Citation Impact
Citing Papers
2013 ACC/AHA Guideline on the Treatment of Blood Cholesterol to Reduce Atherosclerotic Cardiovascular Risk in Adults
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TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
2008 StandoutScience
Induced Pluripotent Stem Cells Generated from Patients with ALS Can Be Differentiated into Motor Neurons
2008 StandoutScience
EglN2 associates with the NRF 1‐ PGC 1α complex and controls mitochondrial function in breast cancer
2015 StandoutNobel
Hypoxia and intra-complex genetic suppressors rescue complex I mutants by a shared mechanism
2024 StandoutNobel
Animal mitochondrial genomes
1999 Standout
Mitochondrial DNA Mutations in Disease, Aging, and Neurodegeneration
2008
Mammalian Mitochondrial Complex I Structure and Disease-Causing Mutations
2018
High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease
2006
Mitochondrial DNA mutations in human cancer
2006
Mitochondrial enzyme activity in amyotrophic lateral sclerosis: Implications for the role of mitochondria in neuronal cell death
1999
Mitochondria: Dynamic Organelles in Disease, Aging, and Development
2006 Standout
Mitochondrial DNA mutations in human colonic crypt stem cells
2003
MtDNA mutations in aging and apoptosis
2003
Critical illness myopathy and neuropathy
2005
Acute axonal Guillain‐Barré syndrome with IgG antibodies against motor axons following parenteral gangliosides
1995
mRNA-based therapeutics — developing a new class of drugs
2014 StandoutNobel
Neuropathological and Histochemical Changes in a Multiple Mitochondrial DNA Deletion Disorder
2000
A nonsense mutation (G15059A) in the cytochromeb gene in a patient with exercise intolerance and myoglobinuria
1999
Pathogenesis and therapy of neuropathies associated with monoclonal gammopathies
1995
Paraneoplastic Syndromes Involving the Nervous System
2003 Standout
The genetics of ageing
2010 StandoutNature
Ageing muscle: clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function
2002
Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia: A syndrome caused by a missense mutation in OPA1
2004
Premature ageing in mice expressing defective mitochondrial DNA polymerase
2004 StandoutNature
Applying genomic and transcriptomic advances to mitochondrial medicine
2021
The Mitochondrial Disulfide Relay System Protein GFER Is Mutated in Autosomal-Recessive Myopathy with Cataract and Combined Respiratory-Chain Deficiency
2009
The Relationship Between the Rate of Molecular Evolution and the Rate of Genome Rearrangement in Animal Mitochondrial Genomes
2006
Hallmarks of aging: An expanding universe
2023 Standout
Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations
2006
Guillain-Barré syndrome
2016 Standout
A Mitochondrial Protein Compendium Elucidates Complex I Disease Biology
2008 Standout
Guillain–Barré Syndrome
2012 Standout
Mitochondrial DNA polymerase-γ and human disease
2006
The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA
2001
Amyotrophic lateral sclerosis
2011 Standout
Mitochondrial DNA and disease
2005
Complete Mitochondrial Genomes Reveal Neolithic Expansion into Europe
2012 StandoutNobel
Nitric Oxide and Peroxynitrite in Health and Disease
2007 Standout
Dysferlin and the plasma membrane repair in muscular dystrophy
2004
Multiple sclerosis
2008 Standout
Mitochondria: In Sickness and in Health
2012 Standout
In Vivo Correction of COX Deficiency by Activation of the AMPK/PGC-1α Axis
2011
DNA Damage, Aging, and Cancer
2009 Standout
Campylobacter jejuni infections and anti‐GM1 antibodies in guillain‐barré syndrome
1996
Mitochondrial Alterations in the Spinal Cord of Patients With Sporadic Amyotrophic Lateral Sclerosis
2007
Muscle biopsy findings in inflammatory myopathies
2002
No Evidence for an mtDNA Role in Sperm Motility: Data from Complete Sequencing of Asthenozoospermic Males
2007
Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA
2001
Energetics in the pathogenesis of neurodegenerative diseases
2000
Autophagy in the Pathogenesis of Disease
2008 Standout
The clinical correlates of high‐titer IgG anti‐GM1 antibodies
1994
Evolutionarily Conserved Multiple C2 Domain Proteins with Two Transmembrane Regions (MCTPs) and Unusual Ca2+ Binding Properties
2004 StandoutNobel
The end of AIDS: HIV infection as a chronic disease
2013 Standout
Understanding the Odd Science of Aging
2005 Standout
Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy
2001
Monoclonal IgM antibodies to GM1 and asialo‐GM1 in chronic neuropathies cross‐react with Compylobacter jejuni lipopolysaccharides
1994
Modified Uridines with C5-methylene Substituents at the First Position of the tRNA Anticodon Stabilize U·G Wobble Pairing during Decoding
2008 StandoutNobel
Immunopathogenesis and treatment of the guillain‐barré syndrome—part I
1995
Antibodies to gangliosides and galactocerebroside in patients with Guillain–Barré syndrome with preceding Campylobacter jejuni and other identical infections
1998
