Anu Suomalainen

Active 1991–2025

107
Papers
22,087
Citations
79
h-index
103
i10-index

Citations

Citations per year for Anu Suomalainen1981: 2 citations1982: 1 citations1987: 1 citations1992: 1 citations1993: 3 citations1994: 8 citations1995: 12 citations1996: 28 citations1997: 21 citations1998: 27 citations1999: 33 citations2000: 28 citations2001: 64 citations2002: 39 citations2003: 83 citations2004: 85 citations2005: 91 citations2006: 115 citations2007: 119 citations2008: 104 citations2009: 126 citations2010: 169 citations2011: 122 citations2012: 173 citations2013: 244 citations2014: 245 citations2015: 239 citations2016: 284 citations2017: 306 citations2018: 327 citations2019: 678 citations2020: 982 citations2021: 911 citations2022: 825 citations2023: 617 citations2024: 1,038 citations2025: 521 citations2026: 13 citations1983–1986: no citations, so these years are not shown1988–1991: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,146 citing papers, 21.8% of this breakdownChina: 1,258 citing papers, 12.8% of this breakdownUnited Kingdom: 878 citing papers, 8.9% of this breakdownGermany: 614 citing papers, 6.2% of this breakdownItaly: 516 citing papers, 5.2% of this breakdownCanada: 323 citing papers, 3.3% of this breakdownSpain: 322 citing papers, 3.3% of this breakdownFrance: 296 citing papers, 3% of this breakdownFinland: 286 citing papers, 2.9% of this breakdownAustralia: 256 citing papers, 2.6% of this breakdownJapan: 249 citing papers, 2.5% of this breakdownSweden: 246 citing papers, 2.5% of this breakdown
0%21.8%Other 25%

Fields

  • Biochemistry, Genetics and Molecular Biology62.7%
  • Medicine27.6%
  • Neuroscience3.7%
  • Immunology and Microbiology1.8%
  • Environmental Science1%
  • Engineering0.6%
  • Other2.6%

Topics

  • Mitochondrial Function and Pathology17.7%
  • Metabolism and Genetic Disorders7.1%
  • ATP Synthase and ATPases Research6.1%
  • Adipose Tissue and Metabolism3.4%
  • Autophagy in Disease and Therapy3.2%
  • RNA modifications and cancer2%
  • Other60.5%

Coauthors

All papers

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  1. Mitochondria: In Sickness and in Health

    Authors: , - Cell 2012 cited by 3,509

  2. Mitochondrial diseases

    Authors: , , , , , , , , , - Nature Reviews Disease Primers 2016 cited by 1,534

  3. Mitochondria at the crossroads of health and disease

    Authors: , - Cell 2024 cited by 452

  4. Mitochondrial diseases: the contribution of organelle stress responses to pathology

    Authors: , - Nature Reviews Molecular Cell Biology 2017 cited by 515

  5. mTORC1 Regulates Mitochondrial Integrated Stress Response and Mitochondrial Myopathy Progression

    Authors: , , , , , , , , , - Cell Metabolism 2017 cited by 412

  6. Niacin Cures Systemic NAD+ Deficiency and Improves Muscle Performance in Adult-Onset Mitochondrial Myopathy

    Authors: , , , , , , , , , , , , , , , , , - Cell Metabolism 2020 cited by 294

  7. Impaired Mitochondrial Biogenesis in Adipose Tissue in Acquired Obesity

    Authors: , , , , , , , , , , , , , , - Diabetes 2015 cited by 367

  8. Fibroblast Growth Factor 21 Drives Dynamics of Local and Systemic Stress Responses in Mitochondrial Myopathy with mtDNA Deletions

    Authors: , , , , , , , , , , , , , , , , , , , - Cell Metabolism 2019 cited by 259

  9. Mitochondrial disease in adults: recent advances and future promise

    Authors: , , , , , , , , , , , - The Lancet Neurology 2021 cited by 217

  10. Mosaic dysfunction of mitophagy in mitochondrial muscle disease

    Authors: , , , , , , - Cell Metabolism 2022 cited by 90

  11. Effective treatment of mitochondrial myopathy by nicotinamide riboside, a vitamin B3

    Authors: , , , , , , , , , , - EMBO Molecular Medicine 2014 cited by 385

  12. Mitochondrial DNA Replication Defects Disturb Cellular dNTP Pools and Remodel One-Carbon Metabolism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Cell Metabolism 2016 cited by 290

  13. FGF21 is a biomarker for mitochondrial translation and mtDNA maintenance disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - Neurology 2016 cited by 220

  14. Mitochondrial myopathy induces a starvation-like response

    Authors: , , , , , , , , , , , , , , - Human Molecular Genetics 2010 cited by 305

  15. Mitochondrial dysfunction compromises ciliary homeostasis in astrocytes

    Authors: , , , , , , , , - The Journal of Cell Biology 2022 cited by 65

  16. FGF-21 as a biomarker for muscle-manifesting mitochondrial respiratory chain deficiencies: a diagnostic study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , - The Lancet Neurology 2011 cited by 421

  17. Phosphorylation of Parkin at serine 65 is essential for its activationin vivo

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Miratul M. K. Muqit - Open Biology 2018 cited by 122

  18. RNA modification landscape of the human mitochondrial tRNALys regulates protein synthesis

    Authors: , , , , , , , , , - Nature Communications 2018 cited by 89

  19. Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice

    Authors: , , , , , , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 2005 cited by 335

  20. SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Communications 2020 cited by 79

  21. Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

    Authors: , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2001 cited by 882

  22. Overexpression of TFAM or Twinkle Increases mtDNA Copy Number and Facilitates Cardioprotection Associated with Limited Mitochondrial Oxidative Stress

    Authors: , , , , , , , , , , , - PLoS ONE 2015 cited by 157

  23. TFPa/HADHA is required for fatty acid beta-oxidation and cardiolipin re-modeling in human cardiomyocytes

    Authors: , , , , , , , , , , , , , , , , , , , , - Nature Communications 2019 cited by 113

  24. Parkinsonism, premature menopause, and mitochondrial DNA polymerase γ mutations: clinical and molecular genetic study

    Authors: , , , , , , , , , , , - The Lancet 2004 cited by 544