Works matching IS 17312302 AND DT 2025 AND VI 23 AND IP 1

Results: 19
    1

    Association analysis of germline mutations in CHEK2, PALB2, NBN and RECQL with the risk of ductal carcinoma in situ in Polish women.

    Published in:
    Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-025-00320-z
    By:
    • Feszak, Sylwia;
    • Kluźniak, Wojciech;
    • Feszak, Igor;
    • Chady, Magdalena;
    • Wokołorczyk, Dominika;
    • Stempa, Klaudia;
    • Rudnicka, Helena;
    • Gliniewicz, Katarzyna;
    • Jakubowska, Anna;
    • Lener, Marcin;
    • Czepukowicz, Maciej;
    • Huzarski, Tomasz;
    • Dębniak, Tadeusz;
    • Gronwald, Jacek;
    • Lubiński, Jan;
    • Cybulski, Cezary
    Publication type:
    Article
    2

    BRCA1 promoter hypermethylation is not associated with germline variants in Polish breast cancer patients.

    Published in:
    Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-025-00317-8
    By:
    • Prajzendanc, Karolina;
    • Domagała, Paweł;
    • Hybiak, Jolanta;
    • Kluźniak, Wojciech;
    • Cybulski, Cezary;
    • Białkowska, Katarzyna;
    • Ogrodniczak, Alicja;
    • Ryś, Janusz;
    • Sejda, Aleksandra;
    • Szwiec, Marek;
    • Tomiczek-Szwiec, Joanna;
    • Kluz, Tomasz;
    • Dwornik, Roksana;
    • Cylwik, Dagmara;
    • Gronwald, Jacek;
    • Lubiński, Jan;
    • Jakubowska, Anna
    Publication type:
    Article
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    Chemotherapy receipt in affected BRCA1/2 and PALB2 carriers with operable breast cancer: the impact of early detection and pre-diagnostic awareness on clinical outcomes and treatment.

    Published in:
    Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-025-00314-x
    By:
    • Wong, Stephanie M.;
    • Apostolova, Carla;
    • Ferroum, Amina;
    • Alhassan, Basmah;
    • Prakash, Ipshita;
    • Basik, Mark;
    • Martel, Karyne;
    • Meterissian, Sarkis;
    • Fleiszer, David;
    • Wong, Nora;
    • Sadinsky, Michaela Bercovitch;
    • Malagon, Talia;
    • Boileau, Jean Francois;
    • Foulkes, William D.
    Publication type:
    Article
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    Assessing germline TP53 mutations in cancer patients: insights into Li-Fraumeni syndrome and genetic testing guidelines.

    Published in:
    Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-025-00307-w
    By:
    • Danishevich, Anastasiia;
    • Fedorova, Daria;
    • Bodunova, Natalia;
    • Makarova, Maria;
    • Byakhova, Maria;
    • Semenova, Anna;
    • Galkin, Vsevolod;
    • Litvinova, Maria;
    • Nikolaev, Sergey;
    • Efimova, Irina;
    • Osinin, Pavel;
    • Lisitsa, Tatyana;
    • Khakhina, Anastasiya;
    • Shipulin, German;
    • Nasedkina, Tatiana;
    • Shumilova, Syuykum;
    • Gusev, Oleg;
    • Bilyalov, Airat;
    • Shagimardanova, Elena;
    • Shigapova, Leyla
    Publication type:
    Article
    16
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    Colorectal carcinogenesis in the Lynch syndromes and familial adenomatous polyposis: trigger events and downstream consequences.

    Published in:
    Hereditary Cancer in Clinical Practice, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s13053-025-00305-y
    By:
    • Møller, Pål;
    • Ahadova, Aysel;
    • Kloor, Matthias;
    • Seppälä, Toni T.;
    • Burn, John;
    • Haupt, Saskia;
    • Macrae, Finlay;
    • Dominguez-Valentin, Mev;
    • Möslein, Gabriela;
    • Lindblom, Annika;
    • sunde, Lone;
    • Winship, Ingrid;
    • Capella, Gabriel;
    • Monahan, Kevin;
    • Buchanan, Daniel D.;
    • Evans, D. Gareth;
    • Hovig, Eivind;
    • Sampson, Julian R.
    Publication type:
    Article
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