Jacqueline Schoumans
- Genetics top 1%
- Molecular Biology top 10%
- Plant Science top 5%
- Pediatrics, Perinatology and Child Health top 2%
- Genetics top 5%
- Co-authors
- Elisabeth BlennowMagnus NordenskjöldBritt‐Marie AnderlidAnn NordgrenSigrid SahlénNicole de LeeuwJohan StaafGöran Annerén
- Topics
- Genomic variations and chromosomal abnormalities (42 papers)Genomics and Rare Diseases (13 papers)Genetics and Neurodevelopmental Disorders (13 papers)
- Journals
- Nature GeneticsThe Journal of Experimental MedicineSHILAP Revista de lepidopterología
- Partner nations
- SwedenSwitzerlandNetherlands
In The Last Decade
Jacqueline Schoumans
70 papers receiving 2.4k citations
Peers
Comparison fields: 5 of 96
- Genetics 1.6k
- Molecular Biology 1.2k
- Plant Science 458
- Pediatrics, Perinatology and Child Health 442
- Genetics 238
Countries citing papers authored by Jacqueline Schoumans
This map shows the geographic impact of Jacqueline Schoumans'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 Jacqueline Schoumans with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jacqueline Schoumans more than expected).
Fields of papers citing papers by Jacqueline Schoumans
This network shows the impact of papers produced by Jacqueline Schoumans. 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 Jacqueline Schoumans. The network helps show where Jacqueline Schoumans may publish in the future.
Co-authorship network of co-authors of Jacqueline Schoumans
This figure shows the co-authorship network connecting the top 25 collaborators of Jacqueline Schoumans. A scholar is included among the top collaborators of Jacqueline Schoumans 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 Jacqueline Schoumans. Jacqueline Schoumans 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 | 0 | |
| 3 | 1 | |
| 4 | 3 | |
| 5 | 7 | |
| 6 | 85 | |
| 7 | 14 | |
| 8 | 88 | |
| 9 | 29 | |
| 10 | 32 | |
| 11 | 52 | |
| 12 | 19 | |
| 13 | 10 | |
| 14 | 22 | |
| 15 | 305 | |
| 16 | 11 | |
| 17 | 3 | |
| 18 | 21 | |
| 19 | 89 | |
| 20 | 64 |
About Jacqueline Schoumans
Jacqueline Schoumans is a scholar working on Genetics, Hematology and Developmental Biology, having authored 73 papers that have together received 2.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (42 papers), Genomics and Rare Diseases (13 papers) and Genetics and Neurodevelopmental Disorders (13 papers). The work is most often cited by research in Genetics (1.6k citations), Pediatrics, Perinatology and Child Health (442 citations) and Genetics (238 citations). Jacqueline Schoumans has collaborated with scholars based in Sweden, Switzerland and Netherlands. Frequent co-authors include Elisabeth Blennow, Magnus Nordenskjöld, Britt‐Marie Anderlid, Ann Nordgren, Sigrid Sahlén, Nicole de Leeuw, Johan Staaf, Göran Annerén, Josephine Wincent and Britt-Marie Anderlid. Their work appears in journals such as Nature Genetics, The Journal of Experimental Medicine and SHILAP Revista de lepidopterología.
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.