1. Tole, Soumitra, Dhir, Priya, Pugi, Jakob, Kirby-Allen, Melanie, Carcao, Manuel D. 2020. Genotype-phenotype correlation in children with hereditary spherocytosis. In British journal of haematology, 191, 486-496. doi:10.1111/bjh.16750. https://pubmed.ncbi.nlm.nih.gov/32436265/
2. More, Tejashree Anil, Devendra, Rati, Dongerdiye, Rashmi, Warang, Prashant, Kedar, Prabhakar. 2023. Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum. In Molecular genetics and genomics : MGG, 298, 427-439. doi:10.1007/s00438-022-01984-1. https://pubmed.ncbi.nlm.nih.gov/36598564/
3. Xue, Jinsong, Li, Fan, Dai, Peng. 2023. The Potential of ANK1 to Predict Parkinson's Disease. In Genes, 14, . doi:10.3390/genes14010226. https://pubmed.ncbi.nlm.nih.gov/36672967/
4. Kang, Meiyun, Li, Huimin, Zhu, Jun, Hong, Yue, Fang, Yongjun. 2023. Clinical manifestations of 17 Chinese children with hereditary spherocytosis caused by novel mutations of the ANK1 gene and phenotypic analysis. In Frontiers in genetics, 14, 1088985. doi:10.3389/fgene.2023.1088985. https://pubmed.ncbi.nlm.nih.gov/36816036/
5. Spracklen, Cassandra N, Horikoshi, Momoko, Kim, Young Jin, Mohlke, Karen L, Sim, Xueling. 2020. Identification of type 2 diabetes loci in 433,540 East Asian individuals. In Nature, 582, 240-245. doi:10.1038/s41586-020-2263-3. https://pubmed.ncbi.nlm.nih.gov/32499647/
6. Huang, Yiming, Wang, Aimin, Wang, Fenglin, Shi, Fuyan, Wang, Suzhen. . Screening of key immune-related gene in Parkinson's disease based on WGCNA and machine learning. In Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences, 49, 207-219. doi:10.11817/j.issn.1672-7347.2024.230307. https://pubmed.ncbi.nlm.nih.gov/38755717/
智鼠故事 
