Sandra Jansen

3.9k total citations
41 papers, 1.9k citations indexed

About

Sandra Jansen is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Sandra Jansen has authored 41 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 16 papers in Molecular Biology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Sandra Jansen's work include Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (9 papers) and Genetic and phenotypic traits in livestock (6 papers). Sandra Jansen is often cited by papers focused on Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (9 papers) and Genetic and phenotypic traits in livestock (6 papers). Sandra Jansen collaborates with scholars based in Germany, Netherlands and United States. Sandra Jansen's co-authors include Peter Carmeliet, Lieve Moons, Mieke Dewerchin, Lars‐Ove Brandenburg, Thomas Pufe, Ruedi Fries, Hubert Pausch, Yin‐Shan Ng, Désiré Collen and Dan Hicklin and has published in prestigious journals such as Circulation, Journal of Clinical Investigation and Nature Medicine.

In The Last Decade

Sandra Jansen

40 papers receiving 1.9k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Sandra Jansen Germany 23 1.1k 484 292 264 233 41 1.9k
James D. Eudy United States 24 1.2k 1.1× 302 0.6× 165 0.6× 188 0.7× 223 1.0× 46 2.1k
Sally H. Cross United Kingdom 26 2.3k 2.1× 844 1.7× 102 0.3× 203 0.8× 128 0.5× 49 3.0k
David M. Alvarado United States 27 997 0.9× 422 0.9× 317 1.1× 262 1.0× 186 0.8× 55 2.4k
Yvonne Boyd United Kingdom 28 1.8k 1.7× 1.0k 2.1× 178 0.6× 210 0.8× 127 0.5× 84 3.1k
Tushar Bhangale United States 20 1.0k 1.0× 647 1.3× 221 0.8× 160 0.6× 150 0.6× 30 2.6k
Orly Goldstein United States 21 1.1k 1.0× 446 0.9× 145 0.5× 148 0.6× 163 0.7× 60 1.6k
Thérèse M.F. Tuohy United States 22 2.0k 1.9× 542 1.1× 245 0.8× 221 0.8× 353 1.5× 41 3.8k
Dean Nižetić United Kingdom 35 1.8k 1.7× 977 2.0× 107 0.4× 264 1.0× 227 1.0× 92 3.5k
Yumi Sato Japan 24 1.2k 1.1× 673 1.4× 340 1.2× 235 0.9× 94 0.4× 104 2.4k
Pascale Giraudon France 28 536 0.5× 280 0.6× 352 1.2× 82 0.3× 135 0.6× 67 2.1k

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-authorship network of co-authors of Sandra Jansen

