Human Genome Epidemiology Literature Finder
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Records 1 - 25 (of 25 Records) |
| Query Trace: Neoplasms and FANCL[original query] |
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| FANCD2 associated with sporadic breast cancer risk. Carcinogenesis 2006 Sep 27 (9): 1930-7. Barroso E, Milne R L, Fernández L P, Zamora P, Arias J I, Benítez J, Ribas |
| Mutational analysis of FANCL, FANCM and the recently identified FANCI suggests that among the 13 known Fanconi Anemia genes, only FANCD1/BRCA2 plays a major role in high-risk breast cancer predisposition. Carcinogenesis 2009 Nov 30 (11): 1898-902. García María J, Fernández Victoria, Osorio Ana, Barroso Alicia, Fernández Fernando, Urioste Miguel, Benítez Javi |
| 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 |
| Evaluation of Fanconi anaemia genes FANCA, FANCC and FANCL in cervical cancer susceptibility. Gynecologic oncology 2011 May . Juko-Pecirep I, Ivansson EL, Gyllensten UB |
| Determining the frequency of pathogenic germline variants from exome sequencing in patients with castrate-resistant prostate cancer. BMJ open 2016 6 (4): e010332. Hart Steven N, Ellingson Marissa S, Schahl Kim, Vedell Peter T, Carlson Rachel E, Sinnwell Jason P, Barman Poulami, Sicotte Hugues, Eckel-Passow Jeanette E, Wang Liguo, Kalari Krishna R, Qin Rui, Kruisselbrink Teresa M, Jimenez Rafael E, Bryce Alan H, Tan Winston, Weinshilboum Richard, Wang Liewei, Kohli Mani |
| Hereditary truncating mutations of DNA repair and other genes in BRCA1/BRCA2/PALB2-negatively tested breast cancer patients. Clinical genetics 2016 Jan . Lhota Filip, Zemankova Petra, Kleiblova Petra, Soukupova Jana, Vocka Michal, Stranecky Viktor, Janatova Marketa, Hartmannova Hana, Hodanova Katerina, Kmoch Stanislav, Kleibl Zden |
| Germline whole exome sequencing and large-scale replication identifies FANCM as a likely high grade serous ovarian cancer susceptibility gene. Oncotarget 2017 (31): 50930-50940. Dicks Ed, Song Honglin, Ramus Susan J, Oudenhove Elke Van, Tyrer Jonathan P, Intermaggio Maria P, Kar Siddhartha, Harrington Patricia, Bowtell David D, Group Aocs Study, Cicek Mine S, Cunningham Julie M, Fridley Brooke L, Alsop Jennifer, Jimenez-Linan Mercedes, Piskorz Anna, Goranova Teodora, Kent Emma, Siddiqui Nadeem, Paul James, Crawford Robin, Poblete Samantha, Lele Shashi, Sucheston-Campbell Lara, Moysich Kirsten B, Sieh Weiva, McGuire Valerie, Lester Jenny, Odunsi Kunle, Whittemore Alice S, Bogdanova Natalia, Dürst Matthias, Hillemanns Peter, Karlan Beth Y, Gentry-Maharaj Aleksandra, Menon Usha, Tischkowitz Marc, Levine Douglas, Brenton James D, Dörk Thilo, Goode Ellen L, Gayther Simon A, Pharoah D P Pa |
| Assessing the spectrum of germline variation in Fanconi anemia genes among patients with head and neck carcinoma before age 50. Cancer 2017 Jul . Chandrasekharappa Settara C, Chinn Steven B, Donovan Frank X, Chowdhury Naweed I, Kamat Aparna, Adeyemo Adebowale A, Thomas James W, Vemulapalli Meghana, Hussey Caroline S, Reid Holly H, Mullikin James C, Wei Qingyi, Sturgis Erich |
| Benchmarking of Whole Exome Sequencing and Ad Hoc Designed Panels for Genetic Testing of Hereditary Cancer. Scientific reports 2017 1 7 37984. Feliubadaló Lídia, Tonda Raúl, Gausachs Mireia, Trotta Jean-Rémi, Castellanos Elisabeth, López-Doriga Adriana, Teulé Àlex, Tornero Eva, Del Valle Jesús, Gel Bernat, Gut Marta, Pineda Marta, González Sara, Menéndez Mireia, Navarro Matilde, Capellá Gabriel, Gut Ivo, Serra Eduard, Brunet Joan, Beltran Sergi, Lázaro Con |
| Somatic mutations in early onset luminal breast cancer. Oncotarget 2018 Apr 9 (32): 22460-22479. Encinas Giselly, Sabelnykova Veronica Y, de Lyra Eduardo Carneiro, Hirata Katayama Maria Lucia, Maistro Simone, de Vasconcellos Valle Pedro Wilson Mompean, de Lima Pereira Gláucia Fernanda, Rodrigues Lívia Munhoz, de Menezes Pacheco Serio Pedro Adolpho, de Gouvêa Ana Carolina Ribeiro Chaves, Geyer Felipe Correa, Basso Ricardo Alves, Pasini Fátima Solange, Del Pilar Esteves Diz Maria, Brentani Maria Mitzi, Guedes Sampaio Góes João Carlos, Chammas Roger, Boutros Paul C, Koike Folgueira Maria Aparecida Azeve |
| 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 |
