Laura Davis‐Keppen
- Molecular Biology
- Genetics
- Cellular and Molecular Neuroscience
- Pediatrics, Perinatology and Child Health
- Plant Science
- Co-authors
- Lior CohenMingyan FangMarco CappaXun XuLina Basel‐VanagaiteAntonella CelluzziBruno DallapiccolaAndrea Masotti
- Topics
- Metabolism and Genetic Disorders (6 papers)Genomics and Rare Diseases (2 papers)Folate and B Vitamins Research (2 papers)
- Partner nations
- United StatesFinlandNetherlands
In The Last Decade
Laura Davis‐Keppen
10 papers receiving 155 citations
Peers
Comparison fields: 5 of 41
- Molecular Biology 105
- Genetics 58
- Cellular and Molecular Neuroscience 32
- Pediatrics, Perinatology and Child Health 32
- Plant Science 32
Countries citing papers authored by Laura Davis‐Keppen
This map shows the geographic impact of Laura Davis‐Keppen'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 Laura Davis‐Keppen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laura Davis‐Keppen more than expected).
Fields of papers citing papers by Laura Davis‐Keppen
This network shows the impact of papers produced by Laura Davis‐Keppen. 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 Laura Davis‐Keppen. The network helps show where Laura Davis‐Keppen may publish in the future.
Co-authorship network of co-authors of Laura Davis‐Keppen
This figure shows the co-authorship network connecting the top 25 collaborators of Laura Davis‐Keppen. A scholar is included among the top collaborators of Laura Davis‐Keppen based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Laura Davis‐Keppen. Laura Davis‐Keppen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 7 | |
| 3 | 3 | |
| 4 | The State of Newborn Screening in South Dakota. | 1 |
| 5 | 0 | |
| 6 | 2 | |
| 7 | 4 | |
| 8 | 86 | |
| 9 | 4 | |
| 10 | Identification of a founder mutation for maple syrup urine disease in Hutterites. | 1 |
| 11 | 6 | |
| 12 | Molecular mapping of the Edwards syndrome phenotype to two noncontiguous regions on chromosome 18. | 41 |
About Laura Davis‐Keppen
Laura Davis‐Keppen is a scholar working on Clinical Biochemistry, Genetics and Pediatrics, Perinatology and Child Health, having authored 12 papers that have together received 155 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (6 papers), Genomics and Rare Diseases (2 papers) and Folate and B Vitamins Research (2 papers). The work is most often cited by research in Genetics (58 citations), Clinical Biochemistry (13 citations) and Cellular and Molecular Neuroscience (32 citations). Laura Davis‐Keppen has collaborated with scholars based in United States, Finland and Netherlands. Frequent co-authors include Lior Cohen, Mingyan Fang, Marco Cappa, Xun Xu, Lina Basel‐Vanagaite, Antonella Celluzzi, Bruno Dallapiccola, Andrea Masotti, Paolo Uva and Elisa Pisaneschi. Their work appears in journals such as PEDIATRICS, The American Journal of Human Genetics and Molecular Genetics and Metabolism.
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.