Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: WNT9A[original query] |
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Association between polymorphisms in Wnt signaling pathway genes and bone mineral density in postmenopausal Korean women. Menopause (New York, N.Y.) 0 17 (5): 1064-70. Lee Dong-Yun, Kim Hoon, Ku Seung Yup, Kim Seok Hyun, Choi Young Min, Kim Jung |
A Pooling Genome-Wide Association Study Combining a Pathway Analysis for Typical Sporadic Parkinson's Disease in the Han Population of Chinese Mainland.
Molecular neurobiology 2015 Jul . Hu Yakun, Deng Libing, Zhang Jie, Fang Xin, Mei Puming, Cao Xuebing, Lin Jiari, Wei Yi, Zhang Xiong, Xu Rens |
The lncRNA myocardial infarction associated transcript-centric competing endogenous RNA network in non-small-cell lung cancer. Cancer management and research 2018 10 1155-1162. Zheng Chang, Li Xuelian, Qian Biyun, Feng Nannan, Gao Sumeng, Zhao Yuxia, Zhou Baos |
[Study regarding the parent-of-origin effect of WNT pathway genes on non-syndromic cleft lip with or without cleft palate among the Chinese population]. Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi 2019 6 40 (6): 670-675. Wang S Y, Wang M Y, Li W Y, Zhou R, Zheng H C, Liu D J, Li N, Zhou Z B, Zhu H P, Wu |
Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify WNT9A as novel osteoarthritis gene.
Annals of the rheumatic diseases 2020 10 . Boer Cindy Germaine, Yau Michelle S, Rice Sarah J, Coutinho de Almeida Rodrigo, Cheung Kathleen, Styrkarsdottir Unnur, Southam Lorraine, Broer Linda, Wilkinson Jeremy Mark, Uitterlinden André G, Zeggini Eleftheria, Felson David, Loughlin John, Young Mariel, Capellini Terence Dante, Meulenbelt Ingrid, van Meurs Joyce |
Common genetic variation in alcohol-related hepatocellular carcinoma: a case-control genome-wide association study.
The Lancet. Oncology 2021 12 23 (1): 161-171. Trépo Eric, Caruso Stefano, Yang Jie, Imbeaud Sandrine, Couchy Gabrielle, Bayard Quentin, Letouzé Eric, Ganne-Carrié Nathalie, Moreno Christophe, Oussalah Abderrahim, Féray Cyrille, Blanc Jean Frédéric, Clément Bruno, Hillon Patrick, Boursier Jérôme, Paradis Valérie, Calderaro Julien, Gnemmi Viviane, Nault Jean-Charles, Guéant Jean-Louis, Devière Jacques, Archambeaud Isabelle, Vitellius Carole, Turlin Bruno, Bronowicki Jean-Pierre, Gustot Thierry, Sutton Angela, , Ziol Marianne, Nahon Pierre, Zucman-Rossi Jessi |
Disorders of Sex Development in Individuals Harbouring MAMLD1 Variants: WES and Interactome Evidence of Oligogenic Inheritance. Frontiers in endocrinology 2021 1 11 582516. Li Lele, Gao Fenqi, Fan Lijun, Su Chang, Liang Xuejun, Gong ChunX |
Identification of novel susceptibility genes for non-syndromic cleft lip with or without cleft palate using NGS-based multigene panel testing. Molecular genetics and genomics : MGG 2022 Jul . D?browska Justyna, Biedziak Barbara, Szponar-?urowska Anna, Budner Margareta, Jagodzi?ski Pawe? P, P?oski Rafa?, Mostowska Adrian |
Integrating genetic variants into clinical models for hepatocellular carcinoma risk stratification in cirrhosis. Journal of hepatology 2022 11 . Nahon Pierre, Bamba-Funck Jessica, Layese Richard, Trépo Eric, Zucman-Rossi Jessica, Cagnot Carole, Ganne-Carrié Nathalie, Chaffaut Cendrine, Guyot Erwan, Ziol Marianne, Sutton Angela, Audureau Etienne, |
Genetic polymorphism of WNT9A is functionally associated with thumb osteoarthritis in the Chinese population. Advances in rheumatology (London, England) 2024 1 64 (1): 12. Jian Dai, Haitao Jiang, Zhang Cheng, Yao Li, Zhaoqi Yang, Chuan Cheng, Xiaoming Ta |
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- Page last updated:Apr 22, 2024
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