1. Mann, Nina, Mzoughi, Slim, Schneider, Ronen, Zenker, Martin, Hildebrandt, Friedhelm. 2021. Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome. In Journal of the American Society of Nephrology : JASN, 32, 580-596. doi:10.1681/ASN.2020040490. https://pubmed.ncbi.nlm.nih.gov/33593823/
2. Mzoughi, Slim, Di Tullio, Federico, Low, Diana H P, Messerschmidt, Daniel M, Guccione, Ernesto. 2020. PRDM15 loss of function links NOTCH and WNT/PCP signaling to patterning defects in holoprosencephaly. In Science advances, 6, eaax9852. doi:10.1126/sciadv.aax9852. https://pubmed.ncbi.nlm.nih.gov/31950080/
3. Saumweber, Ernestine, Mzoughi, Slim, Khadra, Arin, Schmeisser, Michael J, Kühl, Susanne J. 2024. Prdm15 acts upstream of Wnt4 signaling in anterior neural development of Xenopus laevis. In Frontiers in cell and developmental biology, 12, 1316048. doi:10.3389/fcell.2024.1316048. https://pubmed.ncbi.nlm.nih.gov/38444828/
4. Mzoughi, Slim, Zhang, Jingxian, Hequet, Delphine, Messerschmidt, Daniel M, Guccione, Ernesto. 2017. PRDM15 safeguards naive pluripotency by transcriptionally regulating WNT and MAPK-ERK signaling. In Nature genetics, 49, 1354-1363. doi:10.1038/ng.3922. https://pubmed.ncbi.nlm.nih.gov/28740264/
5. Hosgood Iii, H Dean, Díaz-Peña, Roberto, Blansky, Deanna, Silva, Rafael S, Olloquequi, Jordi. 2020. PRDM15 Is Associated with Risk of Chronic Obstructive Pulmonary Disease in a Rural Population in Chile. In Respiration; international review of thoracic diseases, 99, 307-315. doi:10.1159/000506649. https://pubmed.ncbi.nlm.nih.gov/32222710/
6. Khan, Arshad H, Lee, Lydia K, Smith, Desmond J. 2022. Single-cell analysis of gene expression in the substantia nigra pars compacta of a pesticide-induced mouse model of Parkinson's disease. In Translational neuroscience, 13, 255-269. doi:10.1515/tnsci-2022-0237. https://pubmed.ncbi.nlm.nih.gov/36117858/
智鼠故事 
