Ronald J. A. Wanders

Active 1984–2024

Also published as
Ronald J.A. Wanders
282
Papers
42,523
Citations
125
h-index
279
i10-index

Citations

Citations per year for Ronald J. A. Wanders1984: 6 citations1985: 19 citations1986: 36 citations1987: 30 citations1988: 40 citations1989: 29 citations1990: 15 citations1991: 31 citations1992: 44 citations1993: 16 citations1994: 41 citations1995: 50 citations1996: 46 citations1997: 54 citations1998: 117 citations1999: 167 citations2000: 157 citations2001: 181 citations2002: 181 citations2003: 262 citations2004: 280 citations2005: 193 citations2006: 413 citations2007: 209 citations2008: 295 citations2009: 263 citations2010: 409 citations2011: 266 citations2012: 452 citations2013: 445 citations2014: 347 citations2015: 559 citations2016: 433 citations2017: 400 citations2018: 369 citations2019: 1,215 citations2020: 1,499 citations2021: 1,273 citations2022: 1,136 citations2023: 700 citations2024: 1,224 citations2025: 562 citations2026: 16 citations

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,401 citing papers, 24.8% of this breakdownChina: 1,326 citing papers, 9.7% of this breakdownGermany: 950 citing papers, 6.9% of this breakdownUnited Kingdom: 907 citing papers, 6.6% of this breakdownNetherlands: 845 citing papers, 6.2% of this breakdownCanada: 566 citing papers, 4.1% of this breakdownFrance: 538 citing papers, 3.9% of this breakdownItaly: 532 citing papers, 3.9% of this breakdownJapan: 405 citing papers, 3% of this breakdownSpain: 342 citing papers, 2.5% of this breakdownAustralia: 316 citing papers, 2.3% of this breakdownSwitzerland: 286 citing papers, 2.1% of this breakdown
0%24.8%Other 24%

Fields

  • Biochemistry, Genetics and Molecular Biology57.5%
  • Medicine29.2%
  • Neuroscience3.4%
  • Agricultural and Biological Sciences1.9%
  • Immunology and Microbiology1.7%
  • Nursing1.5%
  • Other4.8%

Topics

  • Mitochondrial Function and Pathology6.9%
  • Metabolism and Genetic Disorders6.3%
  • Peroxisome Proliferator-Activated Receptors6%
  • Adipose Tissue and Metabolism3.2%
  • ATP Synthase and ATPases Research2.3%
  • Metabolomics and Mass Spectrometry Studies2.1%
  • Other73.2%

Coauthors

All papers

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  1. The Biochemistry and Physiology of Mitochondrial Fatty Acid β-Oxidation and Its Genetic Disorders

    Authors: , , , - Annual Review of Physiology 2015 cited by 894

  2. A general introduction to the biochemistry of mitochondrial fatty acid β‐oxidation

    Authors: , - Journal of Inherited Metabolic Disease 2010 cited by 982

  3. The physiological functions of human peroxisomes

    Authors: , , , , - Physiological Reviews 2022 cited by 211

  4. The Secret Life of NAD+: An Old Metabolite Controlling New Metabolic Signaling Pathways

    Authors: , , , - Endocrine Reviews 2010 cited by 882

  5. NAD+ homeostasis in human health and disease

    Authors: , , , - EMBO Molecular Medicine 2021 cited by 244

  6. Biochemistry of Mammalian Peroxisomes Revisited

    Authors: , - Annual Review of Biochemistry 2006 cited by 992

  7. Modeling the mitochondrial cardiomyopathy of Barth syndrome with induced pluripotent stem cell and heart-on-chip technologies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Medicine 2014 cited by 841

  8. Systematic mapping of contact sites reveals tethers and a function for the peroxisome-mitochondria contact

    Authors: , , , , , , , , , , , , , , , , , , - Nature Communications 2018 cited by 320

  9. Metabolic Interplay between Peroxisomes and Other Subcellular Organelles Including Mitochondria and the Endoplasmic Reticulum

    Authors: , , - Frontiers in Cell and Developmental Biology 2016 cited by 359

  10. Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle

    Authors: , , , , , , , , - Reviews in Endocrine and Metabolic Disorders 2018 cited by 334

  11. X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management

    Authors: , , , , , , - Orphanet Journal of Rare Diseases 2012 cited by 573

  12. N -lactoyl-amino acids are ubiquitous metabolites that originate from CNDP2-mediated reverse proteolysis of lactate and amino acids

    Authors: , , , , , , , , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 2015 cited by 152

  13. Metabolic interactions between peroxisomes and mitochondria with a special focus on acylcarnitine metabolism

    Authors: , , - Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 2020 cited by 166

  14. A Lethal Defect of Mitochondrial and Peroxisomal Fission

    Authors: , , , , , - New England Journal of Medicine 2007 cited by 743

  15. The malate-aspartate shuttle is important for de novo serine biosynthesis

    Authors: , , , , , , , , , , , - Cell Reports 2023 cited by 62

  16. Human disorders of peroxisome metabolism and biogenesis

    Authors: , , - Biochimica et Biophysica Acta (BBA) - Molecular Cell Research 2015 cited by 375

  17. Adrenoleukodystrophy – neuroendocrine pathogenesis and redefinition of natural history

    Authors: , , , , - Nature Reviews Endocrinology 2016 cited by 272

  18. Sodium taurocholate cotransporting polypeptide (SLC10A1) deficiency: Conjugated hypercholanemia without a clear clinical phenotype

    Authors: , , , , , , , , , , , , - Hepatology 2014 cited by 212

  19. Proteomic and Biochemical Studies of Lysine Malonylation Suggest Its Malonic Aciduria-associated Regulatory Role in Mitochondrial Function and Fatty Acid Oxidation

    Authors: , , , , , , , , , , , , , , , - Molecular & Cellular Proteomics 2015 cited by 197

  20. Mitochondrial protein acetylation is driven by acetyl-CoA from fatty acid oxidation

    Authors: , , , , , , , - Human Molecular Genetics 2014 cited by 165

  21. Clinical, biochemical, and mutational spectrum of peroxisomal acyl–coenzyme A oxidase deficiency

    Authors: , , , , , , , , - Human Mutation 2007 cited by 152

  22. Metabolic functions of peroxisomes in health and disease

    Authors: - Biochimie 2013 cited by 233

  23. X-linked adrenoleukodystrophy in women: a cross-sectional cohort study

    Authors: , , , , , , , , , , , , - Brain 2014 cited by 230

  24. Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in GLS

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Youdong Wang, Michel van Weeghel, Galen E.B. Wright, Xiaohong Xu, Ryan K. C. Yuen, Jinqiu Zhang, Colin J.D. Ross, Wyeth W. Wasserman, Michael T. Geraghty, Saikat Santra, Ronald J. A. Wanders, Xiao‐Yan Wen, Hans R. Waterham, Karen Usdin, Clara D. van Karnebeek - New England Journal of Medicine 2019 cited by 105