Ulrike Orth

2.5k citations
38 papers · 1.7k indexed · 1 hit paper · h-index 18
Topics
Retinal Development and Disorders (8 papers)Neurological diseases and metabolism (5 papers)Hereditary Neurological Disorders (5 papers)

In The Last Decade

Ulrike Orth

38 papers receiving 1.7k citations

Hit Papers

Mutations in MERTK, the human orthologue of the RCS rat r...20002026200820172000100200300400500

Peers

Ulrike Orth
Comparison fields: 5 of 85
  • Molecular Biology 1.2k
  • Cellular and Molecular Neuroscience 453
  • Genetics 446
  • Ophthalmology 313
  • Cell Biology 233
Replace Arnold Munnich with:
Arnold Munnich France
Neena B. Haider United States
Marion A. Maw New Zealand
John Neidhardt Germany
Zhengmao Hu China
Arpad Palfi Ireland
M. M. LaVail United States
Jacqueline L. Vanderluit Canada
Pete Humphries Ireland
Minzhong Yu United States
Ulrike Orth relative to Arnold Munnich France Arnold Munnich's profile →
Citations per field
00.5×1.5×
Arnold Munnich · 1×
Citations per year

Countries citing papers authored by Ulrike Orth

Since Specialization
Citations

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

Fields of papers citing papers by Ulrike Orth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ulrike Orth

This figure shows the co-authorship network connecting the top 25 collaborators of Ulrike Orth. A scholar is included among the top collaborators of Ulrike Orth 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 Ulrike Orth. Ulrike Orth 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
#WorkIndexed citations
1 7
2 29
3 81
4 10
5
Analysis of the frizzled–4 gene in patients with autosomal dominant exudative vitreoretinopathy (FEVR) suggests a mutation hot spot and a high penetrance of the mutated allele.
1
6 8
7 7
8
Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosabreakdown →
539
9 289
10 13
11 3
12 18
13 3
14 7
15 18
16 34
17 7
18 1
19 35
20 167

About Ulrike Orth

Ulrike Orth is a scholar working on Neurology, Cellular and Molecular Neuroscience and Ophthalmology, having authored 38 papers that have together received 1.7k indexed citations. Recurring topics across this work include Retinal Development and Disorders (8 papers), Neurological diseases and metabolism (5 papers) and Hereditary Neurological Disorders (5 papers). The work is most often cited by research in Ophthalmology (313 citations), Cellular and Molecular Neuroscience (453 citations) and Molecular Biology (1.2k citations). Ulrike Orth has collaborated with scholars based in Germany, United States and Netherlands. Frequent co-authors include Andreas Gal, Eckart Apfelstedt-Sylla, Yun Li, Debra A. Thompson, Samuel G. Jacobson, Douglas Vollrath, E. Schwinger, Kerstin Kutsche, Thomas Rosenberg and Wolfgang Baehr. Their work appears in journals such as Nature Genetics, Neuroscience and The American Journal of Human Genetics.

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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