World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
66
Citations
14934
World Ranking
2621
National Ranking
11

Laurence A. Bindoff 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 Laurence A. Bindoff 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: 216 publications — 56th percentile

56% of scientists in this discipline score the same or lower.

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

Laurence A. Bindoff 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 Laurence A. Bindoff 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: 66 D-Index — 41st percentile

41% of scientists in this discipline score the same or lower.

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

Overview

Laurence A. Bindoff is affiliated with Haukeland University Hospital in Norway. The scientist's primary research focus lies in the fields of Biochemistry, Genetics, and Molecular Biology, with a total of 118 publications. Within these fields, Bindoff has contributed significantly to subfields including Molecular Biology, Genetics, Clinical Biochemistry, Cellular and Molecular Neuroscience, and Physiology.

Bindoff's research covers several main topics, notably Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, ATP Synthase and ATPases Research, Pluripotent Stem Cells Research, Genetics and Neurodevelopmental Disorders, RNA Research and Splicing, and Genetic Neurodegenerative Diseases.

Notable recent papers authored by Bindoff include:

  • Mitochondrial disease in adults: recent advances and future promise, 2021, The Lancet Neurology
  • Simplifying the clinical classification of polymerase gamma (POLG) disease based on age of onset; studies using a cohort of 155 cases, 2020, Journal of Inherited Metabolic Disease
  • Safety of drug use in patients with a primary mitochondrial disease: An international Delphi-based consensus, 2020, Journal of Inherited Metabolic Disease
  • Disease-specific phenotypes in iPSC-derived neural stem cells with POLG mutations, 2020, EMBO Molecular Medicine
  • Diagnostic value of serum biomarkers FGF21 and GDF15 compared to muscle sample in mitochondrial disease, 2020, Journal of Inherited Metabolic Disease

Frequent co-authors collaborating with Bindoff include:

  • Kristina Xiao Liang
  • Gareth J. Sullivan
  • Anbin Chen
  • Cecilie Katrin Kristiansen
  • Omar Hikmat

Bindoff's work has been published repeatedly in several venues, including:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Annals of Clinical and Translational Neurology
  • Journal of Inherited Metabolic Disease
  • Journal of Visualized Experiments
  • Experimental Neurology

Best Publications

  • Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease.

    Andrew R.J. Curtis;Constanze Fey;Christopher M Morris;Laurence A. Bindoff

  • Correlation between genetic and geographic structure in Europe.

    Oscar Lao;Timothy T. Lu;Michael Nothnagel;Olaf Junge

  • The epidemiology of pathogenic mitochondrial DNA mutations.

    P. F. Chinnery;M. A. Johnson;T. M. Wardell;R. Singh-Kler

  • Leber Hereditary Optic Neuropathy: Identification of the Same Mitochondrial ND1 Mutation in Six Pedigrees

    N Howell;L A Bindoff;D A McCullough;I Kubacka

  • Multi-system neurological disease is common in patients with OPA1 mutations

    Patrick Yu-Wai-Man;Philip G. Griffiths;Philip G. Griffiths;G. Gorman;C.-M. Lourenco

  • 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

  • The spectrum of clinical disease caused by the A467T and W748S POLG mutations: a study of 26 cases

    Charalampos Tzoulis;Bernt A. Engelsen;Wenche Telstad;Jan Aasly

  • 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

  • An Evaluation of the Measurement of the Activities of Complexes I-IV in the Respiratory Chain of Human Skeletal Muscle Mitochondria

    M.A. Birchmachin;H.L. Briggs;A.A. Saborido;L.A. Bindoff

  • MITOCHONDRIAL FUNCTION IN PARKINSON'S DISEASE

    L.A. Bindoff;M. Birch-Machin;N.E.F. Cartlidge;W.D. Parker

  • Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase γ mutations

    S. Winterthun;G. Ferrari;L. He;R. W. Taylor

  • Risk of developing a mitochondrial DNA deletion disorder

    Patrick F Chinnery;Salvatore DiMauro;Sara Shanske;Eric A Schon

  • Respiratory chain abnormalities in skeletal muscle from patients with Parkinson's disease

    L.A. Bindoff;M.A. Birch-Machin;N.E.F. Cartlidge;W.D. Parker

  • Mutations in ABHD12 Cause the Neurodegenerative Disease PHARC: An Inborn Error of Endocannabinoid Metabolism

    Torunn Fiskerstrand;Dorra H'mida-Ben Brahim;Stefan Johansson;Abderrahim M'zahem

  • A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle.

    K Weber;J N Wilson;L Taylor;E Brierley

  • Defective mitochondrial DNA homeostasis in the substantia nigra in Parkinson disease

    Christian Dölle;Irene Hana Flønes;Irene Hana Flønes;Gonzalo Sanchez Nido;Gonzalo Sanchez Nido;Hrvoje Miletic

  • A multicenter study on Leigh syndrome: Disease course and predictors of survival

    Kalliopi Sofou;Irenaeus F M De Coo;Pirjo Isohanni;Pirjo Isohanni;Elsebet Ostergaard

  • Abnormal RNA processing associated with a novel tRNA mutation in mitochondrial DNA. A potential disease mechanism.

    L A Bindoff;N Howell;J Poulton;D A McCullough

  • Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis

    Zandra A Jenkins;Margriet van Kogelenberg;Tim Morgan;Aaron Jeffs

  • New treatments for mitochondrial disease—no time to drop our standards

    Gerald Pfeffer;Rita Horvath;Thomas Klopstock;Vamsi K. Mootha

Frequent Co-Authors

Douglass M. Turnbull
Douglass M. Turnbull Newcastle University
Robert W. Taylor
Robert W. Taylor Newcastle University
Stefan Johansson
Stefan Johansson University of Bergen
Patrick F. Chinnery
Patrick F. Chinnery University of Cambridge
Massimo Zeviani
Massimo Zeviani University of Padua
Christian A. Vedeler
Christian A. Vedeler University of Bergen
Robert McFarland
Robert McFarland Newcastle University
Mark A. Birch-Machin
Mark A. Birch-Machin Newcastle University
Rita Horvath
Rita Horvath University of Cambridge
Robert N. Lightowlers
Robert N. Lightowlers Newcastle University

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