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BMC Medical Genomics|November 11, 2023
A phenome-wide approach to identify causal risk factors for deep vein thrombosisAndrei-Emil Constantinescu, Caroline J Bull, Lucy J Goudswaard, et al.
BMC Medical Genomics|November 12, 2023
OGM and WES identifies translocation breakpoints in PKD1 gene in an polycystic kidney patient and healthy baby delivered using PGTPeiwen Xu, Lijuan Wang, Jing Li, et al.
BMC Medical Genomics|November 19, 2023
The diagnostic/prognostic roles and biological function of the IFIT family members in acute myeloid leukemiaYiFan Zhao, Yi Zhang, WenYi Lu, et al.
BMC Medical Genomics|October 13, 2023
Origin recognition complex subunit 1(ORC1) is a potential biomarker and therapeutic target in cancerLinling Wu, Hui Chen, Chao Yang
BMC Medical Genomics|October 12, 2023
The potential DNA methylation markers of cardiovascular disease in patients with type 2 diabetesYunbiao He, Xia Chen, Mingliang Liu, et al.
BMC Medical Genomics|October 18, 2023
Interaction, immune infiltration characteristics and prognostic modeling of efferocytosis-related subtypes in glioblastomaSongyun Zhao, Qi Wang, Yuankun Liu, et al.
BMC Medical Genomics|October 19, 2023
Genome-wide analysis revealed the dysregulation of RNA binding protein-correlated alternative splicing events in myocardial ischemia reperfusion injuryNing Ma, Hao Xu, Weihua Zhang, et al.
BMC Medical Genomics|October 3, 2023
Causal effects of gut microbiome on autoimmune liver disease: a two-sample Mendelian randomization studyYugang Fu, Jiacheng Li, Yingying Zhu, et al.
BMC Medical Genomics|October 2, 2023
Insights into the genetics of menopausal vasomotor symptoms: genome-wide analyses of routinely-collected primary care health recordsKatherine S Ruth, Robin N Beaumont, Jonathan M Locke, et al.
BMC Medical Genomics|October 2, 2023
An alpha-helix variant p.Arg156Pro in LMNA as a cause of hereditary dilated cardiomyopathy: genetics and bioinfomatics explorationLei Chang, Rong Huang, Jianzhou Chen, et al.
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