1. Vinci, Mirella, Greco, Donatella, Figura, Maria Grazia, Federico, Concetta, Calì, Francesco. 2024. Exploring the Role of FICD, a New Potential Gene Involved in Borderline Intellectual Functioning, Psychological and Metabolic Disorders. In Genes, 15, . doi:10.3390/genes15121655. https://pubmed.ncbi.nlm.nih.gov/39766922/
2. Gulen, Burak, Blevins, Aubrie, Kinch, Lisa N, Casey, Amanda K, Orth, Kim. 2024. FicD sensitizes cellular response to glucose fluctuations in mouse embryonic fibroblasts. In Proceedings of the National Academy of Sciences of the United States of America, 121, e2400781121. doi:10.1073/pnas.2400781121. https://pubmed.ncbi.nlm.nih.gov/39259589/
3. Gulen, Burak, Kinch, Lisa N, Servage, Kelly A, Casey, Amanda K, Orth, Kim. 2024. FicD Sensitizes Cellular Response to Glucose Fluctuations in Mouse Embryonic Fibroblasts. In bioRxiv : the preprint server for biology, , . doi:10.1101/2024.01.22.576705. https://pubmed.ncbi.nlm.nih.gov/38328056/
4. Rosani, Umberto, De Felice, Sofia, Frizzo, Riccardo, Kawato, Satoshi, Wegner, K Mathias. 2023. FicD genes in invertebrates: A tale of transposons, pathogenic and integrated viruses. In Gene, 893, 147895. doi:10.1016/j.gene.2023.147895. https://pubmed.ncbi.nlm.nih.gov/37832807/
5. Lobato, Amanda G, Ortiz-Vega, Natalie, Canic, Tijana, Syed, Sheyum, Zhai, R Grace. 2024. Loss of Fic causes progressive neurodegeneration in a Drosophila model of hereditary spastic paraplegia. In Biochimica et biophysica acta. Molecular basis of disease, 1870, 167348. doi:10.1016/j.bbadis.2024.167348. https://pubmed.ncbi.nlm.nih.gov/38986817/
6. Perera, Luke A, Hattersley, Andrew T, Harding, Heather P, Ron, David, De Franco, Elisa. 2023. Infancy-onset diabetes caused by de-regulated AMPylation of the human endoplasmic reticulum chaperone BiP. In EMBO molecular medicine, 15, e16491. doi:10.15252/emmm.202216491. https://pubmed.ncbi.nlm.nih.gov/36704923/