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BMC Medical Genomics|August 20, 2025
Long read whole genome sequencing-based discovery of structural variants and their role in aetiology of non-syndromic autism spectrum disorder in IndiaJhanvi Shah, Debasrija Mondal, Deepika Jain, et al.
BMC Medical Genomics|August 22, 2021
Identification of SOFT syndrome caused by a pathogenic homozygous splicing variant of POC1A: a case reportGuoqiang Li, Guoying Chang, Chen Wang, et al.
BMC Medical Genomics|August 26, 2021
Integrative enrichment analysis of gene expression based on an artificial neuronXue Jiang, Weihao Pan, Miao Chen, et al.
BMC Medical Genomics|May 22, 2021
Association between MTNR1B polymorphisms and obesity in African American: findings from the Jackson Heart StudyCynthia Tchio, Solomon K Musani, Alexander Quarshie, et al.
BMC Medical Genomics|July 10, 2025
Integrated analysis reveals key circRNA-mediated regulatory axes related to prognosis and immune infiltration in lung adenocarcinomaYan Pei, Kang Lin
BMC Medical Genomics|July 2, 2025
From gene expression to causal associations: investigating the role of ferroptosis in cataract developmentChen Li, Xian-Bing Yuan, Yi-Cheng Lu, et al.
BMC Medical Genomics|July 27, 2025
Enrichment of tandem repeat element variants near CHD genes identified by short- and long-read genome sequencingAbhilash Suresh, Sarah U Morton, Daniel Quiat, et al.
BMC Medical Genomics|December 19, 2025
Molecular surveillance of antimalarial drug resistance genes in Nigeria: a systematic review and roadmap to malaria eliminationOluwayemi J Bamikole, Ayorinde F Fayehun, Yaaqub A Uthman, et al.
BMC Medical Genomics|December 18, 2025
Heterogeneity study on MiRNA expression in islet cells of rat pancreatic head and tailXuehua Lu, Yunlu Liu, Jinyan Chen, et al.
BMC Medical Genomics|December 19, 2025
Novel LRF/ZBTB7A variants and known HbF-modulating SNPs in transfusion-dependent β-thalassemiaYunus Arikan, Tugba Karaman Mercan, Merve Embel, et al.
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