1. Zhou, Wei, Ye, Dan, Tester, David J, Maginot, Kathleen R, Ackerman, Michael J. 2023. Elucidation of ALG10B as a Novel Long-QT Syndrome-Susceptibility Gene. In Circulation. Genomic and precision medicine, 16, e003726. doi:10.1161/CIRCGEN.122.003726. https://pubmed.ncbi.nlm.nih.gov/37071726/
2. Probst, Frank J, Corrigan, Rebecca R, Del Gaudio, Daniela, Oghalai, John S, Justice, Monica J. 2013. A point mutation in the gene for asparagine-linked glycosylation 10B (Alg10b) causes nonsyndromic hearing impairment in mice (Mus musculus). In PloS one, 8, e80408. doi:10.1371/journal.pone.0080408. https://pubmed.ncbi.nlm.nih.gov/24303013/
3. Gill, Shubhroz, Mandigo, Torrey R, Elmali, Ayse Deniz, Schreiber, Stuart L, Walker, James A. 2024. A conserved role for ALG10/ALG10B and the N -glycosylation pathway in the sleep-epilepsy axis. In medRxiv : the preprint server for health sciences, , . doi:10.1101/2024.12.11.24318624. https://pubmed.ncbi.nlm.nih.gov/39711723/
4. Nakagawa, Shumpei, Nguyen Pham, Khanh Tien, Shao, Xinyan, Doi, Masao. 2020. Time-Restricted G-Protein Signaling Pathways via GPR176, Gz, and RGS16 Set the Pace of the Master Circadian Clock in the Suprachiasmatic Nucleus. In International journal of molecular sciences, 21, . doi:10.3390/ijms21145055. https://pubmed.ncbi.nlm.nih.gov/32709014/
5. Mehboob, Riffat, Kurdi, Maher, Ahmad, Mursleen, Bamaga, Ahmed, Shahzad, Syed Adnan. 2021. Comprehensive Analysis of Genes Associated With Sudden Infant Death Syndrome. In Frontiers in pediatrics, 9, 742225. doi:10.3389/fped.2021.742225. https://pubmed.ncbi.nlm.nih.gov/34722422/