Mette Gilling
Impact in
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- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Hereditary Neurological Disorders
- Neuroscience and Neuropharmacology Research
Papers in
- Genetics 4
- Genomic variations and chromosomal abnormalities 4
- Genetics and Neurodevelopmental Disorders 3
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- Ion channel regulation and function 1
- Co-authors
- Karen Brøndum‐Nielsen (3 shared papers)Niels Tommerup (4 shared papers)Zeynep Tümer (4 shared papers)Vera M. Kalscheuer (3 shared papers)Esben Budtz–Jørgensen (2 shared papers)Reinhard Ullmann (3 shared papers)Rikke S. Møller (1 shared paper)Jakob Christensen (1 shared paper)
- Journals
- European Journal of Medical Genetics (1 paper)The American Journal of Human Genetics (1 paper)European Journal of Neurology (1 paper)Clinical Genetics (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- DenmarkGermanyUnited Kingdom
In The Last Decade
Mette Gilling
7 papers receiving 111 citations
Peers
Comparison fields: 5 of 32
- Genetics 66
- Cellular and Molecular Neuroscience 41
- Neurology 12
- Cognitive Neuroscience 22
- Molecular Biology 64
Countries citing papers authored by Mette Gilling
This map shows the geographic impact of Mette Gilling'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 Mette Gilling with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mette Gilling more than expected).
Fields of papers citing papers by Mette Gilling
This network shows the impact of papers produced by Mette Gilling. 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 Mette Gilling. The network helps show where Mette Gilling may publish in the future.
Co-authors
The 25 scholars most cited alongside Mette Gilling, 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 | 2013 | 40 | |
| 2 | 2006 | 30 | |
| 3 | 2011 | 25 | |
| 4 | 2008 | 14 | |
| 5 | 2011 | 7 | |
| 6 | 2017 | 7 | |
| 7 | Chromosomal Abnormalities and Putative Susceptibility Genes in Autism Spectrum Disorders | 2015 | 1 |
About Mette Gilling
Mette Gilling is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Pediatrics, Perinatology and Child Health and Neuropsychology and Physiological Psychology, having authored 7 papers that have together received 124 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Prenatal Screening and Diagnostics (2 papers), Cardiac electrophysiology and arrhythmias (1 paper), Ion channel regulation and function (1 paper), Hereditary Neurological Disorders (1 paper), Neurological diseases and metabolism (1 paper) and Autism Spectrum Disorder Research (1 paper). The work is most often cited by research in Genetics (66 citations), Cellular and Molecular Neuroscience (41 citations), Neurology (12 citations), Cognitive Neuroscience (22 citations) and Molecular Biology (64 citations). Mette Gilling has collaborated with scholars based in Denmark, Germany and United Kingdom. Frequent co-authors include Karen Brøndum‐Nielsen, Niels Tommerup, Zeynep Tümer, Vera M. Kalscheuer, Esben Budtz–Jørgensen, Reinhard Ullmann, Rikke S. Møller, Jakob Christensen, Susanne E. Boonen and Jørgen E. Nielsen. Their work appears in journals such as European Journal of Medical Genetics, The American Journal of Human Genetics, European Journal of Neurology, Clinical Genetics and European Journal of Human 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.