Robert De Decker

1.4k total citations
28 papers, 1.1k citations indexed

About

Robert De Decker is a scholar working on Physiology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Robert De Decker has authored 28 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Physiology, 10 papers in Molecular Biology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Robert De Decker's work include Alzheimer's disease research and treatments (11 papers), Glycosylation and Glycoproteins Research (4 papers) and Prion Diseases and Protein Misfolding (3 papers). Robert De Decker is often cited by papers focused on Alzheimer's disease research and treatments (11 papers), Glycosylation and Glycoproteins Research (4 papers) and Prion Diseases and Protein Misfolding (3 papers). Robert De Decker collaborates with scholars based in Belgium, France and United States. Robert De Decker's co-authors include Michèle Authelet, Karelle Leroy, Jean‐Pierre Brion, Zehra Yilmaz, Kunié Ando, Alain Boom, Charles Nicaise, Valérie Suain, Roland Pochet and Luc Buée and has published in prestigious journals such as Gut, Brain Research and FEBS Letters.

In The Last Decade

Robert De Decker

27 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Robert De Decker Belgium	17	498	359	340	239	213	28	1.1k
Zhiming Suo United States	18	696 1.4×	464 1.3×	195 0.6×	501 2.1×	283 1.3×	23	1.5k
Jorge Marcondes de Souza Brazil	21	287 0.6×	481 1.3×	414 1.2×	411 1.7×	322 1.5×	70	1.8k
Sonali Joyce United States	19	482 1.0×	631 1.8×	321 0.9×	213 0.9×	302 1.4×	28	1.6k
Chengyuan Mao China	17	255 0.5×	482 1.3×	328 1.0×	188 0.8×	205 1.0×	60	1.1k
Hyun Jin Cho South Korea	19	414 0.8×	736 2.1×	331 1.0×	234 1.0×	220 1.0×	27	1.4k
Béatrice Leveugle United States	13	359 0.7×	344 1.0×	246 0.7×	190 0.8×	127 0.6×	18	948
María V. Andrés Germany	4	465 0.9×	449 1.3×	206 0.6×	116 0.5×	231 1.1×	6	1.0k
Alexandre Henriques Brazil	16	352 0.7×	520 1.4×	725 2.1×	186 0.8×	269 1.3×	57	1.5k
Joseph M. Martinez United States	17	226 0.5×	299 0.8×	108 0.3×	247 1.0×	147 0.7×	26	909
Devika P. Bagchi United States	16	761 1.5×	512 1.4×	410 1.2×	214 0.9×	262 1.2×	26	1.5k

Countries citing papers authored by Robert De Decker

Since Specialization

Citations

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

Fields of papers citing papers by Robert De Decker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert De Decker. 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 Robert De Decker. The network helps show where Robert De Decker may publish in the future.

Co-authorship network of co-authors of Robert De Decker

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

All Works

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20 of 20 papers shown

Yilmaz, Zehra, Robert De Decker, Luc Buée, et al.. (2022). Alzheimer PHF-tau aggregates do not spread tau pathology to the brain via the Retino-tectal projection after intraocular injection in male mouse models. Neurobiology of Disease. 174. 105875–105875. 6 indexed citations

Ando, Kunié, Robert De Decker, Cristina Vergara, et al.. (2020). Picalm reduction exacerbates tau pathology in a murine tauopathy model. Acta Neuropathologica. 139(4). 773–789. 34 indexed citations

Houben, Sarah, Kunié Ando, Luc Poncelet, et al.. (2020). Intravenous Injection of PHF-Tau Proteins From Alzheimer Brain Exacerbates Neuroinflammation, Amyloid Beta, and Tau Pathologies in 5XFAD Transgenic Mice. Frontiers in Molecular Neuroscience. 13. 106–106. 4 indexed citations

Decker, Robert De, et al.. (2019). COMMON LAB ABNORMALITIES FROM AN UNCOMMON SOURCE: A CASE REPORT. CHEST Journal. 156(4). A2185–A2185.

