Jeanette Koht

Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients

Mathieu Anheim, B. Monga, Marie‐Céline Fleury et al. · Brain · 2009 · 248 citations · Full text

Life Sciences, Genetics, Neurology +14

Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study

Anne Kjersti Erichsen, Jeanette Koht, Asbjørg Stray‐Pedersen et al. · Brain · 2009 · 209 citations

Life Sciences, Genetics, Neurology +13

Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene

Domitille Gras, Laurence Jonard, Emmanuel Roze et al. · Journal of Neurology Neurosurgery & Psychiatry · 2012 · 126 citations

Life Sciences, Genetics, Molecular Genetics +17

Prevalence and etiology of epilepsy in a <scp>N</scp>orwegian county—A population based study

Marte Syvertsen, Karl O. Nakken, Astrid Edland et al. · Epilepsia · 2015 · 99 citations

Medicine, Neurology, Disease Surveillance +11

STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity

Ketil Heimdal, Mònica Sánchez-Guixé, Ingvild Aukrust et al. · Orphanet Journal of Rare Diseases · 2014 · 73 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17