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Annals of Clinical and Translational Neurology|March 19, 2026
Cracking the Code: Genotype-Phenotype Correlation Models in SarcoglycanopathiesLeonela Luce, Goknur Selen Kocak, José Verdú-Díaz, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 7, 2014
Rapamycin nanoparticles target defective autophagy in muscular dystrophy to enhance both strength and cardiac functionKristin P Bibee, Ya-Jian Cheng, James K Ching, et al.Neurology|October 28, 2025
Expert Consensus on Genetic Diagnostic Approaches for Patients With Limb-Girdle Muscular DystrophyVolker Straub, Amanda R Clause, Sandra Donkervoort, et al.Research Square|November 1, 2024
Genotype-phenotype correlation in recessive DNAJB4 myopathyMichio Inoue, Divya Jayaraman, Rocio Bengoechea, et al.Acta Neuropathologica Communications|October 29, 2024
Genotype‒phenotype correlation in recessive DNAJB4 myopathyMichio Inoue, Divya Jayaraman, Rocio Bengoechea, et al.Nature Metabolism|March 5, 2020
High-protein diets increase cardiovascular risk by activating macrophage mTOR to suppress mitophagyXiangyu Zhang, Ismail Sergin, Trent D Evans, et al.Nature Metabolism|September 10, 2020
Author Correction: High-protein diets increase cardiovascular risk by activating macrophage mTOR to suppress mitophagyXiangyu Zhang, Ismail Sergin, Trent D Evans, et al.Nature Communications|June 8, 2017
Exploiting macrophage autophagy-lysosomal biogenesis as a therapy for atherosclerosisIsmail Sergin, Trent D Evans, Xiangyu Zhang, et al.Cell Reports|July 21, 2021
Neuronal VCP loss of function recapitulates FTLD-TDP pathologyAbubakar Wani, Jiang Zhu, Jason D Ulrich, et al.Acta Neuropathologica|October 20, 2022
Loss of function variants in DNAJB4 cause a myopathy with early respiratory failureConrad C Weihl, Ana Töpf, Rocio Bengoechea, et al.Pageof 14