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Frontiers in Genetics|October 3, 2022
An integrated platform for Brucella with knowledge graph technology: From genomic analysis to epidemiological projectionFubo Ma, Ming Xiao, Lin Zhu, et al.
Frontiers in Genetics|October 3, 2022
From classical mendelian randomization to causal networks for systematic integration of multi-omicsAzam Yazdani, Akram Yazdani, Raul Mendez-Giraldez, et al.
Frontiers in Genetics|October 3, 2022
A single-center analysis of genotype-phenotype characteristics of Chinese patients with autosomal dominant polycystic kidney disease by targeted exome sequencingZiyan Yan, Yuchen Wang, Wenfeng Deng, et al.
Frontiers in Genetics|October 3, 2022
Uniparental disomy screen of Irish rare disorder cohort unmasks homozygous variants of clinical significance in the TMCO1 and PRKRA genesB Molloy, E R Jones, N D Linhares, et al.
Frontiers in Genetics|October 3, 2022
Evaluation and characterization of expression quantitative trait analysis methods in the Hybrid Rat Diversity PanelJack Pattee, Lauren A Vanderlinden, Spencer Mahaffey, et al.
Frontiers in Genetics|October 3, 2022
Cuproptosis-related gene signature correlates with the tumor immune features and predicts the prognosis of early-stage lung adenocarcinoma patientsYu Tang, Qifan Li, Daoqi Zhang, et al.
Frontiers in Genetics|October 3, 2022
Risk model of hepatocellular carcinoma based on cuproptosis-related genesZhiqiang Liu, Yong Qi, Haibo Wang, et al.
Frontiers in Genetics|October 3, 2022
Super-Enhancer-Associated nine-gene prognostic score model for prediction of survival in chronic lymphocytic leukemia patientsXue Liang, Ye Meng, Cong Li, et al.
Frontiers in Genetics|October 3, 2022
NanoCoV19: An analytical pipeline for rapid detection of severe acute respiratory syndrome coronavirus 2Jidong Lang
Frontiers in Genetics|October 3, 2022
Case Report: Hereditary transthyretin (ATTRv) amyloidosis: The p.G103R mutation of the transthyretin gene in a Han Chinese family is associated with vitreous hemorrhageJunhui Shen, Hao Yu, Jijian Lin, et al.
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