E. Schwinger
Impact in
- Neurology top 1%
- Parkinson's Disease Mechanisms and Treatments
- Neurological disorders and treatments
-
- Genetic Neurodegenerative Diseases
Papers in
-
- Mitochondrial Function and Pathology 16
- Genetics 69
- Genomic variations and chromosomal abnormalities 21
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 17
- Genetics and Neurodevelopmental Disorders 17
- Genetic Syndromes and Imprinting 12
- Co-authors
- Andreas Gal (22 shared papers)Christine Zühlke (19 shared papers)Christine Klein (18 shared papers)Yorck Hellenbroich (15 shared papers)Helga Rehder (13 shared papers)U. Froster‐Iskenius (12 shared papers)Katja Hedrich (14 shared papers)Susanna Bunge (10 shared papers)
- Journals
- Human Genetics (23 papers)European Journal of Human Genetics (9 papers)Prenatal Diagnosis (8 papers)Human Mutation (8 papers)Clinical Genetics (8 papers)
- Partner nations
- GermanyUnited StatesItaly
In The Last Decade
E. Schwinger
199 papers receiving 5.8k citations
Peers
Comparison fields: 5 of 119
- Neurology 934
- Cellular and Molecular Neuroscience 1.2k
- Genetics 1.8k
- Pediatrics, Perinatology and Child Health 681
- Physiology 938
Countries citing papers authored by E. Schwinger
This map shows the geographic impact of E. Schwinger'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 E. Schwinger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites E. Schwinger more than expected).
Fields of papers citing papers by E. Schwinger
This network shows the impact of papers produced by E. Schwinger. 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 E. Schwinger. The network helps show where E. Schwinger may publish in the future.
Co-authors
The 25 scholars most cited alongside E. Schwinger, 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 210 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2004 | 237 | |
| 2 | 2003 | 229 | |
| 3 | 2000 | 183 | |
| 4 | 1994 | 170 | |
| 5 | 2004 | 166 | |
| 6 | 2004 | 150 | |
| 7 | 1996 | 143 | |
| 8 | 2001 | 141 | |
| 9 | 2002 | 118 | |
| 10 | 2002 | 110 | |
| 11 | 1993 | 105 | |
| 12 | 2002 | 104 | |
| 13 | 2002 | 103 | |
| 14 | 2001 | 90 | |
| 15 | 1994 | 87 | |
| 16 | 2000 | 85 | |
| 17 | 2009 | 83 | |
| 18 | 1983 | 78 | |
| 19 | 1993 | 77 | |
| 20 | 2004 | 72 |
About E. Schwinger
E. Schwinger is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience and Physiology, having authored 210 papers that have together received 6.0k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (35 papers), Genetic Neurodegenerative Diseases (22 papers), Genomic variations and chromosomal abnormalities (21 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (17 papers), Genetics and Neurodevelopmental Disorders (17 papers), Mitochondrial Function and Pathology (16 papers), Genetic Syndromes and Imprinting (12 papers) and Chromosomal and Genetic Variations (12 papers). The work is most often cited by research in Neurology (934 citations), Cellular and Molecular Neuroscience (1.2k citations), Genetics (1.8k citations), Pediatrics, Perinatology and Child Health (681 citations) and Physiology (938 citations). E. Schwinger has collaborated with scholars based in Germany, United States and Italy. Frequent co-authors include Andreas Gal, Christine Zühlke, Christine Klein, Yorck Hellenbroich, Helga Rehder, U. Froster‐Iskenius, Katja Hedrich, Susanna Bunge, Joachim Müller–Quernheim and Peter P. Pramstaller. Their work appears in journals such as Human Genetics, European Journal of Human Genetics, Prenatal Diagnosis, Human Mutation 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.