D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Medicine D-index 77 Citations 19,225 391 World Ranking 10888 National Ranking 352

Overview

What is he best known for?

The fields of study he is best known for:

  • Internal medicine
  • Enzyme
  • Gene

His primary scientific interests are in Internal medicine, Endocrinology, Mutation, Genetics and Biochemistry. His Internal medicine research incorporates elements of Gastroenterology, Missense mutation, Compound heterozygosity and Pathology. His work in Missense mutation addresses issues such as Mucopolysaccharidosis III, which are connected to fields such as Sanfilippo syndrome.

His Endocrinology study combines topics from a wide range of disciplines, such as Central nervous system disease and Cerebrospinal fluid. His Mutation study incorporates themes from Dystonia, Molecular biology, Cutis laxa, Intracellular and Hypotonia. In his work, Cerebrotendinous Xanthomatosis is strongly intertwined with Genotype, which is a subfield of Phenotype.

His most cited work include:

  • The frequency of lysosomal storage diseases in The Netherlands (539 citations)
  • Performance of near-infrared spectroscopy in measuring local O(2) consumption and blood flow in skeletal muscle. (425 citations)
  • Mitochondrial creatine kinase: a key enzyme of aerobic energy metabolism (389 citations)

What are the main themes of his work throughout his whole career to date?

Ron A. Wevers mostly deals with Internal medicine, Endocrinology, Pathology, Biochemistry and Genetics. His Internal medicine research is multidisciplinary, relying on both Gastroenterology and Dystonia. His Endocrinology research is multidisciplinary, incorporating perspectives in Homovanillic acid and Epilepsy.

His specific area of interest is Pathology, where Ron A. Wevers studies Cutis laxa. Biochemistry is often connected to Molecular biology in his work. His work in Mutation, Gene, Missense mutation and Exon is related to Genetics.

He most often published in these fields:

  • Internal medicine (39.97%)
  • Endocrinology (34.06%)
  • Pathology (14.17%)

What were the highlights of his more recent work (between 2014-2021)?

  • Internal medicine (39.97%)
  • Endocrinology (34.06%)
  • Metabolomics (3.20%)

In recent papers he was focusing on the following fields of study:

His primary areas of investigation include Internal medicine, Endocrinology, Metabolomics, Biochemistry and Pathology. As a part of the same scientific study, Ron A. Wevers usually deals with the Internal medicine, concentrating on Gastroenterology and frequently concerns with Renal function. His Endocrinology study frequently draws connections between adjacent fields such as 3-Methylglutaconic Aciduria.

His Metabolomics research incorporates themes from Metabolite, Computational biology and Metabolic pathway. The various areas that Ron A. Wevers examines in his Pathology study include Limb-girdle muscular dystrophy, Encephalopathy and Compound heterozygosity. His study in Bioinformatics is interdisciplinary in nature, drawing from both Mutation, Status epilepticus, Genetic testing and Global developmental delay.

Between 2014 and 2021, his most popular works were:

  • Exome Sequencing and the Management of Neurometabolic Disorders (169 citations)
  • NANS-mediated synthesis of sialic acid is required for brain and skeletal development (72 citations)
  • ATP6AP1 deficiency causes an immunodeficiency with hepatopathy, cognitive impairment and abnormal protein glycosylation. (68 citations)

In his most recent research, the most cited papers focused on:

  • Internal medicine
  • Enzyme
  • Gene

Ron A. Wevers focuses on Genetics, Internal medicine, Biochemistry, Endocrinology and Bioinformatics. His work in the fields of Exome sequencing, Missense mutation and Exon overlaps with other areas such as Premature aging. The Internal medicine study combines topics in areas such as Gastroenterology, Aureus infection, Staphylococcus aureus and Pathology.

His study connects Dystrophy and Endocrinology. His Bioinformatics research integrates issues from Tandem mass spectrometry, Phenotype, Molecule, Analytical chemistry and Epilepsy. His biological study spans a wide range of topics, including Bacteria, Enzyme, Glutathione peroxidase and Odor.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

The frequency of lysosomal storage diseases in The Netherlands

B.J.H.M. Poorthuis;R.A. Wevers;W.J. Kleijer;J.E.M. Groener.
Human Genetics (1999)

833 Citations

Performance of near-infrared spectroscopy in measuring local O(2) consumption and blood flow in skeletal muscle.

Mireille C. P. Van Beekvelt;Willy N. J. M. Colier;Ron A. Wevers;Baziel G. M. Van Engelen.
Journal of Applied Physiology (2001)

575 Citations

Mitochondrial creatine kinase: a key enzyme of aerobic energy metabolism

Markus Wyss;Jan Smeitink;Ron A. Wevers;Theo Wallimann.
Biochimica et Biophysica Acta (1992)

508 Citations

Adipose tissue thickness affects in vivo quantitative near-IR spectroscopy in human skeletal muscle.

M. C. P. Van Beekvelt;M. S. Borghuis;B. G. M. Van Engelen;R. A. Wevers.
Clinical Science (2001)

358 Citations

Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2.

Uwe Kornak;Ellen Reynders;Aikaterini Dimopoulou;Jeroen Van Reeuwijk.
Nature Genetics (2008)

357 Citations

Glucose transporter-1 deficiency syndrome: The expanding clinical and genetic spectrum of a treatable disorder

Wilhelmina G. Leen;Joerg Klepper;Marcel M. Verbeek;Maike Leferink.
Brain (2010)

345 Citations

Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man

Karin Tuschl;Peter T. Clayton;Sidney M. Gospe;Shamshad Gulab.
American Journal of Human Genetics (2012)

273 Citations

SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder

Vincent Cantagrel;Dirk J. Lefeber;Bobby G. Ng;Ziqiang Guan.
Cell (2010)

271 Citations

Role of cobalamin intake and atrophic gastritis in mild cobalamin deficiency in older Dutch subjects.

D.Z.B. van Asselt;C.P.G.M. de Groot;W.A. van Staveren;H.J.M. Blom.
The American Journal of Clinical Nutrition (1998)

261 Citations

Elevated plasma chitotriosidase activity in various lysosomal storage disorders.

Yufeng Guo;Wang He;A. M. Boer;R. A. Wevers.
Journal of Inherited Metabolic Disease (1995)

258 Citations

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