Niels Gregersen

α-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy

Jens Mogensen, Ib Christian Klausen, Anders Kirstein Pedersen et al. · Journal of Clinical Investigation · 1999 · 396 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60

Jens Jacob Hansen, Alexandra Dürr, Isabelle Cournu‐Rebeix et al. · The American Journal of Human Genetics · 2002 · 371 citations · Full text

Life Sciences, Genetics, Neurology +14

ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency

Rikke Katrine Jentoft Olsen, S. E. Olpin, Brage Storstein Andresen et al. · Brain · 2007 · 328 citations

Life Sciences, Biochemistry, Molecular Genetics +15

Clear Correlation of Genotype with Disease Phenotype in Very–Long-Chain Acyl-CoA Dehydrogenase Deficiency

Brage Storstein Andresen, S. E. Olpin, Ben J. H. M. Poorthuis et al. · The American Journal of Human Genetics · 1999 · 302 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Oligonucleotide-priming methods for the chromosome-specific labelling of alpha satellite DNA in situ

J�rn E. Koch, Steen K�lvraa, Kirsten Bruun Petersen et al. · Chromosoma · 1989 · 294 citations

Life Sciences, Genetics, Molecular Biology +14