Citation Impact
Citing Papers
Long COVID: major findings, mechanisms and recommendations
2023 Standout
Gut dysbiosis, leaky gut, and intestinal epithelial proliferation in neurological disorders: towards the development of a new therapeutic using amino acids, prebiotics, probiotics, and postbiotics
2018
Mammalian Fe–S cluster biogenesis and its implication in disease
2014
Functional reconstitution of mitochondrial Fe/S cluster synthesis on Isu1 reveals the involvement of ferredoxin
2014
Reactive oxygen species (ROS) as pleiotropic physiological signalling agents
2020 Standout
Hypoxia Rescues Frataxin Loss by Restoring Iron Sulfur Cluster Biogenesis
2019 StandoutNobel
Role of mitochondria, oxidative stress and the response to antioxidants in myalgic encephalomyelitis/chronic fatigue syndrome: A possible approach to SARS‐CoV‐2 ‘long‐haulers’?
2020
Diabetic Cardiomyopathy
2018 Standout
Lipoic acid biosynthesis defects
2014
Maintaining Ancient Organelles
2015
Copper induces cell death by targeting lipoylated TCA cycle proteins
2022 StandoutScience
p53 tumor suppressor and iron homeostasis
2018
Reactive Oxygen Species-Induced Lipid Peroxidation in Apoptosis, Autophagy, and Ferroptosis
2019 Standout
Functional Interplay between Cristae Biogenesis, Mitochondrial Dynamics and Mitochondrial DNA Integrity
2019
Challenges and approaches for production of a healthy and functional mayonnaise sauce
2019 Standout
Works of Devorah Soiferman being referenced
Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy
2013
Mitochondrial complex IV deficiency, caused by mutated COX6B1, is associated with encephalomyopathy, hydrocephalus and cardiomyopathy
2014
The Effects of Ascorbate, N-Acetylcysteine, and Resveratrol on Fibroblasts from Patients with Mitochondrial Disorders
2016
Postnatal microcephaly and pain insensitivity due to a de novo heterozygous DNM1L mutation causing impaired mitochondrial fission and function
2016
Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation
2015