Niels Gregersen
Publications by Year
Research Areas
Metabolism and Genetic Disorders, Mitochondrial Function and Pathology, Biochemical and Molecular Research, Peroxisome Proliferator-Activated Receptors, Diet and metabolism studies
Most-Cited Works
- → α-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy(1999)394 cited
- → Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60(2002)368 cited
- → ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency(2007)327 cited
- → Clear Correlation of Genotype with Disease Phenotype in Very–Long-Chain Acyl-CoA Dehydrogenase Deficiency(1999)300 cited
- → Protein Misfolding and Human Disease(2006)298 cited
- → Oligonucleotide-priming methods for the chromosome-specific labelling of alpha satellite DNA in situ(1989)294 cited
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