This map shows the geographic impact of Birgit Lorenz'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 Birgit Lorenz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Birgit Lorenz more than expected).
This network shows the impact of papers produced by Birgit Lorenz. 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 Birgit Lorenz. The network helps show where Birgit Lorenz may publish in the future.
Co-authorship network of co-authors of Birgit Lorenz
This figure shows the co-authorship network connecting the top 25 collaborators of Birgit Lorenz.
A scholar is included among the top collaborators of Birgit Lorenz 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 Birgit Lorenz. Birgit Lorenz is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Stieger, Knut & Birgit Lorenz. (2010). Gene therapy for vision loss -- recent developments.. PubMed. 10(54). 425–33.20 indexed citations
12.
Preising, Markus N., et al.. (2007). Genetische und klinische Heterogenität bei LCA-Patienten: Das Ende der Einheitlichkeit. Der Ophthalmologe. 104(6). 490–498.1 indexed citations
13.
Lorenz, Birgit, et al.. (2007). Functional Analysis of AIPL1 Mutations and Splice Variants. Investigative Ophthalmology & Visual Science. 48(13). 4667–4667.
14.
Friedburg, Christoph, et al.. (2006). Variation of Phenotype in Patients With Compound Heterozygous Mutations of RetGC1 Depending on the Affected Domains. Investigative Ophthalmology & Visual Science. 47(13). 5802–5802.2 indexed citations
15.
Wegscheider, Erika, Charlotte M. Poloschek, Markus N. Preising, & Birgit Lorenz. (2005). Fundus Autofluorescence in Carriers for Choroideremia. Investigative Ophthalmology & Visual Science. 46(13). 4088–4088.2 indexed citations
16.
Lorenz, Birgit, et al.. (2005). Alternative Splicing of LCA Gene AIPL1 Is Conserved in Mammals. Investigative Ophthalmology & Visual Science. 46(13). 3101–3101.
17.
Munier, Francis L., Béatrice E. Frueh, Philippe Othenin‐Girard, et al.. (2002). BIGH3 mutation spectrum in corneal dystrophies.. PubMed. 43(4). 949–54.178 indexed citations
18.
Lorenz, Birgit, et al.. (2002). Telemedicine in Acute ROP: A Multicenter Study Using a Digital Retinal Imaging System. Investigative Ophthalmology & Visual Science. 43(13). 1243–1243.1 indexed citations
19.
Thompson, Debra A., P Gyürüs, Eve L. Bingham, et al.. (2000). Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration.. PubMed. 41(13). 4293–9.214 indexed citations
20.
Lorenz, Birgit, P Gyürüs, Markus N. Preising, et al.. (2000). Early-onset severe rod-cone dystrophy in young children with RPE65 mutations.. PubMed. 41(9). 2735–42.158 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.