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BMC Medical Genomics|February 13, 2022
Severe phenotypes of B3GAT3-related disorder caused by two heterozygous variants: a case report and literature reviewYing Li, Chuangwen Zhang, Hongyu Zhang, et al.
BMC Medical Genomics|January 22, 2022
Variant analysis of 92 Chinese Han families with hearing lossXiaohua Jin, Shasha Huang, Lisha An, et al.
BMC Medical Genomics|January 30, 2022
Risk stratification of lung adenocarcinoma using a nomogram combined with ferroptosis-related LncRNAs and subgroup analysis with immune and N6-methyladenosine modificationChen Gao, Ning Kong, Fan Zhang, et al.
BMC Medical Genomics|April 26, 2022
Clinically actionable cancer somatic variants (CACSV): a tumor interpreted dataset for analytical workflowsTurki M Sobahy, Ghassan Tashkandi, Donya Bahussain, et al.
BMC Medical Genomics|March 18, 2022
Species composition and overall diversity are significantly correlated between the tongue coating and gastric fluid microbiomes in gastritis patientsJiaxing Cui, Siyu Hou, Bing Liu, et al.
BMC Medical Genomics|March 19, 2022
SARS-CoV-2: tracing the origin, tracking the evolutionKonstantinos Voskarides
BMC Medical Genomics|April 5, 2022
Atypical deletion of Williams-Beuren syndrome reveals the mechanism of neurodevelopmental disordersJianrong Zhou, Ying Zheng, Guiying Liang, et al.
BMC Medical Genomics|April 24, 2022
SARS-COV-2 as potential microRNA sponge in COVID-19 patientsChang Li, Rebecca Wang, Aurora Wu, et al.
BMC Medical Genomics|March 17, 2022
LncRNA PTCSC3 is upregulated in osteoporosis and negatively regulates osteoblast apoptosisXingchao Liu, Mingliang Chen, Qinghe Liu, et al.
BMC Medical Genomics|March 17, 2022
Novel compound heterozygous variants in the PCCB gene causing adult-onset propionic acidemia presenting with neuropsychiatric symptoms: a case report and literature reviewYingxuan Li, Miaomiao Wang, Zhaoyang Huang, et al.
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