Edwin Reyniers

5.6k total citations
67 papers, 3.6k citations indexed

About

Edwin Reyniers is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Edwin Reyniers has authored 67 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Genetics, 35 papers in Molecular Biology and 18 papers in Cognitive Neuroscience. Recurrent topics in Edwin Reyniers's work include Genetics and Neurodevelopmental Disorders (42 papers), Genomic variations and chromosomal abnormalities (23 papers) and Autism Spectrum Disorder Research (18 papers). Edwin Reyniers is often cited by papers focused on Genetics and Neurodevelopmental Disorders (42 papers), Genomic variations and chromosomal abnormalities (23 papers) and Autism Spectrum Disorder Research (18 papers). Edwin Reyniers collaborates with scholars based in Belgium, Netherlands and United States. Edwin Reyniers's co-authors include R. Frank Kooy, Ben A. Oostra, Kristel De Boulle, Patrick J. Willems, Lieve Vits, Annemieke J.M.H. Verkerk, Esther de Graaff, Bernadette Van Roy, C.E. Bakker and Liesbeth Rooms and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Neuroscience.

In The Last Decade

Edwin Reyniers

67 papers receiving 3.5k citations

Peers

Countries citing papers authored by Edwin Reyniers

Since Specialization

Citations

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

Fields of papers citing papers by Edwin Reyniers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Edwin Reyniers

This figure shows the co-authorship network connecting the top 25 collaborators of Edwin Reyniers. A scholar is included among the top collaborators of Edwin Reyniers 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 Edwin Reyniers. Edwin Reyniers 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	RNU4‐2 ‐Related Neurodevelopmental Disorder Is Associated With a Recognisable Facial Gestalt 2024 ·Clinical Genetics ·Jessica Rosenblum, Diane Beysen, Anna Jansen, Marjan De Rademaeker, Edwin Reyniers, Katrien Janssens, Marije Meuwissen	3
2	The Genetic Puzzle of Cerebral Palsy: Results of a Monocentric Study 2024 ·Pediatric Neurology ·(unknown), Diane Beysen, Berten Ceulemans, (unknown), (unknown), Filip Roelens, Edwin Reyniers, Ligia Mateiu, Katrien Janssens, Marije Meuwissen	1
3	Genetic Testing Contributes to Diagnosis in Cerebral Palsy: Aicardi-Goutières Syndrome as an Example 2021 ·Frontiers in Neurology ·Diane Beysen, (unknown), (unknown), Benson Ogunjimi, (unknown), Edwin Reyniers, Katrien Janssens, (unknown)	5
4	PLCB1 epileptic encephalopathies; Review and expansion of the phenotypic spectrum 2016 ·European Journal of Paediatric Neurology ·An‐Sofie Schoonjans, Marije Meuwissen, Edwin Reyniers, R. Frank Kooy, Berten Ceulemans	11
5	Vitamin D-dependent rickets type II: report of a novel mutation in the vitamin D receptor gene. 2008 ·PubMed ·Yousef Shafeghati, (unknown), (unknown), Edwin Reyniers, Wim Wuyts	10
6	Diverse chromosome breakage mechanisms underlie subtelomeric rearrangements, a common cause of mental retardation 2006 ·Human Mutation ·Liesbeth Rooms, Edwin Reyniers, R. Frank Kooy	14
7	A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism 2006 ·Nature Genetics ·David A. Koolen, Lisenka E.L.M. Vissers, Rolph Pfundt, Nicole de Leeuw, Samantha J.L. Knight, Regina Regan, R. Frank Kooy, Edwin Reyniers, Corrado Romano, Marco Fichera, Albert Schinzel, Alessandra Baumer, Britt-Marie Anderlid, Jacqueline Schoumans, Nine V.A.M. Knoers, Ad Geurts van Kessel, Erik A. Sistermans, Joris A. Veltman, Han G. Brunner, Bert B.A. de Vries	305
8	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
9	Somatic and gonadal mosaicism in Hutchinson–Gilford progeria 2005 ·American Journal of Medical Genetics Part A ·Wim Wuyts, Martine Biervliet, Edwin Reyniers, Maria Rosaria D’Apice, Giuseppe Novelli, Katrien Storm	27
10	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
11	Identification of a family with nonspecific mental retardation (MRX79) with the A140V mutation in theMECP2 gene: Is there a need for routine screening? 2002 ·Human Mutation ·Birgitta Winnepenninckx, (unknown), (unknown), Edwin Reyniers, R. Frank Kooy	32
12	Family MRX9 revisited: Further evidence for locus heterogeneity in MRX 2002 ·American Journal of Medical Genetics ·Birgitta Winnepenninckx, (unknown), Edwin Reyniers, Peter Paul De Deyn, Fatima Abidi, Charles E. Schwartz, R. Frank Kooy	2
13	Neuroanatomy of the fragile X knockout mouse brain studied using in vivo high resolution magnetic resonance imaging 1999 ·European Journal of Human Genetics ·R. Frank Kooy, Edwin Reyniers, Marleen Verhoye, Jan Sijbers, Cathy Bakker, Ben A. Oostra, Patrick J. Willems, Annemie Van der Linden	54
14	Mildly impaired water maze performance in maleFmr1 knockout mice 1997 ·Neuroscience ·Rudi D’Hooge, Guy Nagels, F. Franck, C.E. Bakker, Edwin Reyniers, Katrien Storm, R. Frank Kooy, B. A. Oostra, Patrick J. Willems, Peter Paul De Deyn	164
15	Severe mental retardation and macroorchidism without mutation in the FMR1 gene 1996 ·American Journal of Medical Genetics ·Edwin Reyniers, G. Wolff, Gholamali Tariverdian, Kristel De Boulle, Katrien Storm, R. Frank Kooy, (unknown)	7
16	FMR1 Knockout mice: A model to study fragile X mental retardation 1994 ·The American Journal of Human Genetics ·B.A. Oostra, C.E. Bakker, Edwin Reyniers	156
17	MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM 1994 ·Nature Genetics ·Lieve Vits, Guy Van Camp, Paul Coucke, Erik Fransén, Kristel De Boulle, Edwin Reyniers, Bernhard Korn, Annemarie Poustka, Golder N. Wilson, Connie Schrander‐Stumpel, Robin M. Winter, Charles Schwartz, Patrick J. Willems	110
18	Alternative splicing in the fragile X gene FMR1 1993 ·Human Molecular Genetics ·Annemieke J.M.H. Verkerk, Esther de Graaff, Kristel De Boulle, Evan E. Eichler, David Konecki, Edwin Reyniers, Antonella Manca, Annemarie Poustka, Patrick J. Willems, David L. Nelson, B. A. Oostra	114
19	Alternative splicing in the fragile X gene FMR1 1993 ·Human Molecular Genetics ·Annemieke J.M.H. Verkerk, Esther de Graaff, Kristel De Boulle, Evan E. Eichler, David Konecki, Edwin Reyniers, Antonella Manca, Annemarie Poustka, Patrick J. Willems, David L. Nelson, Ben A. Oostra	86
20	A point mutation in the FMR-1 gene associated with fragile X mental retardation 1993 ·Nature Genetics ·Kristel De Boulle, Annemieke J.M.H. Verkerk, Edwin Reyniers, Lieve Vits, Jan Hendrickx, Bernadette Van Roy, (unknown), Esther de Graaff, Ben A. Oostra, (unknown)	484

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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