Liesbeth Rooms

2.1k citations

26 papers · 749 indexed · h-index 17

Genetics top 5%
Molecular Biology
Pediatrics, Perinatology and Child Health top 10%
Cognitive Neuroscience top 10%
Plant Science

Co-authors: R. Frank Kooy Edwin Reyniers J. Wauters Wim Wuyts Rob van Luijk Stefaan Scheers Geert Vandeweyer Winnie Courtens
Topics: Genomic variations and chromosomal abnormalities (19 papers)Genetics and Neurodevelopmental Disorders (17 papers)Autism Spectrum Disorder Research (7 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Cognitive Neuroscience
Journals: PLoS ONE PLoS Genetics BMC Bioinformatics
Partner nations: Belgium Netherlands United Kingdom

In The Last Decade

Liesbeth Rooms

26 papers receiving 723 citations

Peers

Countries citing papers authored by Liesbeth Rooms

Since Specialization

Citations

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

Fields of papers citing papers by Liesbeth Rooms

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Liesbeth Rooms

This figure shows the co-authorship network connecting the top 25 collaborators of Liesbeth Rooms. A scholar is included among the top collaborators of Liesbeth Rooms 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 Liesbeth Rooms. Liesbeth Rooms 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	Impaired GABAergic inhibition in the hippocampus of Fmr1 knockout mice 2016 ·Neuropharmacology ·Victor Sabanov,Sien Braat,Laura D’Andrea,Rob Willemsen,(unknown),Liesbeth Rooms,Claudia Bagni,R. Frank Kooy,Detlef Balschun	56
2	Thoracic dimples and dysmorphic features associated with a partial duplication and triplication of chromosome 12q24 2016 ·Clinical Dysmorphology ·(unknown),Marek Wojciechowski,Sigri Beckers,Liesbeth Rooms,R. Frank Kooy,Marije Meuwissen	1
3	Positron Emission Tomography (PET) Quantification of GABAA Receptors in the Brain of Fragile X Patients 2015 ·PLoS ONE ·Charlotte D’Hulst,Inge Heulens,Nathalie Van der Aa,Karolien Goffin,Michel Koole,Kathleen Porke,Marc Van de Velde,Liesbeth Rooms,Wim Van Paesschen,Hilde Van Esch,Koen Van Laere,R. Frank Kooy	41
4	FRA2A Is a CGG Repeat Expansion Associated with Silencing of AFF3 2014 ·PLoS Genetics ·(unknown),Liesbeth Rooms,Jacqueline K. Rainger,Martin S. Taylor,Hemant Bengani,David I. Wilson,Chandra Sekhar Reddy Chilamakuri,Harris Morrison,Geert Vandeweyer,Edwin Reyniers,Evelyn Douglas,(unknown),Eric Haan,Jozef Gécz,David Fitzpatrick,R. Frank Kooy	29
5	A de novo balanced t(2;6)(p15;p22.3) in a patient with West Syndrome disrupts a lnc-RNA 2012 ·Epilepsy Research ·Geert Vandeweyer,Nathalie Van der Aa,Berten Ceulemans,Bregje W.M. van Bon,Liesbeth Rooms,R. Frank Kooy	9
6	Advances in understanding fragile X syndrome and related disorders 2011 ·Current Opinion in Pediatrics ·Liesbeth Rooms,R. Frank Kooy	17
7	CNV-WebStore: Online CNV Analysis, Storage and Interpretation 2011 ·BMC Bioinformatics ·Geert Vandeweyer,Edwin Reyniers,Wim Wuyts,Liesbeth Rooms,R. Frank Kooy	55
8	Array‐based MLPA to detect recurrent copy number variations in patients with idiopathic mental retardation 2011 ·American Journal of Medical Genetics Part A ·Liesbeth Rooms,Geert Vandeweyer,Edwin Reyniers,(unknown),(unknown),Nathalie Van der Aa,R. Rossau,R. Frank Kooy	10
9	Dandy‐Walker complex in a boy with a 5 Mb deletion of region 1q44 due to a paternal t(1;20)(q44;q13.33) 2007 ·American Journal of Medical Genetics Part A ·Martin Poot,Hester Y. Kroes,(unknown),Marc J. Eleveld,Liesbeth Rooms,Rutger A. J. Nievelstein,Daniël Olde Weghuis,René C. F. M. Vreuls,G. Hageman,R. Frank Kooy,Ron Hochstenbach	31
