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Giacomo P. Comi

Researcher Next ID · RN-034962

Researcher · Biochemistry, Genetics and Molecular Biology

University of Milan

Milan, Italy

Accepting doctoral researchersFunding unknown
Works count
1,056
Citation count
32,007
H-index
92
i10-index
477

Research interests

Biochemistry, Genetics and Molecular Biology
Medicine
Neuroscience
Muscle Physiology and Disorders
Neurogenetic and Muscular Disorders Research
Mitochondrial Function and Pathology
Genetic Neurodegenerative Diseases
Amyotrophic Lateral Sclerosis Research

Publications

  • Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy type 1 (STR1VE-EU): an open-label, single-arm, multicentre, phase 3 trial

    The Lancet Neurology · 2021 · https://doi.org/10.1016/s1474-4422(21)00251-9

  • Neural Stem Cell Transplantation for Neurodegenerative Diseases

    International Journal of Molecular Sciences · 2020 · 10.3390/ijms21093103

  • Neural Stem Cell Transplantation for Neurodegenerative Diseases

    International Journal of Molecular Sciences · 2020 · 10.3390/ijms21093103

  • The Role of Mitochondria in Neurodegenerative Diseases: the Lesson from Alzheimer’s Disease and Parkinson’s Disease

    Molecular Neurobiology · 2020 · 10.1007/s12035-020-01926-1

  • The Role of Mitochondria in Neurodegenerative Diseases: the Lesson from Alzheimer’s Disease and Parkinson’s Disease

    Molecular Neurobiology · 2020 · 10.1007/s12035-020-01926-1

  • Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

    Nature Communications · 2017 · https://doi.org/10.1038/ncomms14774

  • Conversion from clinically isolated syndrome to multiple sclerosis: A large multicentre study

    Multiple Sclerosis Journal · 2015 · https://doi.org/10.1177/1352458514568827

  • Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS

    Neuron · 2014 · https://doi.org/10.1016/j.neuron.2014.09.027

  • Ataluren treatment of patients with nonsense mutation dystrophinopathy

    Muscle & Nerve · 2014 · https://doi.org/10.1002/mus.24332

  • Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease

    Nature Genetics · 2013 · 10.1038/ng.2501

  • Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease

    Nature Genetics · 2013 · 10.1038/ng.2501

  • Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions

    The Journal of Experimental Medicine · 2009 · 10.1084/jem.20082779

  • Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions

    The Journal of Experimental Medicine · 2009 · 10.1084/jem.20082779

  • Reliability of the North Star Ambulatory Assessment in a multicentric setting

    Neuromuscular Disorders · 2009 · https://doi.org/10.1016/j.nmd.2009.06.368

  • Effect of laquinimod on MRI-monitored disease activity in patients with relapsing-remitting multiple sclerosis: a multicentre, randomised, double-blind, placebo-controlled phase IIb study

    The Lancet · 2008 · https://doi.org/10.1016/s0140-6736(08)60918-6

  • Autologous Transplantation of Muscle-Derived CD133+ Stem Cells in Duchenne Muscle Patients

    Cell Transplantation · 2007 · 10.3727/000000007783465064

  • Autologous Transplantation of Muscle-Derived CD133+ Stem Cells in Duchenne Muscle Patients

    Cell Transplantation · 2007 · 10.3727/000000007783465064

  • Identification of a Primitive Brain–Derived Neural Stem Cell Population Based on Aldehyde Dehydrogenase Activity

    Stem Cells · 2005 · 10.1634/stemcells.2005-0217

  • Polyneuropathy in POEMS syndrome: role of angiogenic factors in the pathogenesis

    Brain · 2005 · 10.1093/brain/awh519

  • Polyneuropathy in POEMS syndrome: role of angiogenic factors in the pathogenesis

    Brain · 2005 · 10.1093/brain/awh519

  • Identification of a Primitive Brain–Derived Neural Stem Cell Population Based on Aldehyde Dehydrogenase Activity

    Stem Cells · 2005 · 10.1634/stemcells.2005-0217

  • Mutations of mitochondrial DNA polymerase γA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia

    Annals of Neurology · 2002 · 10.1002/ana.10278

  • Mutations of mitochondrial DNA polymerase γA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia

    Annals of Neurology · 2002 · 10.1002/ana.10278

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

    Nature Genetics · 2001 · https://doi.org/10.1038/90058

  • Role of Adenine Nucleotide Translocator 1 in mtDNA Maintenance

    Science · 2000 · 10.1126/science.289.5480.782

  • Role of Adenine Nucleotide Translocator 1 in mtDNA Maintenance

    Science · 2000 · 10.1126/science.289.5480.782

  • Cytochrome c Oxidase subunit I microdeletion in a patient with motor neuron disease

    Annals of Neurology · 1998 · 10.1002/ana.410430119

  • Cytochrome c Oxidase subunit I microdeletion in a patient with motor neuron disease

    Annals of Neurology · 1998 · 10.1002/ana.410430119

Current projects

    No projects listed.