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BMC Medical Genomics|December 24, 2022
Construction and validation of a metabolic-related genes prognostic model for oral squamous cell carcinoma based on bioinformaticsJingfei Zhang, Chenxi Ma, Han Qin, et al.
BMC Medical Genomics|December 24, 2022
Construction and function analysis of the LncRNA-miRNA-mRNA competing endogenous RNA network in autoimmune hepatitisZhencheng Li, Ying Liu, Yiwen Hou, et al.
BMC Medical Genomics|December 28, 2022
Clinical value and potential mechanisms of BUB1B up-regulation in nasopharyngeal carcinomaLi-Ting Qin, Si-Wei Huang, Zhi-Guang Huang, et al.
BMC Medical Genomics|December 30, 2022
m6A regulator-mediated methylation modification patterns and immune microenvironment infiltration characterization in osteoarthritisShidong Hu, Chen Shen, Xudong Yao, et al.
BMC Medical Genomics|December 31, 2022
Association between PPARγ, PPARGC1A, and PPARGC1B genetic variants and susceptibility of gastric cancer in an Eastern Chinese populationBoyang Chen, Yafeng Wang, Weifeng Tang, et al.
BMC Medical Genomics|January 18, 2023
LRRC superfamily expression in stromal cells predicts the clinical prognosis and platinum resistance of ovarian cancerXiaoying Zhu, Shijing You, Xiuzhen Du, et al.
BMC Medical Genomics|January 19, 2023
Ferroptosis related gene signature in T cell-mediated rejection after kidney transplantationWeixun Zhang, Lian Gong, Di Zhang, et al.
BMC Medical Genomics|January 12, 2023
Disruption of DDX53 coding sequence has limited impact on iPSC-derived human NGN2 neuronsMuhammad Faheem, Eric Deneault, Roumiana Alexandrova, et al.
BMC Medical Genomics|January 16, 2023
Occurrence of variants of unknown clinical significance in genetic testing for hereditary breast and ovarian cancer syndrome and Lynch syndrome: a literature review and analytical observational retrospective cohort studyFelicia Adam, Muriel Fluri, Amina Scherz, et al.
BMC Medical Genomics|June 29, 2021
Discovery of sensorineural hearing loss and ossicle deformity in a Chinese Li nationality family with spondyloepiphyseal dysplasia congenita caused by p.G504S mutation of COL2A1Kan Wu, Zhumei Li, Yuhua Zhu, et al.
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