Griet Van Buggenhout

3.3k total citations · 1 hit paper
63 papers, 1.9k citations indexed

About

Griet Van Buggenhout is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Griet Van Buggenhout has authored 63 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Genetics, 24 papers in Molecular Biology and 15 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Griet Van Buggenhout's work include Genomic variations and chromosomal abnormalities (34 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Prenatal Screening and Diagnostics (13 papers). Griet Van Buggenhout is often cited by papers focused on Genomic variations and chromosomal abnormalities (34 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Prenatal Screening and Diagnostics (13 papers). Griet Van Buggenhout collaborates with scholars based in Belgium, United States and Netherlands. Griet Van Buggenhout's co-authors include Jean‐Pierre Fryns, Joris Vermeesch, Jean‐Pierre Fryns, Koenraad Devriendt, Annick Vogels, Raoul C. M. Hennekam, Thomy de Ravel, Rob de Waal, Ann Swillen and Han G. Brunner and has published in prestigious journals such as Cell, Journal of Clinical Oncology and Cancer Research.

In The Last Decade

Griet Van Buggenhout

58 papers receiving 1.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome

1999 536 citations Jacopo Celli, Pascal H. G. Duijf et al. Cell profile →

Peers

Countries citing papers authored by Griet Van Buggenhout

Since Specialization

Citations

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

Fields of papers citing papers by Griet Van Buggenhout

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Griet Van Buggenhout

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Clinical evaluation of long-read sequencing-based episignature detection in developmental disorders 2025 ·Genome Medicine ·(unknown), (unknown), Erika Souche, Jeroen Breckpot, Koenraad Devriendt, Hilde Peeters, Griet Van Buggenhout, Hilde Van Esch, Kris Van Den Bogaert, Joris Vermeesch	10
2	Consensus recommendations on altered sensory functioning in Phelan-McDermid syndrome 2023 ·European Journal of Medical Genetics ·(unknown), Sarah Jesse, (unknown), Griet Van Buggenhout	7
3	Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledge 2022 ·European Journal of Human Genetics ·Lore Lannoo, (unknown), Jeroen Breckpot, Nathalie Brison, Luc De Catte, Eftychia Dimitriadou, Eric Legius, Hilde Peeters, Ilse Parijs, Olga Tšuiko, Leen Vancoillie, Joris Vermeesch, Griet Van Buggenhout, Kris Van Den Bogaert, Kristel Van Calsteren, Koenraad Devriendt	25
4	Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies 2016 ·Genetics in Medicine ·Nathalie Brison, Kris Van Den Bogaert, Luc Dehaspe, (unknown), Katrien Janssens, Bettina Blaumeiser, Hilde Peeters, Hilde Van Esch, Griet Van Buggenhout, Annick Vogels, Thomy de Ravel, Eric Legius, Koenraad Devriendt, Joris Vermeesch	39
5	Presenting symptoms in adults with the 22q11 deletion syndrome 2014 ·European Journal of Medical Genetics ·Annick Vogels, (unknown), (unknown), (unknown), Griet Van Buggenhout, Ann Swillen, Hilde Van Esch, Thomy de Ravel, (unknown), Koenraad Devriendt	16
6	Adults with Down syndrome: health/care considerations for health professionals 2012 ·Ghent University Academic Bibliography (Ghent University) ·Barbara Delle Chiaie, (unknown), (unknown), (unknown), Roos Leroy, Bert Callewaert, Marek Wojciechowski, Bruce Poppe, Griet Van Buggenhout, (unknown)	0
7	Health problems in children with Down syndrome 2012 ·Ghent University Academic Bibliography (Ghent University) ·Marek Wojciechowski, (unknown), (unknown), Tine Boiy, Bert Callewaert, Barbara Delle Chiaie, (unknown), Marjan De Rademaeker, (unknown), (unknown), (unknown), Griet Van Buggenhout	0
