Emebet Mengesha

Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease

Dermot McGovern, Michelle R. Jones, Kent D. Taylor et al. · Human Molecular Genetics · 2010 · 381 citations · Full text

Missense Mutation in Pseudouridine Synthase 1 (PUS1) Causes Mitochondrial Myopathy and Sideroblastic Anemia (MLASA)

Yelena Bykhovskaya, Kari Casas, Emebet Mengesha et al. · The American Journal of Human Genetics · 2004 · 311 citations · Full text

Mitochondrial Myopathy, Mitochondrial Function, Biochemistry +10

Mutation in TRMU Related to Transfer RNA Modification Modulates the Phenotypic Expression of the Deafness-Associated Mitochondrial 12S Ribosomal RNA Mutations

Min‐Xin Guan, Qingfeng Yan, Xiaoming Li et al. · The American Journal of Human Genetics · 2006 · 222 citations · Full text

Rna Modification, Mitochondrial Biogenesis, Mitochondrial Function +10

Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility

Aleksejs Sazonovs, Christine Stevens, Guhan Venkataraman et al. · Nature Genetics · 2022 · 174 citations · Full text

Genome-wide Association Study, Disease Susceptibility, Autoimmune Disease +8

Mitochondrial Myopathy and Sideroblastic Anemia (MLASA)

Jeffrey R. Patton, Yelena Bykhovskaya, Emebet Mengesha et al. · Journal of Biological Chemistry · 2005 · 149 citations · Full text

Mitochondrial Myopathy, Mitochondrial Biogenesis, Mitochondrial Function +14