Birgit Lorenz

1.0k citations
10 papers · 776 · 1 hit paper · h-index 7

Impact in

    • Retinal Diseases and Treatments
    • Ocular Oncology and Treatments
    • Retinal Development and Disorders
    • Retinoids in leukemia and cellular processes
    • CRISPR and Genetic Engineering
    • Mitochondrial Function and Pathology

Papers in

    • Retinal Development and Disorders 3
    • Mitochondrial Function and Pathology 2
    • Retinal Diseases and Treatments 2
    • Retinal and Optic Conditions 1

Birgit Lorenz

10 papers receiving 748 citations

Birgit Lorenz's Hit Papers

Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy 1997 · 545 citations
5450+9+19Years since publication100200300400500

Peers

Birgit Lorenz
Comparison fields: 5 of 62
  • Ophthalmology 296
  • Molecular Biology 588
  • Cellular and Molecular Neuroscience 127
  • Genetics 95
  • Sensory Systems 14
Replace Gaël Manès with:
Gaël Manès France
F. P. M. Cremers Netherlands
Caroline Thaung United Kingdom
Toshka A. Abrams United States
Sophie Châtelin France
Fatemeh Rajaii United States
Christelle Michiels France
Rajeshwari D. Koilkonda United States
Katherine L. Dry United Kingdom
Imad Ghazi France
Birgit Lorenz relative to Gaël Manès France Gaël Manès's profile →
Citations per field
00.5×1.5×2.1×
Gaël Manès · 1×
Citations per year

Countries citing papers authored by Birgit Lorenz

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authors

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.

Border = papers with Birgit Lorenz Line = papers co-authored together Birgit Lorenz links everyone, so they are left out of the graph.

All Works

10 of 10 papers shown
#Work
1
Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy
Hit paper breakdown →
1997545
2 1997113
3 200240
4 199231
5 201923
6 20049
7 19987
8 20255
9 20022
10 20251

About Birgit Lorenz

Birgit Lorenz is a scholar working on Molecular Biology, Ophthalmology, Pathology and Forensic Medicine, Surgery and Cellular and Molecular Neuroscience, having authored 10 papers that have together received 776 indexed citations. Recurring topics across this work include Retinal Development and Disorders (3 papers), Retinal Diseases and Treatments (2 papers), Mitochondrial Function and Pathology (2 papers), Ophthalmology and Eye Disorders (2 papers), Ophthalmology and Visual Impairment Studies (1 paper), Genomics and Rare Diseases (1 paper), Retinal and Optic Conditions (1 paper) and Amino Acid Enzymes and Metabolism (1 paper). The work is most often cited by research in Ophthalmology (296 citations), Molecular Biology (588 citations), Cellular and Molecular Neuroscience (127 citations), Genetics (95 citations) and Sensory Systems (14 citations). Birgit Lorenz has collaborated with scholars based in Germany, Switzerland and Brazil. Frequent co-authors include Andreas Gal, C.R. Srikumari, Michael J. Denton, Ulrich Finckh, Debra A. Thompson, K. R. Murthy, Sumin Gu, Govindasamy Kumaramanickavel, Dietmar Lohmann and Bernhard Horsthemke. Their work appears in journals such as Nature Genetics, The American Journal of Human Genetics, Human Heredity, Investigative Ophthalmology & Visual Science and Clinical 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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