Works matching IS 17312302 AND DT 2022 AND VI 20 AND IP 1

Results: 38
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    Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium.

    Published in:
    Hereditary Cancer in Clinical Practice, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s13053-022-00241-1
    By:
    • Møller, Pål;
    • Seppälä, Toni;
    • Dowty, James G.;
    • Haupt, Saskia;
    • Dominguez-Valentin, Mev;
    • Sunde, Lone;
    • Bernstein, Inge;
    • Engel, Christoph;
    • Aretz, Stefan;
    • Nielsen, Maartje;
    • Capella, Gabriel;
    • Evans, Dafydd Gareth;
    • Burn, John;
    • Holinski-Feder, Elke;
    • Bertario, Lucio;
    • Bonanni, Bernardo;
    • Lindblom, Annika;
    • Levi, Zohar;
    • Macrae, Finlay;
    • Winship, Ingrid
    Publication type:
    Article
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    Mainstream genetic testing for women with ovarian cancer provides a solid basis for patients to make a well-informed decision about genetic testing.

    Published in:
    Hereditary Cancer in Clinical Practice, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s13053-022-00238-w
    By:
    • Bokkers, Kyra;
    • Bleiker, Eveline M. A.;
    • Hoogendam, Jacob P.;
    • Velthuizen, Mary E.;
    • Schreuder, Henk W. R.;
    • Gerestein, Cornelis G.;
    • Lange, Joost G.;
    • Louwers, Jacqueline A.;
    • Koudijs, Marco J.;
    • Ausems, Margreet G. E. M.;
    • Zweemer, Ronald P.
    Publication type:
    Article
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    Spectrum of germline pathogenic variants using a targeted next generation sequencing panel and genotype-phenotype correlations in patients with suspected hereditary breast cancer at an academic medical centre in Pakistan.

    Published in:
    Hereditary Cancer in Clinical Practice, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s13053-022-00232-2
    By:
    • Akbar, Fizza;
    • Siddiqui, Zahraa;
    • Waheed, Muhammad Talha;
    • Ehsan, Lubaina;
    • Ali, Syed Ibaad;
    • Wiquar, Hajra;
    • Valimohammed, Azmina Tajuddin;
    • Khan, Shaista;
    • Vohra, Lubna;
    • Zeeshan, Sana;
    • Rashid, Yasmin;
    • Moosajee, Munira;
    • Jabbar, Adnan Abdul;
    • Zahir, Muhammad Nauman;
    • Zahid, Naila;
    • Soomro, Rufina;
    • Ullah, Najeeb Niamat;
    • Ahmad, Imran;
    • Haider, Ghulam;
    • Ansari, Uzair
    Publication type:
    Article
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    Literacy-adapted, electronic family history assessment for genetics referral in primary care: patient user insights from qualitative interviews.

    Published in:
    Hereditary Cancer in Clinical Practice, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s13053-022-00231-3
    By:
    • Mittendorf, Kathleen F.;
    • Lewis, Hannah S.;
    • Duenas, Devan M.;
    • Eubanks, Donna J.;
    • Gilmore, Marian J.;
    • Goddard, Katrina A. B.;
    • Joseph, Galen;
    • Kauffman, Tia L.;
    • Kraft, Stephanie A.;
    • Lindberg, Nangel M.;
    • Reyes, Ana A.;
    • Shuster, Elizabeth;
    • Syngal, Sapna;
    • Ukaegbu, Chinedu;
    • Zepp, Jamilyn M.;
    • Wilfond, Benjamin S.;
    • Porter, Kathryn M.
    Publication type:
    Article
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    Lynch syndrome testing of colorectal cancer patients in a high-income country with universal healthcare: a retrospective study of current practice and gaps in seven australian hospitals.

    Published in:
    Hereditary Cancer in Clinical Practice, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s13053-022-00225-1
    By:
    • Steinberg, Julia;
    • Chan, Priscilla;
    • Hogden, Emily;
    • Tiernan, Gabriella;
    • Morrow, April;
    • Kang, Yoon-Jung;
    • He, Emily;
    • Venchiarutti, Rebecca;
    • Titterton, Leanna;
    • Sankey, Lucien;
    • Pearn, Amy;
    • Nichols, Cassandra;
    • McKay, Skye;
    • Hayward, Anne;
    • Egoroff, Natasha;
    • Engel, Alexander;
    • Gibbs, Peter;
    • Goodwin, Annabel;
    • Harris, Marion;
    • Kench, James G
    Publication type:
    Article
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    Association of recurrent mutations in BRCA1, BRCA2, RAD51C, PALB2, and CHEK2 with the risk of borderline ovarian tumor.

    Published in:
    Hereditary Cancer in Clinical Practice, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s13053-022-00218-0
    By:
    • Ogrodniczak, Alicja;
    • Menkiszak, Janusz;
    • Gronwald, Jacek;
    • Tomiczek-Szwiec, Joanna;
    • Szwiec, Marek;
    • Cybulski, Cezary;
    • Dębniak, Tadeusz;
    • Huzarski, Tomasz;
    • Tołoczko-Grabarek, Aleksandra;
    • Byrski, Tomasz;
    • Białkowska, Katarzyna;
    • Prajzendanc, Karolina;
    • Baszuk, Piotr;
    • Lubiński, Jan;
    • Jakubowska, Anna
    Publication type:
    Article
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    Retrospective assessment of barriers and access to genetic services for hereditary cancer syndromes in an integrated health care delivery system.

    Published in:
    Hereditary Cancer in Clinical Practice, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s13053-022-00213-5
    By:
    • Muessig, Kristin R.;
    • Zepp, Jamilyn M.;
    • Keast, Erin;
    • Shuster, Elizabeth E.;
    • Reyes, Ana A.;
    • Arnold, Briana;
    • Ingphakorn, Chalinya;
    • Gilmore, Marian J.;
    • Kauffman, Tia L.;
    • Hunter, Jessica Ezzell;
    • Knerr, Sarah;
    • Feigelson, Heather S.;
    • Goddard, Katrina A. B.
    Publication type:
    Article
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