PRKN and Parkinson disease: While SREBF1 takes center stage as a risk factor for sporadic PD [91], genes such as PARK2, PARK6, and PARK15, encoding Parkin, PINK1, and FBXO7 respectively, claim their roles in the autosomal recessive form of PD, intricately involved in PINK1/Parkin‐mediated mitophagy [92].