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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
Møller, Pål, Haupt, Saskia, Sunde, Lone, Engel, Christoph, Aretz, Stefan, Nielsen, Maartje, Capella, Gabriel, Bertario, Lucio, Lindblom, Annika, Levi, Zohar, Macrae, Finlay, Winship, Ingrid, Plazzer, John-Paul, Sijmons, Rolf, Laghi, Luigi, Heinimann, Karl, Half, Elizabeth, Lopez-Koestner, Francisco, Alvarez-Valenzuela, Karin, Scott, Rodney J., Laish, Ido, Vainer, Elez, Gluck, Nathan, Stakelum, Aine, Winter, Des, Rossi, Benedito Mauro, Greenblatt, Marc, Sheth, Harsh, Tibiletti, Maria Grazia, Nascimento, Ivana, Thomas, Huw, Zaránd, Attila, Mecklin, Jukka-Pekka, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Peltomäki, Päivi, Therkildsen, Christina, Lindberg, Lars Joachim, Thorlacius-Ussing, Ole, Loeffler, Markus, Steinke-Lange, Verena, Schmiegel, Wolff, Vangala, Deepak, Perne, Claudia, Hüneburg, Robert, Gerdes, Anne-Marie, Backman, Ann-Sofie, Snyder, Carrie, Lautrup, Charlotte K., Amor, David, Stoffel, Elena, Duijkers, Floor, Hall, Michael J., Hampel, Heather, Williams, Heinric, Ngeow, Joanne, Guillem, Jose G., Wadt, Karin, Rasmussen, Lene J., van Hest, Liselotte P., Ricciardiello, Luigi, Kohonen-Corish, Maija R. J., Ligtenberg, Marjolijn J. L., Southey, Melissa, Aronson, Melyssa, Samadder, N. Jewel, Morrison, Patrick J., James, Paul, Chen-Shtoyerman, Rakefet, Pai, Rish, Ward, Robyn, Parry, Susan, Dębniak, Tadeusz, van Overeem Hansen, Thomas, Caldés, Trinidad, Yamaguchi, Tatsuro, Barca-Tierno, Verónica, Cavestro, Giulia Martina, Weitz, Jürgen, Heuveline, Vincent, Hopper, John L., Lindor, Noralane, Le Marchand, Loïc, Buchanan, Daniel D., Thibodeau, Stephen N., ten Broeke, Sanne W., Nakken, Sigve, Pineda, Marta, Brunet, Joan, Crosbie, Emma J., Mints, Miriam, Tjandra, Douglas, Neffa, Florencia, Kariv, Revital, Pavicic, Walter Hernán, Torrezan, Giovana Tardin, Bassaneze, Thiago, Kloor, Matthias, Sampson, Julian R., Jenkins, Mark A.
Published in Hereditary cancer in clinical practice (01.10.2022)
Published in Hereditary cancer in clinical practice (01.10.2022)
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Journal Article
Dominantly inherited micro-satellite instable cancer – the four Lynch syndromes - an EHTG, PLSD position statement
Møller, Pal, Seppälä, Toni T., Ahadova, Aysel, Crosbie, Emma J., Holinski-Feder, Elke, Scott, Rodney, Haupt, Saskia, Möslein, Gabriela, Winship, Ingrid, Broeke, Sanne W. Bajwa-ten, Kohut, Kelly E., Ryan, Neil, Bauerfeind, Peter, Thomas, Laura E., Evans, D. Gareth, Aretz, Stefan, Sijmons, Rolf H., Half, Elizabeth, Heinimann, Karl, Horisberger, Karoline, Monahan, Kevin, Engel, Christoph, Cavestro, Giulia Martina, Fruscio, Robert, Abu-Freha, Naim, Zohar, Levi, Laghi, Luigi, Bertario, Lucio, Bonanni, Bernardo, Tibiletti, Maria Grazia, Lino-Silva, Leonardo S., Vaccaro, Carlos, Valle, Adriana Della, Rossi, Benedito Mauro, da Silva, Leandro Apolinário, de Oliveira Nascimento, Ivana Lucia, Rossi, Norma Teresa, Dębniak, Tadeusz, Mecklin, Jukka-Pekka, Bernstein, Inge, Lindblom, Annika, Sunde, Lone, Nakken, Sigve, Heuveline, Vincent, Burn, John, Hovig, Eivind, Kloor, Matthias, Sampson, Julian R., Dominguez-Valentin, Mev
Published in Hereditary cancer in clinical practice (11.10.2023)
Published in Hereditary cancer in clinical practice (11.10.2023)
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Journal Article
The effect of neoadjuvant platinum-based chemotherapy in BRCA mutated triple negative breast cancers -systematic review and meta-analysis
Caramelo, Olga, Silva, Cristina, Caramelo, Francisco, Frutuoso, Cristina, Almeida-Santos, Teresa
Published in Hereditary cancer in clinical practice (25.03.2019)
Published in Hereditary cancer in clinical practice (25.03.2019)
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Journal Article
The role of BRCA1 and BRCA2 mutations in prostate, pancreatic and stomach cancers
Cavanagh, Helen, Rogers, Katherine M.A.
