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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Louise Eksandh

Department of Ophthalmology

University Hospital



Name/email consistency: high



  • Department of Ophthalmology, University Hospital, Sweden. 2000 - 2005


  1. Juvenile X-linked retinoschisis with normal scotopic b-wave in the electroretinogram at an early stage of the disease. Eksandh, L., Andréasson, S., Abrahamson, M. Ophthalmic Genet. (2005) [Pubmed]
  2. Clinical features of achromatopsia in Swedish patients with defined genotypes. Eksandh, L., Kohl, S., Wissinger, B. Ophthalmic Genet. (2002) [Pubmed]
  3. Best's vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene. Eksandh, L., Bakall, B., Bauer, B., Wadelius, C., Andréasson, S. Ophthalmic Genet. (2001) [Pubmed]
  4. Different clinical expressions in two families with Stargardt's macular dystrophy (STGD1). Eksandh, L., Ekström, U., Abrahamson, M., Bauer, B., Andréasson, S. Acta. Ophthalmol. Scand (2001) [Pubmed]
  5. Full-field ERG in patients with Batten/Spielmeyer-Vogt disease caused by mutations in the CLN3 gene. Eksandh, L.B., Ponjavic, V.B., Munroe, P.B., Eiberg, H.E., Uvebrant, P.E., Ehinger, B.E., Mole, S.E., Andréasson, S. Ophthalmic Genet. (2000) [Pubmed]
  6. Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 gene. Eksandh, L.C., Ponjavic, V., Ayyagari, R., Bingham, E.L., Hiriyanna, K.T., Andréasson, S., Ehinger, B., Sieving, P.A. Arch. Ophthalmol. (2000) [Pubmed]
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