M. Leipoldt
- Molecular Biology
- Genetics top 5%
- Plant Science
- Pediatrics, Perinatology and Child Health top 10%
- Cell Biology
- Co-authors
- Wolfgang EngelJudith FischerW. SchemppJörg SchmidtkeJörg T. EpplenWiktor BorozdinJürgen KohlhaseFranz P.W. Radner
- Topics
- Chromosomal and Genetic Variations (11 papers)Genomic variations and chromosomal abnormalities (7 papers)Prenatal Screening and Diagnostics (6 papers)
- Partner nations
- GermanyUnited StatesFrance
In The Last Decade
M. Leipoldt
29 papers receiving 662 citations
Peers
Comparison fields: 5 of 70
- Molecular Biology 445
- Genetics 369
- Plant Science 137
- Pediatrics, Perinatology and Child Health 93
- Cell Biology 79
Countries citing papers authored by M. Leipoldt
This map shows the geographic impact of M. Leipoldt'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. Leipoldt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Leipoldt more than expected).
Fields of papers citing papers by M. Leipoldt
This network shows the impact of papers produced by M. Leipoldt. 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. Leipoldt. The network helps show where M. Leipoldt may publish in the future.
Co-authorship network of co-authors of M. Leipoldt
This figure shows the co-authorship network connecting the top 25 collaborators of M. Leipoldt. A scholar is included among the top collaborators of M. Leipoldt 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 M. Leipoldt. M. Leipoldt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 5 | |
| 2 | 28 | |
| 3 | 37 | |
| 4 | 2 | |
| 5 | 11 | |
| 6 | 42 | |
| 7 | 82 | |
| 8 | 23 | |
| 9 | 38 | |
| 10 | 29 | |
| 11 | 29 | |
| 12 | 22 | |
| 13 | 11 | |
| 14 | 10 | |
| 15 | 7 | |
| 16 | 1 | |
| 17 | 4 | |
| 18 | 29 | |
| 19 | 0 | |
| 20 | 13 |
About M. Leipoldt
M. Leipoldt is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science, having authored 30 papers that have together received 703 indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (11 papers), Genomic variations and chromosomal abnormalities (7 papers) and Prenatal Screening and Diagnostics (6 papers). The work is most often cited by research in Genetics (369 citations), Developmental Biology (28 citations) and Molecular Biology (445 citations). M. Leipoldt has collaborated with scholars based in Germany, United States and France. Frequent co-authors include Wolfgang Engel, Judith Fischer, W. Schempp, Jörg Schmidtke, Jörg T. Epplen, Wiktor Borozdin, Jürgen Kohlhase, Franz P.W. Radner, Slaheddine Marrakchi and Leïla Abid. Their work appears in journals such as Kidney International, Conservation Biology and PLoS 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.