Bert B.A. de Vries

24.7k citations

114 papers · 7.4k · 3 hit papers · h-index 40

Impact in

Genetics top 0.1%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Congenital Ear and Nasal Anomalies
Molecular Biology top 2%
- Congenital heart defects research

Papers in

Genetics 87
- Genomic variations and chromosomal abnormalities 60
- Genetics and Neurodevelopmental Disorders 41
- Genomics and Rare Diseases 34
- Congenital Ear and Nasal Anomalies 6
Molecular Biology 52
- Congenital heart defects research 20
- Epigenetics and DNA Methylation 7

Co-authors: Joris A. Veltman (25 shared papers)Lisenka E.L.M. Vissers (23 shared papers)Han G. Brunner (15 shared papers)Ad Geurts van Kessel (12 shared papers)David A. Koolen (29 shared papers)Irene M. Janssen (5 shared papers)Christian Gilissen (10 shared papers)Alexander Hoischen (7 shared papers)
Journals: European Journal of Human Genetics (13 papers)The American Journal of Human Genetics (10 papers)European Journal of Medical Genetics (6 papers)Human Molecular Genetics (5 papers)Journal of Medical Genetics (5 papers)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Bert B.A. de Vries

109 papers receiving 7.3k citations

Bert B.A. de Vries's Hit Papers

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Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability 2012 · 997 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2012 New England Journal of Medicine
2010 Nature Genetics
2004 Nature Genetics

Peers

Countries citing papers authored by Bert B.A. de Vries

Since Specialization

Citations

This map shows the geographic impact of Bert B.A. 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 B.A. 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 B.A. de Vries more than expected).

