Human Genome Epidemiology Literature Finder
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Records 1 - 17 (of 17 Records) |
| Query Trace: Neoplasms and TRIO[original query] |
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| Genome-wide analysis of chromosomal alterations in patients with esophageal squamous cell carcinoma exposed to tobacco and betel quid from high-risk area in India. Mutation research 2010 Feb 696 (2): 130-8. Chattopadhyay Indranil, Singh Avninder, Phukan Rupkumar, Purkayastha Joydeep, Kataki Amal, Mahanta Jagadish, Saxena Sunita, Kapur Suja |
| Folate pathway gene polymorphisms and risk of childhood brain tumors: results from an Australian case-control study. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2015 Jun 24 (6): 931-7. Greenop Kathryn R, Scott Rodney J, Attia John, Bower Carol, de Klerk Nicholas H, Norris Murray D, Haber Michelle, Jamieson Sarra E, van Bockxmeer Frank M, Gottardo Nicholas G, Ashton Lesley J, Armstrong Bruce K, Milne Elizabe |
Genome-Wide Association Study Identifies a New Locus at 7q21.13 Associated with Hepatitis B Virus-Related Hepatocellular Carcinoma.
Clinical cancer research : an official journal of the American Association for Cancer Research 2018 Feb 24 (4): 906-915. Li Yuanfeng, Zhai Yun, Song Qingfeng, Zhang Haitao, Cao Pengbo, Ping Jie, Liu Xinyi, Guo Bingqian, Liu Guanjun, Song Jin, Zhang Ying, Yang Aiqing, Yan Hongbo, Yang Liang, Cui Ying, Ma Yilong, Xing Jinliang, Shen Xizhong, Liu Taotao, Zhang Hongxin, An Jiaze, Bei Jin-Xin, Jia Weihua, Kang Longli, Liu Lijun, Yuan Dongya, Hu Zhibin, Shen Hongbing, Lu Lei, Wang Xuan, Li Hua, He Fuchu, Zhang Hongxing, Zhou Gangqi |
| A Bayesian Gene-Based Genome-Wide Association Study Analysis of Osteosarcoma Trio Data Using a Hierarchically Structured Prior. Cancer informatics 2018 17 1176935118775103. Yang Yi, Basu Saonli, Mirabello Lisa, Spector Logan, Zhang L |
| Gain-of-function mutations in DNMT3A in patients with paraganglioma. Genetics in medicine : official journal of the American College of Medical Genetics 2018 5 20 (12): 1644-1651. Remacha Laura, Currás-Freixes Maria, Torres-Ruiz Raúl, Schiavi Francesca, Torres-Pérez Rafael, Calsina Bruna, Letón Rocío, Comino-Méndez Iñaki, Roldán-Romero Juan M, Montero-Conde Cristina, Santos María, Pérez Lucía Inglada, Pita Guillermo, Alonso María R, Honrado Emiliano, Pedrinaci Susana, Crespo-Facorro Benedicto, Percesepe Antonio, Falcioni Maurizio, Rodríguez-Perales Sandra, Korpershoek Esther, Ramón-Maiques Santiago, Opocher Giuseppe, Rodríguez-Antona Cristina, Robledo Mercedes, Cascón Alber |
| Robust identification of mosaic variants in congenital heart disease. Human genetics 2018 2 137 (2): 183-193. Manheimer Kathryn B, Richter Felix, Edelmann Lisa J, D'Souza Sunita L, Shi Lisong, Shen Yufeng, Homsy Jason, Boskovski Marko T, Tai Angela C, Gorham Joshua, Yasso Christopher, Goldmuntz Elizabeth, Brueckner Martina, Lifton Richard P, Chung Wendy K, Seidman Christine E, Seidman J G, Gelb Bruce |
| High Yield of Pathogenic Germline Mutations Causative or Likely Causative of the Cancer Phenotype in Selected Children with Cancer. Clinical cancer research : an official journal of the American Association for Cancer Research 2018 1 24 (7): 1594-1603. Diets Illja J, Waanders Esmé, Ligtenberg Marjolijn J, van Bladel Diede A G, Kamping Eveline J, Hoogerbrugge Peter M, Hopman Saskia, Olderode-Berends Maran J, Gerkes Erica H, Koolen David A, Marcelis Carlo, Santen Gijs W, van Belzen Martine J, Mordaunt Dylan, McGregor Lesley, Thompson Elizabeth, Kattamis Antonis, Pastorczak Agata, Mlynarski Wojciech, Ilencikova Denisa, van Silfhout Anneke Vulto-, Gardeitchik Thatjana, de Bont Eveline S, Loeffen Jan, Wagner Anja, Mensenkamp Arjen R, Kuiper Roland P, Hoogerbrugge Nicoline, Jongmans Marjolijn |
| ?-arrestin1/YAP/mutant p53 complexes orchestrate the endothelin A receptor signaling in high-grade serous ovarian cancer. Nature communications 2019 7 10 (1): 3196. Tocci Piera, Cianfrocca Roberta, Di Castro Valeriana, Rosanò Laura, Sacconi Andrea, Donzelli Sara, Bonfiglio Silvia, Bucci Gabriele, Vizza Enrico, Ferrandina Gabriella, Scambia Giovanni, Tonon Giovanni, Blandino Giovanni, Bagnato An |
| The genomic profile of parathyroid carcinoma based on whole-genome sequencing. International journal of cancer 2020 6 147 (9): 2446-2457. Hu Ya, Zhang Xiang, Wang Ou, Bi Yalan, Xing Xiaoping, Cui Ming, Wang Mengyi, Tao Wei, Liao Quan, Zhao Yup |
| Genetics of physiological dysregulation: findings from the long life family study using joint models.
