Peter De Rijk

7.2k citations

64 papers · 5.2k indexed · 1 hit paper · h-index 32

Impact in

Ecology top 1%
- Microbial Community Ecology and Physiology
- Parasite Biology and Host Interactions
Molecular Biology top 2%
- Genomics and Phylogenetic Studies
- RNA and protein synthesis mechanisms
- Protist diversity and phylogeny
- RNA modifications and cancer
- RNA Research and Splicing

Papers in

Endocrinology 4
Molecular Biology 47
- RNA and protein synthesis mechanisms 25
- Genomics and Phylogenetic Studies 21
- RNA modifications and cancer 16
- RNA Research and Splicing 8

Co-authors: Rupert De Wächter Yves Van de Peer Jean‐Marc Neefs Jurgen Del‐Favero Rupert De Wachter Sabine Chapelle J. Wuyts Christine Van Broeckhoven
Journals: Nucleic Acids Research (15 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (4 papers)Bioinformatics (3 papers)Human Molecular Genetics (2 papers)Journal of Molecular Evolution (2 papers)
Partner nations: Belgium Netherlands Sweden

In The Last Decade

Peter De Rijk

64 papers receiving 5.1k citations

Hit Papers

align trajectories log scale

Compilation of small ribosomal subunit RNA sequences 1992 · 756 citations

Peers

Countries citing papers authored by Peter De Rijk

Since Specialization

Citations

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

Fields of papers citing papers by Peter De Rijk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter De Rijk. 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 Peter De Rijk. The network helps show where Peter De Rijk may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Combinatorial optimization of gene expression through recombinase-mediated promoter and terminator shuffling in yeast Nature Communications ·Charlotte Cautereels, Jolien Smets, Peter W. Bircham, Dries De Ruysscher, Anna Zimmermann, Peter De Rijk, Jan Steensels, Anton Gorkovskiy, Joleen Masschelein, Kevin J. Verstrepen	2024	18
2	Mitochondrial DNA methylation in metabolic associated fatty liver disease Frontiers in Nutrition ·Archibold Mposhi, Fabián Cortés-Mancera, Janette Heegsma, (unknown), Bart van de Sluis, Svenja Sydor, Lars P. Bechmann, Claudia Theys, Peter De Rijk, Tim De Pooter, Wim Vanden Berghe, İkbal Agah İnce, Klaas Nico Faber, Marianne G. Rots	2023	14
3	Mitochondrial GpC and CpG DNA Hypermethylation Cause Metabolic Stress-Induced Mitophagy and Cholestophagy International Journal of Molecular Sciences ·Claudia Theys, Joe Ibrahim, Ligia Mateiu, Archibold Mposhi, Laura García-Pupo, Tim De Pooter, Peter De Rijk, Mojca Stražišar, İkbal Agah İnce, Iuliana Vintea, Marianne G. Rots, Wim Vanden Berghe	2023	10
4	Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness PubMed ·Mandy Johnstone, Alan Maclean, Lien Heyrman, An‐Sofie Lenaerts, Annelie Nordin, Lars‐Göran Nilsson, Peter De Rijk, D. Goossens, Rolf Adolfsson, David M. St. Clair, Jérémy Hall, Stephen M. Lawrie, Andrew M. McIntosh, Jurgen Del‐Favero, Douglas Blackwood, Ben Pickard	2015	14
5	Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencing Genetics in Medicine ·Daliya Kancheva, Derek Atkinson, Peter De Rijk, M. Zimoń, Teodora Chamova, Vanio Mitev, Ahmet Yaramış, Gian Maria Fabrizi, Haluk Topaloğlu, Ivailo Tournev, Yesim Parma, Esra Battaloglu, Alejandro Estrada‐Cuzcano, Albena Jordanova	2015	24
6	Genetic variants in microRNA genes: impact on microRNA expression, function, and disease Frontiers in Genetics ·Sophia Cammaerts, Mojca Stražišar, Peter De Rijk, Jurgen Del‐Favero	2015	104
7	CMT-associated mutations in glycyl- and tyrosyl-tRNA synthetases exhibit similar pattern of toxicity and share common genetic modifiers in Drosophila Neurobiology of Disease ·Biljana Ermanoska, William W. Motley, Ricardo Leitão-Gonçalves, Bob Asselbergh, LaTasha H. Lee, Peter De Rijk, Kristel Sleegers, Tinne Ooms, Tanja A. Godenschwege, Vincent Timmerman, Kenneth H. Fischbeck, Albena Jordanova	2014	29
8	Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not? American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Maarten Van Den Bossche, Mandy Johnstone, Mojca Stražišar, Ben Pickard, D. Goossens, An‐Sofie Lenaerts, Sonia De Zutter, Annelie Nordin, Karl‐Fredrik Norrback, Julien Mendlewicz, Daniel Souery, Peter De Rijk, Bernard Sabbe, Rolf Adolfsson, Douglas Blackwood, Jurgen Del‐Favero	2012	26