Antibodies to GT1a ganglioside in patients with Guillain–Barré syndrome
1998
Functional Disability 5 Years after Acute Respiratory Distress Syndrome
2011 Standout
Activated T cells of nonneural specificity open the blood‐nerve barrier to circulating antibody
1995
Mouse models for mitochondrial disease
2001
Role of mitochondrial DNA mutations in human aging: Implications for the central nervous system and muscle
1998
Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases
2006 StandoutNature
Is there a decrease in Guillain–Barré syndrome incidence after bovine ganglioside withdrawal in Italy? A population-based study in the Local Health District of Ferrara, Italy
2003
Progress in the pathogenesis of amyotrophic lateral sclerosis
2001
Recent developments in the molecular genetics of mitochondrial disorders
1998
Mitochondria and ageing
2000
Mitochondrial dysfunction as a cause of optic neuropathies
2004
IgG anti-GM1 antibodies from patients with acute motor neuropathy are predominantly of the IgG1 and IgG3 subclasses
1995
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
2015 Standout
Association of anti-GM2 antibodies in Guillain-Barré syndrome with acute cytomegalovirus infection
1996
Anti‐ganglioside GM1 antibodies in guillain‐barré syndrome and their relationship to Campylobacter jejuni infection
1995
Neuronal degeneration and mitochondrial dysfunction
2003
Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1α
2006 Standout
Ferroptosis: mechanisms, biology and role in disease
2021 Standout
Prevention of Type 2 Diabetes Mellitus by Changes in Lifestyle among Subjects with Impaired Glucose Tolerance
2001 Standout
The Hallmarks of Aging
2013 Standout
High levels of mitochondrial DNA deletions in skeletal muscle of old rhesus monkeys
1995
Natural History of Peripheral Neuropathy in Patients with Non-Insulin-Dependent Diabetes Mellitus
1995
Acquired immune and inflammatory myopathies
2011
A Stop-Codon Mutation in the Human mtDNA Cytochrome c Oxidase I Gene Disrupts the Functional Structure of Complex IV
1999
Molecular biology of amyotrophic lateral sclerosis: insights from genetics
2006
Increased longevity and refractoriness to Ca2+-dependent neurodegeneration in Surf1 knockout mice
2007
Polymyositis and dermatomyositis
2003 Standout
Unbalanced deoxynucleotide pools cause mitochondrial DNA instability in thymidine phosphorylase-deficient mice
2008
Deficiency of the ADP-Forming Succinyl-CoA Synthase Activity Is Associated with Encephalomyopathy and Mitochondrial DNA Depletion
2005
Mitochondrial aging is accelerated by anti-retroviral therapy through the clonal expansion of mtDNA mutations
2011
The role of cytochrome c oxidase deficient hippocampal neurones in Alzheimer's disease
2002
Amyotrophic Lateral Sclerosis
2001 Standout
Cytochrome c oxidase deficient cells accumulate in the hippocampus and choroid plexus with age
2001
Guillain-Barré syndrome
2005 Standout
Mitochondrial defects in acute multiple sclerosis lesions
2008
The cancer genome
2009 StandoutNature
Molecular Biology of Aging
1999
Analysis of 81 genes from 64 plastid genomes resolves relationships in angiosperms and identifies genome-scale evolutionary patterns
2007 Standout
A Mitochondrial Paradigm of Metabolic and Degenerative Diseases, Aging, and Cancer: A Dawn for Evolutionary Medicine
2005 Standout
Induction of anti-GM1 ganglioside antibodies by Campylobacter jejuni lipopolysaccharides
1997
DNA analysis of an early modern human from Tianyuan Cave, China
2013 StandoutNobel
Familial multisystem degeneration with parkinsonism associated with the 11778 mitochondrial DNA mutation
1999
Defective mitochondrial DNA replication and NRTIs: pathophysiological implications in AIDS cardiomyopathy
2003
Inflammatory Muscle Diseases
2015 Standout
DNA Polymerase γ in Mitochondrial DNA Replication and Repair
2005
Inclusion-body myositis
2006
Metabolic control of cell death
2014 Science
Guillain-Barr� syndrome and chronic inflammatory demyelinating polyneuropathy: Immune mechanisms and update on current therapies
1995
Clinical Spectrum, Morbidity, and Mortality in 113 Pediatric Patients With Mitochondrial Disease
2004
Mitochondrial DNA Mutations, Oxidative Stress, and Apoptosis in Mammalian Aging
2005 StandoutScience
2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy
2011 Standout
Thymidine Phosphorylase Gene Mutations in MNGIE, a Human Mitochondrial Disorder
1999 Science
Mitochondrial involvement in the ageing process. Facts and controversies
1997
Mitochondrial Fission, Fusion, and Stress
2012 StandoutScience
Codon-specific translational defect caused by a wobble modification deficiency in mutant tRNA from a human mitochondrial disease
2004
Mitochondrial Disorders in the Nervous System
2008
Mitochondrial complex I: Structure, function and pathology
2006
Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome
2011
Mitochondrial Diseases in Man and Mouse
1999 StandoutScience
A novel Twinkle (PEO1) gene mutation in a Chinese family with adPEO.