8	Wolf–Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter 2011 ·American Journal of Medical Genetics Part A ·Piotr Iwanowski, Barbara Panasiuk, Griet Van Buggenhout, Marina Murdolo, M. Myśliwiec, Nicole Maas, Serena Lattante, L Korniszewski, Renata Posmyk, Jacek Pilch, Stanisław Zajączek, Jean‐Pierre Fryns, Marcella Zollino, Alina T. Midro	4
9	Angelman syndrome (AS, MIM 105830) 2009 ·European Journal of Human Genetics ·Griet Van Buggenhout, Jean‐Pierre Fryns	71
10	Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant 2008 ·Journal of Medical Genetics ·Femke Hannes, Andrew J. Sharp, Heather C. Mefford, Thomy de Ravel, Claudia Ruivenkamp, M.H. Breuning, JP Fryns, Koenraad Devriendt, Griet Van Buggenhout, Annick Vogels, Helen Stewart, Raoul C. M. Hennekam, Gregory M. Cooper, Regina Regan, Samantha J.L. Knight, Evan E. Eichler, Joris Vermeesch	207
11	Chromosome aberrations in ageing mentally retarded persons: a challenge for the clinician 2007 ·Chromosome Research ·Griet Van Buggenhout, (unknown), (unknown), (unknown), Joris Vermeesch, Jean‐Pierre Fryns	1
12	Simple and translation forms of monosomy 4p16.1↔ pter: quantitative syndrome definition and cytogenetic evaluation by FISH 2007 ·Medizinische Genetik ·Alina T. Midro, (unknown), Barbara Panasiuk, Griet Van Buggenhout, (unknown), (unknown), Thomas Eggermann, Ján Pilch, L Korniszewski, Joris Vermeesch, Jean‐Pierre Fryns, Marcella Zollino	1
13	Genotype–phenotype correlation in 21 patients with Wolf–Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH) 2007 ·Journal of Medical Genetics ·Nicole Maas, Griet Van Buggenhout, Femke Hannes, Bernard Thienpont, Damien Sanlaville, Klaas Kok, Alina T. Midro, Joris Andrieux, (unknown), Jacqueline Schoumans, Roel Hordijk, Koenraad Devriendt, JP Fryns, Joris Vermeesch	99
14	The analysis of 4p chromosomal abnormalities using micro-array CGH; genotype-phenotype correlation 2006 ·European Journal of Human Genetics ·(unknown), Cindy Melotte, Griet Van Buggenhout, Jean‐Pierre Fryns, Joris Vermeesch	0
15	MECP2 mutations are an infrequent cause of mental retardation associated with neurological problems in male patients 2006 ·Brain and Development ·Ute Moog, Kees van Roozendaal, Eric Smeets, Demis Tserpelis, Koenraad Devriendt, Griet Van Buggenhout, Jean‐Pierre Frijns, Connie Schrander‐Stumpel	18
16	4q35 deletion and 10p15 duplication associated with immunodeficiency 2006 ·American Journal of Medical Genetics Part A ·Sultan Cingöz, Anne‐Marie Bisgaard, Iben Bache, Thue Bryndorf, (unknown), (unknown), H.H. Ropers, (unknown), Griet Van Buggenhout, Niels Tommerup, Zeynep Tümer	9
17	Micro-array CGH analysis of 4p microdeletions refines the genotype-phenotype map of the region and pinpoints low copy repeats as susceptibility sites for terminal chromosomal deletions 2004 ·European Journal of Human Genetics ·Joris Vermeesch, Nicole Maas, Cindy Melotte, Griet Van Buggenhout, Ronald Thoelen, (unknown), Bhabesh Dutta, Paul Van Hummelen, Peter Marynen, Jean‐Pierre Fryns	0
18	Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome breakdown → 1999 ·Cell ·Jacopo Celli, Pascal H. G. Duijf, Ben C.J. Hamel, Michael J. Bamshad, Bridget Kramer, (unknown), Ruth Newbury‐Ecob, Raoul C. M. Hennekam, Griet Van Buggenhout, Arie van Haeringen, C. Geoffrey Woods, Anthonie J. van Essen, Rob de Waal, Gert Vriend, Daniel A. Haber, Annie Yang, Frank McKeon, Han G. Brunner, Hans van Bokhoven	536
19	Structural chromosome rearrangements in couples with recurrent fetal wastage 1998 ·European Journal of Obstetrics & Gynecology and Reproductive Biology ·Jean‐Pierre Fryns, Griet Van Buggenhout	96
20	Cri du chat syndrome: The changing phenotype in older patients 1996 ·European Journal of Human Genetics ·(unknown), Griet Van Buggenhout, (unknown), (unknown), (unknown), (unknown), Jean‐Pierre Fryns	1

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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