1. Al-Obaide, Mohammed A, Islam, Saimul, Al-Obaidi, Ibtisam, Vasylyeva, Tetyana L. 2023. Novel enhancer mediates the RPL36A-HNRNPH2 readthrough loci and GLA gene expressions associated with fabry disease. In Frontiers in genetics, 14, 1229088. doi:10.3389/fgene.2023.1229088. https://pubmed.ncbi.nlm.nih.gov/38155709/
2. Gonzalez, Joseph Nicho, Goldman, Sylvie, Carter, Melissa T, Bain, Jennifer M. 2023. Rett-like Phenotypes in HNRNPH2-Related Neurodevelopmental Disorder. In Genes, 14, . doi:10.3390/genes14061154. https://pubmed.ncbi.nlm.nih.gov/37372334/
3. Korff, Ane, Yang, Xiaojing, O'Donovan, Kevin, Taylor, J Paul, Kim, Hong Joo. 2023. A murine model of hnRNPH2-related neurodevelopmental disorder reveals a mechanism for genetic compensation by Hnrnph1. In The Journal of clinical investigation, 133, . doi:10.1172/JCI160309. https://pubmed.ncbi.nlm.nih.gov/37463454/
4. Pilch, Jacek, Koppolu, Agnieszka A, Walczak, Anna, Emich-Widera, Ewa, Płoski, Rafał. 2018. Evidence for HNRNPH1 being another gene for Bain type syndromic mental retardation. In Clinical genetics, 94, 381-385. doi:10.1111/cge.13410. https://pubmed.ncbi.nlm.nih.gov/29938792/
5. Al-Obaide, Mohammed A Ibrahim, Al-Obaidi, Ibtisam I, Vasylyeva, Tetyana L. 2020. Unexplored regulatory sequences of divergently paired GLA and HNRNPH2 loci pertinent to Fabry disease in human kidney and skin cells: Presence of an active bidirectional promoter. In Experimental and therapeutic medicine, 21, 154. doi:10.3892/etm.2020.9586. https://pubmed.ncbi.nlm.nih.gov/33456521/
智鼠故事 
