Bert de Vries

2.0k total citations
19 papers, 701 citations indexed

About

Bert de Vries is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Bert de Vries has authored 19 papers receiving a total of 701 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Molecular Biology and 6 papers in Cognitive Neuroscience. Recurrent topics in Bert de Vries's work include Genetics and Neurodevelopmental Disorders (9 papers), Autism Spectrum Disorder Research (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). Bert de Vries is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Autism Spectrum Disorder Research (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). Bert de Vries collaborates with scholars based in Netherlands, France and United Kingdom. Bert de Vries's co-authors include Serieta Mohkamsing, Ben A. Oostra, Rob Willemsen, Martinus F. Niermeijer, Didier Devys, Jean‐Louis Mandel, A. van den Ouweland, Dicky Halley, Ans M.W. van den Ouweland and Aad Tibben and has published in prestigious journals such as The Lancet, The American Journal of Human Genetics and Energy Policy.

In The Last Decade

Bert de Vries

17 papers receiving 682 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Bert de Vries Netherlands	11	592	345	332	32	28	19	701
Serieta Mohkamsing Netherlands	9	639 1.1×	347 1.0×	458 1.4×	19 0.6×	23 0.8×	11	686
Linda S. Weaving Australia	9	619 1.0×	428 1.2×	262 0.8×	18 0.6×	44 1.6×	10	771
Anne Maddalena United States	17	736 1.2×	411 1.2×	375 1.1×	65 2.0×	37 1.3×	27	1.1k
Matthew Pastore United States	12	450 0.8×	605 1.8×	291 0.9×	46 1.4×	38 1.4×	23	940
Marja‐Leena Väisänen Finland	8	336 0.6×	200 0.6×	203 0.6×	26 0.8×	37 1.3×	11	447
Inés Quintela Spain	13	184 0.3×	188 0.5×	59 0.2×	23 0.7×	68 2.4×	29	492
Cara Merusi United Kingdom	10	586 1.0×	753 2.2×	270 0.8×	24 0.8×	30 1.1×	10	915
Catherine M. Watson Australia	12	604 1.0×	659 1.9×	217 0.7×	22 0.7×	70 2.5×	19	1.1k
Marzia Pollazzon Italy	14	494 0.8×	368 1.1×	143 0.4×	43 1.3×	30 1.1×	31	692
Anthony Leotta United States	6	611 1.0×	426 1.2×	490 1.5×	41 1.3×	37 1.3×	8	907

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-authorship network of co-authors of Bert de Vries

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

All Works

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19 of 19 papers shown

Beusekom, Ellen van, Sílvia Albert, Johanna M. van Hagen, et al.. (2024). Generation of induced pluripotent stem cell lines from two unrelated patients affected by intellectual disability carrying homozygous variants in SGIP1. Stem Cell Research. 77. 103442–103442.

Koolen, David A., Bert de Vries, Jean‐Louis Mandel, et al.. (2023). Ocular manifestations in Koolen–de Vries syndrome: an international study. Canadian Journal of Ophthalmology. 59(6). e796–e802. 1 indexed citations

Silfhout, Anneke T. Vulto‐van, Bert de Vries, Bregje W.M. van Bon, et al.. (2013). Mutations in MED12 Cause X-Linked Ohdo Syndrome. The American Journal of Human Genetics. 92(3). 401–406. 67 indexed citations

Silfhout, Anneke T. Vulto-van, Jayne Y. Hehir‐Kwa, Bregje W.M. van Bon, et al.. (2013). Clinical Significance of De Novo and Inherited Copy-Number Variation. Human Mutation. 34(12). 1679–1687. 79 indexed citations

Hoischen, Alexander, Anne Badel, Anne Ronan, et al.. (2012). BDNF and DYRK1A Are Variable and Inversely Correlated in Lymphoblastoid Cell Lines from Down Syndrome Patients. Molecular Neurobiology. 46(2). 297–303. 17 indexed citations

Egger, J.I.M., Ellen Wingbermühle, W.M.A. Verhoeven, et al.. (2012). Hypersociability in the behavioral phenotype of 17q21.31 microdeletion syndrome. American Journal of Medical Genetics Part A. 161(1). 21–26. 19 indexed citations

Vries, Bert de, et al.. (2007). Pseudoarthrosis of the clavicle and copper beaten skull associated with chromosome 10p11.21p12.1 microdeletion. American Journal of Medical Genetics Part A. 146A(2). 233–237. 17 indexed citations

Villeneuve, François, et al.. (2001). Umm El-Jimal, Bourgade de "Frontière" : à propos de Bert De Vries (ed.) Umm el-Jimal. I.. Syria. 78(1). 209–217. 2 indexed citations

Vries, Bert de, et al.. (1998). A frontier town and its landscape in northern Jordan. 5 indexed citations

10.

Vries, Bert de, Ans M.W. van den Ouweland, Serieta Mohkamsing, et al.. (1997). Screening and Diagnosis for the Fragile X Syndrome among the Mentally Retarded: An Epidemiological and Psychological Survey. The American Journal of Human Genetics. 61(3). 660–667. 160 indexed citations

11.

Willemsen, Rob, Serieta Mohkamsing, Bert de Vries, et al.. (1997). Rapid antibody test for diagnosing fragile X syndrome: a validation of the technique. Human Genetics. 99(3). 308–311. 81 indexed citations

12.

Vries, Bert de. (1997). The fragile X syndrome: Clinical, genetic and large scale diagnostic studies among mentally retarded individuals. 2 indexed citations

13.

Graaff, Esther de, et al.. (1996). 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. 64(2). 302–308. 34 indexed citations

14.

Willemsen, Rob, Serieta Mohkamsing, Bert de Vries, et al.. (1995). Rapid antibody test for fragile X syndrome. The Lancet. 345(8958). 1147–1148. 136 indexed citations

15.

Vries, Bert de. (1994). What's in a Name: The Anonymity of Ancient Umm el-Jimal. The Biblical Archaeologist. 57(4). 215–219. 4 indexed citations

16.

Vries, Bert de, Esther de Graaff, Annemieke J.M.H. Verkerk, et al.. (1993). Mental Status and Fragile X Expression in Relation to FMR-1 Gene Mutation. European Journal of Human Genetics. 1(1). 72–79. 57 indexed citations

17.

Vries, Bert de. (1991). Archaeology in Jordan. American Journal of Archaeology. 95(2). 253–280. 18 indexed citations

18.

Vries, Bert de & Jan Kommandeur. (1975). Gas for Western Europe: How much for how long?. Energy Policy. 3(1). 24–37. 2 indexed citations

19.

Vries, Bert de. (1966). Iris missouriensis Nutt. in Southwestern Alberta and in Central and Northern British Columbia. The Canadian Field-Naturalist. 80(3). 158–160.

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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