J. Wauters

5.2k total citations
107 papers, 3.5k citations indexed

About

J. Wauters is a scholar working on Nuclear and High Energy Physics, Atomic and Molecular Physics, and Optics and Genetics. According to data from OpenAlex, J. Wauters has authored 107 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Nuclear and High Energy Physics, 24 papers in Atomic and Molecular Physics, and Optics and 23 papers in Genetics. Recurrent topics in J. Wauters's work include Nuclear physics research studies (43 papers), Nuclear Physics and Applications (19 papers) and Atomic and Molecular Physics (18 papers). J. Wauters is often cited by papers focused on Nuclear physics research studies (43 papers), Nuclear Physics and Applications (19 papers) and Atomic and Molecular Physics (18 papers). J. Wauters collaborates with scholars based in Belgium, United States and Netherlands. J. Wauters's co-authors include P. Van Duppen, Adrien Cremers, Paul Bossuyt, G. Reusen, P. Dendooven, M. Huyse, Wim Wuyts, Patrick J. Willems, Wim Van Hul and M. Huýse and has published in prestigious journals such as Physical Review Letters, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

J. Wauters

106 papers receiving 3.4k citations

Peers

J. Wauters
Tomokazu Fukuda Japan
Deborah J. Henderson United Kingdom
S. Fukuda Japan
Masatoshi Suzuki Japan
H. de Vries Netherlands
G. N. Taylor United States
Noah R. Johnson United States
Cornelius A. Tobias United States
Yoshiya Furusawa Japan
A. Ottolenghi Italy
Tomokazu Fukuda Japan
J. Wauters
Citations per year, relative to J. Wauters J. Wauters (= 1×) peers Tomokazu Fukuda

Countries citing papers authored by J. Wauters

Since Specialization
Citations

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

Fields of papers citing papers by J. Wauters

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Wauters

This figure shows the co-authorship network connecting the top 25 collaborators of J. Wauters. A scholar is included among the top collaborators of J. Wauters 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 J. Wauters. J. Wauters 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.
Sleegers, Kristel, Nathalie Brouwers, Ilse Gijselinck, et al.. (2006). APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy. Brain. 129(11). 2977–2983. 289 indexed citations
2.
Suls, Arvid, Kristl G. Claeys, D. Goossens, et al.. (2006). Microdeletions involving theSCN1A gene may be common inSCN1A-mutation-negative SMEI patients. Human Mutation. 27(9). 914–920. 90 indexed citations
3.
Bever, Yolande van, Liesbeth Rooms, Annick Laridon, et al.. (2005). Clinical report of a pure subtelomeric 1qter deletion in a boy with mental retardation and multiple anomalies adds further evidence for a specific phenotype. American Journal of Medical Genetics Part A. 135A(1). 91–95. 49 indexed citations
4.
Klaassens, Merel, Marieke van Dooren, H. J. Eussen, et al.. (2005). Congenital Diaphragmatic Hernia and Chromosome 15q26: Determination of a Candidate Region by Use of Fluorescent In Situ Hybridization and Array-Based Comparative Genomic Hybridization. The American Journal of Human Genetics. 76(5). 877–882. 113 indexed citations
5.
Rooms, Liesbeth, et al.. (2003). Screening for subtelomeric rearrangements using genetic markers in 70 patients with unexplained mental retardation. Annales de Génétique. 47(1). 53–59. 9 indexed citations
6.
Weng, Lin, Patrick Smits, J. Wauters, et al.. (2003). Isolation and characterization of chondrolectin (Chodl), a novel C-type lectin predominantly expressed in muscle cells. Gene. 308. 21–29. 16 indexed citations
7.
Wuyts, Wim, Dominique Roland, Hermann‐Josef Lüdecke, et al.. (2002). Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion. American Journal of Medical Genetics. 113(4). 326–332. 29 indexed citations
8.
Smits, Patrick, Yves Poumay, Marcel Karperien, et al.. (2000). Differentiation-Dependent Alternative Splicing and Expression of the Extracellular Matrix Protein 1 Gene in Human Keratinocytes. Journal of Investigative Dermatology. 114(4). 718–724. 59 indexed citations
9.
Dhaene, Karl, J. Wauters, Barbara Weyn, Jean‐Pierre Timmermans, & Eric Van Marck. (2000). Expression profile of telomerase subunits in human pleural mesothelioma. The Journal of Pathology. 190(1). 80–85. 23 indexed citations
10.
Wuyts, Wim, Giancarlo Di Gennaro, Federico Bianco, et al.. (1999). Molecular and clinical examination of an Italian DEFECT 11 family. European Journal of Human Genetics. 7(5). 579–584. 22 indexed citations
11.
Hul, Wim Van, Wim Wuyts, Jan Hendrickx, et al.. (1998). Identification of a Third EXT-like Gene (EXTL3) Belonging to the EXT Gene Family. Genomics. 47(2). 230–237. 111 indexed citations
12.
Bingham, C. R., Xintian Xu, J. Wauters, et al.. (1997). Identification of ^180Tl α Decay. APS. 1 indexed citations
13.
Fotiades, Ν., C. N. Davids, D. Seweryniak, et al.. (1997). Spectroscopy of [Formula Presented]Po. Physical review. C. 56(2). 723–728. 6 indexed citations
14.
Smits, Patrick, Jian Ni, Ping Feng, et al.. (1997). The Human Extracellular Matrix Gene 1 (ECM1): Genomic Structure, cDNA Cloning, Expression Pattern, and Chromosomal Localization. Genomics. 45(3). 487–495. 80 indexed citations
15.
Wauters, J., K. Schatteman, Dirk Hendriks, et al.. (1996). The Gene for Human Carboxypeptidase U (CPU)— A Proposed Novel Regulator of Plasminogen Activation— Maps to 13q14.11. Genomics. 38(3). 454–455. 35 indexed citations
16.
Bossuyt, Paul, et al.. (1995). Incidence of low-fluorescence α satellite region on chromosome 21 escaping detection of aneuploidy at interphase by FISH. Cytogenetic and Genome Research. 68(3-4). 203–206. 15 indexed citations
17.
Kotze, Maritha J., Armand V. Peeters, E. Langenhoven, J. Wauters, & Luc F. Van Gaal. (1994). Phenotypic expression and frequency of familial defective apolipoprotein B-100 in Belgian hypercholesterolemics. Atherosclerosis. 111(2). 217–225. 26 indexed citations
18.
Hendrickx, Jan, Paul Coucke, Paul Bossuyt, et al.. (1993). X-linked liver glycogenosis: localization and isolation of a candidate gene. Human Molecular Genetics. 2(5). 583–589. 15 indexed citations
19.
Wauters, J., P. Dendooven, Mark Huyse, et al.. (1992). Fine structure in the α decay of202Rn. Zeitschrift für Physik A Hadrons and Nuclei. 344(1). 29–33. 23 indexed citations
20.
Wauters, J., Jan Hendrickx, Paul Coucke, et al.. (1991). Frequency of the phenylalanine deletion (ΔF508) in the CF gene of Belgian cystic fibrosis patients. Clinical Genetics. 39(2). 89–92. 2 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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