Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 33 Records) |
Query Trace: WNT1[original query] |
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A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation. Translational psychiatry 2013 3 e301. Martin P-M, Yang X, Robin N, Lam E, Rabinowitz J S, Erdman C A, Quinn J, Weiss L A, Hamilton S P, Kwok P-Y, Moon R T, Cheyette B N |
Variation in the Kozak sequence of WNT16 results in an increased translation and is associated with osteoporosis related parameters. Bone 2014 Feb 59 57-65. Hendrickx Gretl, Boudin Eveline, Fija?kowski Igor, Nielsen Torben Leo, Andersen Marianne, Brixen Kim, Van Hul W |
Associations between RNA splicing regulatory variants of stemness-related genes and racial disparities in susceptibility to prostate cancer. International journal of cancer 2017 08 141 (4): 731-743. Wang Yanru, Freedman Jennifer A, Liu Hongliang, Moorman Patricia G, Hyslop Terry, George Daniel J, Lee Norman H, Patierno Steven R, Wei Qing |
WISP1 genetic variants as predictors of tumor development with urothelial cell carcinoma. Urologic oncology 2017 Dec . Lee Hsiang-Lin, Chiou Hui-Ling, Wang Shian-Shiang, Hung Sheng-Chun, Chou Ming-Chih, Yang Shun-Fa, Hsieh Ming-Ju, Chou Ying-E |
Defective WNT signaling associates with bone marrow fibrosis-a cross-sectional cohort study in a family with WNT1 osteoporosis. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2017 11 29 (2): 479-487. Mäkitie R E, Niinimäki R, Kakko S, Honkanen T, Kovanen P E, Mäkitie |
Impacts of WNT1-inducible signaling pathway protein 1 polymorphism on hepatocellular carcinoma development. PloS one 2018 13 (6): e0198967. Chen Chih-Tien, Lee Hsiang-Lin, Chiou Hui-Ling, Chou Chia-Hsuan, Wang Po-Hui, Yang Shun-Fa, Chou Ying-E |
Evaluation of WISP1 as a candidate gene for bone mineral density in the Old Order Amish. Scientific reports 2018 May 8 (1): 7141. Wang Xing, Salimi Shabnam, Deng Zhongliang, Perry James, Ryan Kathleen A, Li Zhizhen, Liu Dongfang, Streeten Elizabeth, Shuldiner Alan R, Fu M |
Diagnostic strategies and genotype-phenotype correlation in a large Indian cohort of osteogenesis imperfecta. Bone 2018 3 110 368-377. Mrosk Julia, Bhavani Gandham SriLakshmi, Shah Hitesh, Hecht Jochen, Krüger Ulrike, Shukla Anju, Kornak Uwe, Girisha Katta Moh |
Association Between Genetic Polymorphisms of WNT1 Inducible Signaling Pathway Protein 1 and Uterine Cervical Cancer. Reproductive sciences (Thousand Oaks, Calif.) 2018 Jan 1933719118756749. Lin Yu-Hsiang, Hsiao Yi-Hsuan, Yang Shun-Fa, Liu Yu-Fan, Hsu Chun-Fang, Wang Po-H |
Primary Osteoporosis in Young Adults: Genetic Basis and Identification of Novel Variants in Causal Genes. JBMR plus 2018 Jan 2 (1): 12-21. Collet Corinne, Ostertag Agnès, Ricquebourg Manon, Delecourt Marine, Tueur Giulia, Isidor Bertrand, Guillot Pascale, Schaefer Elise, Javier Rose-Marie, Funck-Brentano Thomas, Orcel Philippe, Laplanche Jean-Louis, Cohen-Solal Marti |