Fields of papers citing papers by Bert B.A. de Vries

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 114 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability New England Journal of Medicine ·Joep de Ligt, Marjolein H. Willemsen, Bregje W.M. van Bon, Tjitske Kleefstra, Helger G. Yntema, Thessa Kroes, Anneke T. Vulto-van Silfhout, David A. Koolen, Petra de Vries, Christian Gilissen, Marisol del Rosario, Alexander Hoischen, Hans Scheffer, Bert B.A. de Vries, Han G. Brunner, Joris A. Veltman, Lisenka E.L.M. Vissers Hit paper breakdown →	2012	997
2	Mutations in a new member of the chromodomain gene family cause CHARGE syndrome Nature Genetics ·Lisenka E.L.M. Vissers, Conny M.A. van Ravenswaaij, R.J.C. Admiraal, Jane A. Hurst, Bert B.A. de Vries, Irene M. Janssen, W A van der Vliet, Erik Huys, Pieter J. de Jong, Ben C.J. Hamel, Eric Schoenmakers, Han G. Brunner, Joris A. Veltman, Ad Geurts van Kessel Hit paper breakdown →	2004	881
3	A de novo paradigm for mental retardation Nature Genetics ·Lisenka E.L.M. Vissers, Joep de Ligt, Christian Gilissen, Irene M. Janssen, Marloes Steehouwer, Petra de Vries, Bart van Lier, Peer Arts, Nienke Wieskamp, Marisol del Rosario, Bregje W.M. van Bon, Alexander Hoischen, Bert B.A. de Vries, Han G. Brunner, Joris A. Veltman Hit paper breakdown →	2010	530
4	Diagnostic Genome Profiling in Mental Retardation The American Journal of Human Genetics ·Bert B.A. de Vries, Rolph Pfundt, M.A.R. Leisink, David A. Koolen, Lisenka E.L.M. Vissers, Irene M. Janssen, Simon V. van Reijmersdal, Willy M. Nillesen, Erik Huys, Nicole de Leeuw, Dominique Smeets, Erik A. Sistermans, Ton Feuth, Conny M.A. van Ravenswaaij‐Arts, Ad Geurts van Kessel, Eric Schoenmakers, Han G. Brunner, Joris A. Veltman	2005	413
5	Array-Based Comparative Genomic Hybridization for the Genomewide Detection of Submicroscopic Chromosomal Abnormalities The American Journal of Human Genetics ·Lisenka E.L.M. Vissers, Bert B.A. de Vries, Kazutoyo Osoegawa, Irene M. Janssen, Ton Feuth, Chik On Choy, Huub Straatman, Walter van der Vliet, Erik Huys, Anke van Rijk, Dominique Smeets, Conny M.A. van Ravenswaaij‐Arts, Nine V.A.M. Knoers, Ineke van der Burgt, Pieter J. de Jong, Han G. Brunner, Ad Geurts van Kessel, Eric Schoenmakers, Joris A. Veltman	2003	348
6	A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism 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	2006	307
7	CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene Journal of Medical Genetics ·M.C.J. Jongmans, R.J.C. Admiraal, Kim P. van der Donk, Lisenka E.L.M. Vissers, Annette F. Baas, Livia Kapusta, Johanna M. van Hagen, D Donnai, Thomy de Ravel, Joris A. Veltman, Ad Geurts van Kessel, Bert B.A. de Vries, Han G. Brunner, Lies H. Hoefsloot, Conny M.A. van Ravenswaaij	2005	304
8	Loss-of-Function Mutations in Euchromatin Histone Methyl Transferase 1 (EHMT1) Cause the 9q34 Subtelomeric Deletion Syndrome The American Journal of Human Genetics ·Tjitske Kleefstra, Han G. Brunner, Jeanne Amiel, Astrid Oudakker, Willy M. Nillesen, Alex Magee, David Geneviève, Valérie Cormier‐Daire, Hilde Van Esch, Jean‐Pierre Fryns, Ben C.J. Hamel, Erik A. Sistermans, Bert B.A. de Vries, Hans van Bokhoven	2006	279
9	Clinical studies on submicroscopic subtelomeric rearrangements: a checklist Journal of Medical Genetics ·Bert B.A. de Vries, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	2001	190
10	3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome The American Journal of Human Genetics ·Lionel Willatt, James J. Cox, John Barber, Elisabet Dachs Cabanas, Amanda Collins, Dian Donnai, David Fitzpatrick, Eddy Maher, Howard Martin, Josep Parnau, Lesley Pindar, Jacqueline Ramsay, Charles Shaw‐Smith, Erik A. Sistermans, Michael Tettenborn, Dorothy Trump, Bert B.A. de Vries, Kate Walker, F. Lucy Raymond	2005	168
11	Diagnostic Exome Sequencing in Persons With Severe Intellectual Disability Obstetrical & Gynecological Survey ·Joep de Ligt, Marjolein H. Willemsen, Bregje W.M. van Bon, Tjitske Kleefstra, Helger G. Yntema, Thessa Kroes, Anneke T. Vulto-van Silfhout, David A. Koolen, Petra de Vries, Christian Gilissen, Marisol del Rosario, Alexander Hoischen, Hans Scheffer, Bert B.A. de Vries, Han G. Brunner, Joris A. Veltman, Lisenka E.L.M. Vissers	2013	142
12	Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11 Human Molecular Genetics ·Yuan Wu, Peter Heutink, Bert B.A. de Vries, Lodewijk A. Sandkuijl, A.M.W. van den Ouweland, Martinus F. Niermeijer, H. Galjaard, Edwin Reyniers, Patrick J. Willems, D. J. J. Halley	1994	135
13	Characterization of a recurrent 15q24 microdeletion syndrome Human Molecular Genetics ·Andrew J. Sharp, Rebecca R. Selzer, Joris A. Veltman, Stefania Gimelli, Giorgio Gimelli, Pasquale Striano, Antonietta Coppola, Regina Regan, Sue Price, Nine V.A.M. Knoers, Peggy S. Eis, Han G. Brunner, Raoul C. M. Hennekam, Samantha J.L. Knight, Bert B.A. de Vries, Orsetta Zuffardi, Evan E. Eichler	2007	129
14	Fragile X syndrome: diagnosis, treatment and research Human Genetics ·Bert B.A. de Vries	2003	123
15	Screening for subtelomeric rearrangements in 210 patients with unexplained mental retardation using multiplex ligation dependent probe amplification (MLPA) Journal of Medical Genetics ·David A. Koolen, Willy M. Nillesen, Martina H. A. Versteeg, Gerard Merkx, Nine V.A.M. Knoers, Marleen Kets, Sascha Vermeer, Conny M.A. van Ravenswaaij, Carolien G. F. de Kovel, Han G. Brunner, Dominique Smeets, Bert B.A. de Vries, Erik A. Sistermans	2004	122
16	TDP2 protects transcription from abortive topoisomerase activity and is required for normal neural function Nature Genetics ·Fernando Gómez-Herreros, Janneke Schuurs-Hoeijmakers, Mark McCormack, Marie T. Greally, Stuart L. Rulten, Rocío Romero‐Granados, Timothy J. Counihan, Elijah Chaila, Judith Conroy, Sean Ennis, Norman Delanty, Felipe Cortés‐Ledesma, Arjan P.M. de Brouwer, Gianpiero L. Cavalleri, Sherif F. El‐Khamisy, Bert B.A. de Vries, Keith W. Caldecott	2014	116
17	Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture Human Molecular Genetics ·Lisenka E.L.M. Vissers, Samarth Bhatt, Irene M. Janssen, Zhilian Xia, Seema R. Lalani, Rolph Pfundt, Katarzyna Derwińska, Bert B.A. de Vries, Christian Gilissen, Alexander Hoischen, Monika Nesteruk, Barbara Wiśniowiecka‐Kowalnik, Marta Smyk, Han G. Brunner, Sau Wai Cheung, Ad Geurts van Kessel, Joris A. Veltman, Paweł Stankiewicz	2009	114
18	Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosis Journal of Medical Genetics ·Lisenka E.L.M. Vissers, Bert B.A. de Vries, Joris A. Veltman	2009	110
19	Genomic microarrays in mental retardation: A practical workflow for diagnostic applications Human Mutation ·David A. Koolen, Rolph Pfundt, Nicole de Leeuw, Jayne Y. Hehir‐Kwa, Willy M. Nillesen, Ineke Neefs, Ine Scheltinga, Erik A. Sistermans, H.J.M. Smeets, Han G. Brunner, Ad Geurts van Kessel, Joris A. Veltman, Bert B.A. de Vries	2008	103
20	Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype American Journal of Medical Genetics Part A ·Mariëlle E.M. Swinkels, Annet Simons, Dominique Smeets, Lisenka E.L.M. Vissers, Joris A. Veltman, Rolph Pfundt, Bert B.A. de Vries, Brigitte H. W. Faas, Connie T.R.M. Schrander‐Stumpel, Emma McCann, Elizabeth Sweeney, Paul May, Jos Draaisma, Nine V.A.M. Knoers, Ad Geurts van Kessel, Conny M.A. van Ravenswaaij‐Arts	2008	89

