Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Ovarian Neoplasms and FANCI[original query] |
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| The Fanconi anemia family of genes and its correlation with breast cancer susceptibility and breast cancer features. Breast cancer research and treatment 2009 Jun . Barroso E, Pita G, Arias JI, Menendez P, Zamora P, Blanco M, Benitez J, Ribas G |
| The frequency of cancer predisposition gene mutations in hereditary breast and ovarian cancer patients in Taiwan: From BRCA1/2 to multi-gene panels. PloS one 2017 12 (9): e0185615. Sung Pi-Lin, Wen Kuo-Chang, Chen Yi-Jen, Chao Ta-Chung, Tsai Yi-Fang, Tseng Ling-Ming, Qiu Jian-Tai Timothy, Chao Kuan-Chong, Wu Hua-Hsi, Chuang Chi-Mu, Wang Peng-Hui, Huang Chi-Ying |
| Targeted next generation sequencing identifies functionally deleterious germline mutations in novel genes in early-onset/familial prostate cancer. PLoS genetics 2018 Apr 14 (4): e1007355. Paulo Paula, Maia Sofia, Pinto Carla, Pinto Pedro, Monteiro Augusta, Peixoto Ana, Teixeira Manuel |
| Multigene panel testing beyond BRCA1/2 in breast/ovarian cancer Spanish families and clinical actionability of findings. Journal of cancer research and clinical oncology 2018 10 144 (12): 2495-2513. Bonache Sandra, Esteban Irene, Moles-Fernández Alejandro, Tenés Anna, Duran-Lozano Laura, Montalban Gemma, Bach Vanessa, Carrasco Estela, Gadea Neus, López-Fernández Adrià, Torres-Esquius Sara, Mancuso Francesco, Caratú Ginevra, Vivancos Ana, Tuset Noemí, Balmaña Judith, Gutiérrez-Enríquez Sara, Diez Orla |
| Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing. International journal of cancer 2018 Oct . Girard Elodie, Eon-Marchais Séverine, Olaso Robert, Renault Anne-Laure, Damiola Francesca, Dondon Marie-Gabrielle, Barjhoux Laure, Goidin Didier, Meyer Vincent, Le Gal Dorothée, Beauvallet Juana, Mebirouk Noura, Lonjou Christine, Coignard Juliette, Marcou Morgane, Cavaciuti Eve, Baulard Céline, Bihoreau Marie-Thérèse, Cohen-Haguenauer Odile, Leroux Dominique, Penet Clotilde, Fert-Ferrer Sandra, Colas Chrystelle, Frebourg Thierry, Eisinger François, Adenis Claude, Fajac Anne, Gladieff Laurence, Tinat Julie, Floquet Anne, Chiesa Jean, Giraud Sophie, Mortemousque Isabelle, Soubrier Florent, Audebert-Bellanger Séverine, Limacher Jean-Marc, Lasset Christine, Lejeune-Dumoulin Sophie, Dreyfus Hélène, Bignon Yves-Jean, Longy Michel, Pujol Pascal, Venat-Bouvet Laurence, Bonadona Valérie, Berthet Pascaline, Luporsi Elisabeth, Maugard Christine M, Noguès Catherine, Delnatte Capucine, Fricker Jean-Pierre, Gesta Paul, Faivre Laurence, Lortholary Alain, Buecher Bruno, Caron Olivier, Gauthier-Villars Marion, Coupier Isabelle, Servant Nicolas, Boland Anne, Mazoyer Sylvie, Deleuze Jean-François, Stoppa-Lyonnet Dominique, Andrieu Nadine, Lesueur Fabien |
| Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients. Cancers 2020 4 12 (4): . Del Valle Jesús, Rofes Paula, Moreno-Cabrera José Marcos, López-Dóriga Adriana, Belhadj Sami, Vargas-Parra Gardenia, Teulé Àlex, Cuesta Raquel, Muñoz Xavier, Campos Olga, Salinas Mónica, de Cid Rafael, Brunet Joan, González Sara, Capellá Gabriel, Pineda Marta, Feliubadaló Lídia, Lázaro Con |
| Comparison of BRCA versus non-BRCA germline mutations and associated somatic mutation profiles in patients with unselected breast cancer. Aging 2020 Feb 12 . Chen Bo, Zhang Guochun, Li Xuerui, Ren Chongyang, Wang Yulei, Li Kai, Mok Hsiaopei, Cao Li, Wen Lingzhu, Jia Minghan, Li Cheukfai, Guo Liping, Wei Guangnan, Lin Jiali, Li Yingzi, Zhang Yuchen, Han-Zhang Han, Liu Jing, Lizaso Analyn, Liao Ni |
| A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene. Genome medicine 2021 12 13 (1): 186. Fierheller Caitlin T, Guitton-Sert Laure, Alenezi Wejdan M, Revil Timothée, Oros Kathleen K, Gao Yuandi, Bedard Karine, Arcand Suzanna L, Serruya Corinne, Behl Supriya, Meunier Liliane, Fleury Hubert, Fewings Eleanor, Subramanian Deepak N, Nadaf Javad, Bruce Jeffrey P, Bell Rachel, Provencher Diane, Foulkes William D, El Haffaf Zaki, Mes-Masson Anne-Marie, Majewski Jacek, Pugh Trevor J, Tischkowitz Marc, James Paul A, Campbell Ian G, Greenwood Celia M T, Ragoussis Jiannis, Masson Jean-Yves, Tonin Patricia |
| Mutation Landscape of Homologous Recombination Repair Genes in Epithelial Ovarian Cancer in China and Its Relationship With Clinicopathlological Characteristics. Frontiers in oncology 2022 12 709645. Yao Qianlan, Liu Yanhui, Zhang Lihua, Dong Lin, Bao Longlong, Bai Qianming, Cui Qian, Xu Jie, Li Min, Liu Jing, Chuai Shannon, Ying Jianming, Zhang Zhihong, Zhou Xiaoy |
| Molecular Genetic Characteristics of FANCI, a Proposed New Ovarian Cancer Predisposing Gene. Genes 2023 2 14 (2): . Fierheller Caitlin T, Alenezi Wejdan M, Serruya Corinne, Revil Timothée, Amuzu Setor, Bedard Karine, Subramanian Deepak N, Fewings Eleanor, Bruce Jeffrey P, Prokopec Stephenie, Bouchard Luigi, Provencher Diane, Foulkes William D, El Haffaf Zaki, Mes-Masson Anne-Marie, Tischkowitz Marc, Campbell Ian G, Pugh Trevor J, Greenwood Celia M T, Ragoussis Jiannis, Tonin Patricia |
| Methylation marks in blood DNA reveal breast cancer risk in patients fulfilling hereditary disease criteria. NPJ precision oncology 2024 6 8 (1): 136. Miguel Ruiz-De La Cruz, Héctor Martínez-Gregorio, Clara Estela Díaz-Velásquez, Fernando Ambriz-Barrera, Norma Gabriela Resendiz-Flores, Rina Gitler-Weingarten, María Patricia Rojo-Castillo, Didier Pradda, Javier Oliver, Sandra Perdomo, Eva María Gómez-García, Aldo Hugo De La Cruz-Montoya, Luis Ignacio Terrazas, Gabriela Torres-Mejía, Fidel de la Cruz Hernández-Hernández, Felipe Vaca-Paniag |
- Page last reviewed:Feb 1, 2024
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