Prevalence of Genetic Mutations in Patients with Metastatic Prostate Cancer in a Cohort of Mexican Patients by Orión Erenhú Rodríguez González, Edgar Iván Bravo Castro, Jesus Eduardo Osorio, Habiram Pacheco Guerrero, Brenda Suaste Carmona, Luis David Arreola Peralta, Noe Esaul Martinez Juárez, Juan Samuel Izquierdo Luna, José de Jesús Oswaldo Islas García, Omar Dimas Victorio Vargas, Rafael Alberto Valdez Flores, Jesús Javier Torres Gómez, José Gadú Campos Salcedo

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A germline exome analysis reveals harmful POT1 variants in multiple myeloma patients and families by Marja Hakkarainen, Jessica R. Koski, Caroline A. Heckman, Pekka Anttila, Raija Silvennoinen, Juha Lievonen, Outi Kilpivaara, Ulla Wartiovaara‐Kautto

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MPN/MDS OVERLAP SYNDROME ANTICIPATED BY A SEVERE BLEEDING DIATHESIS: HYPOTHESIS OF A PRE-EXISTING PLATELET DISORDER by Paola Ranalli, Stefano Baldoni, Daniela Bruno, Mauro Di Ianni

Subjects: “…Myeloid Neoplasms; Germline mutations…”
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Germline mutations in cancer predisposition genes are frequent in sporadic sarcomas by Chan, Sock Hoai, Lim, Weng Khong, Nur Diana Binte Ishak, Li, Shao-Tzu, Goh, Wei Lin, Tan, Gek San, Lim, Kiat Hon, Teo, Melissa, Ng, Cedric Chuan Young, Malik, Simeen, Tan, Mann Hong, Teh, Jonathan Yi Hui, Chin, Francis Kuok Choon, Kesavan, Sittampalam, Selvarajan, Sathiyamoorthy, Tan, Patrick, Teh, Bin Tean, Soo, Khee Chee, Mohamad Farid, Quek, Richard, Ngeow, Joanne

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A knowledge-based framework for the discovery of cancer-predisposing variants using large-scale sequencing breast cancer data by Giorgio E. M. Melloni, Luca Mazzarella, Loris Bernard, Margherita Bodini, Anna Russo, Lucilla Luzi, Pier Giuseppe Pelicci, Laura Riva

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Germline mutations in patients with oral mucosal leukoplakia and squamous cell carcinoma: a prospective observational study by N. A. Karpuk, S. P. Rubnikovich, O. Ch. Mazur, I. V. Zhyltsov, I. Yu. Karpuk, A. P. Mikhalenka

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Mutations in the von Hippel-Lindau Tumour Suppressor Gene in Central Nervous System Hemangioblastomas by Cybulski Cezary, Matyjasik Joanna, Soroka Marianna, Szymaś Janusz, Górski Bohdan, Dębniak Tadeusz, Jakubowska Anna, Bernaczyk Andrzej, Zimnoch Lech, Bierzyńska-Macyszyn Grażyna, Trojanowski Tomasz, Wierzba-Bobrowicz Teresa, Prudlak Edmund, Markowska-Wojciechowska Alicja, Nowacki Przemysław, Roszkiewicz Andrzej, Kordek Radzisław, Szylberg Tadeusz, Matyja Ewa, Zieliński Krzysztof, Woźniewicz Bogdan, Taraszewska Anna, Kozłowski Wojciech, Lubiński Jan

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Human gene and disease associations for clinical‐genomics and precision medicine research by Zeeshan Ahmed, Saman Zeeshan, Dinesh Mendhe, XinQi Dong

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Germline mutations in penetrant cancer predisposition genes are rare in men with prostate cancer selecting active surveillance by Lauren Brady, Lisa F. Newcomb, Kehao Zhu, Yingye Zheng, Hilary Boyer, Navonil De Sarkar, Jesse K. McKenney, James D. Brooks, Peter R. Carroll, Atreya Dash, William J. Ellis, Christopher P. Filson, Martin E. Gleave, Michael A. Liss, Frances Martin, Todd M. Morgan, Ian M. Thompson, Andrew A. Wagner, Colin C. Pritchard, Daniel W. Lin, Peter S. Nelson

