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Frontiers in Genetics|February 19, 2025
Enhancing the utility of polygenic scores in Alzheimer's disease through systematic curation and annotationSavannah Mwesigwa, Yulin Dai, Nitesh Enduru, et al.Frontiers in Genetics|February 19, 2025
Genome-wide identification of oat TCP gene family and expression patterns under abiotic stressJiaming Nie, Hongbin Zhao, Xiaodong Guo, et al.Frontiers in Genetics|February 7, 2025
Genetic ancestry and the colonial legacies of race in genomics: a cross-disciplinary dialogueErnesto Schwartz-Marin, Tayyaba Jiwani, Sarah Abel, et al.Frontiers in Genetics|August 5, 2024
Keratoconus and inflammatory bowel disease: mendelian randomizationYiheng Jin, Yuanfeng Wang, Xu Qiu, et al.Frontiers in Genetics|August 8, 2024
Case report: First Chinese patient with family partial lipodystrophy type 6 due to novel compound heterozygous mutations in the LIPE geneYimeng Zhou, Lin Zhang, Yang Ding, et al.Frontiers in Genetics|August 5, 2024
Conduction and validation of a novel mitotic spindle assembly related signature in hepatocellular carcinoma: prognostic prediction, tumor immune microenvironment and drug susceptibilityZhao Zhang, Yuezhou Zhang, Gangli Hu, et al.Frontiers in Genetics|July 30, 2024
Screening and the analysis of genotypic and phenotypic characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Fujian province, ChinaJinfu Zhou, Yinglin Zeng, Jianping Tang, et al.Frontiers in Genetics|August 30, 2024
SAFE-MIL: a statistically interpretable framework for screening potential targeted therapy patients based on risk estimationYanfang Guan, Zhengfa Xue, Jiayin Wang, et al.Frontiers in Genetics|August 29, 2024
Genomic insights into prenatal diagnosis of congenital heart defects: value of CNV-seq and WES in clinical practiceShiyu Sun, Yizhen Ji, Di Shao, et al.Frontiers in Genetics|August 29, 2024
Novel PTPRQ variants associated with hearing loss in a Chinese family PTPRQ variants in Chinese hearing lossYuan Hou, Yuanzhen Shi, Longyan Liu, et al.Pageof 1,604