Joris A. Veltman

37.3k total citations · 6 hit papers
201 papers, 15.6k citations indexed

About

Joris A. Veltman is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Joris A. Veltman has authored 201 papers receiving a total of 15.6k indexed citations (citations by other indexed papers that have themselves been cited), including 118 papers in Genetics, 88 papers in Molecular Biology and 26 papers in Cancer Research. Recurrent topics in Joris A. Veltman's work include Genomic variations and chromosomal abnormalities (70 papers), Genomics and Rare Diseases (56 papers) and Genetics and Neurodevelopmental Disorders (28 papers). Joris A. Veltman is often cited by papers focused on Genomic variations and chromosomal abnormalities (70 papers), Genomics and Rare Diseases (56 papers) and Genetics and Neurodevelopmental Disorders (28 papers). Joris A. Veltman collaborates with scholars based in Netherlands, United Kingdom and United States. Joris A. Veltman's co-authors include Han G. Brunner, Lisenka E.L.M. Vissers, Christian Gilissen, Alexander Hoischen, Bert B.A. de Vries, Ad Geurts van Kessel, Irene M. Janssen, Eric Schoenmakers, Rolph Pfundt and Joep de Ligt and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Joris A. Veltman

199 papers receiving 15.3k citations

Hit Papers

5 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability

2012 987 citations Christian Gilissen, Alexander Hoischen et al. profile →
Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

2004 876 citations Lisenka E.L.M. Vissers, R.J.C. Admiraal et al. Nature Genetics profile →
A de novo paradigm for mental retardation

2010 526 citations Lisenka E.L.M. Vissers, Christian Gilissen et al. Nature Genetics profile →
De novo mutations in human genetic disease

2012 514 citations Joris A. Veltman et al. profile →
Genetic studies in intellectual disability and related disorders

2015 448 citations Lisenka E.L.M. Vissers, Christian Gilissen et al. profile →
STAT1 Mutations in Autosomal Dominant Chronic Mucocutaneous Candidiasis

2011 436 citations Alexander Hoischen, Christian Gilissen et al. profile →

Peers

Countries citing papers authored by Joris A. Veltman

Since Specialization

Citations

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

Fields of papers citing papers by Joris A. Veltman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joris A. Veltman. 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 Joris A. Veltman. The network helps show where Joris A. Veltman may publish in the future.

