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BMC Medical Genomics|September 19, 2020
Genome scale analysis of pathogenic variants targetable for single base editingAlexander V Lavrov, Georgi G Varenikov, Mikhail Yu Skoblov
BMC Medical Genomics|October 7, 2020
Fraternal twins with Phelan-McDermid syndrome not involving the SHANK3 gene: case report and literature reviewShan Li, Ke-Wang Xi, Ting Liu, et al.
BMC Medical Genomics|October 7, 2020
Exploring the association of long noncoding RNA expression profiles with intracranial aneurysms, based on sequencing and related bioinformatics analysisYi Sun, Yeying Wen, Qishuang Ruan, et al.
BMC Medical Genomics|October 7, 2020
TOP2A and CENPF are synergistic master regulators activated in cervical cancerBeiwei Yu, Long Chen, Weina Zhang, et al.
BMC Medical Genomics|January 8, 2020
MiR-182-5p and its target HOXA9 in non-small cell lung cancer: a clinical and in-silico exploration with the combination of RT-qPCR, miRNA-seq and miRNA-chipLi Gao, Shi-Bai Yan, Jie Yang, et al.
BMC Medical Genomics|November 29, 2019
Identification and ranking of recurrent neo-epitopes in cancerEric Blanc, Manuel Holtgrewe, Arunraj Dhamodaran, et al.
BMC Medical Genomics|December 5, 2020
The first familial NSD2 cases with a novel variant in a Chinese father and daughter with atypical WHS facial features and a 7.5-year follow-up of growth hormone therapyXuyun Hu, Di Wu, Yuchuan Li, et al.
BMC Medical Genomics|November 29, 2018
Identification of gene expression profiles in myocardial infarction: a systematic review and meta-analysisPanagiota Kontou, Athanasia Pavlopoulou, Georgia Braliou, et al.
BMC Medical Genomics|December 21, 2018
Mapping the landscape of tandem repeat variability by targeted long read single molecule sequencing in familial X-linked intellectual disabilityAlena Zablotskaya, Hilde Van Esch, Kevin J Verstrepen, et al.
BMC Medical Genomics|December 31, 2013
Distinct DNA methylation patterns of cognitive impairment and trisomy 21 in Down syndromeMeaghan J Jones, Pau Farré, Lisa M McEwen, et al.
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