2008
E-Syts, a family of membranous Ca 2+ -sensor proteins with multiple C 2 domains
2007 StandoutNobel
Anti-GalNAc-GD1a antibody-associated Guillain-Barré syndrome with a predominantly distal weakness without cranial nerve impairment and sensory disturbance
1999
Erythropoietin both protects from and reverses experimental diabetic neuropathy
2004
Phase variation of a β‐1,3 galactosyltransferase involved in generation of the ganglioside GM1‐like lipo‐oligosaccharide of Campylobacter jejuni
2000
Approach to the Patient Who Is Intolerant of Statin Therapy
2010
A bacterium lipopolysaccharide that elicits Guillain-Barré syndrome has a GM1 ganglioside-like structure.
1993
Lipopolysaccharides from Campylobacter jejuni O:41 Strains Associated with Guillain-Barre Syndrome Exhibit Mimicry of GM 1 Ganglioside
1998
Lipopolysaccharide Endotoxins
2002 Standout
Nitric oxide prevents axonal degeneration by inducing HIF-1–dependent expression of erythropoietin
2011 StandoutNobel
Neuronal degeneration and mitochondrial dysfunction
2003
Free Radicals in the Physiological Control of Cell Function
2002 Standout
Mitochondrial DNA deletion mutations colocalize with segmental electron transport system abnormalities, muscle fiber atrophy, fiber splitting, and oxidative damage in sarcopenia
2001
Inherited Mitochondrial Diseases of DNA Replication
2007
Immunoglobulin subclass distribution and binding characteristics of anti-GQ1b antibodies in Miller fisher syndrome
1994
Mitochondrial involvement in the ageing process. Facts and controversies
1997
Works of Monica Sciacco being referenced
Paucity of deleted mitochondrial DNAs in brain regions of Huntington's disease patients
1995
Evidence and age-related distribution of mtDNA D-loop point mutations in skeletal muscle from healthy subjects and mitochondrial patients
2002
Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion
2003
Guillain-Barré syndrome associated with high titers of anti-GM1 antibodies
1992
Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA
1993
Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy
1994
A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome
2003
Cytochrome c Oxidase subunit I microdeletion in a patient with motor neuron disease
1998
Clinical, morphological and immunological evaluation of six patients with dysferlin deficiency
2003
[43]Cytochemistry and immunocytochemistry of mitochondria in tissue sections
1996
New Mutations in TK2 Gene Associated With Mitochondrial DNA Depletion
2006
Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: A study of 56 patients
1996
Phenotype-genotype correlations in skeletal muscle of patients with mtDNA deletions
1995
A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsy
2005
Muscle Coenzyme Q10 Level in Statin-Related Myopathy
2005
A novel missense adenine nucleotide translocator-1 gene mutation in a Greek adPEO family
2001
Critically ill patients: immunological evidence of inflammation in muscle biopsy.
1999
Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome
1998
Decrease of nerve Na+,K+-ATPase activity in the pathogenesis of human diabetic neuropathy
1993
Remarkable infidelity of polymerase γA associated with mutations in POLG1 exonuclease domain
2003
Clinical manifestations of mitochondria1 DNA depletion
1998
A mitochondrial tRNA His gene mutation causing pigmentary retinopathy and neurosensorial deafness
2003
Lack of apoptosis in mitochondrial encephalomyopathies
2001