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BMC Medical Genomics|June 30, 2021
Multivariate transcriptome analysis identifies networks and key drivers of chronic lymphocytic leukemia relapse risk and patient survivalTi'ara L Griffen, Eric B Dammer, Courtney D Dill, et al.
BMC Medical Genomics|January 7, 2021
Genome-wide association study of circulating levels of glucagon during an oral glucose tolerance testAnna Jonsson, Sara E Stinson, Signe S Torekov, et al.
BMC Medical Genomics|January 7, 2021
Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohortElisabeth A Rosenthal, David R Crosslin, Adam S Gordon, et al.
BMC Medical Genomics|January 7, 2021
Interactive association between dietary fat and sex on CDH13 cg02263260 methylationBei-Hao Shiu, Wen-Yu Lu, Disline Manli Tantoh, et al.
BMC Medical Genomics|January 7, 2021
Role of ATF3 as a prognostic biomarker and correlation of ATF3 expression with macrophage infiltration in hepatocellular carcinomaLijuan Li, Shaohua Song, Xiaoling Fang, et al.
BMC Medical Genomics|January 7, 2021
Identification of a novel mutation in the KITLG gene in a Chinese family with familial progressive hyper- and hypopigmentationJianbo Wang, Weisheng Li, Naihui Zhou, et al.
BMC Medical Genomics|January 7, 2021
DNA methylation abnormalities of imprinted genes in congenital heart disease: a pilot studyShaoyan Chang, Yubo Wang, Yu Xin, et al.
BMC Medical Genomics|January 13, 2021
Evaluation of chromosomal abnormalities and copy number variations in fetuses with ultrasonic soft markersMeiying Cai, Na Lin, Xuemei Chen, et al.
BMC Medical Genomics|June 9, 2021
Correlating genomic copy number alterations with clinicopathologic findings in 75 cases of hepatocellular carcinomaGang Peng, Hongyan Chai, Weizhen Ji, et al.
BMC Medical Genomics|June 20, 2021
A prenatal diagnosis case of partial duplication 21q21.1-q21.2 with normal phenotype maternally inheritedChunyan Jin, Zhiping Gu, Xiaohan Jiang, et al.
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