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BMC Medical Genomics|October 30, 2021
A novel missense mutation of FOXC1 in an Axenfeld-Rieger syndrome patient with a congenital atrial septal defect and sublingual cyst: a case report and literature reviewKaiming Li, Min Tang, Manhua Xu, et al.BMC Medical Genomics|September 24, 2021
Epigenome-wide association study detects a novel loci associated with central obesity in healthy subjectsTing Xie, Vesna Gorenjak, Maria G Stathopoulou, et al.BMC Medical Genomics|September 26, 2021
Characterization and clinical evaluation of microsatellite instability and loss of heterozygosity within tumor-related genes in colorectal cancerXueyun Huo, Dandan Feng, Shuangyue Zhang, et al.BMC Medical Genomics|October 17, 2019
Transcriptome analysis identified a novel 3-LncRNA regulatory network of transthyretin attenuating glucose induced hRECs dysfunction in diabetic retinopathyJun Shao, Yunbin Zhang, Guangming Fan, et al.BMC Medical Genomics|May 3, 2022
Stratification of lncRNA modulation networks in breast cancerWen-Hsuan Yu, Chia-Lang Hsu, Chen-Ching Lin, et al.BMC Medical Genomics|April 27, 2022
A pancancer analysis of the carcinogenic role of receptor-interacting serine/threonine protein kinase-2 (RIPK2) in human tumoursHanqun Zhang, Yan Ma, Qiuning Zhang, et al.BMC Medical Genomics|June 19, 2019
Retrovirus insertion site analysis of LGL leukemia patient genomesWeiling Li, Lei Yang, Robert S Harris, et al.BMC Medical Genomics|July 3, 2019
Genomic data analysis workflows for tumors from patient-derived xenografts (PDXs): challenges and guidelinesXing Yi Woo, Anuj Srivastava, Joel H Graber, et al.BMC Medical Genomics|July 5, 2019
Next-generation sequencing with comprehensive bioinformatics analysis facilitates somatic mosaic APC gene mutation detection in patients with familial adenomatous polyposisBorahm Kim, Dongju Won, Mi Jang, et al.BMC Medical Genomics|June 5, 2019
Targeted next generation sequencing as a tool for precision medicineMarkus Gulilat, Tyler Lamb, Wendy A Teft, et al.Pageof 278