Human Genome Epidemiology Literature Finder
Records 1 - 25 (of 25 Records) |
Query Trace: FANCG[original query] |
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Evaluation of Fanconi Anemia genes in familial breast cancer predisposition. Cancer research 2003 12 63 (24): 8596-9. Seal Sheila, Barfoot Rita, Jayatilake Hiran, Smith Paula, Renwick Anthony, Bascombe Linda, McGuffog Lesley, Evans D Gareth, Eccles Diana, Easton Douglas F, Stratton Michael R, Rahman Nazneen, |
The genetics of FANCC and FANCG in familial pancreatic cancer. Cancer biology & therapy 2004 1 3 (2): 167-9. Rogers Carmelle D, van der Heijden Michiel S, Brune Kieran, Yeo Charles J, Hruban Ralph H, Kern Scott E, Goggins Micha |
Germ line Fanconi anemia complementation group C mutations and pancreatic cancer. Cancer research 2005 Jan 65 (2): 383-6. Couch Fergus J, Johnson Michele R, Rabe Kari, Boardman Lisa, McWilliams Robert, de Andrade Mariza, Petersen Glor |
FANCA and FANCG are the major Fanconi anemia genes in the Korean population. Clinical genetics 2013 Sep 84 (3): 271-5. Park J, Chung N-G, Chae H, Kim M, Lee S, Kim Y, Lee J-W, Cho B, Jeong D C, Park I |
Founder haplotype analysis of Fanconi anemia in the Korean population finds common ancestral haplotypes for a FANCG variant. Annals of human genetics 2015 May 79 (3): 153-61. Park Joonhong, Kim Myungshin, Jang Woori, Chae Hyojin, Kim Yonggoo, Chung Nack-Gyun, Lee Jae-Wook, Cho Bin, Jeong Dae-Chul, Park In Yang, Park Mi S |
Candidate gene analysis of BRCA1/2 mutation-negative high-risk Russian breast cancer patients. Cancer letters 2015 Apr 359 (2): 259-61. Sokolenko Anna P, Preobrazhenskaya Elena V, Aleksakhina Svetlana N, Iyevleva Aglaya G, Mitiushkina Natalia V, Zaitseva Olga A, Yatsuk Olga S, Tiurin Vladislav I, Strelkova Tatiana N, Togo Alexandr V, Imyanitov Evgeny |
A strategy for molecular diagnostics of Fanconi anemia in Brazilian patients. Molecular genetics & genomic medicine 2017 Jul 5 (4): 360-372. Pilonetto Daniela V, Pereira Noemi F, Bonfim Carmem M S, Ribeiro Lisandro L, Bitencourt Marco A, Kerkhoven Lianne, Floor Karijn, Ameziane Najim, Joenje Hans, Gille Johan J P, Pasquini Ricar |
Functional analysis of Fanconi anemia mutations in China. Experimental hematology 2018 7 66 32-41.e8. Li Niu, Ding Lixia, Li Benshang, Wang Jian, D'Andrea Alan D, Chen Ji |
The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants. International journal of cancer 2018 11 144 (11): 2683-2694. Schubert Stephanie, van Luttikhuizen Jana L, Auber Bernd, Schmidt Gunnar, Hofmann Winfried, Penkert Judith, Davenport Colin F, Hille-Betz Ursula, Wendeburg Lena, Bublitz Janin, Tauscher Marcel, Hackmann Karl, Schröck Evelin, Scholz Caroline, Wallaschek Hannah, Schlegelberger Brigitte, Illig Thomas, Steinemann Dor |
Associations of complementation group, ALDH2 genotype, and clonal abnormalities with hematological outcome in Japanese patients with Fanconi anemia. Annals of hematology 2019 Feb 98 (2): 271-280. Yabe Miharu, Koike Takashi, Ohtsubo Keisuke, Imai Eri, Morimoto Tsuyoshi, Takakura Hiromitsu, Koh Katsuyoshi, Yoshida Kenichi, Ogawa Seishi, Ito Etsuro, Okuno Yusuke, Muramatsu Hideki, Kojima Seiji, Matsuo Keitaro, Mori Minako, Hira Asuka, Takata Minoru, Yabe Hiroma |
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 |
Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation. Molecular genetics & genomic medicine 2020 6 8 (8): e1351. Dillon Bronwyn, Feben Candice, Segal David, du Plessis Johannes, Reynders David, Wainwright Rosalind, Poole Janet, Krause Aman |
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 |
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 |
Clinical, cytogenetic and molecular findings in nine Moroccan patients with Fanconi anemia. The Pan African medical journal 2021 8 39 72. Doubaj Yassamine, Zrhidri Abdelali, Elalaoui Siham Chafai, Lyahyai Jaber, El Kadiri Youssef, Elkassimi Nadia, Sbiti Aziza, El Kababri Maria, Hessissen Laila, Sefiani Abdelaz |
Prevalence of cancer susceptibility variants in patients with multiple Lynch syndrome related cancers. Scientific reports 2021 Jul 11 (1): 14807. Choi Yoon Young, Shin Su-Jin, Lee Jae Eun, Madlensky Lisa, Lee Seung-Tae, Park Ji Soo, Jo Jeong-Hyeon, Kim Hyunki, Nachmanson Daniela, Xu Xiaojun, Noh Sung Hoon, Cheong Jae-Ho, Harismendy Olivi |
Clinicopathological and molecular characterization of chromophobe hepatocellular carcinoma. Liver international : official journal of the International Association for the Study of the Liver 2021 May . Kang Hyo Jeong, Oh Ji-Hye, Kim Yeon Wook, Kim Wonkyung, An Jihyun, Sung Chang Ohk, Kim Jihun, Shim Ju Hyun, Hwang Shin, Yu Eunsil, Heaphy Christopher M, Hong Seung- |
Nitric oxide synthase-2 (NOS2) gene polymorphism c.1832C>T (Ser608Leu) associated with nitrosative stress in Fanconi anaemia. Molecular biology reports 2021 Mar . George Merin, Solanki Avani, Mohanty Purvi, Dhangar Somprakash, Rajendran Aruna, Mohan Sheila, Vundinti Babu R |
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 |
Germline variants in DNA repair genes are associated with young-onset head and neck cancer. Oral oncology 2021 10 122 105545. Cury Sarah Santiloni, Miranda Priscila Mayrink de, Marchi Fabio Albuquerque, Canto Luisa Matos do, Chulam Thiago Celestino, Petersen Annabeth Høgh, Aagaard Mads M, Pinto Clóvis Antonio Lopes, Kowalski Luiz Paulo, Rogatto Silvia Regi |
Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG. International journal of molecular sciences 2022 2 23 (4): . Reyes Pedro, García-de Teresa Benilde, Juárez Ulises, Pérez-Villatoro Fernando, Fiesco-Roa Moisés O, Rodríguez Alfredo, Molina Bertha, Villarreal-Molina María Teresa, Meléndez-Zajgla Jorge, Carnevale Alessandra, Torres Leda, Frias Sa |
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 |
Comprehensive laboratory diagnosis of Fanconi anaemia: comparison of cellular and molecular analysis. Journal of medical genetics 2023 3 . Joshi Gaurav, Arthur Nancy Beryl Janet, Geetha Thenral S, Datari Phaneendra Venkateswara Rao, Modak Kirti, Roy Debanjan, Chaudhury Anurag Dutta, Sundaraganesan Prasanth, Priyanka Sweety, Na Fouzia, Ramprasad Vedam, Abraham Aby, Srivastava Vivi M, Srivastava Alok, Kulkarni Uday Prakash, George Biju, Velayudhan Shaji |
DNA damage response and repair gene mutations are associated with tumor mutational burden and outcomes to platinum-based chemotherapy/immunotherapy in advanced NSCLC patients. Diagnostic pathology 2023 11 18 (1): 119. Weiguang Gu, Wenya Zhuang, Mengxia Zhuang, Minhong He, Zhihua |
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- |
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