Co-authorship network of co-authors of Joris A. Veltman

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Improved phenotypic classification of male infertility to promote discovery of genetic causes 2023 ·Nature Reviews Urology ·Margot J. Wyrwoll, Godfried W. van der Heijden, Csilla Krausz, Kenneth I. Aston, Sabine Kliesch, Robert I. McLachlan, Liliana Ramos, Donald F. Conrad, Moira K. O’Bryan, Joris A. Veltman, Frank Tüttelmann	21
2	A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene–disease relationships 2021 ·Human Reproduction Update ·Brendan J. Houston, Antoni Riera‐Escamilla, Margot J. Wyrwoll, Albert Salas‐Huetos, Miguel J. Xavier, Liina Nagirnaja, Corinna Friedrich, Don F. Conrad, Kenneth I. Aston, Csilla Krausz, Frank Tüttelmann, Moira K. O’Bryan, Joris A. Veltman, Manon S. Oud	140
3	A systematic review and standardized clinical validity assessment of male infertility genes 2019 ·Human Reproduction ·Manon S. Oud, Ludmila Voložonoka, Roos M. Smits, Lisenka E.L.M. Vissers, Liliana Ramos, Joris A. Veltman	126
4	MetaDome: Pathogenicity analysis of genetic variants through aggregation of homologous human protein domains 2019 ·Human Mutation ·Laurens Wiel, Coos Baakman, (unknown), Joris A. Veltman, Gerrit Vriend, Christian Gilissen	115
5	De Novo Mutations Reflect Development and Aging of the Human Germline 2019 ·Trends in Genetics ·Jakob M. Goldmann, Joris A. Veltman, Christian Gilissen	72
6	Germline de novo mutation clusters arise during oocyte aging in genomic regions with high double-strand-break incidence 2018 ·Nature Genetics ·Jakob M. Goldmann, Vladimir B. Seplyarskiy, Wendy S.W. Wong, Thierry Vilboux, Pieter B. Neerincx, Dale L. Bodian, Benjamin D. Solomon, Joris A. Veltman, John F. Deeken, Christian Gilissen, John E. Niederhuber	46
7	A systematic review and standardized clinical validity assessment of male infertility genes 2018 ·bioRxiv (Cold Spring Harbor Laboratory) ·Manon S. Oud, Ludmila Voložonoka, Roos M. Smits, Lisenka E.L.M. Vissers, Liliana Ramos, Joris A. Veltman	20
8	Germline De Novo Mutation Clusters Arise During Oocyte Aging in Genomic Regions With High Double-Strand-Break Incidence 2018 ·Obstetrical & Gynecological Survey ·Jakob M. Goldmann, Vladimir B. Seplyarskiy, Wendy S.W. Wong, Thierry Vilboux, Pieter B. Neerincx, Dale L. Bodian, Benjamin D. Solomon, Joris A. Veltman, John F. Deeken, Christian Gilissen, John E. Niederhuber	4
9	Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment 2017 ·Scientific Reports ·(unknown), (unknown), Alexander Hoischen, Joris A. Veltman, Nuala H. Simpson, Clyde Francks, Dianne F. Newbury, Simon E. Fisher	62
10	Aggregation of population‐based genetic variation over protein domain homologues and its potential use in genetic diagnostics 2017 ·Human Mutation ·Laurens Wiel, Hanka Venselaar, Joris A. Veltman, Gert Vriend, Christian Gilissen	20
11	Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia 2017 ·Human Mutation ·Manon S. Oud, Liliana Ramos, Moira K. O’Bryan, Robert I. McLachlan, Özlem Okutman, Stéphane Viville, Petra F. de Vries, Dominique Smeets, Dorien Lugtenberg, Jayne Y. Hehir‐Kwa, Christian Gilissen, (unknown), Lisenka E.L.M. Vissers, Alexander Hoischen, (unknown), Kathrin Fleischer, Joris A. Veltman, Michiel J. Noordam	44
12	Parent-of-origin-specific signatures of de novo mutations 2016 ·Nature Genetics ·Jakob M. Goldmann, Wendy S.W. Wong, Michele Pinelli, Terry Farrah, Dale L. Bodian, Anna Stittrich, Gustavo Glusman, Lisenka E.L.M. Vissers, Alexander Hoischen, Jared C. Roach, Joseph G. Vockley, Joris A. Veltman, Benjamin D. Solomon, Christian Gilissen, John E. Niederhuber	196
13	A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia 2012 ·Human Molecular Genetics ·Radek Szklarczyk, Bas F.J. Wanschers, Leo Nijtmans, Richard J. Rodenburg, Johannes Zschocke, Nicola Dikow, Mariël A.M. van den Brand, (unknown), Christian Gilissen, Joris A. Veltman, Marco Nooteboom, Werner J.H. Koopman, Peter H.G.M. Willems, Jan Smeıtınk, Martijn A. Huynen, Lambertus P. van den Heuvel	69
14	Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment 2010 ·The American Journal of Human Genetics ·Margit Schraders, Kwanghyuk Lee, Jaap Oostrik, P.L.M. Huygen, Ghazanfar Ali, Lies H. Hoefsloot, Joris A. Veltman, Frans P.M. Cremers, Sulman Basit, Muhammad Ansar, Cor W. R. J. Cremers, Henricus P. M. Kunst, Wasim Ahmad, R.J.C. Admiraal, Suzanne M. Leal, Hannie Kremer	50
15	Functional Differences Between Mesenchymal Stem Cell Populations Are Reflected by Their Transcriptome 2009 ·Stem Cells and Development ·Bas Jansen, Christian Gilissen, Helene Roelofs, Aneta Oziemlak, Joris A. Veltman, Reinier Raymakers, Joop H. Jansen, Gesine Kögler, Carl G. Figdor, Ruurd Torensma, Gosse J. Adema	114
16	Genomic and Expression Profiling of Human Spermatocytic Seminomas: Primary Spermatocyte as Tumorigenic Precursor and DMRT1 as Candidate Chromosome 9 Gene 2006 ·Cancer Research ·Leendert H. J. Looijenga, Remko Hersmus, Ad Gillis, Rolph Pfundt, Hans Stoop, Ruud J. H. L. M. van Gurp, Joris A. Veltman, H. Berna Beverloo, Ellen van Drunen, Ad Geurts van Kessel, Renee A. Reijo Pera, Dominik T. Schneider, Brenda Summersgill, Janet Shipley, Alan McIntyre, Peter J. van der Spek, Eric Schoenmakers, J. Wolter Oosterhuis	170
17	Novel tumor suppressor gene loci on chromosomes 1p, 11q and 22q in insulinomas 2006 ·Cancer Research ·Yvonne M.H. Versleijen‐Jonkers, Sandra M.H. Claessen, Ton Feuth, Ad Geurts van Kessel, Frans C. S. Ramaekers, Joris A. Veltman, Ernst‐Jan M. Speel	1
18	Supervising UAVs: Improving operator performance by optimizing the human factor 2005 ·International Conference on Human-Computer Interaction ·(unknown), Chris Jansen, Joris A. Veltman	1
19	Genome-Wide Array-Based Comparative Genomic Hybridization Reveals Multiple Amplification Targets and Novel Homozygous Deletions in Pancreatic Carcinoma Cell Lines 2004 ·Cancer Research ·Markus Heidenblad, Eric Schoenmakers, Tord Jonson, Ludmila Gorunova, Joris A. Veltman, Ad Geurts van Kessel, Mattias Höglund	73
20	APPLICATION OF A THREE DIMENSIONAL AUDITORY DISPLAY IN A FLIGHT TASK / ADELBERT W. BRONKHORST, J.A. (HANS) VELTMAN AND LEO VAN BREDA.. 1996 ·Human Factors The Journal of the Human Factors and Ergonomics Society ·Adelbert W. Bronkhorst, Joris A. Veltman, (unknown)	1

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.

Explore authors with similar magnitude of impact