Published in Hereditary cancer in clinical practice (01.08.2015)
Published in Hereditary cancer in clinical practice (01.08.2015)
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Journal Article
Gastrointestinal manifestations in patients with gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): a systematic review with analysis of individual patient data
Skat-Rørdam, PA, Kaya, Y, Qvist, N, Hansen, TvO, Jensen, TD, Karstensen, JG, Jelsig, AM
Published in Hereditary cancer in clinical practice (22.07.2024)
Published in Hereditary cancer in clinical practice (22.07.2024)
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Journal Article
Incidences of colorectal adenomas and cancers under colonoscopy surveillance suggest an accelerated “Big Bang” pathway to CRC in three of the four Lynch syndromes
Møller, Pål, Haupt, Saskia, Ahadova, Aysel, Kloor, Matthias, Sampson, Julian R., Sunde, Lone, Seppälä, Toni, Burn, John, Bernstein, Inge, Capella, Gabriel, Evans, D. Gareth, Lindblom, Annika, Winship, Ingrid, Macrae, Finlay, Katz, Lior, Laish, Ido, Vainer, Elez, Monahan, Kevin, Half, Elizabeth, Horisberger, Karoline, da Silva, Leandro Apolinário, Heuveline, Vincent, Therkildsen, Christina, Lautrup, Charlotte, Klarskov, Louise L, Cavestro, Giulia Martina, Möslein, Gabriela, Hovig, Eivind, Dominguez-Valentin, Mev
Published in Hereditary cancer in clinical practice (13.05.2024)
Published in Hereditary cancer in clinical practice (13.05.2024)
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Journal Article
Can harmful lifestyle, obesity and weight changes increase the risk of breast cancer in BRCA 1 and BRCA 2 mutation carriers? A Mini review
Daniele, A., Divella, R., Pilato, B., Tommasi, S., Pasanisi, P., Patruno, M., Digennaro, M., Minoia, C., Dellino, M., Pisconti, S., Casamassima, P., Savino, E., Paradiso, A. V.
Published in Hereditary cancer in clinical practice (27.10.2021)
Published in Hereditary cancer in clinical practice (27.10.2021)
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Journal Article
Medullary breast cancer and germline BRCA1 mutations: a possible criterion for genetic testing
Apostol, Adriana I., Lim, David, Narod, Steven A.
