Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: FMN2[original query] |
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Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure.
PLoS genetics 2013 9 (2): e1003247. Paternoster Lavinia, Lorentzon Mattias, Lehtimäki Terho, Eriksson Joel, Kähönen Mika, Raitakari Olli, Laaksonen Marika, Sievänen Harri, Viikari Jorma, Lyytikäinen Leo-Pekka, Mellström Dan, Karlsson Magnus, Ljunggren Osten, Grundberg Elin, Kemp John P, Sayers Adrian, Nethander Maria, Evans David M, Vandenput Liesbeth, Tobias Jon H, Ohlsson Cla |
Genome-wide association meta-analyses identified 1q43 and 2q32.2 for hip Ward's triangle areal bone mineral density.
Bone 2016 Oct 91 1-10. Pei Yu-Fang, Hu Wen-Zhu, Hai Rong, Wang Xiu-Yan, Ran Shu, Lin Yong, Shen Hui, Tian Qing, , , , Lei Shu-Feng, Zhang Yong-Hong, Papasian Christopher J, Deng Hong-Wen, Zhang L |
Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases. Human reproduction (Oxford, England) 2016 Jun . Tšuiko O, Nõukas M, Žilina O, Hensen K, Tapanainen J S, Mägi R, Kals M, Kivistik P A, Haller-Kikkatalo K, Salumets A, Kurg |
Gene-gene interactions of the Wnt/?-catenin signaling pathway in knee osteoarthritis. Molecular biology reports 2018 Aug . Fernández-Torres Javier, Zamudio-Cuevas Yessica, López-Reyes Alberto, Garrido-Rodríguez Daniela, Martínez-Flores Karina, Lozada Carlos Alberto, Muñóz-Valle José Francisco, Oregon-Romero Edith, Martínez-Nava Gabriela Angéli |
Risk of Wnt/?-catenin signalling pathway gene polymorphisms in primary Sjögren's syndrome. Rheumatology (Oxford, England) 2019 Jul . Fernández-Torres Javier, Pérez-Hernández Nonanzit, Hernández-Molina Gabriela, Martínez-Nava Gabriela A, Garrido-Rodríguez Daniela, López-Reyes Alberto, Rodríguez-Pérez José |
Multi gene mutation signatures in colorectal cancer patients: predict for the diagnosis, pathological classification, staging and prognosis. BMC cancer 2021 4 21 (1): 380. Zhuang Yan, Wang Hailong, Jiang Da, Li Ying, Feng Lixia, Tian Caijuan, Pu Mingyu, Wang Xiaowei, Zhang Jiangyan, Hu Yuanjing, Liu Pengf |
Identification of genetic mutations of cutaneous squamous cell carcinoma using whole exome sequencing in non-Caucasian population. Journal of dermatological science 2022 4 106 (2): 70-77. Lee Soo Young, Lee Minho, Yu Dong Soo, Lee Young B |
Heterozygous FMN2 missense variant found in a family case of premature ovarian insufficiency. Journal of ovarian research 2022 3 15 (1): 31. Li Jie, Peng Tianliu, Wang Le, Long Panpan, Quan Ruping, Tan Hangjing, Zeng Minghua, Wu Xue, Yang Junting, Xiao Hongmei, Shi Xiao |
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