Karen Buysse

2.5k total citations
19 papers, 959 citations indexed

About

Karen Buysse is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Karen Buysse has authored 19 papers receiving a total of 959 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Plant Science. Recurrent topics in Karen Buysse's work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (5 papers) and Genomics and Rare Diseases (3 papers). Karen Buysse is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (5 papers) and Genomics and Rare Diseases (3 papers). Karen Buysse collaborates with scholars based in Belgium, United States and United Kingdom. Karen Buysse's co-authors include Björn Menten, Geert Mortier, Frank Speleman, Heather C. Mefford, Evan E. Eichler, Barbara Delle Chiaie, Sarah von Spiczak, Alain Malafosse, Pierre Genton and Hiltrud Muhle and has published in prestigious journals such as Human Molecular Genetics, PLoS Genetics and BMC Bioinformatics.

In The Last Decade

Karen Buysse

19 papers receiving 938 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Karen Buysse Belgium 15 633 456 169 75 75 19 959
Marianne Till France 17 659 1.0× 556 1.2× 194 1.1× 60 0.8× 70 0.9× 61 1.2k
Roger H. Reeves United States 8 576 0.9× 696 1.5× 95 0.6× 78 1.0× 38 0.5× 10 1.4k
Daniela Orteschi Italy 19 597 0.9× 467 1.0× 101 0.6× 73 1.0× 58 0.8× 37 917
Alexandra Afenjar France 16 621 1.0× 521 1.1× 113 0.7× 106 1.4× 36 0.5× 42 1.0k
Monika Cohen Germany 11 488 0.8× 551 1.2× 98 0.6× 113 1.5× 84 1.1× 13 859
Ute Grasshoff Germany 12 477 0.8× 463 1.0× 100 0.6× 70 0.9× 91 1.2× 29 791
Alice Goldenberg France 20 565 0.9× 678 1.5× 91 0.5× 124 1.7× 34 0.5× 49 1.1k
Audrey Labalme France 19 704 1.1× 629 1.4× 123 0.7× 178 2.4× 84 1.1× 66 1.2k
Carmen Orellana Spain 19 400 0.6× 440 1.0× 115 0.7× 57 0.8× 68 0.9× 65 828
Silvestre Oltra Spain 20 478 0.8× 626 1.4× 109 0.6× 41 0.5× 75 1.0× 69 1.1k

