Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies
if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the
same subfield and year (this is the minimum needed to enter the top 1%, not the average
within it), or reaches the top citation threshold in at least one of its specific research
topics.
Identification of the gene responsible for Best macular dystrophy
1998541 citationsBenjamin Bakall, Sten Andréasson et al.profile →
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late)
cites ·
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Countries citing papers authored by Sten Andréasson
Since
Specialization
Citations
This map shows the geographic impact of Sten Andréasson'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 Sten Andréasson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sten Andréasson more than expected).
This network shows the impact of papers produced by Sten Andréasson. 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 Sten Andréasson. The network helps show where Sten Andréasson may publish in the future.
Co-authorship network of co-authors of Sten Andréasson
This figure shows the co-authorship network connecting the top 25 collaborators of Sten Andréasson.
A scholar is included among the top collaborators of Sten Andréasson 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 Sten Andréasson. Sten Andréasson is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
All Works
20 of 20 papers shown
1.
Andréasson, Sten, et al.. (2022). A five-year follow-up of ABCA4 carriers showing deterioration of retinal function and increased structural changes.. PubMed. 28. 300–316.2 indexed citations
2.
Nikopoulos, Konstantinos, Pietro Farinelli, Béryl Royer‐Bertrand, et al.. (2016). Whole exome sequencing reveals CEP78 as a novel disease gene for cone-rod dystrophy. Investigative Ophthalmology & Visual Science. 57(12).1 indexed citations
3.
Andréasson, Sten, et al.. (2016). Characterization of macular structure and function in two Swedish families with genetically identified autosomal dominant retinitis pigmentosa.. PubMed. 22. 362–73.9 indexed citations
4.
Crafoord, Sven, et al.. (2014). A cross-linked hyaluronic acid hydrogel (Healaflow ®) as a potential vitreous substitute. Investigative Ophthalmology & Visual Science. 55(13). 2338–2338.1 indexed citations
5.
Ghosh, Fredrik, et al.. (2014). Retinal function and morphology in the rabbit eye after intravitreal injection of the TNF alpha inhibitor adalimumab. Investigative Ophthalmology & Visual Science. 55(13). 1921–1921.2 indexed citations
Gränse, Lotta, et al.. (2007). Patients With Diabetic Retinopathy and Neuropathy Showed Lower Amplitudes on the Multifocal Vep Than Diabetic Patients With the Same Level of Retinopathy but No Neuropathy. Investigative Ophthalmology & Visual Science. 48(13). 5010–5010.3 indexed citations
10.
Gränse, Lotta, et al.. (2003). Multifocal Electroretinogram and Multifocal Visual Evoked Potential in a Family With X-Linked Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 44(13). 4935–4935.2 indexed citations
11.
Ghosh, Fredrik, et al.. (2003). Standardized Full-Field and Multifocal Electroretinography in Rabbits. Investigative Ophthalmology & Visual Science. 44(13). 2695–2695.3 indexed citations
12.
Alexander, Suceena, Jan‐Willem Taanman, Susan Sklower Brooks, et al.. (2002). A comprehensive survey of spectrum of mutations in the OPA1 gene in patients with optic atrophy. UCL Discovery (University College London).1 indexed citations
13.
Thiselton, Dawn L., Christiane Alexander, Susan Sklower Brooks, et al.. (2001). OPA1 gene mutations cluster in functional protein domains in ADOA patients and reveal a founder allele in the Danish population.. UCL Discovery (University College London).1 indexed citations
Ponjavic, Vesna, Magnus Abrahamson, Sten Andréasson, et al.. (1997). A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267-Leu.. PubMed. 18(2). 63–70.11 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.