Karen Buysse

2.5k citations

19 papers · 959 indexed · h-index 15

Co-authors: Björn Menten Geert Mortier Frank Speleman Evan E. Eichler Heather C. Mefford P Ostertag Ulrich Stephani Hiltrud Muhle
Topics: Genomic variations and chromosomal abnormalities (11 papers)Chromosomal and Genetic Variations (5 papers)Genomics and Rare Diseases (3 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Molecular Biology
Journals: Human Molecular Genetics PLoS Genetics BMC Bioinformatics
Partner nations: Belgium United States United Kingdom

In The Last Decade

Karen Buysse

19 papers receiving 938 citations

Peers

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

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19 of 19 papers shown

#	Work	Indexed citations
1	Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker–Warburg syndrome 2013 ·Human Molecular Genetics ·Karen Buysse,Moniek Riemersma,Gareth T. Powell,Jeroen van Reeuwijk,David Chitayat,Tony Roscioli,Erik‐Jan Kamsteeg,Christa van den Elzen,Ellen van Beusekom,Susan Blasér,Riyana Babul‐Hirji,W Halliday,Gavin J. Wright,Derek L. Stemple,Yung‐Yao Lin,Dirk J. Lefeber,Hans van Bokhoven	113
2	Reliable noninvasive prenatal testing by massively parallel sequencing of circulating cell-free DNA from maternal plasma processed up to 24 h after venipuncture 2013 ·Clinical Biochemistry ·Karen Buysse,Lean Beulen,(unknown),Christian Gilissen,(unknown),Irene M. Janssen,(unknown),Joep de Ligt,Ilse Feenstra,Mireille N. Bekker,J. M. G. van Vugt,Ad Geurts van Kessel,Lisenka E.L.M. Vissers,Brigitte H. W. Faas	14
3	Five patients with novel overlapping interstitial deletions in 8q22.2q22.3 2011 ·American Journal of Medical Genetics Part A ·Alma Kuechler,Karen Buysse,Jill Clayton‐Smith,Cédric Le Caignec,Albert David,Hartmut Engels,Jürgen Kohlhase,Francesca Mari,Geert Mortier,Alessandra Renieri,Dagmar Wieczorek	22
4	Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN gene 2010 ·American Journal of Medical Genetics Part A ·Karen Buysse,Sarah Vergult,(unknown),Chantal Ceuterick‐de Groote,Frank Speleman,Björn Menten,Willy Lissens,Rudy Van Coster	20
5	Genome-Wide Copy Number Variation in Epilepsy: Novel Susceptibility Loci in Idiopathic Generalized and Focal Epilepsies 2010 ·PLoS Genetics ·Heather C. Mefford,Hiltrud Muhle,P Ostertag,Sarah von Spiczak,Karen Buysse,Carl Baker,André Franke,Alain Malafosse,Pierre Genton,Pierre Thomas,Christina A. Gurnett,Stefan Schreiber,Alexander G. Bassuk,Michel Guipponi,Ulrich Stephani,Katherine L. Helbig,Evan E. Eichler	327
6	Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples 2009 ·BMC Medical Genetics ·Björn Menten,Katrien Swerts,Barbara Delle Chiaie,Sandra Janssens,Karen Buysse,Jan Philippé,Frank Speleman	60
7	Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy 2009 ·Human Molecular Genetics ·Megan Landsverk,Elizabeth K. Ruzzo,Heather C. Mefford,Karen Buysse,Jillian G. Buchan,Evan E. Eichler,Elizabeth M. Petty,Esther A. Peterson,Dana Knutzen,(unknown),Martin R. Farlow,(unknown),G. Parry,Dianna Quan,Kathy Gardner,(unknown),Zachary Simmons,Thomas D. Bird,Phillip F. Chance,Mark Hannibal	22
8	Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy 2009 ·Journal of Medical Genetics ·Angela M. B. Collie,Megan Landsverk,Elizabeth K. Ruzzo,Heather C. Mefford,Karen Buysse,(unknown),Dana Knutzen,(unknown),Robert H. Brown,G. Parry,Sabrina W. Yum,David Simpson,Richard K. Olney,Patrick F. Chinnery,Evan E. Eichler,P. F. Chance,Mark Hannibal	35
9	The 12q14 microdeletion syndrome: Additional patients and further evidence that HMGA2 is an important genetic determinant for human height 2009 ·European Journal of Medical Genetics ·Karen Buysse,William Reardon,Lakshmi Mehta,Teresa Costa,(unknown),D. Kingsbury,(unknown),Barbara McGillivray,Jan Hellemans,Nicole de Leeuw,Bert B.A. de Vries,Frank Speleman,Björn Menten,Geert Mortier	43