Countries citing papers authored by Karen Buysse

Since Specialization
Citations

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

Fields of papers citing papers by Karen Buysse

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karen Buysse

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

All Works

19 of 19 papers shown
1.
Buysse, Karen, Lean Beulen, Christian Gilissen, et al.. (2013). Reliable noninvasive prenatal testing by massively parallel sequencing of circulating cell-free DNA from maternal plasma processed up to 24 h after venipuncture. Clinical Biochemistry. 46(18). 1783–1786. 14 indexed citations
2.
Buysse, Karen, Moniek Riemersma, Gareth T. Powell, et al.. (2013). Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker–Warburg syndrome. Human Molecular Genetics. 22(9). 1746–1754. 113 indexed citations
3.
Kuechler, Alma, Karen Buysse, Jill Clayton‐Smith, et al.. (2011). Five patients with novel overlapping interstitial deletions in 8q22.2q22.3. American Journal of Medical Genetics Part A. 155(8). 1857–1864. 22 indexed citations
4.
Buysse, Karen, Sarah Vergult, Chantal Ceuterick‐de Groote, et al.. (2010). Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN gene. American Journal of Medical Genetics Part A. 152A(11). 2802–2804. 20 indexed citations
5.
Mefford, Heather C., Hiltrud Muhle, P Ostertag, et al.. (2010). Genome-Wide Copy Number Variation in Epilepsy: Novel Susceptibility Loci in Idiopathic Generalized and Focal Epilepsies. PLoS Genetics. 6(5). e1000962–e1000962. 327 indexed citations
6.
Menten, Björn, Katrien Swerts, Barbara Delle Chiaie, et al.. (2009). Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples. BMC Medical Genetics. 10(1). 89–89. 60 indexed citations
7.
Collie, Angela M. B., Megan Landsverk, Elizabeth K. Ruzzo, et al.. (2009). Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy. Journal of Medical Genetics. 47(9). 601–607. 35 indexed citations
8.
Landsverk, Megan, Elizabeth K. Ruzzo, Heather C. Mefford, et al.. (2009). Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy. Human Molecular Genetics. 18(7). 1200–1208. 22 indexed citations
9.
Buysse, Karen, William Reardon, Lakshmi Mehta, et al.. (2009). The 12q14 microdeletion syndrome: Additional patients and further evidence that HMGA2 is an important genetic determinant for human height. European Journal of Medical Genetics. 52(2-3). 101–107. 43 indexed citations
10.
Buysse, Karen, Barbara Delle Chiaie, Rudy Van Coster, et al.. (2009). Challenges for CNV interpretation in clinical molecular karyotyping: Lessons learned from a 1001 sample experience. European Journal of Medical Genetics. 52(6). 398–403. 81 indexed citations
11.
Speleman, Frank, et al.. (2008). Copy number alterations and copy number variation in cancer: close encounters of the bad kind. Cytogenetic and Genome Research. 123(1-4). 176–182. 27 indexed citations
12.
Buysse, Karen, Francesca Antonacci, Bert Callewaert, et al.. (2008). Unusual 8p inverted duplication deletion with telomere capture from 8q. European Journal of Medical Genetics. 52(1). 31–36. 21 indexed citations
13.
Buysse, Karen, et al.. (2008). Delineation of a critical region on chromosome 18 for the del(18)(q12.2q21.1) syndrome. American Journal of Medical Genetics Part A. 146A(10). 1330–1334. 22 indexed citations
14.
Menten, Björn, Karen Buysse, Stefan Vermeulen, et al.. (2007). Report of a female patient with mental retardation and tall stature due to a chromosomal rearrangement disrupting the OPHN1 gene on Xq12. European Journal of Medical Genetics. 50(6). 446–454. 11 indexed citations
15.
Menten, Björn, Karen Buysse, Farah Zahir, et al.. (2007). Osteopoikilosis, short stature and mental retardation as key features of a new microdeletion syndrome on 12q14. Journal of Medical Genetics. 44(4). 264–268. 44 indexed citations
16.
Menten, Björn, Cindy Melotte, Bernard Thienpont, et al.. (2005). Molecular karkyotyping detecs structural low grade mosaics in 4 % of patietns with idiopathic mental retardation and multiple congenital aberrations. European Journal of Human Genetics. 13. 63. 2 indexed citations
17.
Menten, Björn, Karen Buysse, Jo Vandesompele, et al.. (2005). Identification of an unbalanced X-autosome translocation by array CGH in a boy with a syndromic form of chondrodysplasia punctata brachytelephalangic type. European Journal of Medical Genetics. 48(3). 301–309. 12 indexed citations
18.
Menten, Björn, Filip Pattyn, Katleen De Preter, et al.. (2005). arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays. BMC Bioinformatics. 6(1). 124–124. 65 indexed citations
19.
Boeckx, W., S. Gordts, Karen Buysse, & Ivo Brosens. (1986). Reversibility after female sterilization. BJOG An International Journal of Obstetrics & Gynaecology. 93(8). 839–842. 18 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Marianne Till Breakdown of academic impact, for papers by Roger H. Reeves Breakdown of academic impact, for papers by Daniela Orteschi Breakdown of academic impact, for papers by Alexandra Afenjar Breakdown of academic impact, for papers by Monika Cohen Breakdown of academic impact, for papers by Ute Grasshoff Breakdown of academic impact, for papers by Alice Goldenberg Breakdown of academic impact, for papers by Audrey Labalme Breakdown of academic impact, for papers by Carmen Orellana Breakdown of academic impact, for papers by Silvestre Oltra
Rankless by CCL
2026