Anne Kjersti Erichsen

Author

Oslo University Hospital

Also Known As

A Erichsen, A. Erichsen, A. K. Erichsen, A.K. Erichsen, Anne K Erichsen, Anne Kjersti Erichsen, Willeke Van Roon-Mom

Publications

820

Citations

H-Index

Concepts

All Affiliations

Oslo University Hospital University of Oslo Inserm Sorbonne Université Assistance Publique – Hôpitaux de Paris

About

Anne Kjersti Erichsen is an author at Oslo University Hospital specializing in medicine, genetics, and rehabilitation.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	268
2	Neurology	2	2	228
3	Family Medicine	1	1	207
4	Molecular Genetics	1	1	11
5	Neuroscience	1	1	21

Anne Kjersti Erichsen

Publications

736

Citations

H-Index

Page 1

	Year	Citations
Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration Giovanni Stévanin, Hamid Azzedine, Paola S. Denora, Brain	2007	246
Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study Anne Kjersti Erichsen, Jeanette Koht, Asbjørg Stray‐Pedersen, Brain Family MedicineRare DiseasesMendelian DisorderHereditary Ataxia PrevalenceGenetic Disorder	2009	207
STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity Ketil Heimdal, Mònica Sánchez-Guixé, Ingvild Aukrust, Orphanet Journal of Rare Diseases	2014	70
Hereditary Spastic Paraplegia 3A Associated With Axonal Neuropathy Neviana Ivanova, Kristl G. Claeys, Tine Deconinck, Archives of Neurology	2007	51
Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia Anne Kjersti Erichsen, Elin Inderhaug, Morten Mattingsdal, European Journal of Neurology	2007	31
A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42) Nina Schlipf, Christian Beetz, Rebecca Schüle, European Journal of Human Genetics Rare DiseasesGenetic DisorderMedicineGeneticsSlc33a1 Gene	2010	29
CT and MR imaging of the paranasal sinuses in cystic fibrosis. Correlation with microbiological and histopathological results. Heidi B. Eggesbø, S Ringertz, O C Haanaes, PubMed	1999	26
Proton magnetic resonance spectroscopy and cognition in patients with spastin mutations Anne Kjersti Erichsen, Andrés Server, Nils Inge Landrø, Journal of the Neurological Sciences Genetic DisorderGeneticsClinical GeneticsResonanceSpastin Mutations	2008	21
Autosomal Recessive Cerebellar Atrophy and Spastic Ataxia in Patients With Pathogenic Biallelic Variants in GEMIN5 Deepa Rajan, Sukhleen Kour, Tyler R. Fortuna, Frontiers in Cell and Developmental Biology	2022	18
SPG11 – the most common type of recessive spastic paraplegia in Norway? Anne Kjersti Erichsen, Giovanni Stévanin, Paola S. Denora, Acta Neurologica Scandinavica	2008	15

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