Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 43 Records) |
Query Trace: Neoplasms and FANCD2[original query] |
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Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia. Genetics in medicine : official journal of the American College of Medical Genetics 2017 8 20 (4): 458-463. Bogliolo Massimo, Bluteau Dominique, Lespinasse James, Pujol Roser, Vasquez Nadia, d'Enghien Catherine Dubois, Stoppa-Lyonnet Dominique, Leblanc Thierry, Soulier Jean, Surrallés Jor |
Characterization of genetic alterations in brain metastases from non-small cell lung cancer. FEBS open bio 2018 9 8 (9): 1544-1552. Liao Li, Ji Xiaoyu, Ge Mengxi, Zhan Qiong, Huang Ruofan, Liang Xiaohua, Zhou Xin |
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 |
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 |
Mutation Spectrum of Cancer-Associated Genes in Patients With Early Onset of Colorectal Cancer. Frontiers in oncology 2019 8 9 673. Zhunussova Gulnur, Afonin Georgiy, Abdikerim Saltanat, Jumanov Abai, Perfilyeva Anastassiya, Kaidarova Dilyara, Djansugurova Ley |
Somatic variants of potential clinical significance in the tumors of BRCA phenocopies. Hereditary cancer in clinical practice 2019 7 17 21. Buckingham Lela, Mitchell Rachel, Maienschein-Cline Mark, Green Stefan, Hu Vincent Hong, Cobleigh Melody, Rotmensch Jacob, Burgess Kelly, Usha Lyd |
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 |
Clinical importance of FANCD2, BRIP1, BRCA1, BRCA2 and FANCF expression in ovarian carcinomas. Cancer biology & therapy 2019 3 20 (6): 843-854. Moes-Sosnowska Joanna, Rzepecka Iwona K, Chodzynska Joanna, Dansonka-Mieszkowska Agnieszka, Szafron Lukasz M, Balabas Aneta, Lotocka Renata, Sobiczewski Piotr, Kupryjanczyk Jolan |
Association of Single-Nucleotide Polymorphisms in Monoubiquitinated FANCD2-DNA Damage Repair Pathway Genes With Breast Cancer in the Chinese Population. Technology in cancer research & treatment 2018 Jan 17 1533033818819841. Chen Fei-Yu, Wang Hao, Li Hui, Hu Xue-Li, Dai Xu, Wang Shou-Man, Yan Guo-Jiao, Jiang Ping-Lan, Hu Yuan-Ping, Huang Juan, Tang Li- |
A new survival model based on ferroptosis-related genes for prognostic prediction in clear cell renal cell carcinoma. Aging 2020 Jul 12 . Wu Guangzhen, Wang Qifei, Xu Yingkun, Li Quanlin, Cheng Lia |
Frequency of heterozygous germline pathogenic variants in genes for Fanconi anemia in patients with non-BRCA1/BRCA2 breast cancer: a meta-analysis. Breast cancer research and treatment 2020 Jun . Alter Blanche P, Best Ana |
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 |
Polymorphisms and rare variants identified by next-generation sequencing confer risk for lung cancer in han Chinese population. Pathology, research and practice 2020 Feb 152873. Li Xiaoqi, Liu Jinsheng, Wang Ke, Zhou Juan, Zhang Hang, Zhang Mancang, Shi Yongyo |
Whole exome sequencing identifies a novel FANCD2 gene splice site mutation associated with disease progression in chronic myeloid leukemia: Implication in targeted therapy of advanced phase CML. Pakistan journal of pharmaceutical sciences 2020 12 33 (3(Special)): 1419-1426. Absar Muhammad, Mahmood Amer, Akhtar Tanveer, Basit Sulman, Ramzan Khushnooda, Jameel Abid, Afzal Sibtain, Ullah Anhar, Qureshi Kulsoom, Alanazi Nawaf, Iqbal Zaf |
Genomic profiling reveals high frequency of DNA repair genetic aberrations in gallbladder cancer. Scientific reports 2020 12 10 (1): 22087. Abdel-Wahab Reham, Yap Timothy A, Madison Russell, Pant Shubham, Cooke Matthew, Wang Kai, Zhao Haitao, Bekaii-Saab Tanios, Karatas Elif, Kwong Lawrence N, Meric-Bernstam Funda, Borad Mitesh, Javle Mili |