Osteogenesis imperfecta in Brazilian patients. Genetics and molecular biology 2019 8 42 (2): 344-350. Trancozo Maira, Moraes Marcos V D, Silva Dalila A, Soares Jéssica A M, Barbirato Clara, Almeida Márcio G, Santos Lígia R, Rebouças Maria R G O, Akel Akel N, Sipolatti Valentim, Nunes Vanda R R, Errera Flavia I V, Aguena Meire, Passos-Bueno Maria R, Paula Flavia |
NOVEL MUTATIONS IN THE WNT1, TMEM38B, P4HB, AND PLS3 GENES IN FOUR UNRELATED CHINESE FAMILIES WITH OSTEOGENESIS IMPERFECTA. Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2019 3 25 (3): 230-241. Cao Yang-Jia, Zhang Hao, Zhang Zhen-L |
Impact of WNT1-inducible signaling pathway protein-1 (WISP-1) genetic polymorphisms and clinical aspects of breast cancer. Medicine 2019 Nov 98 (44): e17854. Wang Yan, Yang Shi-Hui, Hsu Ping-Wen, Chien Szu-Yu, Wang Chao-Qun, Su Chen-Ming, Dong Xiao-Fang, Zhao Yong-Ming, Tang Chih-Hs |
Associations between WNT1-inducible signaling pathway protein-1 (WISP-1) genetic polymorphisms and clinical aspects of rheumatoid arthritis among Chinese Han subjects. Medicine 2019 Nov 98 (44): e17604. Kuo Shu-Jui, Hsua Ping-Wen, Chien Szu-Yu, Huang Chien-Chung, Hu Sung-Lin, Tsai Chun-Hao, Su Chen-Ming, Tang Chih-Hs |
The role of WNT1 mutant variant (WNT1 ) in osteogenesis imperfecta. Annals of human genetics 2020 8 84 (6): 447-455. Zhang Bashan, Li Rong, Wang Wenfeng, Zhou Xueming, Luo Beijing, Zhu Zinian, Zhang Xibo, Ding Aiji |
Genotypic and Phenotypic Analysis in Chinese Cohort With Autosomal Recessive Osteogenesis Imperfecta. Frontiers in genetics 2020 10 11 984. Li Shan, Cao Yixuan, Wang Han, Li Lulu, Ren Xiuzhi, Mi Huan, Wang Yanzhou, Guan Yun, Zhao Feiyue, Mao Bin, Yang Tao, You Yi, Guan Xin, Yang Yujiao, Zhang Xue, Zhao Xiu |
The Effects of WISP1 Polymorphisms on the Prognosis of Lung Cancer Patients with Platinum-Based Chemotherapy. Pharmacogenomics and personalized medicine 2021 14 1193-1203. He Jia, Wang Zhan, Wang Ying, Zou Ting, Li Xiang-Ping, Cao Lei, Chen Ju |
Association between WNT-1-inducible signaling pathway protein-1 (WISP1) genetic polymorphisms and the risk of gastric cancer in Guangxi Chinese. Cancer cell international 2021 Jul 21 (1): 405. Liu Yanqiong, Qin Weijuan, Zhang Fuyong, Wang Jian, Li Xi, Li Shan, Qin Xue, Lu Yuefe |
Ghrelin modulates dopaminergic neuron formation and attention deficit hyperactivity disorder-like behaviors: From animals to human models. Brain, behavior, and immunity 2021 1 94 327-337. Shi Xulai, Guan Kaiyu, Peng Xuyan, Xu Bingru, Zhou Xianyong, Wang Shao, Xu Shengnan, Zheng Miaomiao, Huang Jing, Wan Xiaoyang, Guan Wanchun, Su Kuan-Pin, Ye Minjie, Gao Xiang, Yin Zhan, Li |
Lipocalin-2 is associated with FGF23 in WNT1 and PLS3 osteoporosis. Frontiers in endocrinology 2022 9 13 954730. Loid Petra, Hauta-Alus Helena, Mäkitie Outi, Magnusson Per, Mäkitie Riikka |
Case report: Early-onset osteoporosis in a patient carrying a novel heterozygous variant of the WNT1 gene. Frontiers in endocrinology 2022 8 13 918682. Campopiano Maria Cristina, Fogli Antonella, Michelucci Angela, Mazoni Laura, Longo Antonella, Borsari Simona, Pardi Elena, Benelli Elena, Sardella Chiara, Pierotti Laura, Dinoi Elisa, Marcocci Claudio, Cetani Filome |
