Sandra Jansen

3.9k citations
41 papers · 1.9k · h-index 23

Impact in

    • Retinal Diseases and Treatments
  • Genetics top 5%
    • Genetic and phenotypic traits in livestock
    • Genetic Mapping and Diversity in Plants and Animals

Papers in

    • Genomic variations and chromosomal abnormalities 9
    • Genomics and Rare Diseases 9
    • Genetic and phenotypic traits in livestock 6
    • Genetics and Neurodevelopmental Disorders 6
    • Genetic Mapping and Diversity in Plants and Animals 4
    • S100 Proteins and Annexins 5

Sandra Jansen

40 papers receiving 1.9k citations

Peers

Sandra Jansen
Comparison fields: 5 of 115
  • Ophthalmology 169
  • Genetics 484
  • Microbiology 104
  • Cell Biology 264
  • Cellular and Molecular Neuroscience 292
Replace James D. Eudy with:
James D. Eudy United States
Sally H. Cross United Kingdom
Thérèse M.F. Tuohy United States
Orly Goldstein United States
Nathalie Labrecque Canada
Rolph Pfundt Netherlands
Yvonne Boyd United Kingdom
Keiko Yamada Japan
H. Maisel United States
Dean Nižetić United Kingdom
Sandra Jansen relative to James D. Eudy United States James D. Eudy's profile →
Citations per field
00.5×5.8×
James D. Eudy · 1×
Citations per year

Countries citing papers authored by Sandra Jansen

Since Specialization
Citations

This map shows the geographic impact of Sandra Jansen'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 Sandra Jansen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sandra Jansen more than expected).

Fields of papers citing papers by Sandra Jansen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandra Jansen. 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 Sandra Jansen. The network helps show where Sandra Jansen may publish in the future.

Co-authors

The 25 scholars most cited alongside Sandra Jansen, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sandra Jansen Line = papers co-authored together Sandra Jansen links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 41 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2002387
2 2002301
3 2014176
4 2009144
5 201479
6 201275
7 201764
8 201558
9 201456
10 201354
11 201148
12 200946
13 201340
14 201140
15 201039
16 200037
17 201437
18 200237
19 201726
20 201625

About Sandra Jansen

Sandra Jansen is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Microbiology and Immunology, having authored 41 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genomics and Rare Diseases (9 papers), Genetic and phenotypic traits in livestock (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), S100 Proteins and Annexins (5 papers), Immune Response and Inflammation (5 papers), Antimicrobial Peptides and Activities (5 papers) and Genetic Mapping and Diversity in Plants and Animals (4 papers). The work is most often cited by research in Ophthalmology (169 citations), Genetics (484 citations), Microbiology (104 citations), Cell Biology (264 citations) and Cellular and Molecular Neuroscience (292 citations). Sandra Jansen has collaborated with scholars based in Germany, Netherlands and United States. Frequent co-authors include Mieke Dewerchin, Lieve Moons, Peter Carmeliet, Lars‐Ove Brandenburg, Thomas Pufe, Ruedi Fries, Hubert Pausch, Bart Hermans, Hans‐Peter Hammes and Patrìcia A. D'Amore. Their work appears in journals such as Journal of Clinical Investigation, BMC Genomics, Genetics in Medicine, PLoS Genetics and Nature Medicine.

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.

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