About Bert B.A. de Vries

Bert B.A. de Vries is a scholar working on Genetics, Molecular Biology, Plant Science, Cognitive Neuroscience and Surgery, having authored 114 papers that have together received 7.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (60 papers), Genetics and Neurodevelopmental Disorders (41 papers), Genomics and Rare Diseases (34 papers), Congenital heart defects research (20 papers), Chromosomal and Genetic Variations (16 papers), Autism Spectrum Disorder Research (12 papers), Epigenetics and DNA Methylation (7 papers) and Congenital Ear and Nasal Anomalies (6 papers). The work is most often cited by research in Genetics (4.7k citations), Genetics (808 citations), Molecular Biology (3.2k citations), Pediatrics, Perinatology and Child Health (612 citations) and Cognitive Neuroscience (562 citations). Bert B.A. de Vries has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Joris A. Veltman, Lisenka E.L.M. Vissers, Han G. Brunner, Ad Geurts van Kessel, David A. Koolen, Irene M. Janssen, Christian Gilissen, Alexander Hoischen, Tjitske Kleefstra and Bregje W.M. van Bon. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, European Journal of Medical Genetics, Human Molecular Genetics and Journal of Medical Genetics.

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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Bert B.A. de Vries

Bert B.A. de Vries's Hit Papers

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