Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Disease and RAD21[original query] |
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| Functional variants at the 21q22.3 locus involved in breast cancer progression identified by screening of genome-wide estrogen response elements. Breast cancer research : BCR 2014 16 (5): 455. Hsiung Chia-Ni, Chu Hou-Wei, Huang Yuan-Ling, Chou Wen-Cheng, Hu Ling-Yueh, Hsu Huan-Ming, Wu Pei-Ei, Hou Ming-Feng, Yu Jyh-Cherng, Shen Chen-Ya |
| Whole-exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia. British journal of haematology 2016 Jul . Shiba Norio, Yoshida Kenichi, Shiraishi Yuichi, Okuno Yusuke, Yamato Genki, Hara Yusuke, Nagata Yasunobu, Chiba Kenichi, Tanaka Hiroko, Terui Kiminori, Kato Motohiro, Park Myoung-Ja, Ohki Kentaro, Shimada Akira, Takita Junko, Tomizawa Daisuke, Kudo Kazuko, Arakawa Hirokazu, Adachi Souichi, Taga Takashi, Tawa Akio, Ito Etsuro, Horibe Keizo, Sanada Masashi, Miyano Satoru, Ogawa Seishi, Hayashi Yasuhi |
| Polymorphisms in mitotic checkpoint-related genes can influence survival outcomes of early-stage non-small cell lung cancer. Oncotarget 2017 Sep 8 (37): 61777-61785. Kang Hyo Gyoung, Yoo Seung Soo, Choi Jin Eun, Hong Mi Jeong, Do Sook Kyung, Jin Cheng Cheng, Kim Soyoun, Lee Won Kee, Choi Sun Ha, Lee So Yeon, Kim Hyun Jung, Lee Shin Yup, Lee Jaehee, Cha Seung Ick, Kim Chang Ho, Seok Yangki, Lee Eungbae, Cho Sukki, Jheon Sanghoon, Park Jae Yo |
| Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies. Genetics in medicine : official journal of the American College of Medical Genetics 2018 8 21 (3): 663-675. Yuan Bo, Neira Juanita, Pehlivan Davut, Santiago-Sim Teresa, Song Xiaofei, Rosenfeld Jill, Posey Jennifer E, Patel Vipulkumar, Jin Weihong, Adam Margaret P, Baple Emma L, Dean John, Fong Chin-To, Hickey Scott E, Hudgins Louanne, Leon Eyby, Madan-Khetarpal Suneeta, Rawlins Lettie, Rustad Cecilie F, Stray-Pedersen Asbjørg, Tveten Kristian, Wenger Olivia, Diaz Jullianne, Jenkins Laura, Martin Laura, McGuire Marianne, Pietryga Marguerite, Ramsdell Linda, Slattery Leah, , Abid Farida, Bertuch Alison A, Grange Dorothy, Immken LaDonna, Schaaf Christian P, Van Esch Hilde, Bi Weimin, Cheung Sau Wai, Breman Amy M, Smith Janice L, Shaw Chad, Crosby Andrew H, Eng Christine, Yang Yaping, Lupski James R, Xiao Rui, Liu Pengf |
| [Analysis of clinical manifestation and genetic mutations in two patients with Cornelia de Lange syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2018 8 35 (4): 493-497. Miao Yequan, Zhu Yueyue, Zhang Qigang, Guo Haowei, Zhao Yuxiang, Cheng Longfei, Han Liangrong, Ning Ying, Pan Qio |
| The effect of aberrant expression and genetic polymorphisms of Rad21 on cervical cancer biology. Cancer medicine 2018 5 7 (7): 3393-3405. Xia Li, Wang Minjie, Li Hongying, Tang Xiangjing, Chen Fei, Cui Jinqu |
| Machine learning derived genomics driven prognostication for acute myeloid leukemia with RUNX1-RUNX1T1. Leukemia & lymphoma 2020 8 61 (13): 3154-3160. Shaikh Anam Fatima, Kakirde Chinmayee, Dhamne Chetan, Bhanshe Prasanna, Joshi Swapnali, Chaudhary Shruti, Chatterjee Gaurav, Tembhare Prashant, Prasad Maya, Roy Moulik Nirmalya, Gokarn Anant, Bonda Avinash, Nayak Lingaraj, Punatkar Sachin, Jain Hasmukh, Bagal Bhausaheb, Shetty Dhanalaxmi, Sengar Manju, Narula Gaurav, Khattry Navin, Banavali Shripad, Gujral Sumeet, P G Subramanian, Patkar Nikh |