This figure shows the co-authorship network connecting the top 25 collaborators of Sandra Jansen. A scholar is included among the top collaborators of Sandra Jansen 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 Sandra Jansen. Sandra Jansen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Dingemans, Alexander J.M., Sandra Jansen, Jeroen van Reeuwijk, et al.. (2024). Prevalence of comorbidities in individuals with neurodevelopmental disorders from the aggregated phenomics data of 51,227 pediatric individuals. Nature Medicine. 30(7). 1994–2003. 4 indexed citations
2.
Kellner, Ulrich, Sandra Jansen, Franziska Bucher, & Katarína Štingl. (2022). Diagnostik erblicher Netzhautdystrophien. Stellenwert molekulargenetischer Diagnostik aus Patientenperspektive. Die Ophthalmologie. 119(8). 820–826. 5 indexed citations
3.
Carvill, Gemma L., Sandra Jansen, Amy Lacroix, et al.. (2021). Genetic convergence of developmental and epileptic encephalopathies and intellectual disability. Developmental Medicine & Child Neurology. 63(12). 1441–1447. 4 indexed citations
4.
Dingemans, Alexander J.M., Max Hinne, Sandra Jansen, et al.. (2021). Phenotype based prediction of exome sequencing outcome using machine learning for neurodevelopmental disorders. Genetics in Medicine. 24(3). 645–653. 7 indexed citations
5.
Jansen, Sandra, Janneke Schuurs-Hoeijmakers, David A. Koolen, et al.. (2018). Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disorders. Genetics in Medicine. 21(8). 1719–1725. 13 indexed citations
6.
Jansen, Sandra, Eugenia Kress, Athanassios Fragoulis, et al.. (2017). Psoriasin has divergent effects on the innate immune responses of murine glial cells. Journal of Neurochemistry. 141(1). 86–99. 5 indexed citations
7.
Lamers, Ideke J.C., Margot R.F. Reijnders, Hanka Venselaar, et al.. (2017). Recurrent De Novo Mutations Disturbing the GTP/GDP Binding Pocket of RAB11B Cause Intellectual Disability and a Distinctive Brain Phenotype. The American Journal of Human Genetics. 101(5). 824–832. 26 indexed citations
8.
Pausch, Hubert, Hermann Schwarzenbacher, Johann Burgstaller, et al.. (2015). Homozygous haplotype deficiency reveals deleterious mutations compromising reproductive and rearing success in cattle. BMC Genomics. 16(1). 312–312. 58 indexed citations
9.
Segelke, Dierck, Helge Täubert, Sandra Jansen, et al.. (2014). Management of Genetic Characteristics. Bulletin - International Bull Evaluation Service/Interbull bulletin. 85–88. 3 indexed citations
10.
Jansen, Sandra, Bernhard Aigner, Hubert Pausch, et al.. (2013). Assessment of the genomic variation in a cattle population by re-sequencing of key animals at low to medium coverage. BMC Genomics. 14(1). 446–446. 54 indexed citations
11.
Kress, Eugenia, Oliver Soehnlein, Sandra Jansen, et al.. (2013). Role of the Cathelicidin-Related Antimicrobial Peptide in Inflammation and Mortality in a Mouse Model of Bacterial Meningitis. Journal of Innate Immunity. 6(2). 205–218. 40 indexed citations
12.
Brandenburg, Lars‐Ove, Sandra Jansen, Christoph Jan Wruck, Ralph Lucius, & Thomas Pufe. (2010). Antimicrobial peptide rCRAMP induced glial cell activation through P2Y receptor signalling pathways. Molecular Immunology. 47(10). 1905–1913. 39 indexed citations
13.
Hellings, Peter W., et al.. (2009). Less inflammatory cell infiltration in the sub-epithelium with fluticasone furoate nasal spray as compared to mometasone furoate nasal spray. Allergy. 64. 69–70. 1 indexed citations
14.
Zacchigna, Serena, Hideyasu Oh, Michaela Wilsch‐Bräuninger, et al.. (2009). Loss of the Cholesterol-Binding Protein Prominin-1/CD133 Causes Disk Dysmorphogenesis and Photoreceptor Degeneration. Journal of Neuroscience. 29(7). 2297–2308. 144 indexed citations
15.
Tjwa, Marc, Nicolai Sidénius, Rute Moura, et al.. (2009). Membrane-anchored uPAR regulates the proliferation, marrow pool size, engraftment, and mobilization of mouse hematopoietic stem/progenitor cells. Journal of Clinical Investigation. 119(4). 1008–18. 46 indexed citations
16.
Tjwa, Marc, Rute Moura, Lieve Moons, et al.. (2008). Fibrinolysis‐independent role of plasmin and its activators in the haematopoietic recovery after myeloablation. Journal of Cellular and Molecular Medicine. 13(11-12). 4587–4595. 22 indexed citations
17.
Tjwa, Marc, Mieke Dewerchin, Sandra Jansen, et al.. (2007). Abstract 330: Mobilization Of Bone Marrow Progenitors By Ischemic Tissues Requires An Interplay Between Hematopoietic Cytokines And Placental Growth Factor (plgf). Circulation. 116(16). 48–48. 1 indexed citations
18.
Stalmans, Ingeborg, Yin‐Shan Ng, Richard M. Rohan, et al.. (2002). Arteriolar and venular patterning in retinas of mice selectively expressing VEGF isoforms. Journal of Clinical Investigation. 109(3). 327–336. 301 indexed citations
19.
Himmelmann, Andreas, et al.. (2000). [Frequency of HFE gene mutations and genotype-phenotype correlations in patients with hereditary hemochromatosis in Switzerland].. PubMed. 130(31-32). 1112–9. 2 indexed citations
20.
Bruin, Natasja de, E.L.J.M. van Luijtelaar, Sandra Jansen, A.R. Cools, & Bart Ellenbroek. (2000). Dopamine characteristics in different rat genotypes: the relation to absence epilepsy. Neuroscience Research. 38(2). 165–173. 37 indexed citations

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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