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Items: 1 to 20 of 797

1.
Analysis of informed consent forms of patients undergoing cancer genetic testing in the era of next-generation sequencing
Tina Kerševan, Tina Kogovšek, Ana Blatnik, Mateja Krajc
Hered Cancer Clin Pract. 2025; 23: 8. Published online 2025 Feb 21. doi: 10.1186/s13053-025-00309-8
PMCID:
PMC11843734
ArticlePDF–1.2M
2.
Assessing germline TP53 mutations in cancer patients: insights into Li-Fraumeni syndrome and genetic testing guidelines
Anastasiia Danishevich, Daria Fedorova, Natalia Bodunova, Maria Makarova, Maria Byakhova, Anna Semenova, Vsevolod Galkin, Maria Litvinova, Sergey Nikolaev, Irina Efimova, Pavel Osinin, Tatyana Lisitsa, Anastasiya Khakhina, German Shipulin, Tatiana Nasedkina, Syuykum Shumilova, Oleg Gusev, Airat Bilyalov, Elena Shagimardanova, Leyla Shigapova, Marina Nemtsova, Olesya Sagaydak, Mary Woroncow, Saida Gadzhieva, Igor Khatkov
Hered Cancer Clin Pract. 2025; 23: 5. Published online 2025 Feb 17. doi: 10.1186/s13053-025-00307-w
PMCID:
PMC11834258
ArticlePDF–1.4M
3.
Time to rethink colorectal cancer prevention strategies for lynch syndrome
Jan Lubinski, Rodney J. Scott
Hered Cancer Clin Pract. 2025; 23: 4. Published online 2025 Feb 7. doi: 10.1186/s13053-024-00295-3
PMCID:
PMC11806523
ArticlePDF–522K
4.
Two independent families with de novo whole APC gene deletion and intellectual disability: a case report
Moriya Iwaizumi, Terumi Taniguchi, Risa Kojima, Harumo Osawa, Kyota Tatsuta, Mayu Sakata, Satoshi Osawa, Kiyotaka Kurachi, Ken Sugimoto
Hered Cancer Clin Pract. 2025; 23: 1. Published online 2025 Jan 8. doi: 10.1186/s13053-024-00297-1
PMCID:
PMC11708175
ArticlePDF–1.2M
5.
BRCA2 germline mutation carrier with five malignancies: a case report
Elena Su, Yann Christinat, Thomas McKee, Silvia Azzarello-Burri, Wolfram Jochum, Stefanie Fischer, Christian Rothermundt
Hered Cancer Clin Pract. 2024; 22: 27. Published online 2024 Dec 19. doi: 10.1186/s13053-024-00302-7
PMCID:
PMC11660894
ArticlePDF–2.0M
6.
Meeting abstracts from the Annual Conference “Clinical Genetics of Cancer 2023”
Hered Cancer Clin Pract. 2024; 22(Suppl 1): 23. Published online 2024 Nov 12. doi: 10.1186/s13053-024-00294-4
PMCID:
PMC11555854
ArticlePDF–923K
7.
Molecular analysis of BRCA1 and BRCA2 genes in La Rioja (Spain): five new variants
Raquel Salazar Saez, Miriam Zorrilla, Rosa Sánchez, Ana Cebollero, Isabel Manrique, Alfonso Martín, Leticia de Ávila, Alejandra Lacalle-Emborujo, Samuel Martin-Rodriguez, Iván Bernardo-González, Martina Alonso
Hered Cancer Clin Pract. 2024; 22: 22. Published online 2024 Oct 22. doi: 10.1186/s13053-024-00296-2
PMCID:
PMC11495111
ArticlePDF–1.2M
8.
PMS2 mutation spectra in Norway and risk of cancer for carriers of pathogenic variants
Wenche Sjursen, Hanne K. Hyldebrandt, Liss Anne S. Lavik, Bjørn Ivar Haukanes, Sarah Ariansen, Siri Briskemyr, Anna E. Sylvander, Marianne T. Haavind, Maren F. Olsen, Elin S. Røyset, Hildegunn Vetti, Astrid Stormorken, Eli Marie Grindedal
Hered Cancer Clin Pract. 2024; 22: 20. Published online 2024 Sep 27. doi: 10.1186/s13053-024-00292-6
PMCID:
PMC11438158
ArticlePDF–1.0M
9.
Adrenal tumours in patients with pathogenic APC mutations: a retrospective study
Lyman Lin, Victoria Beshay, Finlay Macrae
Hered Cancer Clin Pract. 2024; 22: 17. Published online 2024 Sep 3. doi: 10.1186/s13053-024-00289-1
PMCID:
PMC11370095
ArticlePDF–1.1M
10.
Fear of cancer recurrence in breast cancer survivors carrying a BRCA1 or 2 genetic mutation : a cross-sectional study
Alexandra Michel, Michel Dorval, Jocelyne Chiquette, Josée Savard
Hered Cancer Clin Pract. 2024; 22: 16. Published online 2024 Aug 27. doi: 10.1186/s13053-024-00285-5
PMCID:
PMC11350945
ArticlePDF–1.3M
11.
