Radek Szklarczyk

2.5k total citations
36 papers, 1.6k citations indexed

About

Radek Szklarczyk is a scholar working on Molecular Biology, Clinical Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Radek Szklarczyk has authored 36 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Radek Szklarczyk's work include Mitochondrial Function and Pathology (18 papers), ATP Synthase and ATPases Research (11 papers) and Genomics and Phylogenetic Studies (9 papers). Radek Szklarczyk is often cited by papers focused on Mitochondrial Function and Pathology (18 papers), ATP Synthase and ATPases Research (11 papers) and Genomics and Phylogenetic Studies (9 papers). Radek Szklarczyk collaborates with scholars based in Netherlands, United States and Germany. Radek Szklarczyk's co-authors include Martijn A. Huynen, Jaap Heringa, Ricardo De Marco, Ester Perales‐Clemente, Eduardo Balsa, Enrique Calvo, Manuel O. Landázuri, José Antonio Enrı́quez, Leo Nijtmans and Bas F.J. Wanschers and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Bioinformatics.

In The Last Decade

Radek Szklarczyk

36 papers receiving 1.6k citations

Peers

Countries citing papers authored by Radek Szklarczyk

Since Specialization

Citations

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

Fields of papers citing papers by Radek Szklarczyk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Radek Szklarczyk. 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 Radek Szklarczyk. The network helps show where Radek Szklarczyk may publish in the future.

Co-authorship network of co-authors of Radek Szklarczyk

This figure shows the co-authorship network connecting the top 25 collaborators of Radek Szklarczyk. A scholar is included among the top collaborators of Radek Szklarczyk 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 Radek Szklarczyk. Radek Szklarczyk 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	Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers 2019 ·Molecular Genetics & Genomic Medicine ·Job A.J. Verdonschot, Emma Robinson, Kiely N. James, (unknown), Godelieve R.F. Claes, Kari Casas, Els K. Vanhoutte, Mark R. Hazebroek, (unknown), (unknown), Arthur van den Wijngaard, Jan F. C. Glatz, Stéphane Heymans, Ingrid P.C. Krapels, Shareef Nahas, Han G. Brunner, Radek Szklarczyk	12
2	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
3	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
4	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
5	Network topology of NaV1.7 mutations in sodium channel-related painful disorders 2017 ·BMC Systems Biology ·(unknown), (unknown), Jenny Sassone, Yang Yang, Barbara Galbardi, Markos Xenakis, Ronald Westra, Radek Szklarczyk, Patrick Lindsey, Catharina G. Faber, (unknown), Ingemar S. J. Merkies, Sulayman D. Dib‐Hajj, Massimo Mantegazza, (unknown), Giuseppe Lauria	27
6	Selection and Characterization of Palmitic Acid Responsive Patients with an OXPHOS Complex I Defect 2017 ·Frontiers in Molecular Neuroscience ·Tom E. J. Theunissen, Mike Gerards, Debby M.E.I. Hellebrekers, (unknown), Rick Kamps, Suzanne C.E.H. Sallevelt, (unknown), H.R. Scholte, Robert M. Verdijk, Kees Schoonderwoerd, I.F.M. de Coo, Radek Szklarczyk, Hubert J.M. Smeets	7
7	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
8	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
9	WeGET: predicting new genes for molecular systems by weighted co-expression 2015 ·Nucleic Acids Research ·Radek Szklarczyk, Wout Megchelenbrink, Pavel Čížek, (unknown), (unknown), Damian Szklarczyk, Martijn A. Huynen	21
10	Transcriptome analysis of complex I-deficient patients reveals distinct expression programs for subunits and assembly factors of the oxidative phosphorylation system 2015 ·BMC Genomics ·Robin van der Lee, Radek Szklarczyk, Jan Smeıtınk, Hubert J.M. Smeets, Martijn A. Huynen, Rutger O. Vogel	15
11	Mutations in the UQCC1-Interacting Protein, UQCC2, Cause Human Complex III Deficiency Associated with Perturbed Cytochrome b Protein Expression 2013 ·PLoS Genetics ·Elena J. Tucker, Bas F.J. Wanschers, Radek Szklarczyk, Hayley S. Mountford, (unknown), Mariël A.M. van den Brand, (unknown), Richard J. Rodenburg, Boris Reljić, Alison G. Compton, Ann E. Frazier, Damien L. Bruno, John Christodoulou, Hitoshi Endo, Michael T. Ryan, Leo Nijtmans, Martijn A. Huynen, David R. Thorburn	85
12	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
13	BOLA1 Is an Aerobic Protein That Prevents Mitochondrial Morphology Changes Induced by Glutathione Depletion 2012 ·Antioxidants and Redox Signaling ·Peter H.G.M. Willems, Bas F.J. Wanschers, J.J. Esseling, Radek Szklarczyk, Urszula Kudla, Isabel Duarte, Marleen Forkink, Marco Nooteboom, Herman G.P. Swarts, Jolein Gloerich, Leo Nijtmans, Werner J.H. Koopman, Martijn A. Huynen	45
14	Loss, replacement and gain of proteins at the origin of the mitochondria 2012 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Martijn A. Huynen, Isabel Duarte, Radek Szklarczyk	43
15	A Mutation in C2orf64 Causes Impaired Cytochrome c Oxidase Assembly and Mitochondrial Cardiomyopathy 2011 ·The American Journal of Human Genetics ·Merei Huigsloot, Leo Nijtmans, Radek Szklarczyk, Marieke J.H. Baars, Mariël A.M. van den Brand, (unknown), Lambertus P. van den Heuvel, Jan Smeıtınk, Martijn A. Huynen, Richard J. Rodenburg	65
16	Unraveling the human dendritic cell phagosome proteome by organellar enrichment ranking 2011 ·Journal of Proteomics ·Sonja I. Buschow, Edwin Lasonder, Radek Szklarczyk, Machteld M. Oud, I. Jolanda M. de Vries, Carl G. Figdor	23
17	FACIL: Fast and Accurate Genetic Code Inference and Logo 2011 ·Bioinformatics ·Bas E. Dutilh, (unknown), Radek Szklarczyk, Sacha A. F. T. van Hijum, Harry R. Harhangi, Markus Schmid, (unknown), Kees‐Jan Françoijs, Hendrik G. Stunnenberg, Marc Strous, Mike S. M. Jetten, Huub J. M. Op den Camp, Martijn A. Huynen	32
18	Mitochondrial proteome evolution and genetic disease 2009 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Martijn A. Huynen, Mattias de Hollander, Radek Szklarczyk	26
19	Complex fate of paralogs 2008 ·BMC Evolutionary Biology ·Radek Szklarczyk, Martijn A. Huynen, ‎Berend Snel	21
20	A First Look at ARFome: Dual-Coding Genes in Mammalian Genomes 2007 ·PLoS Computational Biology ·Wen‐Yu Chung, Samir Wadhawan, Radek Szklarczyk, Sergei L. Kosakovsky Pond, Anton Nekrutenko	51

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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