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BMC Medical Genomics|November 7, 2022
A novel likely pathogenic variant in the FBXO32 gene associated with dilated cardiomyopathy according to whole‑exome sequencingSerwa Ghasemi, Mohammad Mahdavi, Majid Maleki, et al.BMC Medical Genomics|November 7, 2022
Custom gene expression panel for evaluation of potential molecular markers in hepatocellular carcinomaSrinivas Reddy Pallerla, Nghiem Xuan Hoan, Sivaramakrishna Rachakonda, et al.BMC Medical Genomics|August 15, 2022
High expression of serine and arginine-rich splicing factor 9 (SRSF9) is associated with hepatocellular carcinoma progression and a poor prognosisGuoshun Zhang, Bin Liu, Hua Shang, et al.BMC Medical Genomics|August 22, 2022
A novel signature to predict thyroid cancer prognosis and immune landscape using immune-related LncRNA pairsBo Song, Lijun Tian, Fan Zhang, et al.BMC Medical Genomics|November 11, 2022
A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in GhanaSamuel Mawuli Adadey, Elvis Twumasi Aboagye, Kevin Esoh, et al.BMC Medical Genomics|February 4, 2023
Variants in TPO rs2048722, PTCSC2 rs925489 and SEMA4G rs4919510 affect thyroid carcinoma susceptibility riskZhen Shen, Yingjun Sun, Guohua NiuBMC Medical Genomics|January 26, 2023
Whole-exome sequencing identified recurrent and novel variants in benzene-induced leukemiaDafeng Lin, Dianpeng Wang, Peimao Li, et al.BMC Medical Genomics|February 16, 2023
Case report: a Chinese girl like atypical Rubinstein-Taybi syndrome caused by a novel heterozygous mutation of the EP300 geneZhouxian Bai, Gaopan Li, Xiangdong KongBMC Medical Genomics|February 26, 2025
Targeting RECQL4 in hepatocellular carcinoma: from prognosis to therapeutic potentialYingchen Li, Linan Yin, Bowen Liu, et al.BMC Medical Genomics|February 25, 2025
m6A regulator-based molecular classification and hub genes associated with immune infiltration characteristics and clinical outcomes in diffuse gliomasJie Lu, Siyu Chen, Wanming Hu, et al.Pageof 278