10	A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review 2007 ·Clinical Dysmorphology ·Winnie Courtens,J. Wauters,Marek Wojciechowski,Edwin Reyniers,(unknown),Rob van Luijk,Liesbeth Rooms,R. Frank Kooy,Wim Wuyts	5
11	Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches 2007 ·European Journal of Human Genetics ·David A. Koolen,Erik A. Sistermans,(unknown),Samantha J.L. Knight,Regina Regan,(unknown),R. Frank Kooy,Liesbeth Rooms,Corrado Romano,Marco Fichera,Albert Schinzel,Alessandra Baumer,Britt-Marie Anderlid,Jacqueline Schoumans,Ad Geurts van Kessel,Magnus Nordenskjöld,Bert B.A. de Vries	12
12	Diverse chromosome breakage mechanisms underlie subtelomeric rearrangements, a common cause of mental retardation 2006 ·Human Mutation ·Liesbeth Rooms,Edwin Reyniers,R. Frank Kooy	14
13	A subterminal deletion of the long arm of chromosome 10: A clinical report and review 2006 ·American Journal of Medical Genetics Part A ·Winnie Courtens,Wim Wuyts,Liesbeth Rooms,(unknown),J. Wauters	39
14	TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletions 2006 ·European Journal of Human Genetics ·Liesbeth Rooms,Edwin Reyniers,Stefaan Scheers,Rob van Luijk,J. Wauters,(unknown),Zsuzsanna Callaerts‐Vegh,Rudi D’Hooge,Gabrielle Mengus,Irwin Davidson,Winnie Courtens,R. Frank Kooy	34
15	A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review 2006 ·European Journal of Medical Genetics ·Winnie Courtens,Wim Wuyts,Stefaan Scheers,Rob van Luijk,Edwin Reyniers,Liesbeth Rooms,Berten Ceulemans,R. Frank Kooy,J. Wauters	8
16	Clinical report of a pure subtelomeric 1qter deletion in a boy with mental retardation and multiple anomalies adds further evidence for a specific phenotype 2005 ·American Journal of Medical Genetics Part A ·Yolande van Bever,Liesbeth Rooms,Annick Laridon,Edwin Reyniers,Rob van Luijk,Stefaan Scheers,J. Wauters,R. Frank Kooy	49
17	Multiplex ligation‐dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics 2005 ·Clinical Genetics ·Liesbeth Rooms,Edwin Reyniers,Wim Wuyts,Katrien Storm,Rob van Luijk,Stefaan Scheers,J. Wauters,Jenneke van den Ende,Martine Biervliet,François Eyskens,G. Van Goethem,Annick Laridon,Berten Ceulemans,Winnie Courtens,R. Frank Kooy	51
18	Subtelomeric rearrangements in the mentally retarded: A comparison of detection methods 2005 ·Human Mutation ·Liesbeth Rooms,Edwin Reyniers,R. Frank Kooy	42
19	Screening for subtelomeric rearrangements using genetic markers in 70 patients with unexplained mental retardation 2003 ·Annales de Génétique ·Liesbeth Rooms,Edwin Reyniers,Rob van Luijk,(unknown),J. Wauters,R. Frank Kooy	9
20	Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA) 2003 ·Human Mutation ·Liesbeth Rooms,Edwin Reyniers,Rob van Luijk,Stefaan Scheers,J. Wauters,Berten Ceulemans,Jenneke van den Ende,Yolande van Bever,R. Frank Kooy	79

About Liesbeth Rooms

Liesbeth Rooms is a scholar working on Genetics, Cognitive Neuroscience and Pediatrics, Perinatology and Child Health, having authored 26 papers that have together received 749 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (19 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Autism Spectrum Disorder Research (7 papers). The work is most often cited by research in Genetics (593 citations), Pediatrics, Perinatology and Child Health (133 citations) and Cognitive Neuroscience (118 citations). Liesbeth Rooms has collaborated with scholars based in Belgium, Netherlands and United Kingdom. Frequent co-authors include R. Frank Kooy, Edwin Reyniers, J. Wauters, Wim Wuyts, Rob van Luijk, Stefaan Scheers, Geert Vandeweyer, Winnie Courtens, Berten Ceulemans and Jenneke van den Ende. Their work appears in journals such as PLoS ONE, PLoS Genetics and BMC Bioinformatics.

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