Flemming Juul Hansen

The 11q;22q translocation: A European collaborative analysis of 43 cases

M. Fraccaro, J. Lindsten, C. E. Ford et al. · Human Genetics · 1980 · 203 citations

Life Sciences, Genetics, Molecular Genetics +5

Mitochondrial encephalomyopathy with elevated methylmalonic acid is caused by SUCLA2 mutations

Flemming Juul Hansen, N. Sörensen, John Vissing et al. · Brain · 2007 · 184 citations

Life Sciences, Genetics, Neurology +17

Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletion

Joanna Poulton, Karl Morten, C. Freeman-Emmerson et al. · Human Molecular Genetics · 1994 · 169 citations

Life Sciences, Biochemistry, Genetics +13

A 17q21.31 microduplication, reciprocal to the newly described 17q21.31 microdeletion, in a girl with severe psychomotor developmental delay and dysmorphic craniofacial features

Maria Kirchhoff, Anne‐Marie Bisgaard, Flemming Juul Hansen et al. · European Journal of Medical Genetics · 2007 · 105 citations

Medicine, Genetics, Molecular Genetics +14

An mtDNA mutation, 14453G→A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome

Kirstine Ravn, Flemming Wibrand, Flemming Juul Hansen et al. · European Journal of Human Genetics · 2001 · 100 citations

Life Sciences, Genetics, Molecular Genetics +16