Iris E. Jansen

17.5k total citations
29 papers, 592 citations indexed

About

Iris E. Jansen is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Iris E. Jansen has authored 29 papers receiving a total of 592 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 11 papers in Physiology and 9 papers in Genetics. Recurrent topics in Iris E. Jansen's work include Genetic Associations and Epidemiology (8 papers), Alzheimer's disease research and treatments (8 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). Iris E. Jansen is often cited by papers focused on Genetic Associations and Epidemiology (8 papers), Alzheimer's disease research and treatments (8 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). Iris E. Jansen collaborates with scholars based in Netherlands, Germany and United States. Iris E. Jansen's co-authors include Peter Heutink, Philip Scheltens, Wiesje M. van der Flier, Sven J. van der Lee, Ganqiang Liu, Alexis Brice, Joseph J. Locascio, Sophie Winder‐Rhodes, Bernard Ravina and Florence Cormier‐Dequaire and has published in prestigious journals such as Neurology, Diabetes and Annals of Neurology.

In The Last Decade

Iris E. Jansen

25 papers receiving 588 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Iris E. Jansen Netherlands 14 310 255 170 119 93 29 592
Maryam Shoai United Kingdom 16 395 1.3× 268 1.1× 305 1.8× 243 2.0× 193 2.1× 28 891
Lee Marshall United States 10 167 0.5× 154 0.6× 330 1.9× 95 0.8× 71 0.8× 15 580
Sumitra Chakraverty United States 9 359 1.2× 254 1.0× 273 1.6× 130 1.1× 117 1.3× 13 693
Martin Medrano United States 15 394 1.3× 92 0.4× 251 1.5× 183 1.5× 69 0.7× 23 690
Raffaele Ferrari United Kingdom 14 427 1.4× 660 2.6× 312 1.8× 82 0.7× 253 2.7× 21 980
Toni S. Pearson United States 15 213 0.7× 158 0.6× 303 1.8× 182 1.5× 56 0.6× 39 909
Kiyohiro Yamazaki Japan 16 246 0.8× 86 0.3× 282 1.7× 97 0.8× 160 1.7× 43 693
Priya Gami‐Patel Netherlands 13 224 0.7× 198 0.8× 204 1.2× 45 0.4× 50 0.5× 18 501
Nancy Monroy‐Jaramillo Mexico 15 109 0.4× 76 0.3× 225 1.3× 78 0.7× 39 0.4× 43 577
Lieke Meeter Netherlands 14 397 1.3× 431 1.7× 201 1.2× 32 0.3× 153 1.6× 25 780

Countries citing papers authored by Iris E. Jansen

Since Specialization
Citations

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

Fields of papers citing papers by Iris E. Jansen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Iris E. Jansen

