Bart de Koning

1.0k total citations
29 papers, 520 citations indexed

About

Bart de Koning is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Bart de Koning has authored 29 papers receiving a total of 520 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Bart de Koning's work include Mitochondrial Function and Pathology (5 papers), RNA modifications and cancer (4 papers) and Genomics and Rare Diseases (3 papers). Bart de Koning is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), RNA modifications and cancer (4 papers) and Genomics and Rare Diseases (3 papers). Bart de Koning collaborates with scholars based in Netherlands, United Kingdom and Belgium. Bart de Koning's co-authors include Ambrosius P. Snijders, Phillip C. Wright, Hubert J.M. Smeets, Judith E. Raber‐Durlacher, S. Osanto, A. H. Zwinderman, Nir I. Weijl, I.F.M. de Coo, Rick Kamps and Mike Gerards and has published in prestigious journals such as PLoS ONE, Brain and Biochemical Journal.

In The Last Decade

Bart de Koning

26 papers receiving 503 citations

Peers

Countries citing papers authored by Bart de Koning

Since Specialization

Citations

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

Fields of papers citing papers by Bart de Koning

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bart de Koning. 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 Bart de Koning. The network helps show where Bart de Koning may publish in the future.

Co-authorship network of co-authors of Bart de Koning

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Clinically Irrelevant Terminal 16q21 Deletion Detected by NIPT Is Attributable to Inherited Fragility at FRA16B 2025 ·American Journal of Medical Genetics Part A ·Servi J.C. Stevens, (unknown), Nicole Y. Souren, Merryn Macville, (unknown), Brigitte H. W. Faas, Bart de Koning, Arthur van den Wijngaard, Sonja de Munnik, Masoud Zamani Esteki	0
2	Optimizing freeform lenses for extended sources with algorithmic differentiable ray tracing and truncated hierarchical B-splines 2024 ·Optics Express ·(unknown), Bart de Koning, (unknown), A. J. L. Adam	7
3	Gradient descent-based freeform optics design for illumination using algorithmic differentiable non-sequential ray tracing 2023 ·Optimization and Engineering ·Bart de Koning, (unknown), A. J. L. Adam, Matthias Möller	4
4	Clustering of Cardiac Transcriptome Profiles Reveals Unique 2023 ·JACC Basic to Translational Science ·Job A.J. Verdonschot, Ping Wang, Kasper Derks, Michiel Adriaens, (unknown), Michiel T.H.M. Henkens, Anne G. Raafs, (unknown), Bart de Koning, Arthur van den Wijngaard, Ingrid P.C. Krapels, Miranda Nabben, Han G. Brunner, Stéphane Heymans	8
5	Diagnostic exome-based preconception carrier testing in consanguineous couples: results from the first 100 couples in clinical practice 2021 ·Genetics in Medicine ·Suzanne C.E.H. Sallevelt, Alexander P.A. Stegmann, Bart de Koning, (unknown), Anja Steyls, (unknown), Phillis Lakeman, Helger G. Yntema, Masoud Zamani Esteki, Christine de Die‐Smulders, Christian Gilissen, Arthur van den Wijngaard, Han G. Brunner, Aimée Paulussen	26
6	Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing 2020 ·PLoS ONE ·Rowida Almomani, Margherita Marchi, (unknown), Patrick Lindsey, Erika Salvi, Bart de Koning, Silvia Santoro, Stefania Magri, H.J.M. Smeets, Filippo Martinelli Boneschi, (unknown), Dan Ziegler, Janneke G. J. Hoeijmakers, Gidon J. Bönhof, Sulayman D. Dib‐Hajj, Stephen G. Waxman, Ingemar S.J. Merkies, Giuseppe Lauria, Catharina G. Faber, Monique M. Gerrits, (unknown)	13
7	MON-PO623: Assessment of Feeding Intolerance Definitions in the Pediatric Intensive Care Unit 2019 ·Clinical Nutrition ·R.D. Eveleens, (unknown), Bart de Koning, Jessie M. Hulst, Ilse Vanhorebeek, Greet Van den Berghe, Koen F. M. Joosten, Sascha Verbruggen	1
