M. Durner
Impact in
- Psychiatry and Mental health top 5%
- Epilepsy research and treatment
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 9
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 2
- Genetic Associations and Epidemiology 2
- Diabetes and associated disorders 1
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- Glycogen Storage Diseases and Myoclonus 3
- Folate and B Vitamins Research 1
- Co-authors
- Diéter Janz (4 shared papers)David A. Greenberg (5 shared papers)G. Beck‐Mannagetta (2 shared papers)Antonio V. Delgado‐Escueta (2 shared papers)Keith Johnson (1 shared paper)T. Sander (1 shared paper)M. Anne Spence (1 shared paper)Karen Weissbecker (1 shared paper)
- Journals
- Neurology (2 papers)Epilepsia (1 paper)Genetic Epidemiology (1 paper)American Journal of Medical Genetics (1 paper)PubMed (4 papers)
- Partner nations
- United StatesGermanyCanada
In The Last Decade
M. Durner
9 papers receiving 542 citations
Peers
Comparison fields: 5 of 46
- Psychiatry and Mental health 305
- Genetics 287
- Rheumatology 93
- Cellular and Molecular Neuroscience 119
- Clinical Biochemistry 33
Countries citing papers authored by M. Durner
This map shows the geographic impact of M. Durner'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 M. Durner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Durner more than expected).
Fields of papers citing papers by M. Durner
This network shows the impact of papers produced by M. Durner. 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 M. Durner. The network helps show where M. Durner may publish in the future.
Co-authors
The 16 scholars most cited alongside M. Durner, 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 | 1991 | 156 | |
| 2 | 1991 | 130 | |
| 3 | 1989 | 66 | |
| 4 | Evidence for multiple gene loci in the expression of the common generalized epilepsies. | 1992 | 61 |
| 5 | Inter- and intrafamilial heterogeneity: effective sampling strategies and comparison of analysis methods. | 1992 | 51 |
| 6 | 1995 | 48 | |
| 7 | 1992 | 27 | |
| 8 | Is there a genetic relationship between epilepsy and birth defects? | 1992 | 16 |
| 9 | 2001 | 2 |
About M. Durner
M. Durner is a scholar working on Genetics, Rheumatology, Psychiatry and Mental health, Surgery and Molecular Biology, having authored 9 papers that have together received 557 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Epilepsy research and treatment (4 papers), Glycogen Storage Diseases and Myoclonus (3 papers), Genomics and Rare Diseases (2 papers), Genetic Associations and Epidemiology (2 papers), Folate and B Vitamins Research (1 paper), Neurological disorders and treatments (1 paper) and Diabetes and associated disorders (1 paper). The work is most often cited by research in Psychiatry and Mental health (305 citations), Genetics (287 citations), Rheumatology (93 citations), Cellular and Molecular Neuroscience (119 citations) and Clinical Biochemistry (33 citations). M. Durner has collaborated with scholars based in United States, Germany and Canada. Frequent co-authors include Diéter Janz, David A. Greenberg, G. Beck‐Mannagetta, Antonio V. Delgado‐Escueta, Keith Johnson, T. Sander, M. Anne Spence, Karen Weissbecker, R S Sparkes and A. Scaramelli. Their work appears in journals such as Neurology, Epilepsia, Genetic Epidemiology, American Journal of Medical Genetics and PubMed.
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.