Brain

Papers
(The median citation count of Brain is 7. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-05-01 to 2026-05-01.)
ArticleCitations
Correction to: Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders441
Source-sink connectivity: a novel interictal EEG marker for seizure localization302
PET-MRI biomarkers reveal efficacy of a novel NLRP3 inhibitor in Parkinson’s disease models261
The RAB3A hot spot variant R83W causes spasticity as part of the ataxia-spasticity spectrum230
Cerebral amyloid angiopathy interacts with neuritic amyloid plaques to promote tau and cognitive decline222
Choroid plexus mis-splicing and altered cerebrospinal fluid composition in myotonic dystrophy type 1219
Optogenetic stimulation of the superior colliculus suppresses genetic absence seizures211
Clinical and genetic characterization of a progressive RBL2-associated neurodevelopmental disorder210
Deep brain stimulation: a tale of two targets … and closing the loop207
Dysregulated cortical excitability and tau phosphorylation in a β3 integrin mouse model of autism196
We’re all in this together: a rejoinder to Masud Husain’s (rant) editorial190
Genetically identical twin-pair difference models support the amyloid cascade hypothesis186
Thalamic stereo EEG: a clinically justified extension of hypothesis-driven intracranial exploration177
Reply: Is postural tachycardia syndrome a psychogenic disorder?; Notes on establishing fear conditioning as causal in the postural orthostatic tachycardia syndrome; Patients with POTS fear that data o172
The axon initial segment as a source of neuropathic pain162
Methodological drawbacks in the alleged association between foetal sonographic anomalies and autism157
Somatic variants of MAP3K3 are sufficient to cause cerebral and spinal cord cavernous malformations156
Peripherin is a biomarker of axonal damage in Guillain-Barré syndrome: a pathophysiological annotation152
Clinical dimensions along the non-fluent variant primary progressive aphasia spectrum151
Dysfunction of the magnocellular subdivision of the visual thalamus in developmental dyslexia150
In vivo self-assembled siRNAs ameliorate neurological pathology in TDP-43-associated neurodegenerative disease147
Lesion correlates of impaired acoustic-phonetic perception after unilateral left hemisphere stroke139
Maternal microbiome-derived propionate regulates offspring myelination via histone lactylation136
Global network and local vulnerabilities underlie brain atrophy across Parkinson’s disease stages134
De novo variants in ATXN7L3 lead to developmental delay, hypotonia and distinctive facial features134
Impaired ribosome-associated quality control of C9orf72 arginine-rich dipeptide-repeat proteins133
Thalamostriatal disconnection underpins long-term seizure freedom in frontal lobe epilepsy surgery132
The vascular contribution of apolipoprotein E to Alzheimer’s disease129
Brain cholesterol and Alzheimer's disease: challenges and opportunities in probe and drug development124
Dopamine and the dynamics of subthalamic and leg muscle activities in parkinsonian stepping122
Diffusion MRI tracks cortical microstructural changes during the early stages of Alzheimer’s disease120
‘Hippocampal innate inflammatory gliosis only’ in pharmacoresistant temporal lobe epilepsy120
Apathy, effort-based decisions and brain integrity in Alzheimer's and Parkinson's diseases114
The inferior fronto-occipital fasciculus: bridging phylogeny, ontogeny and functional anatomy113
Trigeminal nerve microstructure is linked with neuroinflammation and brainstem activity in migraine112
Associations between accelerated forgetting, amyloid deposition and brain atrophy in older adults110
From bugs to brain: unravelling the GABA signalling networks in the brain–gut–microbiome axis108
Mapping the peripheral immune landscape of Parkinson’s disease patients with single-cell sequencing107
The use of optical coherence tomography in neurology: a review106
Brain repair mechanisms after cell therapy for stroke104
Speech and language markers of neurodegeneration: a call for global equity104
A data-driven study of Alzheimer's disease related amyloid and tau pathology progression99
Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes99
Correction to: New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy98
Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 4097
Normalization of network activity in an epilepsy model with a constitutively active GABBR2 variant96
Integrative genomics reveals pathogenic mediator of valproate-induced neurodevelopmental disability94
Distinct contribution of spinal neuropeptide Y and NPY1R neurons to morphine analgesia94
Loss of DOT1L disrupts neuronal transcription and leads to a neurodevelopmental disorder94
Demystifying interictal discharges and seizure initiation in focal epilepsy93
The low dimensionality of post-stroke cognitive deficits: it’s the lesion anatomy!93
Reply: Unblinding in the lecanemab trial in Alzheimer’s disease92
Loss-of-function variants inMYCBP2cause neurobehavioural phenotypes and corpus callosum defects91
How COVID-19 affects microvessels in the brain86
Neural stem cell therapies for spinal cord injury repair: an update on recent preclinical and clinical advances85
Clinical features and prognostic factors in adults with brain abscess85
Extra-cranial cholinergic lesions in dementia with Lewy bodies84
New mechanistic insights into hereditary spastic paraplegias84
Preclinical type 2 diabetes mellitus subtypes: new insights into diabetes, depression and dementia82
Biallelic LGI1 and ADAM23 variants cause hippocampal epileptic encephalopathy via the LGI1–ADAM22/23 pathway81
Disruption of DNA methylation underpins the neuroinflammation induced by targeted CNS radiotherapy81
Evolutionary perspectives on mRNA signatures of neurodegeneration-related brain remodelling80
The interictal suppression hypothesis is the dominant differentiator of seizure onset zones in focal epilepsy80
Cytotoxic T cells and plasma cells dominate early in temporal lobe epilepsy with GAD antibodies80
That which we call cortisol awakening response, by any other word would smell as sweet79
Integrative miRNA–mRNA profiling of human epidermis: unique signature of SCN9A painful neuropathy76
Cross-seeding by prion protein inactivates TDP-4376
Synaptic dysregulation in a mouse model of GRIN2D developmental and epileptic encephalopathy75
Defective lipid signalling caused by mutations inPIK3C2Bunderlies focal epilepsy75
Multiple sclerosis in Denmark (1950–2023): mean age, sex distribution, incidence and prevalence75
Is glymphatic clearance the secret to restorative sleep?74
Clinical and MRI measures to identify non-acute MOG-antibody disease in adults74
Hippocampal synaptic failure is an early event in experimental parkinsonism with subtle cognitive deficit74
Multiple lines of evidence for disruption of nuclear lamina and nucleoporins in FUS amyotrophic lateral sclerosis73
Plasma pTau 217/β-amyloid 1–42 ratio for enhanced accuracy and reduced uncertainty in detecting amyloid pathology73
Biallelic null variants in PNPLA8 cause microcephaly by reducing the number of basal radial glia72
The three deceits of bureaucracy72
Routes of precursors’ migration in remyelination72
Rigidity in Parkinson’s disease72
Multifaceted nanoparticles: emerging mechanisms and therapies in neurodegenerative diseases71
Natural experiment on neuroinflammatory disease incidence and infection links pre- and post-COVID-1970
Molecular and clinical spectrum of epilepsy-dyskinesia syndromes: a cross-sectional study of 609 patients69
Extracellular vesicle biomarkers for complement dysfunction in schizophrenia69
Cortical cerebral microinfarcts spark cognitive decline68
Functional network reorganization precedes apathy in Parkinson’s disease: a neural marker of risk?68
Multicentre analysis of seizure outcome predicted by removal of high-frequency oscillations68
GGC repeat expansions in NOTCH2NLC cause uN2CpolyG cerebral amyloid angiopathy68
Multimodal mapping of regional brain vulnerability to focal cortical dysplasia67
A generalizable data-driven model of atrophy heterogeneity and progression in memory clinic settings67
Genome-wide association study of neuropathological features in Lewy body disease67
Midbrain cytotoxic T cells as a distinct neuropathological feature of progressive supranuclear palsy66
