Lynch syndrome mutations in Poland and the Baltic States

per Dymerska, Dagmara, Lubinski, Jan, Kurzawski, Grzegorz
Publicat a Hered Cancer Clin Pract (2015)

DNA and RNA analyses in detection of genetic predisposition to cancer

per Kurzawski, Grzegorz, Dymerska, Dagmara, Serrano-Fernández, Pablo, Trubicka, Joanna, Masojć, Bartłomiej, Jakubowska, Anna, Scott, Rodney J
Publicat 2012

Pedigree based DNA sequencing pipeline for germline genomes of cancer families

per Försti, Asta, Kumar, Abhishek, Paramasivam, Nagarajan, Schlesner, Matthias, Catalano, Calogerina, Dymerska, Dagmara, Lubinski, Jan, Eils, Roland, Hemminki, Kari
Publicat a Hered Cancer Clin Pract (2016)

Identification of Familial Hodgkin Lymphoma Predisposing Genes Using Whole Genome Sequencing

per Srivastava, Aayushi, Giangiobbe, Sara, Kumar, Abhishek, Paramasivam, Nagarajan, Dymerska, Dagmara, Behnisch, Wolfgang, Witzens-Harig, Mathias, Lubinski, Jan, Hemminki, Kari, Försti, Asta, Bandapalli, Obul Reddy
Publicat a Front Bioeng Biotechnol (2020)

Cancer Predisposition Genes in Cancer-Free Families

per Zheng, Guoqiao, Catalano, Calogerina, Bandapalli, Obul Reddy, Paramasivam, Nagarajan, Chattopadhyay, Subhayan, Schlesner, Matthias, Sijmons, Rolf, Hemminki, Akseli, Dymerska, Dagmara, Lubinski, Jan, Hemminki, Kari, Försti, Asta
Publicat a Cancers (Basel) (2020)

A rare large duplication of MLH1 identified in Lynch syndrome

per Kumar, Abhishek, Paramasivam, Nagarajan, Bandapalli, Obul Reddy, Schlesner, Matthias, Chen, Tianhui, Sijmons, Rolf, Dymerska, Dagmara, Golebiewska, Katarzyna, Kuswik, Magdalena, Lubinski, Jan, Hemminki, Kari, Försti, Asta
Publicat a Hered Cancer Clin Pract (2021)

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

per Skopelitou, Diamanto, Miao, Beiping, Srivastava, Aayushi, Kumar, Abhishek, Kuswick, Magdalena, Dymerska, Dagmara, Paramasivam, Nagarajan, Schlesner, Matthias, Lubinski, Jan, Hemminki, Kari, Försti, Asta, Bandapalli, Obul Reddy
Publicat a Int J Mol Sci (2021)

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

per Skopelitou, Diamanto, Miao, Beiping, Srivastava, Aayushi, Kumar, Abhishek, Kuświk, Magdalena, Dymerska, Dagmara, Paramasivam, Nagarajan, Schlesner, Matthias, Lubiński, Jan, Hemminki, Kari, Försti, Asta, Bandapalli, Obul Reddy
Publicat a J Pers Med (2021)

Combined iPLEX and TaqMan Assays to Screen for 45 Common Mutations in Lynch Syndrome and FAP Patients

per Dymerska, Dagmara, Serrano-Fernández, Pablo, Suchy, Janina, Pławski, Andrzej, Słomski, Ryszard, Kąklewski, Krzysztof, Scott, Rodney J., Gronwald, Jacek, Kładny, Józef, Byrski, Tomasz, Huzarski, Tomasz, Lubiński, Jan, Kurzawski, Grzegorz
Publicat 2010

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

per Dębniak, Tadeusz, Gromowski, Tomasz, Scott, Rodney J, Gronwald, Jacek, Huzarski, Tomasz, Byrski, Tomasz, Kurzawski, Grzegorz, Dymerska, Dagmara, Górski, Bohdan, Paszkowska-Szczur, Katarzyna, Cybulski, Cezary, Serrano-Fernandez, Pablo, Lubiński, Jan
Publicat a Hered Cancer Clin Pract (2015)

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

per Paszkowska-Szczur, Katarzyna, Scott, Rodney J., Górski, Bohdan, Cybulski, Cezary, Kurzawski, Grzegorz, Dymerska, Dagmara, Gupta, Satish, van de Wetering, Thierry, Masojć, Bartłomiej, Kashyap, Aniruddh, Gapska, Paulina, Gromowski, Tomasz, Kładny, Józef, Lubiński, Jan, Dębniak, Tadeusz
Publicat a Mol Biol Rep (2014)

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

per Serrano-Fernandez, Pablo, Dymerska, Dagmara, Kurzawski, Grzegorz, Derkacz, Róża, Sobieszczańska, Tatiana, Banaszkiewicz, Zbigniew, Roomere, Hanno, Oitmaa, Eneli, Metspalu, Andres, Janavičius, Ramūnas, Elsakov, Pavel, Razumas, Mindaugas, Petrulis, Kestutis, Irmejs, Arvīds, Miklaševičs, Edvīns, Scott, Rodney J., Lubiński, Jan
Publicat a Gastroenterol Res Pract (2015)

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

per Wiik, Mariann Unhjem, Evans, Tiffany-Jane, Belhadj, Sami, Bolton, Katherine A., Dymerska, Dagmara, Jagmohan-Changur, Shantie, Capellá, Gabriel, Kurzawski, Grzegorz, Wijnen, Juul T., Valle, Laura, Vasen, Hans F. A., Lubinski, Jan, Scott, Rodney J., Talseth-Palmer, Bente A.
Publicat a Sci Rep (2021)