Gert‐Jan B. van Ommen

29.1k total citations · 5 hit papers
185 papers, 12.8k citations indexed

About

Gert‐Jan B. van Ommen is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Gert‐Jan B. van Ommen has authored 185 papers receiving a total of 12.8k indexed citations (citations by other indexed papers that have themselves been cited), including 142 papers in Molecular Biology, 45 papers in Genetics and 30 papers in Cellular and Molecular Neuroscience. Recurrent topics in Gert‐Jan B. van Ommen's work include Muscle Physiology and Disorders (64 papers), RNA Research and Splicing (36 papers) and Genetic Neurodegenerative Diseases (28 papers). Gert‐Jan B. van Ommen is often cited by papers focused on Muscle Physiology and Disorders (64 papers), RNA Research and Splicing (36 papers) and Genetic Neurodegenerative Diseases (28 papers). Gert‐Jan B. van Ommen collaborates with scholars based in Netherlands, United Kingdom and United States. Gert‐Jan B. van Ommen's co-authors include Johan T. den Dunnen, Annemieke Aartsma‐Rus, J.C.T. van Deutekom, Peter A.C. ’t Hoen, George W. Padberg, Ivo F.A.C. Fokkema, Anneke A. M. Janson, Rune R. Frants, Jan J.G.M. Verschuuren and Lodewijk A. Sandkuijl and has published in prestigious journals such as Nature, New England Journal of Medicine and Cell.

In The Last Decade

Gert‐Jan B. van Ommen

182 papers receiving 12.6k 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.

Deep sequencing-based expression analysis shows major advances in robustness, resolution and inter-lab portability over five microarray platforms

2008 617 citations Peter A.C. ’t Hoen, Rolf H. A. M. Vossen et al. profile →
Local Dystrophin Restoration with Antisense Oligonucleotide PRO051

2007 577 citations Anneke A. M. Janson, Annemieke Aartsma‐Rus et al. profile →
Entries in the Leiden Duchenne muscular dystrophy mutation database: An overview of mutation types and paradoxical cases that confirm the reading‐frame rule

2006 531 citations Annemieke Aartsma‐Rus, J.C.T. van Deutekom et al. Muscle & Nerve profile →
Systemic Administration of PRO051 in Duchenne's Muscular Dystrophy

2011 518 citations Anneke A. M. Janson, Annemieke Aartsma‐Rus et al. profile →
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

1992 514 citations Cisca Wijmenga, Gert‐Jan B. van Ommen et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gert‐Jan B. van Ommen Netherlands	58	10.2k	3.2k	1.6k	1.5k	1.4k	185	12.8k
Egbert Bakker Netherlands	62	7.2k 0.7×	4.1k 1.3×	1.1k 0.7×	1.4k 0.9×	1.4k 1.0×	246	12.3k
Raju Kucherlapati United States	69	13.2k 1.3×	4.2k 1.3×	859 0.5×	1.0k 0.7×	960 0.7×	230	19.4k
Johan T. den Dunnen Netherlands	72	14.8k 1.5×	5.9k 1.8×	1.4k 0.9×	2.2k 1.5×	1.9k 1.3×	300	20.6k
Thomas Meitinger Germany	69	11.2k 1.1×	5.5k 1.7×	1.7k 1.0×	481 0.3×	1.2k 0.8×	319	19.1k
André Reis Germany	60	7.7k 0.8×	4.4k 1.4×	1.4k 0.8×	451 0.3×	470 0.3×	320	13.6k
Tim M. Strom Germany	63	8.0k 0.8×	6.0k 1.8×	1.5k 0.9×	649 0.4×	518 0.4×	216	16.6k
En Li United States	57	17.0k 1.7×	4.7k 1.5×	1.7k 1.0×	635 0.4×	534 0.4×	119	22.4k
Chad A. Shaw United States	65	7.7k 0.8×	5.7k 1.8×	1.2k 0.7×	609 0.4×	536 0.4×	193	13.9k
Karl V. Voelkerding United States	32	11.2k 1.1×	9.8k 3.0×	1.1k 0.7×	1.6k 1.0×	2.2k 1.6×	86	23.1k
Gert Matthijs Belgium	60	8.3k 0.8×	3.3k 1.0×	640 0.4×	771 0.5×	505 0.4×	332	13.1k

Countries citing papers authored by Gert‐Jan B. van Ommen

Since Specialization

Citations

This map shows the geographic impact of Gert‐Jan B. van Ommen'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 Gert‐Jan B. van Ommen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gert‐Jan B. van Ommen more than expected).

Fields of papers citing papers by Gert‐Jan B. van Ommen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gert‐Jan B. van Ommen. 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 Gert‐Jan B. van Ommen. The network helps show where Gert‐Jan B. van Ommen may publish in the future.

