Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Disease and CTNNA1[original query] |
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| Exome sequencing reveals three novel candidate predisposition genes for diffuse gastric cancer. Familial cancer 2015 Jun 14 (2): 241-6. Donner Iikki, Kiviluoto Tuula, Ristimäki Ari, Aaltonen Lauri A, Vahteristo P |
| Exome Sequencing of Extended Families with Alzheimer's Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function. Journal of Alzheimer's disease & Parkinsonism 2017 11 7 (4): . Cukier H N, Kunkle B K, Hamilton K L, Rolati S, Kohli M A, Whitehead P L, Jaworski J, Vance J M, Cuccaro M L, Carney R M, Gilbert J R, Farrer L A, Martin E R, Beecham G W, Haines J L, Pericak-Vance M |
| Mutations in TFAP2B and previously unimplicated genes of the BMP, Wnt, and Hedgehog pathways in syndromic craniosynostosis. Proceedings of the National Academy of Sciences of the United States of America 2019 7 116 (30): 15116-15121. Timberlake Andrew T, Jin Sheng Chih, Nelson-Williams Carol, Wu Robin, Furey Charuta G, Islam Barira, Haider Shozeb, Loring Erin, Galm Amy, , Steinbacher Derek M, Larysz Dawid, Staffenberg David A, Flores Roberto L, Rodriguez Eduardo D, Boggon Titus J, Persing John A, Lifton Richard |
| Whole Exome Sequencing Identifies Candidate Genes Associated with Hereditary Predisposition to Uveal Melanoma. Ophthalmology 2019 Nov . Abdel-Rahman Mohamed H, Sample Klarke M, Pilarski Robert, Walsh Tomas, Grosel Timothy, Kinnamon Daniel, Boru Getachew, Massengill James B, Schoenfield Lynn, Kelly Ben, Gordon David, Johansson Peter, DeBenedictis Meghan J, Singh Arun, Casadei Silvia, Davidorf Frederick H, White Peter, Stacey Andrew W, Scarth James, Fewings Ellie, Tischkowitz Marc, King Mary-Claire, Hayward Nicholas K, Cebulla Colleen |
| Novel somatic variants in CTNNA1 gene in Iranian patients with diffuse gastric cancer. Gastroenterology and hepatology from bed to bench 2021 4 14 (1): 17-24. Naghi Vishteh Mohadeseh, Salmani Tayyeb Ali, Javadi Mamaghani Amirreza, Seyyed Tabaei Seyyed Javad, Kheirollahi Maj |
| Hereditary diffuse gastric cancer (HDGC). An overview. Clinics and research in hepatology and gastroenterology 2021 10 46 (4): 101820. Taja-Chayeb L, Vidal-Millán S, Trejo-Becerril C, Pérez-Cárdenas E, Chávez-Blanco A, Domínguez-Gómez G, González-Fierro A, Romo-Pérez A, Dueñas-González |
| Evaluating the Occurrence of Rare Variants in the Complement Factor H Gene in Patients With Early-Onset Drusen Maculopathy. JAMA ophthalmology 2021 Oct . de Breuk Anita, Heesterbeek Thomas J, Bakker Bjorn, Verzijden Timo, Lechanteur Yara T E, Klaver Caroline C W, den Hollander Anneke I, Hoyng Carel |
| [Hereditary gastric cancer syndromes and their association with specific histological subtypes]. Bulletin du cancer 2022 8 . Dardenne Antoine, Sirmai Laura, Metras Julie, Enea Diana, Svrcek Magali, Benusiglio Patrick |
| Mutation spectrum in a cohort with familial exudative vitreoretinopathy. Molecular genetics & genomic medicine 2022 Jul e2021. Qu Ning, Li Wei, Han Dong-Ming, Gao Jia-Yu, Yang Zheng-Tao, Jiang Li, Liu Tian-Bin, Chen Yan-Xian, Jiang Xiao-Sen, Zhou Liang, Wu Ji-Hong, Huang X |
| Whole-Exome Sequencing Among Chinese Patients With Hereditary Diffuse Gastric Cancer. JAMA network open 2022 Dec 5 (12): e2245836. Liu Ze-Xian, Zhang Xiao-Long, Zhao Qi, Chen Yungchang, Sheng Hui, He Cai-Yun, Sun Yu-Ting, Lai Ming-Yu, Wu Min-Qing, Zuo Zhi-Xiang, Wang Wei, Zhou Zhi-Wei, Wang Feng-Hua, Li Yu-Hong, Xu Rui-Hua, Qiu Miao-Zh |
| Somatic mutation of targeted sequencing identifies risk stratification in advanced ovarian clear cell carcinoma. Gynecologic oncology 2024 9 191 56-66. Shimeng Wan, Yang Gao, Sisi Wu, Hua Wang, Jiyu Tong, Wei Wei, Hang Ren, Danni Yang, Hao He, Hong Ye, Hongbing C |
- Page last reviewed:Feb 1, 2024
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