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CDH1 mutations in gastric cancer patients from northern Brazil identified by Next- Generation Sequencing (NGS) by Antonette El-Husny, Milene Raiol-Moraes, Marcos Amador, André M. Ribeiro-dos-Santos, André Montagnini, Silvanira Barbosa, Artur Silva, Paulo Assumpção, Geraldo Ishak, Sidney Santos, Pablo Pinto, Aline Cruz, Ândrea Ribeiro-dos-Santos

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Assessing germline TP53 mutations in cancer patients: insights into Li-Fraumeni syndrome and genetic testing guidelines by 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

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CDH1 mutations in gastric cancer patients from northern Brazil identified by Next- Generation Sequencing (NGS) by Antonette El-Husny, Milene Raiol-Moraes, Marcos Amador, André M. Ribeiro-dos-Santos, André Montagnini, Silvanira Barbosa, Artur Silva, Paulo Assumpção, Geraldo Ishak, Sidney Santos, Pablo Pinto, Aline Cruz, Ândrea Ribeiro-dos-Santos

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Spectrum and prevalence of BRCA1/2 germline mutations in Pakistani breast cancer patients: results from a large comprehensive study by Muhammad Usman Rashid, Noor Muhammad, Humaira Naeemi, Faiz Ali Khan, Mariam Hassan, Saima Faisal, Sidra Gull, Asim Amin, Asif Loya, Ute Hamann

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<i>BRCA1/2</i> Mutation Types Do Not Affect Prognosis in Ovarian Cancer Patients by Michalis Liontos, Eleni Zografos, Panagiotis Zoumpourlis, Angeliki Andrikopoulou, Anna Svarna, Oraianthi Fiste, Elena Kunadis, Alkistis Maria Papatheodoridi, Maria Kaparelou, Konstantinos Koutsoukos, Nikoloas Thomakos, Dimitrios Haidopoulos, Alexandros Rodolakis, Meletios-Athanasios Dimopoulos, Flora Zagouri

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Mutation spectrum of germline cancer susceptibility genes among unselected Chinese colorectal cancer patients by Gong R, He Y, Liu XY, Wang HY, Sun LY, Yang XH, Li B, Cao XK, Ye ZL, Kong LH, Zhang DD, Li YH, Xu RH, Shao JY

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Ethical frameworks for obtaining informed consent in tumour profiling: an evidence-based case for Singapore by Yasmin Bylstra, Tamra Lysaght, Jyothi Thrivikraman, Sangeetha Watson, Patrick Tan

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BRIP1 loss-of-function mutations confer high risk for familial ovarian cancer, but not familial breast cancer by Nana Weber-Lassalle, Jan Hauke, Juliane Ramser, Lisa Richters, Eva Groß, Britta Blümcke, Andrea Gehrig, Anne-Karin Kahlert, Clemens R. Müller, Karl Hackmann, Ellen Honisch, Konstantin Weber-Lassalle, Dieter Niederacher, Julika Borde, Holger Thiele, Corinna Ernst, Janine Altmüller, Guido Neidhardt, Peter Nürnberg, Kristina Klaschik, Christopher Schroeder, Konrad Platzer, Alexander E. Volk, Shan Wang-Gohrke, Walter Just, Bernd Auber, Christian Kubisch, Gunnar Schmidt, Judit Horvath, Barbara Wappenschmidt, Christoph Engel, Norbert Arnold, Bernd Dworniczak, Kerstin Rhiem, Alfons Meindl, Rita K. Schmutzler, Eric Hahnen

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Germline RECQL gene mutations in Chinese patients with breast cancer by Jun Hu, Jun Hu, Yong Shen, Kun Zhang, Yiding Chen

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Germline mutations in BRCA1 and BRCA2 among Brazilian women with ovarian cancer treated in the Public Health System by Caroline de Oliveira Ferreira, Vandré Cabral Gomes Carneiro, Carolline Araujo Mariz

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Intronic <it>TP53 </it>Germline Sequence Variants Modify the Risk in German Breast/Ovarian Cancer Families by Liu Xuan, Sinn Hans-Peter, Ulmer Hans, Scott Rodney J, Hamann Ute

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