D. Dymerska

发表

Management of ovarian and endometrial cancers in women belonging to HNPCC carrier families: review of the literature and results of cancer risk assessment in Polish HNPCC families

R. Scott, J. Lubiński, C. Cybulski, 2015, Hereditary cancer in clinical practice.

A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants

R. Scott, G. Capellá, J. Lubiński, 2021, Scientific Reports.

Cancer Predisposition Genes in Cancer-Free Families

M. Schlesner, K. Hemminki, J. Lubiński, 2020, Cancers.

Whole exome sequencing identifies novel germline variants of SLC15A4 gene as potentially cancer predisposing in familial colorectal cancer

M. Schlesner, K. Hemminki, J. Lubiński, 2021, Zeitschrift für Induktive Abstammungs- und Vererbungslehre.

Germline MBD4 deficiency causes a multi-tumor predisposition syndrome

M. Christie, D. Wedge, N. López-Bigas, 2022, American journal of human genetics.

Whole exome sequencing identifies novel germline variants of SLC15A4 gene as potentially cancer predisposing in familial colorectal cancer

M. Schlesner, K. Hemminki, J. Lubiński, 2021, Molecular Genetics and Genomics.

Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype.

W. Foulkes, G. Capellá, I. Tomlinson, 2019, Cancer cell.

Skin layer-specific Melan-A expression during progression of human cutaneous melanoma: implications for diagnostic applications of the marker

Anna Sztramska, B. Chwirot, D. Dymerska, 2008, Melanoma research.

Germline Variants of CYBA and TRPM4 Predispose to Familial Colorectal Cancer

M. Schlesner, K. Hemminki, J. Lubiński, 2021, Cancers.

Pedigree based DNA sequencing pipeline for germline genomes of cancer families

Abhishek Kumar, R. Eils, M. Schlesner, 2016, Hereditary Cancer in Clinical Practice.

Polymorphisms in nucleotide excision repair genes and susceptibility to colorectal cancer in the Polish population

J. Kładny, R. Scott, J. Lubiński, 2014, Molecular Biology Reports.

New EPCAM founder deletion in Polish population

A. Pławski, T. Byrski, T. Huzarski, 2017, Clinical genetics.

DNA and RNA analyses in detection of genetic predisposition to cancer

R. Scott, A. Jakubowska, J. Trubicka, 2008, Hereditary Cancer in Clinical Practice.

Whole Exome Sequencing Identifies APCDD1 and HDAC5 Genes as Potentially Cancer Predisposing in Familial Colorectal Cancer

M. Schlesner, K. Hemminki, J. Lubiński, 2021, International journal of molecular sciences.

MLK4 regulates DNA damage response and promotes triple-negative breast cancer chemoresistance

D. Nowis, Anna A. Marusiak, E. Iżycka-Świeszewska, 2021, Cell Death & Disease.

A Novel Low-Risk Germline Variant in the SH2 Domain of the SRC Gene Affects Multiple Pathways in Familial Colorectal Cancer

M. Schlesner, K. Hemminki, J. Lubiński, 2021, Journal of personalized medicine.

Identification of Familial Hodgkin Lymphoma Predisposing Genes Using Whole Genome Sequencing

K. Hemminki, W. Behnisch, J. Lubiński, 2019, Frontiers in Bioengineering and Biotechnology.

Cumulative Small Effect Genetic Markers and the Risk of Colorectal Cancer in Poland, Estonia, Lithuania, and Latvia

R. Scott, A. Metspalu, J. Lubiński, 2015, Gastroenterology research and practice.

Polymorphisms in nucleotide excision repair genes and susceptibility to colorectal cancer in the Polish population

J. Kładny, R. Scott, J. Lubiński, 2014, Molecular Biology Reports.

Whole-Exome Sequencing Identifies a Novel Germline Variant in PTK7 Gene in Familial Colorectal Cancer

Abhishek Kumar, M. Schlesner, K. Hemminki, 2022, International journal of molecular sciences.

Management of ovarian and endometrial cancers in women belonging to HNPCC carrier families: review of the literature and results of cancer risk assessment in Polish HNPCC families

R. Scott, J. Lubiński, C. Cybulski, 2015, Hereditary cancer in clinical practice.

Lynch syndrome mutations shared by the Baltic States and Poland

J. Kładny, A. Metspalu, T. Byrski, 2014, Clinical genetics.

Germline loss-of-function variants in the base-excision repair gene MBD4 cause a Mendelian recessive syndrome of adenomatous colorectal polyposis and acute myeloid leukaemia

M. Christie, D. Wedge, N. López-Bigas, 2021, bioRxiv.

Pedigree based DNA sequencing pipeline for germline genomes of cancer families

Abhishek Kumar, R. Eils, M. Schlesner, 2016, Hereditary cancer in clinical practice.

A rare large duplication of MLH1 identified in Lynch syndrome

M. Schlesner, K. Hemminki, J. Lubiński, 2021, Hereditary cancer in clinical practice.

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

J. Kładny, J. Lubiński, R. Słomski, 2011, The Journal of molecular diagnostics : JMD.

Fast diagnostic test for the identification of an increased genetic predisposition to colon cancer (exemplified on a DNA test for recurrent mutations of the gene MMR)

T. Dębniak, G. Kurzawski, J. Suchy, 2012, Hereditary Cancer in Clinical Practice.

Fast diagnostic test for the identification of an increased genetic predisposition to colon cancer (exemplified on a DNA test for recurrent mutations of the gene MMR)

T. Dębniak, G. Kurzawski, J. Suchy, 2012, Hereditary Cancer in Clinical Practice.

A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants

G. Capellá, J. Lubiński, B. Talseth-Palmer, 2021, Scientific Reports.

Lynch syndrome (HNPCC)

J. Kładny, J. Lubiński, T. Dębniak, 2015 .

Drivers of cancer metastasis - Arise early and remain present.

Anna A. Marusiak, D. Dymerska, 2023, Biochimica et biophysica acta. Reviews on cancer.