Possible link between familial susceptibility to cancer and the level of oxidative stress in thyroid cancer patients
Ivane Javakhishvili, Kote Mardaleishvili, Maka Buleishvili, Maia Mantskava, Irakli Chkhikvishvili, Sophio Kalmakhelidze, Nina Kipiani, Tamar Sanikidze
Hered Cancer Clin Pract. 2024; 22: 15. Published online 2024 Aug 23. doi: 10.1186/s13053-024-00287-3
PMCID:
PMC11342469
ArticlePDF–934K
12.
Universal testing in endometrial cancer in Sweden
Emil Andersson, Anne Keränen, Kristina Lagerstedt-Robinson, Sam Ghazi, Annika Lindblom, Emma Tham, Miriam Mints
Hered Cancer Clin Pract. 2024; 22: 14. Published online 2024 Aug 22. doi: 10.1186/s13053-024-00288-2
PMCID:
PMC11342736
ArticlePDF–1.0M
13.
Benefits of osimertinib treat a lung adenocarcinoma patient with germline EGFR T790M, somatic EGFR 19-Del, TP53 and PIK3CA mutations
Yingxue Li, Guangqi Li, Zheng Zheng, Wenjuan Wen, Haihui Zhao, Xia Liu, Jiaping Xie, Lin Han
Hered Cancer Clin Pract. 2024; 22: 13. Published online 2024 Aug 19. doi: 10.1186/s13053-024-00286-4
PMCID:
PMC11331667
ArticlePDF–1.9M
14.
Two Japanese families with familial pancreatic cancer with suspected pathogenic variants of CDKN2A: a case report
Yoshimi Kiyozumi, Hiroyuki Matsubayashi, Akiko Todaka, Ryo Ashida, Seiichiro Nishimura, Nobuhiro Kado, Satomi Higashigawa, Rina Harada, Eiko Ishihara, Yasue Horiuchi, Goichi Honda, Hirotsugu Kenmotsu, Masakuni Serizawa, Kenichi Urakami
Hered Cancer Clin Pract. 2024; 22: 11. Published online 2024 Jul 3. doi: 10.1186/s13053-024-00283-7
PMCID:
PMC11223274
ArticlePDF–1.0M
15.
Mutations in Helicobacter pylori infected patients with chronic gastritis, intestinal type of gastric cancer and familial gastric cancer
Andrzej Hnatyszyn, Marlena Szalata, Aleksandra Zielińska, Karolina Wielgus, Mikołaj Danielewski, Piotr Tomasz Hnatyszyn, Andrzej Pławski, Jarosław Walkowiak, Ryszard Słomski
Hered Cancer Clin Pract. 2024; 22: 9. Published online 2024 Jun 12. doi: 10.1186/s13053-024-00282-8
PMCID:
PMC11167877
ArticlePDF–1.1M
16.
A second hereditary cancer predisposition syndrome in a patient with lynch syndrome and three primary cancers
Annmarie Taheny, Haylie McSwaney, Julia Meade
Hered Cancer Clin Pract. 2024; 22: 8. Published online 2024 Jun 12. doi: 10.1186/s13053-024-00281-9
PMCID:
PMC11167841
ArticlePDF–850K
17.
Preoperative multimodal ultrasonic imaging in a case of Peutz-Jeghers syndrome complicated by atypical lobular endocervical glandular hyperplasia: a case report and literature review
Liwen Yang, Duan Duan, Ying Xiong, Tianjiao Liu, Lijun Zhao, Fan Lai, Dingxian Gu, Liuying Zhou
Hered Cancer Clin Pract. 2024; 22: 3. Published online 2024 Feb 28. doi: 10.1186/s13053-024-00275-7
PMCID:
PMC10900695
ArticlePDF–2.5M
18.
Li-Fraumeni syndrome presenting with de novo TP53 mutation, severe phenotype and advanced paternal age: a case report
Juan Pablo Arango-Ibañez, Luis Gabriel Parra-Lara, Ángela R. Zambrano, Lisa Ximena Rodríguez-Rojas
Hered Cancer Clin Pract. 2024; 22: 1. Published online 2024 Jan 18. doi: 10.1186/s13053-023-00272-2
PMCID:
PMC10797758
ArticlePDF–828K
19.
Experiences of patients and family members with follow-up care, information needs and provider support after identification of Lynch Syndrome
Ryan Mooney, Yelena P. Wu, Kelsey Kehoe, Molly Volkmar, Wendy Kohlmann, Cathryn Koptiuch, Kimberly A Kaphingst
Hered Cancer Clin Pract. 2023; 21: 28. Published online 2023 Dec 19. doi: 10.1186/s13053-023-00273-1
PMCID:
PMC10731879
ArticlePDF–945K
20.
Progression of duodenal neoplasia to advanced adenoma in patients with familial adenomatous polyposis
Hiroko Nakahira, Yoji Takeuchi, Yusaku Shimamoto, Shingo Ishiguro, Hiroshi Yunokizaki, Yasumasa Ezoe, Fumie Fujisawa, Ryu Ishihara, Tetsuji Takayama, Teruhiko Yoshida, Michihiro Mutoh, Hideki Ishikawa
Hered Cancer Clin Pract. 2023; 21: 25. Published online 2023 Nov 27. doi: 10.1186/s13053-023-00264-2
PMCID:
PMC10683362
ArticlePDF–1.4M

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