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John Vissing

Researcher Next ID · RN-038575

Researcher · Biochemistry, Genetics and Molecular Biology

University of Copenhagen

Copenhagen, Denmark

Accepting doctoral researchersFunding unknown
Works count
883
Citation count
20,339
H-index
73
i10-index
350

Research interests

Biochemistry, Genetics and Molecular Biology
Medicine
Neuroscience
Muscle Physiology and Disorders
Glycogen Storage Diseases and Myoclonus
Genetic Neurodegenerative Diseases
Mitochondrial Function and Pathology
Metabolism and Genetic Disorders

Publications

  • OxPhos defects cause hypermetabolism and reduce lifespan in cells and in patients with mitochondrial diseases

    Communications Biology · 2023 · 10.1038/s42003-022-04303-x

  • Safety, efficacy, and tolerability of efgartigimod in patients with generalised myasthenia gravis (ADAPT): a multicentre, randomised, placebo-controlled, phase 3 trial

    The Lancet Neurology · 2021 · https://doi.org/10.1016/s1474-4422(21)00159-9

  • Bimagrumab vs Optimized Standard of Care for Treatment of Sarcopenia in Community-Dwelling Older Adults

    JAMA Network Open · 2020 · 10.1001/jamanetworkopen.2020.20836

  • Efficacy and Safety of Rozanolixizumab in Moderate to Severe Generalized Myasthenia Gravis

    Neurology · 2020 · 10.1212/wnl.0000000000011108

  • Guidance for the management of myasthenia gravis (MG) and Lambert-Eaton myasthenic syndrome (LEMS) during the COVID-19 pandemic

    Journal of the Neurological Sciences · 2020 · 10.1016/j.jns.2020.116803

  • Long‐term safety and efficacy of eculizumab in generalized myasthenia gravis

    Muscle & Nerve · 2019 · 10.1002/mus.26447

  • 229th ENMC international workshop: Limb girdle muscular dystrophies – Nomenclature and reformed classification Naarden, the Netherlands, 17–19 March 2017

    Neuromuscular Disorders · 2018 · https://doi.org/10.1016/j.nmd.2018.05.007

  • Congenital Titinopathy: Comprehensive characterization and pathogenic insights

    Annals of Neurology · 2018 · 10.1002/ana.25241

  • Safety and efficacy of eculizumab in anti-acetylcholine receptor antibody-positive refractory generalised myasthenia gravis (REGAIN): a phase 3, randomised, double-blind, placebo-controlled, multicentre study

    The Lancet Neurology · 2017 · https://doi.org/10.1016/s1474-4422(17)30369-1

  • European consensus for starting and stopping enzyme replacement therapy in adult patients with Pompe disease: a 10‐year experience

    European Journal of Neurology · 2017 · 10.1111/ene.13285

  • Quantitative Muscle MRI as an Assessment Tool for Monitoring Disease Progression in LGMD2I: A Multicentre Longitudinal Study

    PLoS ONE · 2013 · 10.1371/journal.pone.0070993

  • Cardiac manifestations of myotonic dystrophy type 1

    International Journal of Cardiology · 2011 · 10.1016/j.ijcard.2011.08.037

  • McArdle disease: a clinical review

    Journal of Neurology Neurosurgery & Psychiatry · 2010 · 10.1136/jnnp.2009.195040

  • Mitochondrial encephalomyopathy with elevated methylmalonic acid is caused by SUCLA2 mutations

    Brain · 2007 · 10.1093/brain/awl383

  • High prevalence and phenotype–genotype correlations of limb girdle muscular dystrophy type 2I in Denmark

    Annals of Neurology · 2006 · 10.1002/ana.20824

  • Aerobic conditioning: An effective therapy in McArdle's disease

    Annals of Neurology · 2006 · 10.1002/ana.20881

  • Aerobic training is safe and improves exercise capacity in patients with mitochondrial myopathy

    Brain · 2006 · 10.1093/brain/awl149

  • Aerobic training improves exercise performance in facioscapulohumeral muscular dystrophy

    Neurology · 2005 · 10.1212/01.wnl.0000150584.45055.27

  • Recombination of Human Mitochondrial DNA

    Science · 2004 · https://doi.org/10.1126/science.1096342

  • Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy

    European Journal of Human Genetics · 2003 · 10.1038/sj.ejhg.5201002

  • Identification and Characterization of a Common Set of Complex I Assembly Intermediates in Mitochondria from Patients with Complex I Deficiency

    Journal of Biological Chemistry · 2003 · 10.1074/jbc.m304998200

  • The Effect of Oral Sucrose on Exercise Tolerance in Patients with McArdle's Disease

    New England Journal of Medicine · 2003 · 10.1056/nejmoa031836

  • Spontaneous "Second Wind" and Glucose-Induced Second "Second Wind" in McArdle Disease

    Archives of Neurology · 2002 · 10.1001/archneur.59.9.1395

  • Paternal Inheritance of Mitochondrial DNA

    New England Journal of Medicine · 2002 · https://doi.org/10.1056/nejmoa020350

  • Exercise-Induced Changes in Local Cerebral Glucose Utilization in the Rat

    Journal of Cerebral Blood Flow & Metabolism · 1996 · 10.1097/00004647-199607000-00025

Current projects

    No projects listed.