Vergara, Cristina, Sarah Houben, Valérie Suain, et al.. (2018). Amyloid-β pathology enhances pathological fibrillary tau seeding induced by Alzheimer PHF in vivo. Acta Neuropathologica. 137(3). 397–412. 89 indexed citations

Pierrot, Nathalie, Zehra Yilmaz, Valérie Suain, et al.. (2017). Amyloid precursor protein reduction enhances the formation of neurofibrillary tangles in a mutant tau transgenic mouse model. Neurobiology of Aging. 55. 202–212. 20 indexed citations

Audouard, Emilie, Sarah Houben, Zehra Yilmaz, et al.. (2016). High–Molecular-Weight Paired Helical Filaments from Alzheimer Brain Induces Seeding of Wild-Type Mouse Tau into an Argyrophilic 4R Tau Pathology in Vivo. American Journal Of Pathology. 186(10). 2709–2722. 47 indexed citations

Héraud, Céline, Kunié Ando, Karelle Leroy, et al.. (2013). Increased misfolding and truncation of tau in APP/PS1/tau transgenic mice compared to mutant tau mice. Neurobiology of Disease. 62. 100–112. 52 indexed citations

Ando, Kunié, Karelle Leroy, Céline Héraud, et al.. (2011). Accelerated Human Mutant Tau Aggregation by Knocking Out Murine Tau in a Transgenic Mouse Model. American Journal Of Pathology. 178(2). 803–816. 64 indexed citations

10.

Leroy, Karelle, Kunié Ando, Céline Héraud, et al.. (2010). Lithium Treatment Arrests the Development of Neurofibrillary Tangles in Mutant Tau Transgenic Mice with Advanced Neurofibrillary Pathology. Journal of Alzheimer s Disease. 19(2). 705–719. 78 indexed citations

11.

Nicaise, Charles, Dinko Mitrečić, Pieter Demetter, et al.. (2009). Impaired blood–brain and blood–spinal cord barriers in mutant SOD1-linked ALS rat. Brain Research. 1301. 152–162. 143 indexed citations

12.

Nicaise, Charles, Robert De Decker, A. Mangas, et al.. (2008). Gemals, a new drug candidate, extends lifespan and improves electromyographic parameters in a rat model of amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis. 9(2). 85–90. 7 indexed citations

13.

Nicaise, Charles, Muhammad Shahnawaz Soyfoo, Michèle Authelet, et al.. (2008). Aquaporin‐4 Overexpression in Rat ALS Model. The Anatomical Record. 292(2). 207–213. 54 indexed citations

14.

Daubie, Valéry, Robert De Decker, Charles Nicaise, & Roland Pochet. (2007). Osteosarcoma cell‐calcium signaling through tissue factor–factor VIIa complex and factor Xa. FEBS Letters. 581(14). 2611–2615. 8 indexed citations

15.

Leroy, Karelle, Alexis Bretteville, Katharina Schindowski, et al.. (2007). Early Axonopathy Preceding Neurofibrillary Tangles in Mutant Tau Transgenic Mice. American Journal Of Pathology. 171(3). 976–992. 107 indexed citations

16.

Remmelink, Myriam, Francis Darro, Christine Decaestecker, et al.. (1999). In vitro influence of lectins and neoglycoconjugates on the growth of three human sarcoma cell lines. Journal of Cancer Research and Clinical Oncology. 125(5). 275–285. 19 indexed citations

17.

Barr, William, et al.. (1998). New-Onset Psychogenic Seizures After Surgery for Epilepsy. Archives of Neurology. 55(5). 726–726. 37 indexed citations

18.

Kiss, Róbert, Isabelle Camby, Carrie A. Duckworth, et al.. (1997). In vitro influence of Phaseolus vulgaris, Griffonia simplicifolia, concanavalin A, wheat germ, and peanut agglutinins on HCT-15, LoVo, and SW837 human colorectal cancer cell growth.. Gut. 40(2). 253–261. 50 indexed citations

19.

Pétein, Michel, Roland van Velthoven, Robert De Decker, et al.. (1997). Coregulatory effects of epidermal growth factor, dihydrotestosterone, and prolactin on benign human prostatic hyperplasia tissue culture proliferation. The Prostate. 30(1). 47–52. 10 indexed citations

20.

Camby, Isabelle, Isabelle Salmon, Robert De Decker, et al.. (1997). Lectin histochemistry of astrocytic tumors and in vitro characterization of lectin-induced modifications on the proliferation of the SW1088, U373 and U87 human astrocytic cell lines. Journal of Neuro-Oncology. 34(2). 111–122. 5 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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