Paul Bossuyt

992 total citations
15 papers, 796 citations indexed

About

Paul Bossuyt is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Paul Bossuyt has authored 15 papers receiving a total of 796 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Rheumatology. Recurrent topics in Paul Bossuyt's work include Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic factors in colorectal cancer (3 papers). Paul Bossuyt is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic factors in colorectal cancer (3 papers). Paul Bossuyt collaborates with scholars based in Belgium, United Kingdom and Germany. Paul Bossuyt's co-authors include J. Wauters, Patrick J. Willems, Jan Hendrickx, Wim Van Hul, Wim Wuyts, Frank Speleman, Kristel De Boulle, Nadine Van Roy, Richard J. Smith and Lut Van Laer and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Paul Bossuyt

15 papers receiving 776 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paul Bossuyt Belgium 13 440 177 157 117 114 15 796
Axel Bohring Germany 13 361 0.8× 88 0.5× 203 1.3× 65 0.6× 17 0.1× 17 609
Luís Garcia Alonso Brazil 17 541 1.2× 74 0.4× 621 4.0× 33 0.3× 18 0.2× 56 1.1k
Megana Prasad United States 14 379 0.9× 49 0.3× 124 0.8× 19 0.2× 11 0.1× 19 550
Abdulrahman Alswaid Saudi Arabia 16 509 1.2× 159 0.9× 698 4.4× 6 0.1× 34 0.3× 29 1.1k
Véronique Geoffroy France 12 559 1.3× 58 0.3× 510 3.2× 28 0.2× 17 0.1× 17 775
Hsiao‐Man Ivy Yu United States 13 814 1.9× 51 0.3× 373 2.4× 16 0.1× 9 0.1× 14 992
Stuart W. Tompson United States 12 482 1.1× 55 0.3× 429 2.7× 12 0.1× 20 0.2× 16 716
Lorne Lonie United Kingdom 10 591 1.3× 213 1.2× 153 1.0× 123 1.1× 2 0.0× 12 1.1k
Jiangxia Li China 18 478 1.1× 85 0.5× 119 0.8× 4 0.0× 27 0.2× 40 755
Debra J. Gilbert United States 13 390 0.9× 47 0.3× 106 0.7× 6 0.1× 9 0.1× 17 597

Countries citing papers authored by Paul Bossuyt

Since Specialization
Citations

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

Fields of papers citing papers by Paul Bossuyt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paul Bossuyt

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

All Works

15 of 15 papers shown
1.
Winnepenninckx, Birgitta, Edwin Reyniers, Paul Bossuyt, et al.. (2001). Precise mapping of the fragile siteFRA12Aon chromosome 12q13.1. 1(3). 131–137. 1 indexed citations
2.
Holinski‐Feder, Elke, Edwin Reyniers, Sabine Uhrig, et al.. (2000). Familial Mental Retardation Syndrome ATR-16 Due to an Inherited Cryptic Subtelomeric Translocation, t(3;16)(q29;p13.3). The American Journal of Human Genetics. 66(1). 16–25. 43 indexed citations
3.
Pittois, Karen, et al.. (1999). Genomic organization and chromosomal localization of the Itm2a gene. Mammalian Genome. 10(1). 54–56. 26 indexed citations
4.
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
5.
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
6.
Laer, Lut Van, E. H. Huizing, Margriet Verstreken, et al.. (1998). Nonsyndromic hearing impairment is associated with a mutation in DFNA5. Nature Genetics. 20(2). 194–197. 315 indexed citations
7.
Wuyts, Wim, Wim Van Hul, Jan Hendrickx, et al.. (1998). Identification and characterization of a novel member of the EXT gene family, EXTL2.. PubMed. 5(6). 382–9. 85 indexed citations
8.
Wuyts, Wim, Wim Van Hul, Jan Hendrickx, et al.. (1997). Identification and Characterization of a Novel Member of the EXT Gene Family, EXTL2. European Journal of Human Genetics. 5(6). 382–389. 75 indexed citations
9.
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
10.
Goossens, Filip, J. Wauters, Greet Vanhoof, et al.. (1996). Subregional mapping of the human lymphocyte prolyl oligopeptidase gene (PREP) to human chromosome 6q22. Cytogenetic and Genome Research. 74(1-2). 99–101. 12 indexed citations
11.
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
12.
13.
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
14.
Wauters, J., Paul Bossuyt, Jordan Davidson, et al.. (1992). Regional mapping of a liver α-subunit gene of phosphorylase kinase (PHKA) to the distal region of human chromosome Xp. Cytogenetic and Genome Research. 60(3-4). 194–196. 17 indexed citations
15.
Coucke, Paul, Kathelijne Mangelschots, Frank Speleman, et al.. (1991). Assignment of the fucosidase pseudogene FUCA1P to chromosome region 2q31→q32. Cytogenetic and Genome Research. 57(2-3). 120–122. 1 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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