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Genetics
Finland
2026
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Genetics and Molecular Biology
Finland
2024

D-Index & Metrics

Genetics

D-Index
85
Citations
28341
World Ranking
1306
National Ranking
8

Medicine

D-Index
85
Citations
28472
World Ranking
14540
National Ranking
166

Anu Suomalainen publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Anu Suomalainen sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 235 publications — 62nd percentile

62% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

Anu Suomalainen D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Anu Suomalainen sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 85 D-Index — 71st percentile

71% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

Research.com Recognitions

  • 2026 - Research.com Genetics in Finland Leader Award
  • 2025 - Research.com Genetics in Finland Leader Award
  • 2024 - Research.com Genetics in Finland Leader Award
  • 2024 - Research.com Genetics and Molecular Biology in Finland Leader Award
  • 2023 - Research.com Genetics and Molecular Biology in Finland Leader Award
  • 2022 - Research.com Genetics and Molecular Biology in Finland Leader Award

Overview

Anu Suomalainen is affiliated with the University of Helsinki in Finland and has contributed extensively to the field of Biochemistry, Genetics and Molecular Biology, with a total of 117 publications. Their research primarily focuses on Molecular Biology, Clinical Biochemistry, Genetics, Cellular and Molecular Neuroscience, and Physiology.

The main topics covered in their work include:

  • Mitochondrial Function and Pathology
  • Metabolism and Genetic Disorders
  • ATP Synthase and ATPases Research
  • Genetic Neurodegenerative Diseases
  • RNA modifications and cancer
  • Genomics and Rare Diseases
  • RNA Research and Splicing

Suomalainen has published several recent papers, some of which include:

  • Mitochondria at the crossroads of health and disease, 2024, Cell
  • Mitochondrial disease in adults: recent advances and future promise, 2021, The Lancet Neurology
  • Vegan diet in young children remodels metabolism and challenges the statuses of essential nutrients, 2021, EMBO Molecular Medicine
  • Mosaic dysfunction of mitophagy in mitochondrial muscle disease, 2022, Cell Metabolism
  • Niacin Cures Systemic NAD+ Deficiency and Improves Muscle Performance in Adult-Onset Mitochondrial Myopathy, 2020, Cell Metabolism

Frequent collaborators in Suomalainen's research include:

  • Pirjo Isohanni
  • Mari Auranen
  • Nahid Khan
  • Juan C. Landoni
  • Virginia Brilhante

The scientist's work has been disseminated in multiple venues, including:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Nature Communications
  • Cell Metabolism
  • The Journal of Cell Biology
  • Annals of Clinical and Translational Neurology

Best Publications

  • Mitochondria: In Sickness and in Health

    Jodi Nunnari;Anu Suomalainen;Anu Suomalainen

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

    Johannes N. Spelbrink;Fang Yuan Li;Valeria Tiranti;Kaisu Nikali

  • Role of Adenine Nucleotide Translocator 1 in mtDNA Maintenance

    Jyrki Kaukonen;Jukka K. Juselius;Valeria Tiranti;Aija Kyttälä

  • Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.

    Petri Luoma;Atle Melberg;Juha O Rinne;Jyrki A Kaukonen

  • Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.

    Gavin Hudson;Patrizia Amati-Bonneau;Emma L. Blakely;Joanna D. Stewart

  • Mitochondrial diseases: the contribution of organelle stress responses to pathology

    Anu Suomalainen;Brendan J Battersby

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

    Anu Suomalainen;Anu Suomalainen;Jenni M Elo;Kirsi H Pietiläinen;Anna H Hakonen

  • Phenotypic spectrum associated with mutations of the mitochondrial polymerase γ gene

    R Horvath;G Hudson;G Ferrari;N Futterer

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

    Nahid A Khan;Mari Auranen;Mari Auranen;Ilse Paetau;Eija Pirinen;Eija Pirinen

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

    Henna Tyynismaa;Katja Peltola Mjosund;Sjoerd Wanrooij;Ilse Lappalainen

  • Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin

    Anna H. Hakonen;Silja Heiskanen;Vesa Juvonen;Ilse Lappalainen

  • mTORC1 Regulates Mitochondrial Integrated Stress Response and Mitochondrial Myopathy Progression

    Nahid A. Khan;Joni Nikkanen;Shuichi Yatsuga;Shuichi Yatsuga;Christopher Jackson

  • Mitochondrial myopathy induces a starvation-like response

    Henna Tyynismaa;Christopher J. Carroll;Nuno Raimundo;Sofia Tuulikki Ahola-Erkkilä

  • Global Transcript Profiles of Fat in Monozygotic Twins Discordant for BMI: Pathways behind Acquired Obesity

    Kirsi H Pietiläinen;Jussi Naukkarinen;Aila Rissanen;Juha Saharinen

  • Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia.

    A Suomalainen;A Majander;M Haltia;H Somer

  • Comparison of solution-based exome capture methods for next generation sequencing.

    Anna-Maija Sulonen;Pekka Ellonen;Henrikki Almusa;Maija Lepistö

  • GRACILE Syndrome, a Lethal Metabolic Disorder with Iron Overload, Is Caused by a Point Mutation in BCS1L

    Ilona Visapää;Ilona Visapää;Vineta Fellman;Jouni Vesa;Ayan Dasvarma

  • An autosomal locus predisposing to deletions of mitochondrial DNA

    Anu Suomalainen;Jyrki Kaukonen;Patrizia Amati;Ritva Timonen

  • Twinkle helicase is essential for mtDNA maintenance and regulates mtDNA copy number

    Henna Tyynismaa;Hiroshi Sembongi;Monika Bokori-Brown;Caroline Granycome

  • Phenotypic spectrum associated with mutations of the mitochondrial polymerase γ gene. Commentary

    Salvatore Dimauro;Guido Davidzon;Michio Hirano;Rita Horvath

Frequent Co-Authors

Anders Paetau
Anders Paetau University of Helsinki
Kirsi H. Pietiläinen
Kirsi H. Pietiläinen University of Helsinki
Leena Peltonen
Leena Peltonen University of Helsinki
Jaakko Kaprio
Jaakko Kaprio University of Helsinki
Massimo Zeviani
Massimo Zeviani University of Padua
Laurence A. Bindoff
Laurence A. Bindoff Haukeland University Hospital
Robert W. Taylor
Robert W. Taylor Newcastle University
Johannes N. Spelbrink
Johannes N. Spelbrink Radboud University
Aila Rissanen
Aila Rissanen University of Helsinki
Ann-Christine Syvänen
Ann-Christine Syvänen Uppsala University

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