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BMC Medical Genomics|September 13, 2022
KCNJ14 knockdown significantly inhibited the proliferation and migration of colorectal cellsBin Li, Ning Ge, Zhongping Pan, et al.
BMC Medical Genomics|January 4, 2022
The frequency of the known mitochondrial variants associated with drug-induced toxicity in a Korean populationVinh Hoa Pham, Van Lam Nguyen, Hye-Eun Jung, et al.
BMC Medical Genomics|October 19, 2022
Turning up the heat on non-immunoreactive tumors: autophagy influences the immune microenvironment in pancreatic cancerSi-Yuan Lu, Jie Hua, Jiang Liu, et al.
BMC Medical Genomics|October 26, 2022
An asparagine metabolism-based classification reveals the metabolic and immune heterogeneity of hepatocellular carcinomaJianguo Bai, Ruifeng Tang, Keyu Zhou, et al.
BMC Medical Genomics|July 21, 2016
Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rateWu-Lin Charng, Ender Karaca, Zeynep Coban Akdemir, et al.
BMC Medical Genomics|June 4, 2020
Identification of genes and miRNA associated with idiopathic recurrent pregnancy loss: an exploratory data mining studyWael Bahia, Ismael Soltani, Anouar Abidi, et al.
BMC Medical Genomics|June 4, 2020
Using Ethereum blockchain to store and query pharmacogenomics data via smart contractsGamze Gürsoy, Charlotte M Brannon, Mark Gerstein
BMC Medical Genomics|August 11, 2021
A novel USH2A variant in a patient with hearing loss and prenatal diagnosis of a familial fetus: a case reportCong Zhou, Yuanyuan Xiao, Hanbing Xie, et al.
BMC Medical Genomics|September 8, 2021
A missense variant rs2585405 in clock gene PER1 is associated with the increased risk of noise-induced hearing loss in a Chinese occupational populationHao Chen, Xuexue Ding, Enmin Ding, et al.
BMC Medical Genomics|September 8, 2021
The effect of CYP7B1 polymorphisms on the risk of coronary heart disease in Hainan Han populationTiebiao Liang, Xianbo Zhang, Anshan Liang, et al.
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