Mutational Screening of Skeletal Genes in 14 Chinese Children with Osteogenesis Imperfecta Using Targeted Sequencing. Journal of immunology research 2022 6 2022 5068523. Tan Wei, Ji Yuelun, Qian Yuepeng, Lin Yongchang, Ye Ruolian, Wu Weiping, Li Yibin, Sun Yongjian, Pan Jiany |
Genotype-Phenotype Relationship and Follow-up Analysis of a Chinese Cohort With Osteogenesis Imperfecta. Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2022 May . Wei Shuoshuo, Yao Yangyang, Shu Meng, Gao Ling, Zhao Jiajun, Li Tianyou, Wang Yanzhou, Xu Ch |
Genetic Diagnostics in Routine Osteological Assessment of Adult Low Bone Mass Disorders. The Journal of clinical endocrinology and metabolism 2022 3 107 (7): e3048-e3057. Oheim Ralf, Tsourdi Elena, Seefried Lothar, Beller Gisela, Schubach Max, Vettorazzi Eik, Stürznickel Julian, Rolvien Tim, Ehmke Nadja, Delsmann Alena, Genest Franca, Krüger Ulrike, Zemojtel Tomasz, Barvencik Florian, Schinke Thorsten, Jakob Franz, Hofbauer Lorenz C, Mundlos Stefan, Kornak U |
Osteoporosis related to WNT1 variants: a not infrequent cause of osteoporosis. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2022 11 34 (2): 405-411. Peris Pilar, Monegal Ana, Mäkitie Riikka E, Guañabens Nuria, González-Roca E |
Suppression of Wnt/?-Catenin Signaling Is Associated with Downregulation of Wnt1, PORCN, and Rspo2 in Alzheimer's Disease. Molecular neurobiology 2022 10 60 (1): 26-35. Macyczko Jesse R, Wang Na, Zhao Jing, Ren Yingxue, Lu Wenyan, Ikezu Tadafumi C, Zhao Na, Liu Chia-Chen, Bu Guojun, Li Yong |
Scoliosis in osteogenesis imperfecta: identifying the genetic and non-genetic factors affecting severity and progression from longitudinal data of 290 patients. Orphanet journal of rare diseases 2023 9 18 (1): 295. Peikai Chen, Yapeng Zhou, Zhijia Tan, Yunzhi Lin, Daniel Li-Liang Lin, Jingwei Wu, Zeluan Li, Hiu Tung Shek, Jianbin Wu, Yong Hu, Feng Zhu, Danny Chan, Kenneth Man-Chee Cheung, Michael Kai-Tsun |
Genotype-phenotype relationship and comparison between eastern and western patients with osteogenesis imperfecta. Journal of endocrinological investigation 2023 6 . X Lin, J Hu, B Zhou, Q Zhang, Y Jiang, O Wang, W Xia, X Xing, M |
Multifactor dimensionality reduction method identifies novel SNP interactions in the WNT protein interaction networks that are associated with recurrence risk in colorectal cancer. Frontiers in oncology 2023 3 13 1122229. Curtis Aaron A, Yu Yajun, Carey Megan, Parfrey Patrick, Yilmaz Yildiz E, Savas Sevt |
Genotypic and phenotypic spectrum and pathogenesis of WNT1 variants in a large cohort of patients with OI/osteoporosis. The Journal of clinical endocrinology and metabolism 2023 1 . Hu Jing, Lin Xiaoyun, Gao Peng, Zhang Qian, Zhou Bingna, Wang Ou, Jiang Yan, Xia Weibo, Xing Xiaoping, Li M |
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- Page last updated:Mar 25, 2024
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