Published in Hereditary cancer in clinical practice (01.09.2025)
Published in Hereditary cancer in clinical practice (01.09.2025)
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Journal Article
Association analysis of germline mutations in CHEK2, PALB2, NBN and RECQL with the risk of ductal carcinoma in situ in Polish women
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
Published in Hereditary cancer in clinical practice (06.08.2025)
Published in Hereditary cancer in clinical practice (06.08.2025)
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Journal Article
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report
Seppälä, Toni T., Ahadova, Aysel, Dominguez-Valentin, Mev, Macrae, Finlay, Evans, D. Gareth, Therkildsen, Christina, Sampson, Julian, Scott, Rodney, Burn, John, Möslein, Gabriela, Bernstein, Inge, Holinski-Feder, Elke, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Lepistö, Anna, Lautrup, Charlotte Kvist, Lindblom, Annika, Plazzer, John-Paul, Winship, Ingrid, Tjandra, Douglas, Katz, Lior H., Aretz, Stefan, Hüneburg, Robert, Holzapfel, Stefanie, Heinimann, Karl, Valle, Adriana Della, Neffa, Florencia, Gluck, Nathan, de Vos tot Nederveen Cappel, Wouter H., Vasen, Hans, Morak, Monika, Steinke-Lange, Verena, Engel, Christoph, Rahner, Nils, Schmiegel, Wolff, Vangala, Deepak, Thomas, Huw, Green, Kate, Lalloo, Fiona, Crosbie, Emma J., Hill, James, Capella, Gabriel, Pineda, Marta, Navarro, Matilde, Blanco, Ignacio, ten Broeke, Sanne, Nielsen, Maartje, Ljungmann, Ken, Nakken, Sigve, Lindor, Noralane, Frayling, Ian, Hovig, Eivind, Sunde, Lone, Kloor, Matthias, Mecklin, Jukka-Pekka, Kalager, Mette, Møller, Pål
Published in Hereditary cancer in clinical practice (28.02.2019)
Published in Hereditary cancer in clinical practice (28.02.2019)
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Journal Article
Endoscopic surveillance for colorectal cancer and its precursor lesions in Lynch syndrome; time for some policy shifts?
Kuipers, Romy N, Burggraaff, Marissa F, Maas, Michiel HJ, van der Biessen – van Beek, Dorien TJ, van Kouwen, Mariëtte CA, Bisseling, Tanya M
Published in Hereditary cancer in clinical practice (16.04.2025)
Published in Hereditary cancer in clinical practice (16.04.2025)
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Journal Article
BRCA1 promoter hypermethylation is not associated with germline variants in Polish breast cancer patients
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
Published in Hereditary cancer in clinical practice (10.06.2025)
Published in Hereditary cancer in clinical practice (10.06.2025)
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Journal Article
Association between single nucleotide polymorphisms of DNA repair genes (BRCA1, BRCA2, and PALB2) and breast cancer incidence in a subset of Iranian population
Jahangiri, Sepideh, Abdan, Zahra, Houshmand, Massoud, Souroush, Ali, Aznab, Mozaffar
Published in Hereditary cancer in clinical practice (29.03.2025)
Published in Hereditary cancer in clinical practice (29.03.2025)
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Journal Article
SMAD4 variants and its genotype–phenotype correlations to juvenile polyposis syndrome
Cao, Kimberley, Plazzer, John-Paul, Macrae, Finlay
Published in Hereditary cancer in clinical practice (08.12.2023)
Published in Hereditary cancer in clinical practice (08.12.2023)
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Journal Article
Knowledge and perceptions of genetic testing for patients with breast cancer in Nigeria: a survey of healthcare providers
Wuraola, Funmilola Olanike, Dare, Anna, Ramruthan, Jenine, Reel, Emma, Santiago, Anna T., Sharif, Folorunso, Olayide, Agodirin, Sunday-Nweke, Nneka, Alatise, Olusegun, Cil, Tulin D.
Published in Hereditary cancer in clinical practice (19.05.2025)
Published in Hereditary cancer in clinical practice (19.05.2025)
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Journal Article
Translation, cultural adaptation, and pilot testing of the German cancer worry scale among BRCA1/2 pathogenic variant carriers in Austria
Parger, Anna-Maria, Muhr, Daniela, Singer, Christian F., Tan, Yen Y.
Published in Hereditary cancer in clinical practice (19.05.2025)
Published in Hereditary cancer in clinical practice (19.05.2025)
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Journal Article