Ruth Riise

2.0k total citations
44 papers, 1.3k citations indexed

About

Ruth Riise is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Ruth Riise has authored 44 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 16 papers in Molecular Biology and 11 papers in Epidemiology. Recurrent topics in Ruth Riise's work include Genetic and Kidney Cyst Diseases (14 papers), Ophthalmology and Visual Impairment Studies (10 papers) and Genetic Syndromes and Imprinting (8 papers). Ruth Riise is often cited by papers focused on Genetic and Kidney Cyst Diseases (14 papers), Ophthalmology and Visual Impairment Studies (10 papers) and Genetic Syndromes and Imprinting (8 papers). Ruth Riise collaborates with scholars based in Norway, Sweden and Denmark. Ruth Riise's co-authors include Kristina Törnqvist, Thomas Rosenberg, Uri T. Eden, Esben Søvsø Szocska Hansen, T Flage, Sirkka‐Liisa Rudanko, Karen Brøndum‐Nielsen, Kari Storhaug, Sten Andréasson and Val C. Sheffield and has published in prestigious journals such as Nature Genetics, Human Molecular Genetics and Investigative Ophthalmology & Visual Science.

In The Last Decade

Ruth Riise

43 papers receiving 1.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Ruth Riise Norway	19	694	609	373	281	216	44	1.3k
Sachiko Nishina Japan	20	533 0.8×	230 0.4×	455 1.2×	481 1.7×	100 0.5×	82	1.2k
I Russell‐Eggitt United Kingdom	21	531 0.8×	194 0.3×	228 0.6×	563 2.0×	221 1.0×	38	1.2k
J.W. Delleman Netherlands	17	360 0.5×	275 0.5×	142 0.4×	196 0.7×	81 0.4×	45	872
Barbara Käsmann‐Kellner Germany	20	417 0.6×	105 0.2×	455 1.2×	452 1.6×	82 0.4×	100	1.3k
Victor Godel Israel	15	210 0.3×	174 0.3×	160 0.4×	322 1.1×	62 0.3×	64	738
Emin Cumhur Şener Türkiye	15	395 0.6×	184 0.3×	94 0.3×	289 1.0×	175 0.8×	38	1.0k
Keith Bradshaw United Kingdom	15	580 0.8×	89 0.1×	159 0.4×	376 1.3×	44 0.2×	26	728
Roberta La Piana Canada	19	475 0.7×	93 0.2×	124 0.3×	57 0.2×	213 1.0×	62	1.1k
Oliver Puk Germany	17	404 0.6×	158 0.3×	127 0.3×	186 0.7×	32 0.1×	30	681
Mary Z. Pelias United States	17	536 0.8×	238 0.4×	37 0.1×	54 0.2×	32 0.1×	35	1.1k

Countries citing papers authored by Ruth Riise

Since Specialization

Citations

This map shows the geographic impact of Ruth Riise'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 Ruth Riise with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ruth Riise more than expected).

Fields of papers citing papers by Ruth Riise

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ruth Riise. 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 Ruth Riise. The network helps show where Ruth Riise may publish in the future.

Co-authorship network of co-authors of Ruth Riise

This figure shows the co-authorship network connecting the top 25 collaborators of Ruth Riise. A scholar is included among the top collaborators of Ruth Riise 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 Ruth Riise. Ruth Riise is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Lagali, Neil, Uri T. Eden, Tor Paaske Utheim, et al.. (2013). In Vivo Morphology of the Limbal Palisades of Vogt Correlates With Progressive Stem Cell Deficiency in Aniridia-Related Keratopathy. Investigative Ophthalmology & Visual Science. 54(8). 5333–5333. 83 indexed citations

Hjortshøj, Tina Duelund, Karen Grønskov, Alisdair R. Philp, et al.. (2010). Bardet-Biedl syndrome in Denmark-report of 13 novel sequence variations in six genes. Human Mutation. 31(4). 429–436. 60 indexed citations

Selmer, Kaja Kristine, et al.. (2009). Autosomal dominant pericentral retinal dystrophy caused by a novel missense mutation in the TOPORS gene. Acta Ophthalmologica. 88(3). 323–328. 15 indexed citations

Coccia, Margherita, Simon P. Brooks, Tom R. Webb, et al.. (2009). X-linked cataract and Nance-Horan syndrome are allelic disorders. Human Molecular Genetics. 18(14). 2643–2655. 50 indexed citations

Eden, Uri T., et al.. (2008). Aniridia among children and teenagers in Sweden and Norway. Acta Ophthalmologica. 86(7). 730–734. 27 indexed citations

Riise, Ruth, et al.. (2005). [Visual problems in cerebral stroke].. PubMed. 125(2). 176–7. 5 indexed citations

Haugen, Olav H., Gunnar Høvding, & Ruth Riise. (2004). Øyeforandringer ved Downs syndrom. Tidsskrift for Den Norske Laegeforening. 2 indexed citations

Riise, Ruth. (2002). The Phenotype in Norwegian Patients With Bardet-Biedl Syndrome With Mutations in the BBS4 Gene. Archives of Ophthalmology. 120(10). 1364–1364. 28 indexed citations

Riise, Ruth, Kari Storhaug, & Karen Brøndum‐Nielsen. (2001). Rieger syndrome is associated with PAX6 deletion. Acta Ophthalmologica Scandinavica. 79(2). 201–203. 58 indexed citations

10.

Riise, Ruth. (1998). Laurence-Moon-Bardet-Biedl syndrome. Clinical, electrophysiological and genetic aspects.. PubMed. 1–28. 12 indexed citations

11.

Riise, Ruth, Sten Andréasson, Alan F. Wright, et al.. (1997). Intrafamilial variation of the phenotype in Bardet-Biedl syndrome. British Journal of Ophthalmology. 81(5). 378–385. 53 indexed citations

12.

Riise, Ruth, et al.. (1996). Anomalies in the permanent dentition and other oral findings in 29 individuals with Laurence‐Moon‐Bardet‐Biedl syndrome. Journal of Oral Pathology and Medicine. 25(2). 86–89. 22 indexed citations

13.

Riise, Ruth. (1996). The cause of death in Laurence‐Moon‐Bardet‐Biedl syndrome. Acta Ophthalmologica Scandinavica. 74(S219). 45–47. 14 indexed citations

14.

Riise, Ruth, et al.. (1993). Visual impairment due to retinopathy of prematurity in Nordic children. Acta Ophthalmologica. 71(S210). 9–11. 10 indexed citations

15.

Fannemel, Madeleine, et al.. (1993). High‐resolution chromosome analysis in autosomal recessive disorders: Laurence‐Moon‐Bardet‐Biedl syndrome. Clinical Genetics. 43(2). 111–112. 3 indexed citations

16.

Flage, T, et al.. (1993). Visual impairment in Nordic children. Acta Ophthalmologica. 71(5). 586–589. 9 indexed citations

17.

Riise, Ruth, T Flage, Esben Søvsø Szocska Hansen, et al.. (1992). Visual impairment in Nordic children. Acta Ophthalmologica. 70(2). 145–154. 71 indexed citations

18.

Riise, Ruth, et al.. (1990). [Laurence-Moon-Bardet-Biedl syndrome].. PubMed. 105(5). 146–8. 13 indexed citations

19.

Riise, Ruth. (1987). Visual Function in Laurence‐Moon‐Bardet‐Biedl Syndrome A Survey of 26 Cases. Acta Ophthalmologica. 65(S182). 128–131. 18 indexed citations

20.

Riise, Ruth. (1986). [Visual function in Down's syndrome].. PubMed. 106(4). 317–9. 6 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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