Julie M. Rochelle

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

Stephan Züchner, Irina Mersiyanova, M. Muglia et al. · Nature Genetics · 2004 · 1.5K citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Mitochondrial Function +9

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21

Rachel V. Baxter, Kamel Ben Othmane, Julie M. Rochelle et al. · Nature Genetics · 2001 · 367 citations

Disease Mechanism, Pathogenesis, Experimental Pathology +7

Genetic analysis of MRL-lpr mice: relationship of the Fas apoptosis gene to disease manifestations and renal disease-modifying loci.

M. Watson, Jayasimha Rao, Gary S. Gilkeson et al. · The Journal of Experimental Medicine · 1992 · 336 citations · Full text

Genetics, Renal Pathology, Apoptosis +24

Cloning, pharmacological characterization, and genomic localization of the human creatine transporter.

Stuart Nash, Bruno Giros, Stephen F. Kingsmore et al. · PubMed · 1994 · 150 citations

Pharmacological Characterization, Creatine Transporter, Translational Physiology +16

Protocadherin Pcdh2 shows properties similar to, but distinct from, those of classical cadherins

Shuichi Obata, Haruhiko Sago, Nozomu Mori et al. · Journal of Cell Science · 1995 · 110 citations