Birgit Lorenz
- Ophthalmology top 1%
- Retinal Diseases and Treatments 3
- Retinal and Optic Conditions 1
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- Retinal Development and Disorders 3
- Mitochondrial Function and Pathology 3
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- Genomics and Rare Diseases 1
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- Ophthalmology and Eye Disorders 2
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- Amino Acid Enzymes and Metabolism 1
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- interferon and immune responses 1
- Co-authors
- C.R. SrikumariGovindasamy KumaramanickavelSumin GuAndreas GalDebra A. ThompsonMichael J. DentonK. R. MurthyUlrich Finckh
- Journals
- The American Journal of Human Genetics (1 paper)Nature Genetics (1 paper)Clinical Genetics (1 paper)
- Partner nations
- GermanyFinlandNew Zealand
In The Last Decade
Birgit Lorenz
10 papers receiving 710 citations
Hit Papers
Peers
Comparison fields: 5 of 64
- Ophthalmology 383
- Molecular Biology 588
- Cellular and Molecular Neuroscience 148
- Cell Biology 65
- Genetics 105
Countries citing papers authored by Birgit Lorenz
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).
Fields of papers citing papers by Birgit Lorenz
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
The 25 scholars most cited alongside Birgit Lorenz, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 1 | |
| 2 | 2025 | 1 | |
| 3 | 2019 | 20 | |
| 4 | 2004 | 8 | |
| 5 | 2002 | 38 | |
| 6 | 2002 | 2 | |
| 7 | 1998 | 7 | |
| 8 | 1997 | 109 | |
| 9 | Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophybreakdown → | 1997 | 504 |
| 10 | 1992 | 30 |
About Birgit Lorenz
Birgit Lorenz is a scholar working on Ophthalmology, Biochemistry, Pathology and Forensic Medicine, Molecular Biology and Neurology, having authored 10 papers that have together received 720 indexed citations. Recurring topics across this work include Retinal Development and Disorders (3 papers), Mitochondrial Function and Pathology (3 papers), Retinal Diseases and Treatments (3 papers), Ophthalmology and Eye Disorders (2 papers), Amino Acid Enzymes and Metabolism (1 paper), Genomics and Rare Diseases (1 paper), Retinal and Optic Conditions (1 paper) and interferon and immune responses (1 paper). The work is most often cited by research in Ophthalmology (383 citations), Molecular Biology (588 citations), Cellular and Molecular Neuroscience (148 citations), Cell Biology (65 citations) and Genetics (105 citations). Birgit Lorenz has collaborated with scholars based in Germany, Finland and New Zealand. Frequent co-authors include C.R. Srikumari, Govindasamy Kumaramanickavel, Sumin Gu, Andreas Gal, Debra A. Thompson, Michael J. Denton, K. R. Murthy, Ulrich Finckh, Eberhard Passarge and Dietmar Lohmann. Their work appears in journals such as The American Journal of Human Genetics, Nature Genetics, Clinical Genetics, Investigative Ophthalmology & Visual Science and Human Heredity.
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.