| Analysis of polymorphisms in genes associated with the FA/BRCA pathway in three patients with multiple primary malignant neoplasms. Artificial cells, nanomedicine, and biotechnology 2019 Dec 47 (1): 1101-1112. Wang Le, Wang Hao, Wang Ting, Liu Jinhui, Chen Wei, Wang Yamin, Chen Chao, Zhu Hongli, Dai Pengg |
| 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 |
| Mutations in DNA Repair Genes and Clinical Outcomes of Patients With Metastatic Colorectal Cancer Receiving Oxaliplatin or Irinotecan-containing Regimens. American journal of clinical oncology 2020 Dec . Marks Eric I, Matera Robert, Olszewski Adam J, Yakirevich Evgeny, El-Deiry Wafik S, Safran Howard, Carneiro Benedito |
| A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects. Human mutation 2021 Sep . George Merin, Solanki Avani, Chavan Niranjan, Rajendran Aruna, Raj Revathi, Mohan Sheila, Nemani Sandeep, Kanvinde Shailesh, Munirathnam Deendayalan, Rao Sudha, Radhakrishnan Nita, Lashkari Harsha Prasada, Ghildhiyal Radha Gulati, Manglani Mamta, Shanmukhaiah Chandrakala, Bhat Sunil, Ramesh Sowmyashree, Cherian Anchu, Junagade Pritesh, Vundinti Babu R |
| Germline variants predictive of tumor mutational burden and immune checkpoint inhibitor efficacy. iScience 2021 3 24 (3): 102248. Chatrath Ajay, Ratan Aakrosh, Dutta Anind |
| [Application of next-generation sequencing in detection of BRCA1/2 and homologous recombination repair pathway multi-genes germline mutation and correlation analysis]. Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine] 2022 4 56 (3): 302-311. Chen Y L, Zhuo Z L, Liu C, Xie F, Yang Z Y, Liu P F, Wang S, Zhao X |
| Role of Homologous Recombination Repair (HRR) Genes in Uterine Leiomyosarcomas: A Retrospective Analysis. Cancers 2022 4 14 (8): . Ciccarone Francesca, Bruno Matteo, De Paolis Elisa, Piermattei Alessia, De Bonis Maria, Lorusso Domenica, Zannoni Gian Franco, Normanno Nicola, Minucci Angelo, Scambia Giovanni, Ferrandina Gabriel |
| Canonical and uncanonical pathogenic germline variants in colorectal cancer patients by next-generation sequencing in a European referral center. ESMO open 2022 11 7 (6): 100607. Poliani L, Greco L, Barile M, Dal Buono A, Bianchi P, Basso G, Giatti V, Genuardi M, Malesci A, Laghi L, |
| Concurrent BRAFV600E and BRCA Mutations in MSS Metastatic Colorectal Cancer: Prevalence and Case Series of mCRC patients with prolonged OS. Cancer treatment and research communications 2022 Apr 32 100569. Cannon Timothy Lewis, Randall Jamie N, Sokol Ethan S, Alexander Sonja M, Wadlow Raymond C, Winer Arthur A, Barnett Daniel M, Rayes Danny L, Nimeiri Halla S, McGregor Kimberly |
| Next generation sequencing reveals a high prevalence of pathogenic mutations in homologous recombination DNA damage repair genes among patients with uterine sarcoma. Gynecologic oncology 2023 8 177 14-19. Dimitrios Nasioudis, Nawar A Latif, Emily M Ko, Lori Cory, Sarah H Kim, Lainie Martin, Fiona Simpkins, Robert Giunto |
| Mutations of TP53 and genes related to homologous recombination repair in breast cancer with germline BRCA1/2 mutations. Human genomics 2023 1 17 (1): 2. Kim Jinyong, Jeong Kyeonghun, Jun Hyeji, Kim Kwangsoo, Bae Jeong Mo, Song Myung Geun, Yi Hanbaek, Park Songyi, Woo Go-Un, Lee Dae-Won, Kim Tae-Yong, Lee Kyung-Hun, Im Seock- |
| DNA-Damaging Therapies in Patients With Prostate Cancer and Pathogenic Alterations in Homologous Recombination Repair Genes. JCO precision oncology 2024 8 8 e2400014. Laura S Graham, Nicholas C Henderson, Olesia Kellezi, Clara Hwang, Pedro C Barata, Mehmet A Bilen, Deepak Kilari, Michael Pierro, Bicky Thapa, Abhishek Tripathi, George Mo, Matthew Labriola, Joseph J Park, Shoshana Rothstein, Rohan Garje, Vadim S Koshkin, Vaibhav G Patel, Tanya Dorff, Andrew J Armstrong, Rana R McKay, Ajjai Alva, Michael T Schweiz |
| SMARCA4 Mutations in Gastroesophageal Adenocarcinoma: An Observational Study via a Next-Generation Sequencing Panel. Cancers 2024 4 16 (7): . Kohei Yamashita, Matheus Sewastjanow-Silva, Katsuhiro Yoshimura, Jane E Rogers, Ernesto Rosa Vicentini, Melissa Pool Pizzi, Yibo Fan, Gengyi Zou, Jenny J Li, Mariela Blum Murphy, Qiong Gan, Rebecca E Waters, Linghua Wang, Jaffer A Aja |
- Page last reviewed:Feb 1, 2024
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