Bert de Vries

2.0k citations

19 papers · 703 · h-index 11

Impact in

Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research

Papers in

Genetics 10
- Genetics and Neurodevelopmental Disorders 9
- Genomic variations and chromosomal abnormalities 3
Molecular Biology 7
- Congenital heart defects research 3
- Epigenetics and DNA Methylation 2

Co-authors: Serieta Mohkamsing (4 shared papers)Ben A. Oostra (3 shared papers)Rob Willemsen (3 shared papers)Martinus F. Niermeijer (2 shared papers)Jean‐Louis Mandel (2 shared papers)A. van den Ouweland (1 shared paper)Didier Devys (1 shared paper)Hugo J. Duivenvoorden (1 shared paper)
Journals: The American Journal of Human Genetics (2 papers)Canadian Journal of Ophthalmology (1 paper)Human Genetics (1 paper)Energy Policy (1 paper)Molecular Neurobiology (1 paper)
Partner nations: Netherlands France Belgium

In The Last Decade

Bert de Vries

17 papers receiving 685 citations

Peers

Countries citing papers authored by Bert de Vries

Since Specialization

Citations

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

Fields of papers citing papers by Bert de Vries

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bert de Vries. 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 Bert de Vries. The network helps show where Bert de Vries may publish in the future.

Co-authors

The 25 scholars most cited alongside Bert de Vries, 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 Bert de Vries Line = papers co-authored together Bert de Vries links everyone, so they are left out of the graph.