Co-authorship network of co-authors of Gert‐Jan B. van Ommen

This figure shows the co-authorship network connecting the top 25 collaborators of Gert‐Jan B. van Ommen. A scholar is included among the top collaborators of Gert‐Jan B. van Ommen 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 Gert‐Jan B. van Ommen. Gert‐Jan B. van Ommen 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

Fest, Jesse, Lisanne S. Vijfhuizen, Jelle J. Goeman, et al.. (2019). Search for Early Pancreatic Cancer Blood Biomarkers in Five European Prospective Population Biobanks Using Metabolomics. Endocrinology. 160(7). 1731–1742. 20 indexed citations

Törnwall, Outi, et al.. (2018). Role of Academic Biobanks in Public–Private Partnerships in the European Biobanking and BioMolecular Resources Research Infrastructure Community. Biopreservation and Biobanking. 17(1). 46–51. 7 indexed citations

Brennan, Paul, Markus Perola, Gert‐Jan B. van Ommen, & Elio Ríboli. (2017). Chronic disease research in Europe and the need for integrated population cohorts. European Journal of Epidemiology. 32(9). 741–749. 64 indexed citations

Li, Mingkun, Rebecca Rothwell, Martijn Vermaat, et al.. (2016). Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck. Genome Research. 26(4). 417–426. 64 indexed citations

Francioli, Laurent C., Paz Polak, Amnon Koren, et al.. (2015). Genome-wide patterns and properties of de novo mutations in humans. Nature Genetics. 47(7). 822–826. 238 indexed citations

Passtoors, Willemijn M., Erik B. van den Akker, Joris Deelen, et al.. (2015). IL7R gene expression network associates with human healthy ageing. Immunity & Ageing. 12(1). 21–21. 42 indexed citations

Ommen, Gert‐Jan B. van, Outi Törnwall, Christian Bréchot, et al.. (2014). BBMRI-ERIC as a resource for pharmaceutical and life science industries: the development of biobank-based Expert Centres. European Journal of Human Genetics. 23(7). 893–900. 55 indexed citations

Vojinović, Dina, Hieab H.H. Adams, Sven J. van der Lee, et al.. (2014). The dystrophin gene and cognitive function in the general population. European Journal of Human Genetics. 23(6). 837–843. 5 indexed citations

Iterson, Maarten van, Floor A.M. Duijkers, Jules P.P. Meijerink, et al.. (2012). A Novel and Fast Normalization Method for High-Density Arrays. Statistical Applications in Genetics and Molecular Biology. 11(4). 2 indexed citations

10.

Evers, Melvin M., Barry A. Pepers, J.C.T. van Deutekom, et al.. (2011). Targeting Several CAG Expansion Diseases by a Single Antisense Oligonucleotide. PLoS ONE. 6(9). e24308–e24308. 78 indexed citations

11.

Inouye, Michael, Kaisa Silander, Eija Hämäläinen, et al.. (2010). An Immune Response Network Associated with Blood Lipid Levels. PLoS Genetics. 6(9). e1001113–e1001113. 78 indexed citations

12.

Aartsma‐Rus, Annemieke, J.C.T. van Deutekom, Ivo F.A.C. Fokkema, Gert‐Jan B. van Ommen, & Johan T. den Dunnen. (2006). Entries in the Leiden Duchenne muscular dystrophy mutation database: An overview of mutation types and paradoxical cases that confirm the reading‐frame rule. Muscle & Nerve. 34(2). 135–144. 531 indexed citations breakdown →

13.

Cong, Shuyan, Barry A. Pepers, Raymund A.C. Roos, Gert‐Jan B. van Ommen, & Josephine C. Dorsman. (2005). Small N-terminal mutant huntingtin fragments, but not wild type, are mainly present in monomeric form: Implications for pathogenesis. Experimental Neurology. 199(2). 257–264. 6 indexed citations

14.

Cong, Shuyan, Barry A. Pepers, Raymund A.C. Roos, Gert‐Jan B. van Ommen, & Josephine C. Dorsman. (2005). Epitope Mapping of Monoclonal Antibody 4C8 Recognizing the Protein Huntingtin. Hybridoma. 24(5). 231–235. 15 indexed citations

15.

Aartsma‐Rus, Annemieke, Emile J. de Meijer, Anneke A. M. Janson, et al.. (2004). Targeted Exon Skipping in Transgenic hDMD Mice: A Model for Direct Preclinical Screening of Human-Specific Antisense Oligonucleotides. Molecular Therapy. 10(2). 232–240. 95 indexed citations

16.

Ommen, Gert‐Jan B. van. (1998). The Human Genome Project and the Role of Genetics in Health Care. Clinical Chemistry and Laboratory Medicine (CCLM). 36(8). 515–517.

17.

Roelfsema, Jeroen, Lia Spruit, Jasper J. Saris, et al.. (1997). Mutation Detection in the Repeated Part of the PKD1 Gene. The American Journal of Human Genetics. 61(5). 1044–1052. 35 indexed citations

18.

Hoogeveen, A. T., et al.. (1993). Characterization and localization of the Huntington disease gene product. Human Molecular Genetics. 2(12). 2069–2073. 152 indexed citations

19.

Cobben, Jan M., Hans Scheffer, Marjolein Visser, et al.. (1993). Linkage and apparent heterogeneity in proximal spinal muscular atrophies. Neuromuscular Disorders. 3(4). 327–333. 8 indexed citations

20.

Rooij, Karien E. de, et al.. (1993). Defining the Proximal Border of the Huntington Disease Candidate Region by Multipoint Recombination Analyses. Genomics. 16(3). 599–604. 3 indexed citations

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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