Chaya Miller

Deficiency of the ADP-Forming Succinyl-CoA Synthase Activity Is Associated with Encephalomyopathy and Mitochondrial DNA Depletion

Orly Elpeleg, Chaya Miller, Eli Hershkovitz et al. · The American Journal of Human Genetics · 2005 · 311 citations · Full text

Cellular Enzymology, Mitochondrial Function, Biochemistry +7

Defective mitochondrial translation caused by a ribosomal protein (MRPS16) mutation

Chaya Miller, Ann Saada, Nava Shaul et al. · Annals of Neurology · 2004 · 228 citations

C6ORF66 Is an Assembly Factor of Mitochondrial Complex I

Ann Saada, Simon Edvardson, Matan Rapoport et al. · The American Journal of Human Genetics · 2008 · 159 citations · Full text

Mitochondrial Function, Biochemistry, Natural Sciences +2

The <i>trithorax</i> Group Gene <i>moira</i> Encodes a Brahma-Associated Putative Chromatin-Remodeling Factor in <i>Drosophila melanogaster</i>

Madeline A. Crosby, Chaya Miller, Kellie L. Watson et al. · Molecular and Cellular Biology · 1999 · 124 citations

Mitochondrial complex IV deficiency, caused by mutated COX6B1, is associated with encephalomyopathy, hydrocephalus and cardiomyopathy

Ulla Najwa Abdulhag, Devorah Soiferman, Ora Schueler‐Furman et al. · European Journal of Human Genetics · 2014 · 102 citations · Full text

Mitochondrial Myopathy, Cardiomyopathy, Mitochondrial Biogenesis +7