Louise Eksandh

400 total citations
8 papers, 265 citations indexed

About

Louise Eksandh is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Louise Eksandh has authored 8 papers receiving a total of 265 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Ophthalmology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Louise Eksandh's work include Retinal Development and Disorders (8 papers), Retinal Diseases and Treatments (6 papers) and Photoreceptor and optogenetics research (2 papers). Louise Eksandh is often cited by papers focused on Retinal Development and Disorders (8 papers), Retinal Diseases and Treatments (6 papers) and Photoreceptor and optogenetics research (2 papers). Louise Eksandh collaborates with scholars based in Sweden, Germany and United States. Louise Eksandh's co-authors include Sten Andréasson, Magnus Abrahamson, Vesna Ponjavic, Bernd Wissinger, Susanne Kohl, Benjamin Bakall, Claes Wadelius, Birgitta Bauer, Berndt Ehinger and Sofie Ingvast and has published in prestigious journals such as Ophthalmic Genetics, Archives of Ophthalmology and Acta Ophthalmologica Scandinavica.

In The Last Decade

Louise Eksandh

8 papers receiving 261 citations

Peers

Louise Eksandh

MB

OPHTH

RNMI

CMN

CB

Ascensión Giménez Spain

Renate C. Zekveld-Vroon Netherlands

Meira R. Meltzer United States

Linda Rose United States

Stephen H. Tsang United States

Megan F. Jones United Kingdom

Monika Andrassi Germany

Magali Loyer Canada

Demelza Koehn United States

Raquel Pérez-Carro Spain

Ascensión Giménez Spain

Louise Eksandh

335 ×1.4

MB

183 ×1.0

OPHTH

43 ×0.4

RNMI

53 ×1.2

CMN

34 ×1.0

CB

Citations per year, relative to Louise Eksandh Louise Eksandh (= 1×) peers Ascensión Giménez

Countries citing papers authored by Louise Eksandh

Since Specialization

Citations

This map shows the geographic impact of Louise Eksandh's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Louise Eksandh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Louise Eksandh more than expected).

Fields of papers citing papers by Louise Eksandh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Louise Eksandh. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Louise Eksandh. The network helps show where Louise Eksandh may publish in the future.

Co-authorship network of co-authors of Louise Eksandh

This figure shows the co-authorship network connecting the top 25 collaborators of Louise Eksandh. A scholar is included among the top collaborators of Louise Eksandh based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Louise Eksandh. Louise Eksandh is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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8 of 8 papers shown

1.

Eksandh, Louise, Sten Andréasson, & Magnus Abrahamson. (2005). Juvenile X-Linked Retinoschisis with Normal Scotopic b-Wave in the Electroretinogram at an Early Stage of the Disease. Ophthalmic Genetics. 26(3). 111–117. 21 indexed citations

2.

Andréasson, Sten, Debra K. Breuer, Louise Eksandh, et al.. (2003). Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes. Ophthalmic Genetics. 24(4). 215–223. 25 indexed citations

3.

Schatz, Patrik, Magnus Abrahamson, Louise Eksandh, Vesna Ponjavic, & Sten Andréasson. (2003). Macular appearance by means of OCT and electrophysiology in members of two families with different mutations in RDS (the peripherin/RDS gene). Acta Ophthalmologica Scandinavica. 81(5). 500–507. 22 indexed citations

4.

Eksandh, Louise, Susanne Kohl, & Bernd Wissinger. (2002). Clinical features of achromatopsia in Swedish patients with defined genotypes. Ophthalmic Genetics. 23(2). 109–120. 36 indexed citations

5.

Eksandh, Louise, Benjamin Bakall, Birgitta Bauer, Claes Wadelius, & Sten Andréasson. (2001). Best’s vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene. Ophthalmic Genetics. 22(2). 107–115. 30 indexed citations

6.

Eksandh, Louise, Ulf Ekström, Magnus Abrahamson, Birgitta Bauer, & Sten Andréasson. (2001). Different clinical expressions in two families with Stargardt’s macular dystrophy (STGD1). Acta Ophthalmologica Scandinavica. 79(5). 524–530. 14 indexed citations

7.

Eksandh, Louise. (2000). Phenotypic Expression of Juvenile X-linked Retinoschisis in Swedish Families With Different Mutations in the XLRS1 Gene. Archives of Ophthalmology. 118(8). 1098–1098. 81 indexed citations

8.

Ponjavic, Vesna, Louise Eksandh, Sten Andréasson, et al.. (1999). Clinical expression of Best's vitelliform macular dystrophy in Swedish families with mutations in the bestrophin gene. Ophthalmic Genetics. 20(4). 251–257. 36 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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