1. Mamishi, Setareh, Pourakbari, Babak, Sadeghi, Reihaneh Hosseinpour, Marjani, Majid, Mahmoudi, Shima. . Differential Gene Expression of ASUN, NEMF, PTPRC and DHX29: Candidate Biomarkers for the Diagnosis of Active and Latent Tuberculosis. In Infectious disorders drug targets, 21, 268-273. doi:10.2174/1871526520666200313144951. https://pubmed.ncbi.nlm.nih.gov/32167431/
2. Ahmed, Ashfaque, Wang, Meng, Bergant, Gaber, Xia, Kun, Hu, Zhengmao. 2020. Biallelic loss-of-function variants in NEMF cause central nervous system impairment and axonal polyneuropathy. In Human genetics, 140, 579-592. doi:10.1007/s00439-020-02226-3. https://pubmed.ncbi.nlm.nih.gov/33048237/
3. Lee, Shih-Wei, Wu, Lawrence Shih-Hsin, Huang, Guan-Mau, Lee, Tzong-Yi, Weng, Julia Tzu-Ya. 2016. Gene expression profiling identifies candidate biomarkers for active and latent tuberculosis. In BMC bioinformatics, 17 Suppl 1, 3. doi:10.1186/s12859-015-0848-x. https://pubmed.ncbi.nlm.nih.gov/26818387/
4. Plessis-Belair, Jonathan, Ravano, Kathryn, Han, Ellen, Molina, Catalina, Sher, Roger B. 2024. NEMF mutations in mice illustrate how Importin-β specific nuclear transport defects recapitulate neurodegenerative disease hallmarks. In PLoS genetics, 20, e1011411. doi:10.1371/journal.pgen.1011411. https://pubmed.ncbi.nlm.nih.gov/39312574/
5. Anazi, S, Maddirevula, S, Faqeih, E, Shaheen, R, Alkuraya, F S. 2016. Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield. In Molecular psychiatry, 22, 615-624. doi:10.1038/mp.2016.113. https://pubmed.ncbi.nlm.nih.gov/27431290/
6. Dos Santos, Otávio Augusto Leitão, Carneiro, Rodolfo L, Requião, Rodrigo D, Domitrovic, Tatiana, Palhano, Fernando L. 2024. Transcriptional profile of ribosome-associated quality control components and their associated phenotypes in mammalian cells. In Scientific reports, 14, 1439. doi:10.1038/s41598-023-50811-z. https://pubmed.ncbi.nlm.nih.gov/38228636/