10	Challenges for CNV interpretation in clinical molecular karyotyping: Lessons learned from a 1001 sample experience 2009 ·European Journal of Medical Genetics ·Karen Buysse,Barbara Delle Chiaie,Rudy Van Coster,Bart Loeys,Anne De Paepe,Geert Mortier,Frank Speleman,Björn Menten	81
11	Copy number alterations and copy number variation in cancer: close encounters of the bad kind 2008 ·Cytogenetic and Genome Research ·Frank Speleman,Candy Kumps,Karen Buysse,(unknown),Björn Menten,Katleen De Preter	27
12	Delineation of a critical region on chromosome 18 for the del(18)(q12.2q21.1) syndrome 2008 ·American Journal of Medical Genetics Part A ·Karen Buysse,Björn Menten,Ann Oostra,(unknown),Geert Mortier,Frank Speleman	22
13	Unusual 8p inverted duplication deletion with telomere capture from 8q 2008 ·European Journal of Medical Genetics ·Karen Buysse,Francesca Antonacci,Bert Callewaert,Bart Loeys,(unknown),Victoria Mok Siu,Geert Mortier,Frank Speleman,Björn Menten	21
14	Report of a female patient with mental retardation and tall stature due to a chromosomal rearrangement disrupting the OPHN1 gene on Xq12 2007 ·European Journal of Medical Genetics ·Björn Menten,Karen Buysse,Stefan Vermeulen,(unknown),Jo Vandesompele,Bee Ling Ng,Nigel P. Carter,Geert Mortier,Frank Speleman	11
15	Osteopoikilosis, short stature and mental retardation as key features of a new microdeletion syndrome on 12q14 2007 ·Journal of Medical Genetics ·Björn Menten,Karen Buysse,Farah Zahir,Jan Hellemans,Sara Hamilton,Teresa Costa,Cecilia Fagerström,(unknown),D. Kingsbury,Barbara McGillivray,Marco A. Marra,Jan M. Friedman,Frank Speleman,Geert Mortier	44
16	Molecular karkyotyping detecs structural low grade mosaics in 4 % of patietns with idiopathic mental retardation and multiple congenital aberrations 2005 ·European Journal of Human Genetics ·(unknown),Björn Menten,Cindy Melotte,Bernard Thienpont,Karen Buysse,(unknown),Peter Marynen,Anne De Paepe,Jean‐Pierre Fryns,Geert Mortier,Koenraad Devriendt,Frank Speleman,Joris Vermeesch	2
17	Identification of an unbalanced X-autosome translocation by array CGH in a boy with a syndromic form of chondrodysplasia punctata brachytelephalangic type 2005 ·European Journal of Medical Genetics ·Björn Menten,Karen Buysse,Jo Vandesompele,Els De Smet,Anne De Paepe,Frank Speleman,Geert Mortier	12
18	arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays 2005 ·BMC Bioinformatics ·Björn Menten,Filip Pattyn,Katleen De Preter,(unknown),Evi Michels,Karen Buysse,Geert Mortier,Anne De Paepe,Steven Van Vooren,Joris Vermeesch,Yves Moreau,Bart De Moor,Stefan Vermeulen,Frank Speleman,Jo Vandesompele	65
19	Reversibility after female sterilization 1986 ·BJOG An International Journal of Obstetrics & Gynaecology ·W. Boeckx,S. Gordts,Karen Buysse,Ivo Brosens	18

About Karen Buysse

Karen Buysse is a scholar working on Genetics, Cancer Research and Genetics, having authored 19 papers that have together received 959 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (5 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Genetics (633 citations), Pediatrics, Perinatology and Child Health (169 citations) and Molecular Biology (456 citations). Karen Buysse has collaborated with scholars based in Belgium, United States and United Kingdom. Frequent co-authors include Björn Menten, Geert Mortier, Frank Speleman, Evan E. Eichler, Heather C. Mefford, P Ostertag, Ulrich Stephani, Hiltrud Muhle, Pierre Thomas and Alexander G. Bassuk. Their work appears in journals such as Human Molecular Genetics, PLoS Genetics and BMC Bioinformatics.

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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