Treatment-resistant recurrent unipolar and bipolar depression: associative learning abnormalities66
Activation and sensitization of meningeal nociceptors by PACAP-38: implications for migraine headache66
Periventricular remyelination failure in multiple sclerosis: a substrate for neurodegeneration65
Novel insight into TRPV1-induced mitochondrial dysfunction in neuropathic pain65
From phenomena to phrasing: rethinking seizure classification through history65
A sensory neuron-specific long non-coding RNA reduces neuropathic pain by rescuing KCNN1 expression65
Structural covariance analysis for neurodegenerative and neuroinflammatory brain disorders65
Deciphering the impact of coding and non-coding SCN1A gene variants on RNA splicing65
Long-term neuropsychological trajectories in children with epilepsy: does surgery halt decline?64
From shadows to spotlight: the evolution of migraine stigma since the 17th century64
How modular are modules in visual cortex?64
Correction to: Blood–brain barrier opening of the default mode network in Alzheimer's disease with magnetic resonance-guided focused ultrasound62
Correction to: Sex-specific modulation of amyloid-β on tau phosphorylation underlies faster tangle accumulation in females62
Correction to: Remyelination of chronic demyelinated lesions with directly induced neural stem cells62
Distinct cerebellar networks underpin clinical improvement in adolescent Tourette disorder61
Endosomal 2Cl−/H+ exchangers regulate neuronal excitability by tuning Kv7/KCNQ channel density61
Reply: Lecanemab: turning point, or status quo? An ethics perspective61
Delineation of functionally essential protein regions for 242 neurodevelopmental genes60
Correction to: Expanded clinical phenotype spectrum correlates with variant function in SCN2A-related disorders60
Sleep and seizure risk in epilepsy: bed and wake times are more important than sleep duration60
Decoding inflammatory pathways in spinal muscular atrophy: implications for next-generation therapies60
Untangling white matter fibre changes in Alzheimer's disease and small vessel disease59
A journey towards the pot of gold59
Neuromelanin as a nidus for neurodegeneration58
Age-related and amyloid-beta-independent tau deposition and its downstream effects57
Reply: Do we need new MRI criteria for the diagnosis of radiologically isolated syndrome?57
Reply: The correlation of behavioural deficits post-stroke: a trivial issue?57
Role of CD5 signalling for pro-inflammatory Th17 response in multiple sclerosis57
JC virus spread is potentiated by glial replication and demyelination-linked glial proliferation57
Occludin modulates HIV and ischaemic stroke response via the mitochondrial antiviral signalling pathway56
Early onset hereditary neuronopathies: an update on non-5qmotor neuron diseases56
Neural basis of speech and grammar symptoms in non-fluent variant primary progressive aphasia spectrum56
Misdirected yet intact TREX1 exonuclease activity causes human cerebral and systemic small vessel disease56
Impaired value-based decision-making in Parkinson’s disease apathy56
Estimating the time course of biomarker changes in Alzheimer’s disease55
The use of animals in neuroscience research55
A novel eye-movement impairment in multiple sclerosis indicating widespread cortical damage55
Multicompartmental models and diffusion abnormalities in paediatric mild traumatic brain injury55
Failure of C9orf72 sense repeat-targeting antisense oligonucleotides: lessons learned and the path forward55
Cdc42GAP deficiency contributes to the Alzheimer’s disease phenotype54
Nigrostriatal tau pathology in parkinsonism and Parkinson’s disease54
Basal forebrain integrity, cholinergic innervation and cognition in idiopathic Parkinson’s disease54
Plasma VEGFA and PGF impact longitudinal tau and cognition in preclinical Alzheimer’s disease54
The human subthalamic nucleus transiently inhibits active attentional processes54
Effort avoidance as a core mechanism of apathy in frontotemporal dementia54
In silico versus functional characterization of genetic variants: lessons from muscle channelopathies54
