Curt Scharfe
Publications by Year
Research Areas
Metabolism and Genetic Disorders, Genomics and Rare Diseases, Mitochondrial Function and Pathology, Metabolomics and Mass Spectrometry Studies, Genomics and Phylogenetic Studies
Most-Cited Works
- → Role of duplicate genes in genetic robustness against null mutations(2003)940 cited
- → Evolutionary Rate in the Protein Interaction Network(2002)894 cited
- → Systematic screen for human disease genes in yeast(2002)554 cited
- → The Role of Selection in the Evolution of Human Mitochondrial Genomes(2005)462 cited
- → The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein(2000)259 cited
- → Integrative Analysis of the Mitochondrial Proteome in Yeast(2004)215 cited
- → Massively parallel discovery of human-specific substitutions that alter enhancer activity(2020)116 cited
- → Mitochondrial Disease Sequence Data Resource (MSeqDR): A global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communities(2014)89 cited
- → Proteome analysis of mitochondrial outer membrane from Neurospora crassa (2005)87 cited
- → Mapping Gene Associations in Human Mitochondria using Clinical Disease Phenotypes(2009)87 cited