients with deletions of the entire VHL gene

artículo científico publicado en 2002

Impact of BRCA1 mutation on survival after early onset breast cancer.

artículo científico publicado en 2012

Increased risk of breast cancer in relatives of malignant melanoma patients from families with strong cancer familial aggregation

artículo científico publicado en 2003

LDL-R and Apo-B-100 gene mutations in Polish familial hypercholesterolemias ⬇️

artículo científico publicado el 1 de mayo de 1998

Meeting abstracts from the Annual Conference on Hereditary Cancers 2016: Szczecin, Poland. 14-15 September 2016.

artículo científico publicado en 2017

Mutations predisposing to breast cancer in 12 candidate genes in breast cancer patients from Poland.

artículo científico publicado en 2014

NBS1 is a prostate cancer susceptibility gene

artículo científico publicado en 2004

NOD2 variants and the risk of malignant melanoma

artículo científico publicado en 2005

Neoadjuvant therapy with cisplatin in BRCA1-positive breast cancer patients

New diagnostic test for high risk of breast cancer in Poland

article

Non-random transmission of mutant alleles to female offspring of BRCA1 carriers in Poland

artículo científico publicado en 2003

Optimization of experimental conditions for RNA-based sequencing of MLH1 and MSH2 genes

artículo científico publicado en 2001

Pleomorphic adenoma of salivary glands does not appear to be a BRCA-1-dependent tumour in a Polish cohort.

artículo científico publicado en 2008

Rapid test for detection of high risk of breast cancer

artículo científico publicado en 2012

Recurrent mutations of BRCA1 and BRCA2 in Poland: an update

artículo científico publicado en 2014

Response to neoadjuvant therapy with cisplatin in BRCA1-positive breast cancer patients

artículo científico publicado en 2008

Selenium and the risk of cancer in BRCA1 carriers

artículo científico publicado en 2011

Serum YKL-40 levels in patients with ovarian cancer and women with BRCA1 gene mutation--comparison to CA 125 antigen

artículo científico publicado en 2009

The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions

artículo científico publicado en 2008

The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions.

artículo científico publicado en 2008

The contribution of founder mutations in BRCA1 to breast and ovarian cancer in Lithuania

artículo científico publicado en 2010

Value of pedigree/clinical data, immunohistochemistry and microsatellite instability analyses in reducing the cost of determining hMLH1 and hMSH2 gene mutations in patients with colorectal cancer

artículo científico publicado en 2000

Vascular endothelial growth factor (VEGF) levels and mutation of the BRCA1 gene in breast cancer patients

artículo científico publicado en 2004

Vitamin D receptor variants and breast cancer risk in the Polish population

artículo científico publicado en 2008

Vitamin D receptor variants and the malignant melanoma risk: a population-based study

artículo científico publicado en 2009

XPD common variants and their association with melanoma and breast cancer risk

artículo científico publicado en 2006

Xeroderma pigmentosum genes and melanoma risk

artículo científico publicado en 2013

[HPV virus infections and other promotion factors of the carcinogenic process in girls]

scientific article published on 01 July 1993

[VNTR-PCR in diagnosis of inherited Rb gene mutation]

artículo científico publicado en 1994

Lista de obras de

A Range of Cancers Is Associated with the rs6983267 Marker on Chromosome 8

A common variant of CDKN2A (p16) predisposes to breast cancer

A large germline deletion in the Chek2 kinase gene is associated with an increased risk of prostate cancer

A personalised approach to prostate cancer screening based on genotyping of risk founder alleles

A protein truncating BRCA1 allele with a low penetrance of breast cancer

An inherited NBN mutation is associated with poor prognosis prostate cancer

Attitudes toward preventive oophorectomy among BRCA1 mutation carriers in Poland

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies

BRCA1 mutation, leptin and estrogen levels in breast cancer patients

BRCA1-positive breast cancers in young women from Poland.

Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies

Breast cancer predisposing alleles in Poland

CHEK2 is a multiorgan cancer susceptibility gene

CHEK2 variants predispose to benign, borderline and low-grade invasive ovarian tumors

Cancer risks in first-degree relatives of CHEK2 mutation carriers: effects of mutation type and cancer site in proband

Clinical characteristics of breast cancer in patients with an NBS1 mutation

Clinical characteristics of laryngeal cancer in BRCA-1 mutation carriers

Clinical features of familial ovarian cancer lacking mutations in BRCA1 or BRCA2

Common variants of DNA repair genes and malignant melanoma

Comparison of Alu-PCR, microsatellite instability, and immunohistochemical analyses in finding features characteristic for hereditary nonpolyposis colorectal cancer

Detection of germline mutations in the BRCA1 gene by RNA-based sequencing

Effect of CHEK2 missense variant I157T on the risk of breast cancer in carriers of other CHEK2 or BRCA1 mutations

Electroretinographic Changes in Eyes of Patients with BRCA1 Gene Mutation ⬇️

Estrogen receptor status in CHEK2-positive breast cancers: implications for chemoprevention

Founder mutations in the BRCA1 gene in Polish families with breast-ovarian cancer

Founder mutations in the BRCA1 gene in west Belarusian breast-ovarian cancer families

Frequency and nature of germline Rb-1 gene mutations in a series of patients with sporadic unilateral retinoblastoma

Frequency of three BRCA1 gene founder mutations in breast/ovarian cancer families from the Pomerania-Kujawy region of Poland

Germline mutations in the von Hippel-Lindau (VHL) gene in patients from Poland: disease presentation in patients with deletions of the entire VHL gene

Impact of BRCA1 mutation on survival after early onset breast cancer.

Increased risk of breast cancer in relatives of malignant melanoma patients from families with strong cancer familial aggregation

LDL-R and Apo-B-100 gene mutations in Polish familial hypercholesterolemias ⬇️

Meeting abstracts from the Annual Conference on Hereditary Cancers 2016: Szczecin, Poland. 14-15 September 2016.

Mutations predisposing to breast cancer in 12 candidate genes in breast cancer patients from Poland.

NBS1 is a prostate cancer susceptibility gene

NOD2 variants and the risk of malignant melanoma

Neoadjuvant therapy with cisplatin in BRCA1-positive breast cancer patients

New diagnostic test for high risk of breast cancer in Poland

Non-random transmission of mutant alleles to female offspring of BRCA1 carriers in Poland

Optimization of experimental conditions for RNA-based sequencing of MLH1 and MSH2 genes

Pleomorphic adenoma of salivary glands does not appear to be a BRCA-1-dependent tumour in a Polish cohort.

Rapid test for detection of high risk of breast cancer

Recurrent mutations of BRCA1 and BRCA2 in Poland: an update

Response to neoadjuvant therapy with cisplatin in BRCA1-positive breast cancer patients

Selenium and the risk of cancer in BRCA1 carriers

Serum YKL-40 levels in patients with ovarian cancer and women with BRCA1 gene mutation--comparison to CA 125 antigen

The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions

The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions.

The contribution of founder mutations in BRCA1 to breast and ovarian cancer in Lithuania

Value of pedigree/clinical data, immunohistochemistry and microsatellite instability analyses in reducing the cost of determining hMLH1 and hMSH2 gene mutations in patients with colorectal cancer

Vascular endothelial growth factor (VEGF) levels and mutation of the BRCA1 gene in breast cancer patients

Vitamin D receptor variants and breast cancer risk in the Polish population

Vitamin D receptor variants and the malignant melanoma risk: a population-based study

XPD common variants and their association with melanoma and breast cancer risk

Xeroderma pigmentosum genes and melanoma risk

[HPV virus infections and other promotion factors of the carcinogenic process in girls]

[VNTR-PCR in diagnosis of inherited Rb gene mutation]