1. Liu, Zhenqiu, Elcheva, Irina. 2022. A six-gene prognostic signature for both adult and pediatric acute myeloid leukemia identified with machine learning. In American journal of translational research, 14, 6210-6221. doi:. https://pubmed.ncbi.nlm.nih.gov/36247279/
2. Mahamdallie, Shazia, Yost, Shawn, Poyastro-Pearson, Emma, Ruark, Elise, Rahman, Nazneen. 2019. Identification of new Wilms tumour predisposition genes: an exome sequencing study. In The Lancet. Child & adolescent health, 3, 322-331. doi:10.1016/S2352-4642(19)30018-5. https://pubmed.ncbi.nlm.nih.gov/30885698/
3. Tambi, Richa, Zehra, Binte, Nandkishore, Sharon, Uddin, Mohammed, Berdiev, Bakhrom K. 2023. Single-cell reconstruction and mutation enrichment analysis identifies dysregulated cardiomyocyte and endothelial cells in congenital heart disease. In Physiological genomics, 55, 634-646. doi:10.1152/physiolgenomics.00070.2023. https://pubmed.ncbi.nlm.nih.gov/37811720/
4. Chai, Tianci, Wang, Zhisheng, Yang, Xiaojie, Qiu, Zhihuang, Chen, Liangwan. 2022. PSRC1 May Affect Coronary Artery Disease Risk by Altering CELSR2, PSRC1, and SORT1 Gene Expression and Circulating Granulin and Apolipoprotein B Protein Levels. In Frontiers in cardiovascular medicine, 9, 763015. doi:10.3389/fcvm.2022.763015. https://pubmed.ncbi.nlm.nih.gov/35252377/
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