The C/A polymorphism in intron 11 of the XPC gene plays a crucial role in the modulation of an individual’s susceptibility to sporadic colorectal cancer von Gil, Justyna, Ramsey, Dave, Stembalska, Agnieszka, Karpinski, Pawel, Pesz, Karolina A., Laczmanska, Izabela, Leszczynski, Przemyslaw, Grzebieniak, Zygmunt, Sasiadek, Maria Malgorzata

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Cancer stem cells: the theory and perspectives in cancer therapy von Gil, Justyna, Stembalska, Agnieszka, Pesz, Karolina A., Sąsiadek, Maria M.

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Basal cell carcinoma of the skin: whole genome screening by comparative genome hybridization revisited von Pesz, Karolina A., Bieniek, Andrzej, Makowska, Izabela, Sąsiadek, Maria M.

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May autophagy be a novel biomarker and antitumor target in colorectal cancer? von Gil, Justyna, Pesz, Karolina A, S siadek, Maria M

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Personalized medicine in oncology. New perspectives in management of gliomas von Gil, Justyna, Laczmanska, Izabela, Pesz, Karolina A., Sasiadek, Maria M.

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Polymorphisms in nucleotide excision repair genes and basal cell carcinoma of the skin von Pesz, Karolina A., Bieniek, Andrzej, Gil, Justyna, Laczmanska, Izabela, Karpinski, Pawel, Makowska, Izabela, Trusewicz, Alicja, Sasiadek, Maria M.

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Indices of Insulin Resistance and Dyslipidemia Are Correlated with Lymphocyte Proneness to Apoptosis in Obese or Overweight Low Birth Weight Children von Barg, Ewa, Szopa, Jan, Pesz, Karolina A., Gąsiorowski, Kazimierz

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Assessment of chromosomal imbalances in CIMP-high and CIMP-low/CIMP-0 colorectal cancers von Kozlowska, Joanna, Karpinski, Pawel, Szmida, Elzbieta, Laczmanska, Izabela, Misiak, Blazej, Ramsey, David, Bebenek, Marek, Kielan, Wojciech, Pesz, Karolina A., Sasiadek, Maria M.

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Rapid-FISH--fast and reliable method of detecting common numerical chromosomal aberrations in prenatal diagnosis von Laczmańska, Izabela, Stembalska, Agnieszka, Slezak, Ryszard, Kozłowska, Joanna, Makowska, Izabela, Czemarmazowicz, Halina, Pesz, Karolina A, Smigiel, Robert, Jakiel, Anna, Sasiadek, Maria Małgorzata

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The role of genetic counselling in oncology von Stembalska, Agnieszka, Pesz, Karolina

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Genetic variants in ATM, H2AFX and MRE11 genes and susceptibility to breast cancer in the polish population von Podralska, Marta, Ziółkowska-Suchanek, Iwona, Żurawek, Magdalena, Dzikiewicz-Krawczyk, Agnieszka, Słomski, Ryszard, Nowak, Jerzy, Stembalska, Agnieszka, Pesz, Karolina, Mosor, Maria

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Pan-cancer analysis reveals presence of pronounced DNA methylation drift in CpG island methylator phenotype clusters von Karpinski, Pawel, Pesz, Karolina, Sasiadek, Maria M

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Clinical characteristics of Polish patients with molecularly confirmed Mowat-Wilson syndrome von Jakubiak, Aleksandra, Szczałuba, Krzysztof, Badura-Stronka, Magdalena, Kutkowska-Kaźmierczak, Anna, Jakubiuk-Tomaszuk, Anna, Chilarska, Tatiana, Pilch, Jacek, Braun-Walicka, Natalia, Castaneda, Jennifer, Wołyńska, Katarzyna, Wiśniewska, Marzena, Kugaudo, Monika, Bielecka, Monika, Pesz, Karolina, Wierzba, Jolanta, Latos-Bieleńska, Anna, Obersztyn, Ewa, Krajewska-Walasek, Małgorzata, Śmigiel, Robert

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Selected syndromes of hamartomatous polyposis of the gastrointestinal tract – clinical and genetic aspects von Pytrus, Tomasz, Pesz, Karolina, Kofla-Dlubacz, Anna, Stawarski, Andrzej, Gil, Justyna

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DNA methylation abundantly associates with fetal alcohol spectrum disorder and its subphenotypes von Cobben, Jan Maarten, Krzyzewska, Izabela M, Venema, Andrea, Mul, Adri N, Polstra, Abeltje, Postma, Alex V, Smigiel, Robert, Pesz, Karolina, Niklinski, Jacek, Chomczyk, Monika A, Henneman, Peter, Mannens, Marcel MAM

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Interfamilial clinical variability in four Polish families with cranioectodermal dysplasia and identical compound heterozygous variants in WDR35 von Walczak‐Sztulpa, Joanna, Wawrocka, Anna, Stańczyk, Małgorzata, Pesz, Karolina, Dudarewicz, Lech, Chrul, Sławomir, Bukowska‐Olech, Ewelina, Wieczorek‐Cichecka, Nina, Arts, Heleen H., Oud, Machteld M., Śmigiel, Robert, Grenda, Ryszard, Obersztyn, Ewa, Chrzanowska, Krystyna H., Latos‐Bieleńska, Anna

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The Role of the Reanalysis of Genetic Test Results in the Diagnosis of Dysmorphic Syndrome Caused by Inherited Xq24 Deletion including the UBE2A and CXorf56 Genes von Wolanska, Ewelina, Pollak, Agnieszka, Rydzanicz, Malgorzata, Pesz, Karolina, Klaniewska, Magdalena, Rozensztrauch, Anna, Skiba, Pawel, Stawinski, Piotr, Ploski, Rafal, Smigiel, Robert

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Phenotypic consequences of gene disruption by a balanced de novo translocation involving SLC6A1 and NAA15 von Pesz, Karolina, Pienkowski, Victor Murcia, Pollak, Agnieszka, Gasperowicz, Piotr, Sykulski, Maciej, Kosińska, Joanna, Kiszko, Magdalena, Krzykwa, Bogusława, Bartnik-Głaska, Magdalena, Nowakowska, Beata, Rydzanicz, Małgorzata, Sasiadek, Maria Małgorzata, Płoski, Rafał

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Multiplex ligation-dependent probe amplification as a screening test in children with autism spectrum disorders von Laczmanska, Izabela, Stembalska, Agnieszka, Zlocinska, Magdalena, Korlowska, Joanna, Skiba, Pawel, Pesz, Karolina, Slezak, Ryszard, Smigiel, Robert, Jakubiak, Aleksandra, Misiak, Blazej, Sasiadek, Maria M.

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Polymorphism in nucleotide excision repair gene XPC correlates with bleomycin-induced chromosomal aberrations von Laczmanska, Izabela, Gil, Justyna, Karpinski, Pawel, Stembalska, Agnieszka, Trusewicz, Alicja, Pesz, Karolina, Ramsey, David, Schlade-Bartusiak, Kamilla, Blin, Nikolaus, Sasiadek, Maria Malgorzata

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