Citation Impact
Citing Papers
2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy
2014 Standout
2017 Standout
Cerebral cortex expansion and folding: what have we learned?
2016
Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
2022 Standout
Activation of the Keap1/Nrf2 stress response pathway in autophagic vacuolar myopathies
2016
Band-like calcification with simplified gyration and polymicrogyria: report of 10 new families and identification of five novel OCLN mutations
2017
Desmosomes in the Heart: A Review of Clinical and Mechanistic Analyses
2014
Mechanical stress activates NMDA receptors in the absence of agonists
2017
Desmin-related myopathy: clinical, electrophysiological, radiological, neuropathological and genetic studies
2004
Malformations of cortical development: clinical features and genetic causes
2014
Nrf2-Keap1 signaling in oxidative and reductive stress
2018 Standout
The Neurovascular Unit Coming of Age: A Journey through Neurovascular Coupling in Health and Disease
2017 Standout
Sporadic inclusion-body myositis: A degenerative muscle disease associated with aging, impaired muscle protein homeostasis and abnormal mitophagy
2014
Viscoelastic parameter identification of human brain tissue
2017
Effects of extracellular matrix viscoelasticity on cellular behaviour
2020 StandoutNature
Blood–brain barrier breakdown in Alzheimer disease and other neurodegenerative disorders
2018 Standout
Piezos thrive under pressure: mechanically activated ion channels in health and disease
2017 StandoutNobel
Finding twinkle in the eyes of a 71‐year‐old lady: A case report and review of the genotypic and phenotypic spectrum of TWINKLE‐related dominant disease
2009
Establishment and Dysfunction of the Blood-Brain Barrier
2015
Broadening horizons: the role of ferroptosis in cancer
2021 Standout
Metabolic control through the PGC-1 family of transcription coactivators
2005 Standout
The intestinal epithelial barrier: a therapeutic target?
2016 Standout
Anti-Aβ Drug Screening Platform Using Human iPS Cell-Derived Neurons for the Treatment of Alzheimer's Disease
2011 StandoutNobel
Targeting ferroptosis as a vulnerability in cancer
2022 Standout
Zika Virus and Birth Defects — Reviewing the Evidence for Causality
2016 Standout
Fetal Infections and Brain Development
2009
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
2015 Standout
Ferroptosis: mechanisms, biology and role in disease
2021 Standout
Neocortical Layer Formation of Human Developing Brains and Lissencephalies: Consideration of Layer-Specific Marker Expression
2010
Delineation of the Clinical, Molecular and Cellular Aspects of Novel JAM 3 Mutations Underlying the Autosomal Recessive Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts
2012
Cytosolic 5′‐nucleotidase 1A autoimmunity in sporadic inclusion body myositis
2012
Inflammatory Muscle Diseases
2015 Standout
Materials and technologies for soft implantable neuroprostheses
2016
PGC-1-Related Coactivator, a Novel, Serum-Inducible Coactivator of Nuclear Respiratory Factor 1-Dependent Transcription in Mammalian Cells
2001
Peroxisome Proliferator-Activated Receptor-γ Coactivator 1α (PGC-1α): Transcriptional Coactivator and Metabolic Regulator
2003 Standout
Hydrogel bioelectronics
2018 Standout
Brown Adipose Tissue: Function and Physiological Significance
2004 Standout
Hydrogel ionotronics
2018 Standout
Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals
2022 StandoutScienceNobel
How neuroinflammation contributes to neurodegeneration
2016 StandoutScience
A novel Twinkle (PEO1) gene mutation in a Chinese family with adPEO.
2008
SLC7A11 expression is associated with seizures and predicts poor survival in patients with malignant glioma
2015
Deafness in occludin-deficient mice with dislocation of tricellulin and progressive apoptosis of the hair cells
2014
Alzheimer’s disease: A matter of blood–brain barrier dysfunction?
2017
Works of Waney Squier being referenced
A retrospective cohort study identifying the principal pathological features useful in the diagnosis of inclusion body myositis
2014
Long-term observational study of sporadic inclusion body myositis
2011
Genotypically Defined Lissencephalies Show Distinct Pathologies
2005
Recessive Mutations in the Gene Encoding the Tight Junction Protein Occludin Cause Band-like Calcification with Simplified Gyration and Polymicrogyria
2010
Respiratory insufficiency in desminopathy patients caused by introduction of proline residues in desmin c‐terminal α‐helical segment
2003
Mechanics of the brain: perspectives, challenges, and opportunities
2015
Band‐like intracranial calcification with simplified gyration and polymicrogyria: A distinct “pseudo‐TORCH” phenotype
2008
Expression patterns of glial fibrillary acidic protein (GFAP)‐delta in epilepsy‐associated lesional pathologies
2009
Polymicrogyria: pathology, fetal origins and mechanisms
2014
Mapping of autosomal dominant progressive external ophthalmoplegia to a 7-cM critical region on 10q24
1999