H.R. Scholte

5.1k total citations · 1 hit paper
100 papers, 3.7k citations indexed

About

H.R. Scholte is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, H.R. Scholte has authored 100 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 78 papers in Molecular Biology, 66 papers in Clinical Biochemistry and 19 papers in Physiology. Recurrent topics in H.R. Scholte's work include Metabolism and Genetic Disorders (66 papers), Mitochondrial Function and Pathology (62 papers) and ATP Synthase and ATPases Research (17 papers). H.R. Scholte is often cited by papers focused on Metabolism and Genetic Disorders (66 papers), Mitochondrial Function and Pathology (62 papers) and ATP Synthase and ATPases Research (17 papers). H.R. Scholte collaborates with scholars based in Netherlands, United States and France. H.R. Scholte's co-authors include I. E. M. Luyt‐Houwen, E.M. Wit-Peeters, Ruud CW Vermeulen, Pieter H.E. Groot, P. G. Barth, J.A. Berden, J. M. van der Klei‐van Moorsel, M.A. Sobotka-Plojhar, J.J. van der Harten and W.C. Hülsmann and has published in prestigious journals such as Brain, Hepatology and Neurology.

In The Last Decade

H.R. Scholte

100 papers receiving 3.6k citations

Hit 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.

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

1983 548 citations P. G. Barth, H.R. Scholte et al. Journal of the Neurological Sciences profile →

Peers

Countries citing papers authored by H.R. Scholte

Since Specialization

Citations

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

Fields of papers citing papers by H.R. Scholte

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H.R. Scholte. 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 H.R. Scholte. The network helps show where H.R. Scholte may publish in the future.