Aging 2020 Apr 12 (7): 5920-5947. Arbeev Konstantin G, Bagley Olivia, Ukraintseva Svetlana V, Wu Deqing, Duan Hongzhe, Kulminski Alexander M, Stallard Eric, Christensen Kaare, Lee Joseph H, Thyagarajan Bharat, Zmuda Joseph M, Yashin Anatoliy |
| Nearly Half of TP53 Germline Variants Predicted To Be Pathogenic in Patients With Osteosarcoma Are De Novo: A Report From the Children's Oncology Group. JCO precision oncology 2020 4 . Diessner Brandon J, Pankratz Nathan, Hooten Anthony J, Mirabello Lisa, Sarver Aaron L, Mills Lauren J, Malkin David, Kelley Ava C, Spector Logan |
| De novo variants in the Helicase-C domain of CHD8 are associated with severe phenotypes including autism, language disability and overgrowth. Human genetics 2020 1 139 (4): 499-512. An Yu, Zhang Linna, Liu Wenwen, Jiang Yunyun, Chen Xue, Lan Xiaoping, Li Gan, Hang Qiang, Wang Jian, Gusella James F, Du Yasong, Shen Yipi |
| Comprehensive germline-genomic and clinical profiling in 160 unselected children and adolescents with cancer. European journal of human genetics : EJHG 2021 4 29 (8): 1301-1311. Wagener Rabea, Taeubner Julia, Walter Carolin, Yasin Layal, Alzoubi Deya, Bartenhagen Christoph, Attarbaschi Andishe, Classen Carl-Friedrich, Kontny Udo, Hauer Julia, Fischer Ute, Dugas Martin, Kuhlen Michaela, Borkhardt Arndt, Brozou Triantafyll |
| Investigating the relationship between cancer and orofacial clefts using GWAS significant loci for cancers: A case-control and case-triad study. Frontiers in oral health 2022 3 915361. Fashina Azeez, Busch Tamara, Young Mary, Adamson Olawale, Awotoye Waheed, Alade Azeez, Adeleke Chinyere, Hassan Mohaned, Oladayo Abimbola M, Gowans Lord J J, Eshete Mekonen, Naicker Thirona, Olotu Joy, Adeyemo Wasiu L, Butali Aze |
| Clinical trio genome sequencing facilitates the interpretation of variants in cancer predisposition genes in paediatric tumour patients. European journal of human genetics : EJHG 2023 7 . Christopher Schroeder, Ulrike Faust, Luisa Krauße, Alexandra Liebmann, Michael Abele, German Demidov, Leon Schütz, Olga Kelemen, Alexandra Pohle, Silja Gauß, Marc Sturm, Cristiana Roggia, Monika Streiter, Rebecca Buchert, Sorin Armenau-Ebinger, Dominik Nann, Rudi Beschorner, Rupert Handgretinger, Martin Ebinger, Peter Lang, Ursula Holzer, Julia Skokowa, Stephan Ossowski, Tobias B Haack, Ulrike A Mau-Holzmann, Andreas Dufke, Olaf Riess, Ines B Brec |
| Genetic Trio of BRAF and TERT Mutations and rs2853669TT in Papillary Thyroid Cancer Aggressiveness. Journal of the National Cancer Institute 2023 12 . Rengyun Liu, Guangwu Zhu, Jie Tan, Xiaopei Shen, Mingzhao Xi |
| Spatial architectures of somatic mutations in normal prostate, benign prostatic hyperplasia and coexisting prostate cancer. Experimental & molecular medicine 2024 1 . Jeesoo Chae, Seung-Hyun Jung, Eun Ji Choi, Jae Woong Kim, Na Yung Kim, Sung Won Moon, Ji Youl Lee, Yeun-Jun Chung, Sug Hyung L |
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