8	Genetic defects in mtDNA-encoded protein translation cause pediatric, mitochondrial cardiomyopathy with early-onset brain disease 2018 ·European Journal of Human Genetics ·Rick Kamps, Radek Szklarczyk, Tom E. J. Theunissen, Debby M.E.I. Hellebrekers, Suzanne C.E.H. Sallevelt, (unknown), Bart de Koning, B.J.C. van den Bosch, Gajja S. Salomons, (unknown), Robert M. Verdijk, Kees Schoonderwoerd, I.F.M. de Coo, Jo Vanoevelen, Hubert J.M. Smeets	22
9	Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause 2018 ·Frontiers in Genetics ·Tom E. J. Theunissen, (unknown), Rick Kamps, Alexandra T.M. Hendrickx, Suzanne C.E.H. Sallevelt, Ralph W.H. Gottschalk, (unknown), Alphons P. M. Stassen, Bart de Koning, (unknown), Kees Schoonderwoerd, Sabine A. Fuchs, Yvonne Hilhorst‐Hofstee, Marjolein Visser, Jo Vanoevelen, Radek Szklarczyk, Mike Gerards, I.F.M. de Coo, Debby M.E.I. Hellebrekers, Hubert J.M. Smeets	62
10	De VVD en integriteit: Over woorden en daden 2018 ·Data Archiving and Networked Services (DANS) ·L.W.J.C. Huberts, Muel Kaptein, Bart de Koning	1
11	Rapid Resolution of Blended or Composite Multigenic Disease in Infants by Whole-Exome Sequencing 2017 ·The Journal of Pediatrics ·Tom E. J. Theunissen, Suzanne C.E.H. Sallevelt, Debby M.E.I. Hellebrekers, Bart de Koning, Alexandra T.M. Hendrickx, B.J.C. van den Bosch, Rick Kamps, Kees Schoonderwoerd, Radek Szklarczyk, (unknown), I.F.M. de Coo, Hubert J.M. Smeets	6
12	Medication review using a Systematic Tool to Reduce Inappropriate Prescribing (STRIP) in adults with an intellectual disability: A pilot study 2016 ·Research in Developmental Disabilities ·Rianne J. Zaal, (unknown), (unknown), Bart de Koning, (unknown), (unknown), Hans Vollaard, Patricia M. L. A. van den Bemt, Heleen M. Evenhuis	19
13	Specific MRI Abnormalities Reveal Severe Perrault Syndrome due to CLPP Defects 2016 ·Frontiers in Neurology ·Tom E. J. Theunissen, Radek Szklarczyk, Mike Gerards, Debby M.E.I. Hellebrekers, (unknown), Jo Vanoevelen, Rick Kamps, Bart de Koning, S. Lane Rutledge, Thomas Schmitt‐Mechelke, Carola G.M. van Berkel, Marjo S. van der Knaap, I.F.M. de Coo, Hubert J.M. Smeets	21
14	A comprehensive strategy for exome-based preconception carrier screening 2016 ·Genetics in Medicine ·Suzanne C.E.H. Sallevelt, Bart de Koning, Radek Szklarczyk, Aimée Paulussen, Christine de Die‐Smulders, Hubert J.M. Smeets	22
15	Pathogenic CWF19L1 variants as a novel cause of autosomal recessive cerebellar ataxia and atrophy 2015 ·European Journal of Human Genetics ·(unknown), (unknown), Debby M.E.I. Hellebrekers, Jo Vanoevelen, Rick Kamps, Bart de Koning, I.F.M. de Coo, Mike Gerards, Hubert J.M. Smeets	18
16	Exome sequencing reveals a novel Moroccan founder mutation inSLC19A3as a new cause of early-childhood fatal Leigh syndrome 2013 ·Brain ·Mike Gerards, Rick Kamps, (unknown), (unknown), (unknown), Bart de Koning, H.R. Scholte, (unknown), Kees Schoonderwoerd, Abdelaziz Sefiani, Ilham Ratbi, Wouter Coppieters, Latifa Karim, I.F.M. de Coo, (unknown), Hubert J.M. Smeets	69
17	Fidelity in Archaeal Information Processing 2010 ·Archaea ·Bart de Koning, Fabian Blombach, Stan J. J. Brouns, John van der Oost	4
18	A fast method for quantitative proteomics based on a combination between two‐dimensional electrophoresis and ¹⁵N‐metabolic labelling 2005 ·Electrophoresis ·Ambrosius P. Snijders, Marjon G. J. de Vos, Bart de Koning, Phillip C. Wright	28
19	Oral mucositis in patients treated with chemotherapy for solid tumors: a retrospective analysis of 150 cases 2000 ·Supportive Care in Cancer ·Judith E. Raber‐Durlacher, Nir I. Weijl, (unknown), Bart de Koning, A. H. Zwinderman, S. Osanto	92
20	Arthroscopic Meniscus Repair: Clinical and Isokinetic Results 1997 ·Diagnostic and therapeutic endoscopy ·Christoph Erggelet, (unknown), (unknown), Bart de Koning	5

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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