All Works

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19 of 19 papers shown

#	Work
1	Screening and Diagnosis for the Fragile X Syndrome among the Mentally Retarded: An Epidemiological and Psychological Survey The American Journal of Human Genetics ·Bert de Vries, Ans M.W. van den Ouweland, Serieta Mohkamsing, Hugo J. Duivenvoorden, Esther Mol, Kirsten Gelsema, Monique van Rijn, Dicky Halley, Lodewijk A. Sandkuijl, Ben A. Oostra, Aad Tibben, Martinus F. Niermeijer	1997	159
2	Rapid antibody test for fragile X syndrome The Lancet ·Rob Willemsen, Serieta Mohkamsing, Bert de Vries, A. van den Ouweland, H. Galjaard, Ben A. Oostra, Didier Devys, Jean‐Louis Mandel	1995	136
3	Rapid antibody test for diagnosing fragile X syndrome: a validation of the technique Human Genetics ·Rob Willemsen, Arie Smits, Serieta Mohkamsing, H. van Beerendonk, Anton de Haan, Bert de Vries, Ans van den Ouweland, Erik A. Sistermans, H. Galjaard, B. A. Oostra	1997	81
4	Clinical Significance of De Novo and Inherited Copy-Number Variation Human Mutation ·Anneke T. Vulto-van Silfhout, Jayne Y. Hehir‐Kwa, Bregje W.M. van Bon, Janneke Schuurs-Hoeijmakers, Stephen Meader, Claudia J.M. Hellebrekers, Ilse J.M. Thoonen, Arjan P.M. de Brouwer, Han G. Brunner, Caleb Webber, Rolph Pfundt, Nicole de Leeuw, Bert de Vries	2013	79
5	Mutations in MED12 Cause X-Linked Ohdo Syndrome The American Journal of Human Genetics ·Anneke T. Vulto‐van Silfhout, Bert de Vries, Bregje W.M. van Bon, Alexander Hoischen, Martina Ruiterkamp‐Versteeg, Christian Gilissen, Fangjian Gao, Marloes van Zwam, Cornelis L. Harteveld, Anthonie J. van Essen, Ben C.J. Hamel, Tjitske Kleefstra, Michèl A.A.P. Willemsen, Helger G. Yntema, Hans van Bokhoven, Han G. Brunner, Thomas Boyer, Arjan P.M. de Brouwer	2013	67
6	Mental Status and Fragile X Expression in Relation to FMR-1 Gene Mutation European Journal of Human Genetics ·Bert de Vries, Agnes M. Wiegers, Esther de Graaff, Annemieke J.M.H. Verkerk, J. O. Van Hemel, D. J. J. Halley, Jean‐Pierre Fryns, Leopold Curfs, Martinus F. Niermeijer, Ben A. Oostra	1993	57
7	The fragile X phenotype in a mosaic male with a deletion showing expression of theFMR1 protein in 28% of the cells American Journal of Medical Genetics ·Esther de Graaff, Bert de Vries, Rob Willemsen, J. O. Van Hemel, Serieta Mohkamsing, Ben A. Oostra, Ans M. W. van den Ouweland	1996	35
8	Hypersociability in the behavioral phenotype of 17q21.31 microdeletion syndrome American Journal of Medical Genetics Part A ·J.I.M. Egger, Ellen Wingbermühle, W.M.A. Verhoeven, Marije Dijkman, Sina Radke, Ellen R. A. de Bruijn, Bert de Vries, Roy P. C. Kessels, David A. Koolen	2012	19
9	Pseudoarthrosis of the clavicle and copper beaten skull associated with chromosome 10p11.21p12.1 microdeletion American Journal of Medical Genetics Part A ·Raveen Shahdadpuri, Bert de Vries, Rolph Pfundt, Nicole de Leeuw, William Reardon	2007	18
10	Archaeology in Jordan American Journal of Archaeology ·Bert de Vries	1991	18
11	BDNF and DYRK1A Are Variable and Inversely Correlated in Lymphoblastoid Cell Lines from Down Syndrome Patients Molecular Neurobiology ·Asma Tlili, Alexander Hoischen, Clémentine Ripoll, Eva Benabou, Anne Badel, Anne Ronan, Renaud Touraine, Yann Grattau, Samantha Stora, Bregje W.M. van Bon, Bert de Vries, Björn Menten, Nele Bockaert, (unknown), Stylianos E. Antonarakis, Dominique Campion, Marie‐Claude Potier, Henri Bléhaut, Jean‐Maurice Delabar, Nathalie Janel	2012	17
12	A frontier town and its landscape in northern Jordan Bert de Vries, John W. Betlyon	1998	5
13	What's in a Name: The Anonymity of Ancient Umm el-Jimal The Biblical Archaeologist ·Bert de Vries	1994	4
14	Gas for Western Europe: How much for how long? Energy Policy ·Bert de Vries, Jan Kommandeur	1975	2
15	Ocular manifestations in Koolen–de Vries syndrome: an international study Canadian Journal of Ophthalmology ·D. Shalev, David A. Koolen, Bert de Vries, Sharon Blum Meirovitch, Jean‐Louis Mandel, Pauline Burger, Alik Rosenfeld, Guy J. Ben Simon, Daphna Landau Prat	2023	2
16	The fragile X syndrome: Clinical, genetic and large scale diagnostic studies among mentally retarded individuals Bert de Vries	1997	2
17	Umm El-Jimal, Bourgade de "Frontière" : à propos de Bert De Vries (ed.) Umm el-Jimal. I. Syria ·François Villeneuve, S. Thomas Parker, Bert de Vries, J. D. SAUER, R.F. Brown, John W. Betlyon, M. Toplyn	2001	2
18	Iris missouriensis Nutt. in Southwestern Alberta and in Central and Northern British Columbia The Canadian Field-Naturalist ·Bert de Vries	1966	0
19	Generation of induced pluripotent stem cell lines from two unrelated patients affected by intellectual disability carrying homozygous variants in SGIP1 Stem Cell Research ·Lieke Dillen, Neelam Fatima, Marina P. Hommersom, Ece Çepni, Fareeha Fatima, Ellen van Beusekom, Sílvia Albert, Johanna M. van Hagen, Bert de Vries, (unknown), Arjan P.M. de Brouwer, Hans van Bokhoven	2024	0

About Bert de Vries

Bert de Vries is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Archeology and Surgery, having authored 19 papers that have together received 703 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (9 papers), Autism Spectrum Disorder Research (6 papers), Archaeology and Historical Studies (4 papers), Congenital heart defects research (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Epigenetics and DNA Methylation (2 papers), Botany and Plant Ecology Studies (1 paper) and Botany, Ecology, and Taxonomy Studies (1 paper). The work is most often cited by research in Genetics (567 citations), Cognitive Neuroscience (280 citations), Molecular Biology (311 citations), Developmental Neuroscience (13 citations) and Archeology (26 citations). Bert de Vries has collaborated with scholars based in Netherlands, France and Belgium. Frequent co-authors include Serieta Mohkamsing, Ben A. Oostra, Rob Willemsen, Martinus F. Niermeijer, Jean‐Louis Mandel, A. van den Ouweland, Didier Devys, Hugo J. Duivenvoorden, Aad Tibben and Ans M.W. van den Ouweland. Their work appears in journals such as The American Journal of Human Genetics, Canadian Journal of Ophthalmology, Human Genetics, Energy Policy and Molecular Neurobiology.

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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