| High Throughput Molecular Characterization of Normal Karyotype Acute Myeloid Leukemia in the Context of the Prospective Trial 02/06 of the Northern Italy Leukemia Group (NILG). Cancers 2020 8 12 (8): . Salmoiraghi Silvia, Cavagna Roberta, Zanghì Pamela, Pavoni Chiara, Michelato Anna, Buklijas Ksenija, Elidi Lara, Intermesoli Tamara, Lussana Federico, Oldani Elena, Caprioli Chiara, Stefanoni Paola, Gianfaldoni Giacomo, Audisio Ernesta, Terruzzi Elisabetta, De Paoli Lorella, Borlenghi Erika, Cavattoni Irene, Mattei Daniele, Scattolin Annamaria, Tajana Monica, Ciceri Fabio, Todisco Elisabetta, Campiotti Leonardo, Corradini Paolo, Fracchiolla Nicola, Bassan Renato, Rambaldi Alessandro, Spinelli Oriet |
| [Genetic variant analysis of a neonate with Cornelia de Lange syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 3 37 (4): 449-451. Sun Yuanyuan, Chen Cuie, Di Tianwei, Shao Haoran, Zhu Ronghe, Zhu Yanke, Zhou Aihua, Wang Q |
| Clinicopathologic and Genomic Landscape of Breast Carcinoma Brain Metastases. The oncologist 2021 Jun . Huang Richard S P, Haberberger James, McGregor Kimberly, Mata Douglas A, Decker Brennan, Hiemenz Matthew C, Lechpammer Mirna, Danziger Natalie, Schiavone Kelsie, Creeden James, Graf Ryon P, Strowd Roy, Lesser Glenn J, Razis Evangelia D, Bartsch Rupert, Giannoudis Athina, Bhogal Talvinder, Lin Nancy U, Pusztai Lajos, Ross Jeffrey S, Palmieri Carlo, Ramkissoon Shakti |
| Integrated Clinical Genotype-Phenotype Characteristics of Blastic Plasmacytoid Dendritic Cell Neoplasm. Cancers 2021 12 13 (23): . Yin C Cameron, Pemmaraju Naveen, You M James, Li Shaoying, Xu Jie, Wang Wei, Tang Zhenya, Alswailmi Omar, Bhalla Kapil N, Qazilbash Muzaffar H, Konopleva Marina, Khoury Joseph |
| Early-onset metastatic and clinically advanced prostate cancer is a distinct clinical and molecular entity characterized by increased TMPRSS2-ERG fusions. Prostate cancer and prostatic diseases 2021 Jan . Chalmers Zachary R, Burns Michael C, Ebot Ericka M, Frampton Garrett M, Ross Jeffrey S, Hussain Maha H A, Abdulkadir Sarki |
| PTPN11 mutations in adult acute myeloid leukaemia: Prevalence and clinical implications in the context of NPM1 mutation. Leukemia research 2022 5 118 106859. Liu Jie, Qin Wei, Wang Biao, Wang Zheng, Hua Haiying, Zhou Feng, Jia Zhuxia, Wu Pin, Chao Hongying, Lu Xuzha |
Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes.
Communications biology 2022 11 5 (1): 1175. Lee Chia-Jung, Chen Ting-Huei, Lim Aylwin Ming Wee, Chang Chien-Ching, Sie Jia-Jyun, Chen Pei-Lung, Chang Su-Wei, Wu Shang-Jung, Hsu Chia-Lin, Hsieh Ai-Ru, Yang Wei-Shiung, Fann Cathy S |
| Recurrent Somatic Copy Number Alterations and Their Association with Oncogene Expression Levels in High-Grade Ovarian Serous Carcinoma. Life (Basel, Switzerland) 2023 11 13 (11): . Hillary P Esplen, Richard K Yang, Awdhesh Kalia, Zhenya Tang, Guilin Tang, L Jeffrey Medeiros, Gokce A Torun |
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