Co-authorship network of co-authors of H.R. Scholte

This figure shows the co-authorship network connecting the top 25 collaborators of H.R. Scholte. A scholar is included among the top collaborators of H.R. Scholte 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 H.R. Scholte. H.R. Scholte 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	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
2	Two Novel Mutations in the SLC25A4 Gene in a Patient with Mitochondrial Myopathy 2015 ·JIMD Reports ·(unknown), Marjolein Visser, H. D. Bakker, Ronald J. A. Wanders, Fleur Vansenne, H.R. Scholte, L. Dorland, Gerry A. F. Nicolaes, (unknown), Hubert J.M. Smeets, Alexandra T.M. Hendrickx, B.J.C. van den Bosch	25
3	Patients with chronic fatigue syndrome performed worse than controls in a controlled repeated exercise study despite a normal oxidative phosphorylation capacity 2010 ·Journal of Translational Medicine ·Ruud CW Vermeulen, (unknown), Frans C. Visser, Wim J. Sluiter, H.R. Scholte	115
4	Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome 2009 ·Journal of Medical Genetics ·Mike Gerards, Wim J. Sluiter, B.J.C. van den Bosch, L. Elly A. de Wit, (unknown), (unknown), (unknown), Kees Schoonderwoerd, H.R. Scholte, R. J. E. Jongbloed, Alexandra T.M. Hendrickx, I.F.M. de Coo, Hubert J.M. Smeets	59
5	Azithromycin in Chronic Fatigue Syndrome (CFS), an analysis of clinical data 2006 ·Journal of Translational Medicine ·Ruud CW Vermeulen, H.R. Scholte	16
6	Transmission and prenatal diagnosis of the T9176C mitochondrial DNA mutation 2004 ·Molecular Human Reproduction ·L.J.A.M. Jacobs, I.F.M. de Coo, Jeroen G. Nijland, R. J. H. Galjaard, Frans J. Los, Kees Schoonderwoerd, Martinus F. Niermeijer, Joep Geraedts, H.R. Scholte, Hubert J.M. Smeets	31
7	Chronic fatigue syndrome and sexual dysfunction 2004 ·Journal of Psychosomatic Research ·Ruud CW Vermeulen, H.R. Scholte	10
8	Efficacy of carnitine in the treatment of children with attention-deficit hyperactivity disorder 2002 ·Prostaglandins Leukotrienes and Essential Fatty Acids ·(unknown), H.R. Scholte	45
9	Immunological Phenotyping of Fibroblast Cultures from Patients with a Mitochondrial Respiratory Chain Deficit 2001 ·Laboratory Investigation ·Siôn L. Williams, H.R. Scholte, R. G. F. Gray, James V. Leonard, Anthony H.V. Schapira, Jan‐Willem Taanman	15
10	Treatment and molecular analysis of neonatal carnitine palmitoyltransferase II deficiency. 1999 ·Pediatric Research ·Jan Smeıtınk, B. A. Semmekrot, (unknown), H.R. Scholte, Lambertus P. van den Heuvel, Carla Costa, U. Wendel, W. Ruitenbeek, (unknown), (unknown), (unknown), Jennifer Jager, (unknown), (unknown), R. C. A. Sengers, C. Jakobs, J. M. F. Trijbels	2
11	Clear Correlation of Genotype with Disease Phenotype in Very–Long-Chain Acyl-CoA Dehydrogenase Deficiency 1999 ·The American Journal of Human Genetics ·Brage Storstein Andresen, S. E. Olpin, Ben J. H. M. Poorthuis, H.R. Scholte, Christine Vianey‐Saban, Ronald Wanders, Lodewijk IJlst, Andrew A.M. Morris, Morteza Pourfarzam, K. Bartlett, E. R. Baumgartner, (unknown), Lisbeth Dahl Schroeder, Thomas J. Corydon, Hans Lund, Vibeke Winter, Peter Bross, Lars Bolund, Niels Gregersen	233
12	Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch families 1998 ·Neuromuscular Disorders ·P. G. Barth, Ronald J. A. Wanders, W. Ruitenbeek, Charles R. Roe, H.R. Scholte, (unknown), (unknown), Marinus Duran, K. P. Dingemans	11
13	Effect of lamivudine on morphology and function of mitochondria in patients with chronic hepatitis B 1997 ·Hepatology ·Pieter Honkoop, Robert A. de Man, H.R. Scholte, Pieter E. Zondervan, (unknown), L. H. P. M. Rademakers, Solko W. Schalm	42
14	Depletion of mitochondrial DNA in the liver of a patient with lactic acidemia and hypoketotic hypoglycemia 1996 ·The Journal of Pediatrics ·P. D. Maaswinkel‐Mooij, Coby Van den Bogert, H.R. Scholte, W. Onkenhout, P. Brederoo, Ben J. H. M. Poorthuis	51
15	Deficiency of the Adenine Nucleotide Translocator in Muscle of a Patient with Myopathy and Lactic Acidosis: A New Mitochondrial Defect 1993 ·Pediatric Research ·H. D. Bakker, H.R. Scholte, Coby Van den Bogert, W. Ruitenbeek, Jeroen A. L. Jeneson, Ronald J. A. Wanders, N. G. G. M. Abeling, Bert Dorland, R. C. A. Sengers, Albert H. Gennip	38
16	Problems with the biochemical diagnosis in mitochondrial (encephalo-)myopathies 1993 ·European Journal of Pediatrics ·J. M. F. Trijbels, H.R. Scholte, W. Ruitenbeek, R. C. A. Sengers, A.J.M. Janssen, H. F. M. Busch	36
17	Defect in succinate oxidation by isolated muscle mitochondria in a patient with symmetrical lesions in the basal ganglia 1988 ·Journal of the Neurological Sciences ·Jean‐Jacques Martin, Frank L. Van de Vyver, H.R. Scholte, (unknown), C. Ceuterick, (unknown), I. E. M. Luyt‐Houwen	27
18	Mitochondrial Myopathies with Necrotizing Encephalopathy of the Leigh Type 1988 ·Pathology - Research and Practice ·J. Peiffer, B. Kustermann‐Kuhn, W. Mortier, M. Poremba, Wolfgang Roggendorf, H.R. Scholte, J. M. Schröder, (unknown), K. Wessel, (unknown)	17
19	The role of the carnitine system in myocardial fatty acid oxidation: carnitine deficiency, failing mitochondria and cardiomyopathy 1987 ·Steinkopff eBooks ·H.R. Scholte, I. E. M. Luyt‐Houwen, (unknown)	22
20	Neurologic Action of Megadoses of Vitamins 1986 ·Forum of nutrition/Bibliotheca Nutritio et dieta ·W. Blom, (unknown), J. G. M. Huijmans, Hildegard Przyrembel, José O. Fernandes, H.R. Scholte, J. A. R. Sanders‐Woudstra	3

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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