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 |
Distinct Somatic Alteration Features Identified by Gene Panel Sequencing in Korean Triple-Negative Breast Cancer with High Ki67 Expression. Diagnostics (Basel, Switzerland) 2021 4 11 (3): . Sun Woo Young, Lee Jina, Kim Bong Kyun, Kim Jong Ok, Park Joonho |
Genomic Landscape of Primary and Recurrent Anal Squamous Cell Carcinomas in Relation to HPV Integration, Copy-Number Variation, and DNA Damage Response Genes. Molecular cancer research : MCR 2021 4 19 (8): 1308-1321. Aldersley Jordan, Lorenz David R, Mouw Kent W, D'Andrea Alan D, Gabuzda Da |
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 |
Fanconi anemia gene-associated germline predisposition in aplastic anemia and hematologic malignancies. Frontiers of medicine 2021 Nov . Nie Daijing, Zhang Jing, Wang Fang, Li Xvxin, Liu Lili, Zhang Wei, Cao Panxiang, Chen Xue, Zhang Yang, Chen Jiaqi, Ma Xiaoli, Zhou Xiaosu, Wu Qisheng, Liu Ming, Liu Mingyue, Tian Wenjun, Liu Hongxi |
Prevalence and Spectrum of Predisposition Genes With Germline Mutations Among Chinese Patients With Bowel Cancer. Frontiers in genetics 2022 2 12 755629. Xie Zhengyong, Ke Yongli, Chen Junyong, Li Zehang, Wang Changzheng, Chen Yuhong, Ding Hongliang, Cheng Liya |
A pan-cancer analysis of the oncogenic role of zinc finger protein 419 in human cancer. Frontiers in oncology 2022 12 12 1042118. Zhu Weizhen, Feng Dechao, Shi Xu, Li Dengxiong, Wei Qiang, Yang |
Genomic characterization of metastatic castration-resistant prostate cancer patients undergoing PSMA radioligand therapy: A single-center experience. The Prostate 2022 Oct . Satapathy Swayamjeet, Das Chandan K, Aggarwal Piyush, Sood Ashwani, Parihar Ashwin S, Singh Shrawan K, Mittal Bhagwant |
The Spectrum of Germline Nucleotide Variants in Gastric Cancer Patients in the Kyrgyz Republic. Current issues in molecular biology 2023 8 45 (8): 6383-6394. Airat Bilyalov, Sergey Nikolaev, Anastasiia Danishevich, Igor Khatkov, Komron Makhmudov, Zhainagul Isakova, Nurbek Bakirov, Ernis Omurbaev, Alena Osipova, Ramaldan Ramaldanov, Elena Shagimardanova, Andrey Kiyasov, Oleg Gusev, Natalia Boduno |
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 |
A comprehensive analysis of Fanconi anemia genes in Chinese patients with high-risk hereditary breast cancer. Journal of cancer research and clinical oncology 2023 8 . Qiao-Yan Zhu, Pu-Chun Li, Yi-Fan Zhu, Jia-Ni Pan, Rong Wang, Xiao-Lin Li, Wei-Wu Ye, Xiao-Wen Ding, Xiao-Jia Wang, Wen-Ming C |
New pathogenic germline variants identified in mesothelioma. Lung cancer (Amsterdam, Netherlands) 2023 3 179 107172. Belcaid Laila, Bertelsen Birgitte, Wadt Karin, Tuxen Ida, Spanggaard Iben, Højgaard Martin, Benn Sørensen Jens, Ravn Jesper, Lassen Ulrik, Cilius Nielsen Finn, Rohrberg Kristoffer, Westmose Yde Christi |
Association of Reported Candidate Monogenic Genes With Lung Cancer Risk. Clinical lung cancer 2023 2 . Rifkin Andrew S, Less Ethan M, Wei Jun, Shi Zhuqing, Zheng Siqun Lilly, Helfand Brian T, Hulick Peter J, Krantz Seth B, Xu Jianfe |
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- |
Whole-exome sequencing and bioinformatic analyses revealed differences in gene mutation profiles in papillary thyroid cancer patients with and without benign thyroid goitre background. Frontiers in endocrinology 2023 1 13 1039494. Eng Zing Hong, Abdullah Mardiaty Iryani, Ng Khoon Leong, Abdul Aziz Azlina, Arba'ie Nurul Hannis, Mat Rashid Nurullainy, Mat Junit Sar |
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- Page last updated:Apr 22, 2024
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