9	Evaluation of a multiplex-PCR detection in combination with an isolation method for STEC O26, O103, O111, O145 and sorbitol fermenting O157 in food Food Microbiology ·Karen Verstraete, Joris Robyn, Jurgen Del‐Favero, Peter De Rijk, Maria-Adelheid Joris, Lieve Herman, Marc Heyndrickx, Lieven De Zutter, Koen De Reu	2011	21
10	SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles Human Molecular Genetics ·Dries Castermans, Karolien Volders, An Crepel, Liesbeth Backx, Rita De Vos, Kathleen Freson, Sandra Meulemans, Joris Vermeesch, Connie Schrander‐Stumpel, Peter De Rijk, Jurgen Del‐Favero, Chris Van Geet, Wim J.M. Van de Ven, Jean Steyaert, Koenraad Devriendt, John W.M. Creemers	2010	72
11	novoSNP, a novel computational tool for sequence variation discovery Genome Research ·Stefan Weckx, Jurgen Del‐Favero, Rosa Rademakers, Lieve Claes, Marc Cruts, Peter De Jonghe, Christine Van Broeckhoven, Peter De Rijk	2005	214
12	Linkage and Association Studies Identify a Novel Locus for Alzheimer Disease at 7q36 in a Dutch Population-Based Sample The American Journal of Human Genetics ·Rosa Rademakers, Marc Cruts, Kristel Sleegers, Bart Dermaut, Jessie Theuns, Yurii S. Aulchenko, Stefan Weckx, Tim De Pooter, Marleen Van den Broeck, Ellen Corsmit, Peter De Rijk, Jurgen Del‐Favero, John C. van Swieten, Cornelia M. van Duijn, Christine Van Broeckhoven	2005	35
13	Database on the structure of large ribosomal subunit RNA Nucleic Acids Research ·Peter De Rijk	1998	32
14	Database on the structure of large ribosomal subunit RNA Nucleic Acids Research ·Peter De Rijk, Yves Van de Peer, Rupert De Wächter	1997	27
15	Phylogenetic study of the genus Plasmodium based on the secondary structure-based alignment of the small subunit ribosomal RNA Molecular and Biochemical Parasitology ·Ananías A. Escalante, Ira F. Goldman, Peter De Rijk, Rupert De Wächter, William E. Collins, Shoukat H. Qari, Altaf A. Lal	1997	26
16	Database on the structure of large ribosomal subunit RNA Nucleic Acids Research ·Peter De Rijk	1996	474
17	Evolution according to large ribosomal subunit RNA Journal of Molecular Evolution ·Peter De Rijk, Yves Van de Peer, I. Van den Broeck, Rupert De Wächter	1995	93
18	The phylogeny of the Hyphochytriomycota as deduced from ribosomal RNA sequences of Hyphochytrium catenoides. Molecular Biology and Evolution ·Gert Van der Auwera, R. De Baere, Yves Van de Peer, Peter De Rijk, I. Van den Broeck, Rupert De Wächter	1995	42
19	Ribosomal RNA as a tool for studying evolution Ghent University Academic Bibliography (Ghent University) ·Yves Van de Peer, Jean‐Marc Neefs, Peter De Rijk, R. De Baere, Anne Goris, Lydia Hendriks, Rupert De Wächter	1992	1
20	Compilation of small ribosomal subunit RNA sequences Nucleic Acids Research ·Jean‐Marc Neefs, Yves Van de Peer, Peter De Rijk, Anne Goris, Rupert De Wächter	1991	173

About Peter De Rijk

Peter De Rijk is a scholar working on Endocrinology, Molecular Biology, Genetics, Cancer Research and Ecology, having authored 64 papers that have together received 5.2k indexed citations. Recurring topics across this work include RNA and protein synthesis mechanisms (25 papers), Genomics and Phylogenetic Studies (21 papers), RNA modifications and cancer (16 papers), Genomics and Rare Diseases (10 papers), RNA Research and Splicing (8 papers), Genomic variations and chromosomal abnormalities (7 papers), Bacteriophages and microbial interactions (5 papers) and Microbial Community Ecology and Physiology (5 papers). The work is most often cited by research in Ecology (1.4k citations), Molecular Biology (3.3k citations), Parasitology (300 citations), Endocrinology (193 citations) and Genetics (871 citations). Peter De Rijk has collaborated with scholars based in Belgium, Netherlands and Sweden. Frequent co-authors include Rupert De Wächter, Yves Van de Peer, Jean‐Marc Neefs, Jurgen Del‐Favero, Rupert De Wachter, Sabine Chapelle, J. Wuyts, Christine Van Broeckhoven, Mojca Stražišar and I. Van den Broeck. Their work appears in journals such as Nucleic Acids Research, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Bioinformatics, Human Molecular Genetics and Journal of Molecular Evolution.

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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