Cancer predisposition syndromes in children by D. Yu. Kachanov, R. T. Abdullaev, T. V. Shamanskaya, Ye. V. Inyushkina, K. V. Dobrenkov, R. F. Savkova, S. R. Varfolomeeva

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Model of care for individuals with rare cancer predisposition syndromes in Germany by Valentina Härter, Birte Sänger, Josephine C. Gieseke, Tanja Gerasimov, Beatrice Hoffmann, Carolin Huisinga, Anja Karow, Lucas J. Müntnich, Natalie E. Palmaers, Stefanie Paquet, Judith Penkert, Diane M. Renz, Tim Ripperger, Farina J. Silchmüller, Christina M. Dutzmann, Christian P. Kratz

Subjects: “…Cancer predisposition syndromes…”
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High prevalence of constitutional BRCA1 epimutation in patients with early-onset triple-negative breast cancer by Mathias Schwartz, Sabrina Ibadioune, Hélène Delhomelle, Solenn Barraud, Sandrine M. Caputo, Olfa Trabelsi-Grati, Marie-Charlotte Villy, Anthony Laugé, Roseline Tang, Etienne Rouleau, Emmanuelle Mouret-Fourme, Dominique Stoppa-Lyonnet, Éric Pasmant, Lisa Golmard, Chrystelle Colas, Ivan Bièche

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Synchronous childhood T-lymphoblastic lymphoma and B-cell precursor acute lymphoblastic leukemia associated with constitutional MMR deficiency syndrome –a case report by Joanna Bulsa, Agata Karolina Pastorczak, Joanna Taha, Wojciech Mlynarski, Łukasz Sędek, Tomasz Szczepanski

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Impact of germline variants on breast and ovarian cancer risk in Japanese women: an original cohort study and meta-analysisResearch in context by Shu Yazaki, Megumi Hori, Hisaki Aiba, Yukihide Momozawa, Masayuki Yoshida, Sho Shiino, Kenichi Harano, Chisako Yamauchi, Takashi Yamanaka, Maiko Miwa, Koichi Matsuda, Yosuke Kawai, Mayumi Kobayashi-Kato, Masakazu Kitagawa, Motonobu Saito, Hiroshi Nakagomi, Kazunoshin Tachibana, Ikuko Sakamoto, Kazuaki Takahashi, Yuka Asami, Kota Katanoda, Aya Kuchiba, Hiroshi Yoshida, Mitsuya Ishikawa, Tastunori Shimoi, Kazuki Sudo, Chikako Shimizu, Akihiko Shimomura, Takeshi Murata, Yuji Yamashita, Takahiro Kogawa, Saori Fujiwara, Haruya Saji, Hisamori Kato, Etsuko Miyagi, Yusuke Iwasaki, Tomomi Aoi, Sadaaki Takata, Aiko Ogasawara, Tohru Ohtake, Keiya Fujimori, Yosuke Hirotsu, Minoru Nagashima, Masaaki Komatsu, Ryuji Hamamoto, Makoto Hirata, Teruhiko Yoshida, Takayuki Honda, Kengo Hiranuma, Maiko Matsuda, Yoko Shimada, Kuniko Sunami, Eisei Noiri, Yosuke Omae, Koji Matsumoto, Aikou Okamoto, Masao Omata, Takafumi Watanabe, Yohei Miyagi, Yoshinori Murakami, Katsushi Tokunaga, Kosei Hasegawa, Tomoyasu Kato, Tatsuya Onishi, Toshinari Yamashita, Yoichi Naito, Akihiko Suto, Kan Yonemori, Takashi Kohno, Kouya Shiraisihi, Yukihide Momozawa, Koichi Matsuda, Yusuke Iwasaki, Tomomi Aoi, Sadaaki Takata, Yoshinori Murakami, Yosuke Kawai, Eisei Noiri, Yosuke Omae, Katsushi Tokunaga

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Genetic characterization of Lynch syndrome germline variants in a LATAM cohort using a customized NGS gene panel by Cecilia Mathó, Cecilia Mathó, Santiago Chávez, Santiago Chávez, Rafael Sebastián Fort, Rafael Sebastián Fort, Adriana Della Valle, Florencia Neffa, José Roberto Sotelo-Silveira, José Roberto Sotelo-Silveira, Nora Artagaveytia, María Ana Duhagon, María Ana Duhagon

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Distinct pathways for genetic and epigenetic predisposition in familial and bilateral Wilms tumor by Jenny Wegert, Silke Appenzeller, Taryn D. Treger, Heike Streitenberger, Barbara Ziegler, Sabrina Bausenwein, Christian Vokuhl, Conor Parks, Eva Jüttner, Susanne Gramlich, Karen Ernestus, Steven W. Warman, Jörg Fuchs, Jochen Hubertus, Dietrich von Schweinitz, Birgit Fröhlich, Norbert Jorch, Ralf Knöfler, Carsten Friedrich, Selim Corbacioglu, Michael C. Frühwald, Arnulf Pekrun, Dominik T. Schneider, Jörg Faber, Jana Stursberg, Markus Metzler, Nils Welter, Kathy Pritchard-Jones, Norbert Graf, Rhoikos Furtwängler, Sam Behjati, Manfred Gessler

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Social vulnerability and genetic service utilization among unaffected BRIDGE trial patients with inherited cancer susceptibility by Jemar R. Bather, Melody S. Goodman, Adrian Harris, Guilherme Del Fiol, Rachel Hess, David W. Wetter, Daniel Chavez-Yenter, Lingzi Zhong, Lauren Kaiser-Jackson, Rachelle Chambers, Richard Bradshaw, Wendy Kohlmann, Sarah Colonna, Whitney Espinel, Rachel Monahan, Saundra S. Buys, Ophira Ginsburg, Kensaku Kawamoto, Kimberly A. Kaphingst, on behalf of the BRIDGE research team

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Feasibility of whole‐body MRI for cancer screening in children and young people with ataxia telangiectasia: A mixed methods cross‐sectional study by Renata Neves, Rafal Panek, Katie Clarkson, Ouliana Panagioti, Natasha Schneider Fernandez, Sophie Wilne, Mohnish Suri, William P. Whitehouse, Sumit Jagani, Madhumita Dandapani, Cris Glazebrook, Robert A. Dineen

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Prevalence and clinical relavance of germline mutations in Chinese patients with pancreatic cancer by Yu Jiang, Dan Li, Yang Liu, Jiejie Qin, Hao Chen, Jun Zhang, Yijin Gu, Baiyong Shen, Jiabin Jin

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Living with rare genetic disease during the COVID-19 pandemic: A qualitative study of adolescents and young adults with Li-Fraumeni syndrome by Allison Werner-Lin, Payal P. Khincha, Ashley S. Thompson, Camella Rising, Alix Sleight, Catherine Wilsnack, Patrick Boyd, Alexandra Feldman, Rowan Forbes Shepherd, Sharon A. Savage

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Clinician perspectives on designing and implementing a hereditary cancer transition clinic by Jazmine L. Gabriel, Victoria Schlieder, Jessica M. Goehringer, Tracey Leitzel, Emily Ann Sugrue, Sarah Zultevicz, Thomas W. Davis, Gemme Campbell-Salome, Katrina Romagnoli

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