Bernadette Van Roy

1.1k total citations
10 papers, 837 citations indexed

About

Bernadette Van Roy is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Bernadette Van Roy has authored 10 papers receiving a total of 837 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Bernadette Van Roy's work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Syndromes and Imprinting (3 papers). Bernadette Van Roy is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Syndromes and Imprinting (3 papers). Bernadette Van Roy collaborates with scholars based in Belgium, Netherlands and Israel. Bernadette Van Roy's co-authors include Annemieke J.M.H. Verkerk, Lieve Vits, Kristel De Boulle, Edwin Reyniers, Ben A. Oostra, Esther de Graaff, Jan Hendrickx, Patrick J. Willems, John Darby and Jan E. Dumon and has published in prestigious journals such as Nature Genetics, Human Molecular Genetics and Journal of the American Academy of Dermatology.

In The Last Decade

Bernadette Van Roy

10 papers receiving 817 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bernadette Van Roy Belgium 6 687 601 295 96 45 10 837
Doris Wöhrle Germany 6 492 0.7× 425 0.7× 193 0.7× 89 0.9× 47 1.0× 8 619
P. Goonewardena Sweden 11 491 0.7× 377 0.6× 238 0.8× 88 0.9× 19 0.4× 23 613
Zhou Xp China 5 306 0.4× 416 0.7× 227 0.8× 47 0.5× 34 0.8× 8 634
Roberta Pietrobono Italy 11 442 0.6× 515 0.9× 188 0.6× 93 1.0× 13 0.3× 20 641
Jean-Louis Mandel France 3 588 0.9× 481 0.8× 291 1.0× 48 0.5× 11 0.2× 4 660
Anna Bergo Italy 11 532 0.8× 453 0.8× 158 0.5× 39 0.4× 21 0.5× 11 653
Aaron Cheung Canada 9 326 0.5× 656 1.1× 151 0.5× 95 1.0× 15 0.3× 12 777
Tetsushi Yamagata Japan 12 276 0.4× 448 0.7× 82 0.3× 221 2.3× 69 1.5× 14 736
Liesbeth Rooms Belgium 17 593 0.9× 388 0.6× 118 0.4× 67 0.7× 99 2.2× 26 749
Kali Witherspoon United States 2 446 0.6× 283 0.5× 279 0.9× 35 0.4× 17 0.4× 2 568

Countries citing papers authored by Bernadette Van Roy

Since Specialization
Citations

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

Fields of papers citing papers by Bernadette Van Roy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bernadette Van Roy. 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 Bernadette Van Roy. The network helps show where Bernadette Van Roy may publish in the future.

Co-authorship network of co-authors of Bernadette Van Roy

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

All Works

10 of 10 papers shown
1.
Stinissen, Piet, Bernadette Van Roy, Guy Van Camp, et al.. (2005). Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphisms. American Journal of Medical Genetics. 37(S7). 133–136. 1 indexed citations
2.
Beuten, Joke, Raoul C. M. Hennekam, Bernadette Van Roy, et al.. (1996). Angelman syndrome in an inbred family. Human Genetics. 97(3). 294–298. 3 indexed citations
3.
Camp, Guy Van, Bernadette Van Roy, V. Sree Hari Rao, et al.. (1995). Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.. Journal of Medical Genetics. 32(7). 531–536. 27 indexed citations
4.
Willems, Patrick J., et al.. (1994). Becker's nevus associated with chromosomal mosaicism and congenital adrenal hyperplasia. Journal of the American Academy of Dermatology. 30(4). 655–657. 23 indexed citations
5.
Boulle, Kristel De, Annemieke J.M.H. Verkerk, Edwin Reyniers, et al.. (1993). A point mutation in the FMR-1 gene associated with fragile X mental retardation. Nature Genetics. 3(1). 31–35. 484 indexed citations
6.
7.
Reyniers, Edwin, Lieve Vits, Kristel De Boulle, et al.. (1993). The full mutation in the FMR–1 gene of male fragile X patients is absent in their sperm. Nature Genetics. 4(2). 143–146. 225 indexed citations
8.
Willems, Patrick J., Bernadette Van Roy, Kristel De Boulle, et al.. (1992). Segregation of the fragile X mutation from an affected male to his normal daughter. Human Molecular Genetics. 1(7). 511–515. 46 indexed citations
9.
10.
Neetens, A, Jan E. Dumon, & Bernadette Van Roy. (1990). [Hereditary paracentric inversion of chromosome 3].. PubMed. 3(1). 69–72. 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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