Giacomo P. Comi
Researcher Next ID · RN-034962
Researcher · Biochemistry, Genetics and Molecular Biology
Milan, Italy
- Works count
- 1,056
- Citation count
- 32,007
- H-index
- 92
- i10-index
- 477
Research interests
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.