Human Genome Epidemiology Literature Finder
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Records 1 - 14 (of 14 Records) |
| Query Trace: Disease and PAX3[original query] |
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| A genome-wide association study identifies five loci influencing facial morphology in Europeans. PLoS genetics 2012 Sep 8 (9): 9. Liu F, van der Lijn F, Schurmann C, Zhu G, Chakravarty MM, Hysi PG, Wollstein A, Lao O, de Bruijne M, Ikram MA, van der Lugt A, Rivadeneira F, Uitterlinden AG, Hofman A, Niessen WJ, Homuth G, de Zubicaray G, McMahon KL, Thompson PM, Daboul A, Puls R, Hegenscheid K, Bevan L, Pausova Z, Medland SE, Montgomery GW, Wright MJ, Wicking C, Boehringer S, Spector TD, Paus T, Martin NG, Biffar R, Kayser M |
Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls.
Nature communications 0 6 8355. Zhu Zezhang, Tang Nelson Leung-Sang, Xu Leilei, Qin Xiaodong, Mao Saihu, Song Yueming, Liu Limin, Li Fangcai, Liu Peng, Yi Long, Chang Jiang, Jiang Long, Ng Bobby Kin-Wah, Shi Benlong, Zhang Wen, Qiao Jun, Sun Xu, Qiu Xusheng, Wang Zhou, Wang Fei, Xie Dingding, Chen Ling, Chen Zhonghui, Jin Mengran, Han Xiao, Hu Zongshan, Zhang Zhen, Liu Zhen, Zhu Feng, Qian Bang-Ping, Yu Yang, Wang Bing, Lee K M, Lee Wayne Y W, Lam T P, Qiu Yong, Cheng Jack Chun-Y |
| Clinical and genetic investigation of families with type II Waardenburg syndrome. Molecular medicine reports 2016 Jan . Chen Yong, Yang Fuwei, Zheng Hexin, Zhou Jianda, Zhu Ganghua, Hu Peng, Wu Weiji |
| Variants in the host genome may inhibit tumour growth in devil facial tumours: evidence from genome-wide association. Scientific reports 2017 Mar 7 (1): 423. Wright Belinda, Willet Cali E, Hamede Rodrigo, Jones Menna, Belov Katherine, Wade Claire |
| Replication Study for the Association of GWAS-associated Loci With Adolescent Idiopathic Scoliosis Susceptibility and Curve Progression in a Chinese Population. Spine 2018 Sep . Man Gene Chi-Wai, Tang Nelson Leung-Sang, Chan Ting Fung, Lam Tsz Ping, Li Jing Woei, Ng Bobby Kin-Wah, Zhu Zezhang, Qiu Yong, Cheng Jack Chun-Y |
| A Genetic Predictive Model Estimating the Risk of Developing Adolescent Idiopathic Scoliosis. Current genomics 2019 May 20 (4): 246-251. Xu Leilei, Wu Zhichong, Xia Chao, Tang Nelson, Cheng Jack C Y, Qiu Yong, Zhu ZeZha |
| The Interaction Analysis of SNP Variants and DNA Methylation Identifies Novel Methylated Pathogenesis Genes in Congenital Heart Diseases. Frontiers in cell and developmental biology 2021 5 9 665514. Wang Jing, Ma Xiaoqin, Zhang Qi, Chen Yinghui, Wu Dan, Zhao Pengjun, Yu |
| Acquired mutations and transcriptional remodeling in long-term estrogen-deprived locoregional breast cancer recurrences. Breast cancer research : BCR 2021 1 23 (1): 1. Priedigkeit Nolan, Ding Kai, Horne William, Kolls Jay K, Du Tian, Lucas Peter C, Blohmer Jens-Uwe, Denkert Carsten, Machleidt Anna, Ingold-Heppner Barbara, Oesterreich Steffi, Lee Adrian |
| Molecular etiology study of hearing loss in 13 Chinese Han families. Frontiers in neurology 2022 12 13 1048218. Sun Lianhua, Lin Zhengyu, Wang Xiaowen, Shen Jiali, Li Yue, Huang Yuyu, Yang J |
| Molecular Characterization of Circulating Tumor DNA in Pediatric Rhabdomyosarcoma: A Feasibility Study. JCO precision oncology 2022 10 6 e2100534. Ruhen Olivia, Lak Nathalie S M, Stutterheim Janine, Danielli Sara G, Chicard Mathieu, Iddir Yasmine, Saint-Charles Alexandra, Di Paolo Virginia, Tombolan Lucia, Gatz Susanne A, Aladowicz Ewa, Proszek Paula, Jamal Sabri, Stankunaite Reda, Hughes Deborah, Carter Paul, Izquierdo Elisa, Wasti Ajla, Chisholm Julia C, George Sally L, Pace Erika, Chesler Louis, Aerts Isabelle, Pierron Gaelle, Zaidi Sakina, Delattre Olivier, Surdez Didier, Kelsey Anna, Hubank Michael, Bonvini Paolo, Bisogno Gianni, Di Giannatale Angela, Schleiermacher Gudrun, Schäfer Beat W, Tytgat Godelieve A M, Shipley Jan |
| Preimplantation genetic testing for hereditary hearing loss in Chinese population. Journal of assisted reproduction and genetics 2023 4 . Bi Qingling, Huang Shasha, Wang Hui, Gao Xue, Ma Minyue, Han Mingyu, Lu Sijia, Kang Dongyang, Nourbakhsh Aida, Yan Denise, Blanton Susan, Liu Xuezhong, Yuan Yongyi, Yao Yuanqing, Dai |
| DNA Copy Number Alterations and Copy Neutral Loss of Heterozygosity in Adult Ph-Negative Acute B-Lymphoblastic Leukemia: Focus on the Genes Involved. International journal of molecular sciences 2023 12 24 (24): . Natalya Risinskaya, Maria Gladysheva, Abdulpatakh Abdulpatakhov, Yulia Chabaeva, Valeriya Surimova, Olga Aleshina, Anna Yushkova, Olga Dubova, Nikolay Kapranov, Irina Galtseva, Sergey Kulikov, Tatiana Obukhova, Andrey Sudarikov, Elena Parovichniko |
| Role of Abelson Helper Integration Site 1, Nebulin, and Paired Box 3 Genes in the Development of Nonsyndromic Strabismus in a Series of Iranian Families: Sequence Analysis and Systematic Review of the Genetics of Nonsyndromic Strabismus. Journal of current ophthalmology 2024 4 35 (3): 216-225. Maliheh Rahpeyma, Aliakbar Sabermoghaddam, Mohammad Yaser Kiarudi, Amirsaeed Sabeti Aghabozorgi, Alireza Pasd |
| Prognostic factors in patients with localized and metastatic alveolar rhabdomyosarcoma. A report from two studies and two registries of the Cooperative Weichteilsarkom Studiengruppe CWS. Cancer medicine 2025 1 14 (1): e70215. Ewa Koscielniak, Sabine Stegmaier, Gustaf Ljungman, Bernarda Kazanowska, Felix Niggli, Ruth Ladenstein, Bernd Blank, Erika Hallmen, Christian Vokuhl, Claudia Blattmann, Monika Sparber-Sauer, Thomas Klingebi |
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