Cathy Obringer
Impact in
- Genetics top 10%
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
-
- DNA Repair Mechanisms
- Hedgehog Signaling Pathway Studies
- Retinal Development and Disorders
- CRISPR and Genetic Engineering
Papers in
-
- DNA Repair Mechanisms 10
- CRISPR and Genetic Engineering 4
- Epigenetics and DNA Methylation 2
- Genetics 13
- Genetic and Kidney Cyst Diseases 7
- Genetic Syndromes and Imprinting 5
- Genetics and Neurodevelopmental Disorders 3
- Co-authors
- Vincent Marion (10 shared papers)Hélène Dollfus (10 shared papers)Corinne Stoetzel (6 shared papers)Nadège Calmels (12 shared papers)Vincent Laugel (12 shared papers)M. Durand (4 shared papers)Nadia Messaddeq (4 shared papers)Nikolai Petrovsky (2 shared papers)
- Journals
- European Journal of Medical Genetics (2 papers)Orphanet Journal of Rare Diseases (2 papers)Clinical Genetics (2 papers)Diabetes (2 papers)Experimental Eye Research (1 paper)
- Partner nations
- FranceUnited KingdomGermany
In The Last Decade
Cathy Obringer
22 papers receiving 411 citations
Peers
Comparison fields: 5 of 48
- Genetics 236
- Molecular Biology 275
- Cell Biology 51
- Ophthalmology 17
- Cellular and Molecular Neuroscience 27
Countries citing papers authored by Cathy Obringer
This map shows the geographic impact of Cathy Obringer'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 Cathy Obringer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Cathy Obringer more than expected).
Fields of papers citing papers by Cathy Obringer
This network shows the impact of papers produced by Cathy Obringer. 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 Cathy Obringer. The network helps show where Cathy Obringer may publish in the future.
Co-authors
The 25 scholars most cited alongside Cathy Obringer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 71 | |
| 2 | 2015 | 51 | |
| 3 | 2018 | 50 | |
| 4 | 2012 | 41 | |
| 5 | 2013 | 30 | |
| 6 | 2015 | 25 | |
| 7 | 2020 | 24 | |
| 8 | 2021 | 16 | |
| 9 | 2020 | 16 | |
| 10 | 2021 | 13 | |
| 11 | 2020 | 11 | |
| 12 | 2022 | 8 | |
| 13 | 2020 | 8 | |
| 14 | 2019 | 7 | |
| 15 | 2022 | 7 | |
| 16 | 2021 | 7 | |
| 17 | 2018 | 7 | |
| 18 | 2021 | 6 | |
| 19 | 2019 | 6 | |
| 20 | 2020 | 5 |
About Cathy Obringer
Cathy Obringer is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Pediatrics, Perinatology and Child Health and Cell Biology, having authored 22 papers that have together received 412 indexed citations. Recurring topics across this work include DNA Repair Mechanisms (10 papers), Genetic and Kidney Cyst Diseases (7 papers), Genetic Syndromes and Imprinting (5 papers), CRISPR and Genetic Engineering (4 papers), Biomedical Research and Pathophysiology (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Epigenetics and DNA Methylation (2 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Genetics (236 citations), Molecular Biology (275 citations), Cell Biology (51 citations), Ophthalmology (17 citations) and Cellular and Molecular Neuroscience (27 citations). Cathy Obringer has collaborated with scholars based in France, United Kingdom and Germany. Frequent co-authors include Vincent Marion, Hélène Dollfus, Corinne Stoetzel, Nadège Calmels, Vincent Laugel, M. Durand, Nadia Messaddeq, Nikolai Petrovsky, Wouter H. Lamers and Jean‐Philippe Loeffler. Their work appears in journals such as European Journal of Medical Genetics, Orphanet Journal of Rare Diseases, Clinical Genetics, Diabetes and Experimental Eye Research.
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.