Rob van Luijk

473 citations

9 papers · 345 indexed · h-index 8

Impact in

Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders

Papers in ⓘ

Genetics 9
- Genomic variations and chromosomal abnormalities 8
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 3
Plant Science 3
- Chromosomal and Genetic Variations 3

Co-authors: Stefaan Scheers (7 shared papers)J. Wauters (8 shared papers)R. Frank Kooy (8 shared papers)Edwin Reyniers (7 shared papers)Liesbeth Rooms (7 shared papers)Berten Ceulemans (4 shared papers)Yolande van Bever (2 shared papers)Jenneke van den Ende (2 shared papers)
Journals: Human Mutation (2 papers)European Journal of Human Genetics (1 paper)European Journal of Medical Genetics (1 paper)Clinical Genetics (1 paper)Cytogenetic and Genome Research (1 paper)
Partner nations: Belgium Croatia India

In The Last Decade

Rob van Luijk

9 papers receiving 336 citations

Peers

Countries citing papers authored by Rob van Luijk

Since Specialization

Citations

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

Fields of papers citing papers by Rob van Luijk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rob van Luijk. 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 Rob van Luijk. The network helps show where Rob van Luijk may publish in the future.

Co-authors

The 25 scholars most cited alongside Rob van Luijk, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Rob van Luijk Line = papers co-authored together Rob van Luijk links everyone, so they are left out of the graph.

All Works

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9 of 9 papers shown

#	Work
1	Microdeletions involving theSCN1A gene may be common inSCN1A-mutation-negative SMEI patients Human Mutation ·Arvid Suls, Kristl G. Claeys, D. Goossens, B Harding, Rob van Luijk, Stefaan Scheers, Liesbet Deprez, Dominique Audenaert, Tine Van Dyck, Sabine Beeckmans, Iris Smouts, Berten Ceulemans, Lieven Lagae, Gunnar Buyse, Nina Barišić, Jean‐Paul Misson, J. Wauters, Jurgen Del‐Favero, Peter De Jonghe, Lieve Claes	2006	90
2	Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA) 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	2003	79
3	Multiplex ligation‐dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics 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	2005	51
4	Clinical report of a pure subtelomeric 1qter deletion in a boy with mental retardation and multiple anomalies adds further evidence for a specific phenotype 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	2005	49
5	TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletions European Journal of Human Genetics ·Liesbeth Rooms, Edwin Reyniers, Stefaan Scheers, Rob van Luijk, J. Wauters, Leen Van Aerschot, Zsuzsanna Callaerts‐Vegh, Rudi D’Hooge, Gabrielle Mengus, Irwin Davidson, Winnie Courtens, R. Frank Kooy	2006	34
6	The molecular basis of the folate-sensitive fragile site FRA11A at 11q13 Cytogenetic and Genome Research ·Kim Debacker, Birgitta Winnepenninckx, Cheryl Longman, J. Colgan, JL Tolmie, Ronald S. Murray, Rob van Luijk, Stefaan Scheers, David Fitzpatrick, R. Frank Kooy	2007	20
7	Screening for subtelomeric rearrangements using genetic markers in 70 patients with unexplained mental retardation Annales de Génétique ·Liesbeth Rooms, Edwin Reyniers, Rob van Luijk, Stefan Scheers, J. Wauters, R. Frank Kooy	2003	9
8	A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review 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	2006	8
9	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 Clinical Dysmorphology ·Winnie Courtens, J. Wauters, Marek Wojciechowski, Edwin Reyniers, Stefan Scheers, Rob van Luijk, Liesbeth Rooms, R. Frank Kooy, Wim Wuyts	2007	5

About Rob van Luijk

Rob van Luijk is a scholar working on Genetics, Plant Science, Psychiatry and Mental health, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 9 papers that have together received 345 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (3 papers), Chromosomal and Genetic Variations (3 papers), Congenital heart defects research (1 paper), Advanced biosensing and bioanalysis techniques (1 paper), Chromatin Remodeling and Cancer (1 paper) and Epilepsy research and treatment (1 paper). The work is most often cited by research in Genetics (276 citations), Pediatrics, Perinatology and Child Health (90 citations), Psychiatry and Mental health (61 citations), Molecular Biology (153 citations) and Plant Science (66 citations). Rob van Luijk has collaborated with scholars based in Belgium, Croatia and India. Frequent co-authors include Stefaan Scheers, J. Wauters, R. Frank Kooy, Edwin Reyniers, Liesbeth Rooms, Berten Ceulemans, Yolande van Bever, Jenneke van den Ende, Annick Laridon and Winnie Courtens. Their work appears in journals such as Human Mutation, European Journal of Human Genetics, European Journal of Medical Genetics, Clinical Genetics and Cytogenetic and Genome Research.

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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