This figure shows the co-authorship network connecting the top 25 collaborators of Iris E. Jansen. A scholar is included among the top collaborators of Iris E. 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 Iris E. Jansen. Iris E. 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.
Fernández‐Quintero, Monica L., Marta Campiglio, Petronel Tuluc, et al.. (2025). Two pairs of CACNA1I (CaV3.3) variants with opposite effects on channel function cause neurodevelopmental disorders of varying severity. PLoS Genetics. 21(8). e1011828–e1011828.
2.
Wightman, Douglas P., Jeanne E. Savage, Christiaan de Leeuw, Iris E. Jansen, & Daniëlle Posthuma. (2023). Rare variant aggregation in 148,508 exomes identifies genes associated with proxy dementia. Scientific Reports. 13(1). 2179–2179. 8 indexed citations
3.
Wightman, Douglas P., et al.. (2023). The genetic overlap between Alzheimer’s disease, amyotrophic lateral sclerosis, Lewy body dementia, and Parkinson’s disease. Neurobiology of Aging. 127. 99–112. 9 indexed citations
4.
Tesi, Niccoló, Marc Hulsman, Iris E. Jansen, et al.. (2021). Pathway-specific polygenic risk score of AD-associated genetic variants associated with AD risk, resilience against AD, and progression to AD. Pure Amsterdam UMC. 1 indexed citations
5.
Jansen, Iris E., et al.. (2021). Spatial Building Typology: Vacant Heritage: Department Stores | V&D’s. BK BOOKS. 1. 1 indexed citations
6.
Lee, Sven J. van der, Inger van Steenoven, Marleen van de Beek, et al.. (2021). Genetics Contributes to Concomitant Pathology and Clinical Presentation in Dementia with Lewy Bodies. Journal of Alzheimer s Disease. 83(1). 269–279. 20 indexed citations
7.
Bosch, Karlijn A. van den, Inge M.W. Verberk, Jarith L. Ebenau, et al.. (2021). BDNF-Met polymorphism and amyloid-beta in relation to cognitive decline in cognitively normal elderly: the SCIENCe project. Neurobiology of Aging. 108. 146–154. 5 indexed citations
8.
Tesi, Niccoló, Marc Hulsman, Sven J. van der Lee, et al.. (2021). The Effect of Alzheimer’s Disease-Associated Genetic Variants on Longevity. Frontiers in Genetics. 12. 748781–748781. 7 indexed citations
9.
Ebenau, Jarith L., Sven J. van der Lee, Marc Hulsman, et al.. (2021). Risk of dementia in APOE ε4 carriers is mitigated by a polygenic risk score. Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring. 13(1). e12229–e12229. 16 indexed citations
10.
Tesi, Niccoló, Sven J. van der Lee, Marc Hulsman, et al.. (2020). Immune response and endocytosis pathways are associated with the resilience against Alzheimer’s disease. Translational Psychiatry. 10(1). 332–332. 34 indexed citations
11.
Gardiner, Sarah L., Aster V. E. Harder, Stella Trompet, et al.. (2018). Repeat length variations in ATXN1 and AR modify disease expression in Alzheimer's disease. Neurobiology of Aging. 73. 230.e9–230.e17. 5 indexed citations
12.
Tesi, Niccoló, Sven J. van der Lee, Marc Hulsman, et al.. (2018). Centenarian controls increase variant effect sizes by an average twofold in an extreme case–extreme control analysis of Alzheimer’s disease. European Journal of Human Genetics. 27(2). 244–253. 41 indexed citations
13.
Jansen, Iris E., J. Raphael Gibbs, T. Ryan Price, et al.. (2017). Establishing the role of rare coding variants in known Parkinson's disease risk loci. Neurobiology of Aging. 59. 220.e11–220.e18. 11 indexed citations
14.
Blauwendraat, Cornelis, Carlo Wilke, Javier Simón‐Sánchez, et al.. (2017). The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects. Genetics in Medicine. 20(2). 240–249. 51 indexed citations
15.
Blauwendraat, Cornelis, Margherita Francescatto, J. Raphael Gibbs, et al.. (2016). Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe. Genome Medicine. 8(1). 65–65. 14 indexed citations
16.
Liu, Ganqiang, Brendon Boot, Joseph J. Locascio, et al.. (2016). Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's. Annals of Neurology. 80(5). 674–685. 180 indexed citations
17.
Nichols, Noah, José Brás, Dena G. Hernandez, et al.. (2015). EIF4G1 mutations do not cause Parkinson's disease. Neurobiology of Aging. 36(8). 2444.e1–2444.e4. 15 indexed citations
18.
Blauwendraat, Cornelis, Carlo Wilke, Iris E. Jansen, et al.. (2015). Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variants. Neurobiology of Aging. 37. 208.e11–208.e17. 39 indexed citations
19.
Heutink, Peter, Iris E. Jansen, & Emily M. Lynes. (2014). C9orf72; abnormal RNA expression is the key. Experimental Neurology. 262. 102–110. 12 indexed citations
20.
Huppertz, Charlotte, Meike Bartels, Iris E. Jansen, et al.. (2013). A Twin-Sibling Study on the Relationship Between Exercise Attitudes and Exercise Behavior. Behavior Genetics. 44(1). 45–55. 25 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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