White matter connections within the central sulcus subserving the somato-cognitive action network53
Anatomo-functional basis of emotional and motor resonance elicited by facial expressions53
Common and distinct fronto-striatal volumetric changes in heroin and cocaine use disorders53
Interferon-γ controls aquaporin 4-specific Th17 and B cells in neuromyelitis optica spectrum disorder53
The lysosomal β-glucocerebrosidase strikes mitochondria: implications for Parkinson’s therapeutics53
Genetic variability in sporadic amyotrophic lateral sclerosis52
Large-scale rare variant burden testing in Parkinson's disease52
Reduced striatal dopamine transmission as a transdiagnostic substrate of psychomotor retardation52
Widespread white matter oedema in subacute COVID-19 patients with neurological symptoms52
Amyloid-β predominant Alzheimer’s disease neuropathologic change52
Localizing epileptogenic tissues in epilepsy: are we losing (the) focus?51
Is it time to rename hereditary cases of cerebral palsy?51
Imaging chronic active lesions in multiple sclerosis: a consensus statement51
Interleukin-17B is a new biomarker of human muscle regeneration in dystrophinopathies51
Tiam1 is part of a novel mechanism for morphine tolerance and hyperalgesia51
A foothold in detection of limbic-predominant age-related TDP-43 encephalopathy51
Shedding light on a novel circuit within primary motor cortex as a target for neuromodulation50
The visual cortex in the blind but not the auditory cortex in the deaf becomes multiple-demand regions50
Bridging the gaps between JCV infection models and human disease50
The ageing central nervous system in multiple sclerosis: the imaging perspective50
Surgical white matter disruption leads to downstream atrophy in the non-resected human brain50
Correction to: Bidirectional gut-to-brain and brain-to-gut propagation of synucleinopathy in non-human primates50
C-terminal TMEM106B fragments in human brain correlate with disease-associated TMEM106B haplotypes50
Understanding brain calcification via N-terminal acetylation at the Golgi apparatus50
Seeding, maturation and propagation of amyloid β-peptide aggregates in Alzheimer’s disease49
Four dimensions of naturalistic language production in aphasia after stroke49
Biomarker evidence of neurodegeneration in mid-life former rugby players49
USP25 in genetic generalized epilepsy: a gene under scrutiny49
The ‘secret connections’ of the brain: a connectomic reserve for neuroplasticity?49
Synaptic and cognitive impairment associated with L444P heterozygous glucocerebrosidase mutation48
Motor compensation in Parkinson’s disease: an empirical challenge with clinical implications48
Sleep circuit modulation: from animal models to human translation48
CGRP signalling in migraine: time to look downstream?47
Thalamic stereo-EEG in epilepsy surgery: where do we stand?47
HDAC6 regulates BACE1 stability and NLRP3 inflammasome activation in Alzheimer’s disease47
Precision dynamics of predictive coding in functional neurological disorder47
Brain accumulation of lactosylceramide characterizes GALC deficiency in a zebrafish model of Krabbe disease47
Amyloid-β-activated microglia can induce compound proteinopathies47
Cul-4 inhibition rescues spastin levels and reduces defects in hereditary spastic paraplegia models47
Clinical and biochemical characterization of amyotrophic lateral sclerosis in a CHCHD10 R15L family47
Imaging progenitor cell differentiation during central nervous system remyelination using an MRI gene reporter46
Alzheimer proteopathic tau seeds are biochemically a forme fruste of mature paired helical filaments46
PTPA variants and the risk for Parkinson’s disease in diverse ancestry populations46
Ageing and remyelination failure in people with multiple sclerosis46
Satellite glial GLRX3 drives ageing-biased neuropathic pain via HMGB145
The basal forebrain cholinergic system as target for cell replacement therapy in Parkinson’s disease45
Machine learning model based on plasma proteomics for the identification of Parkinson’s disease45
Characterizing proteomic and transcriptomic features of missense variants in amyotrophic lateral sclerosis genes45
Emotional bias modification weakens game-related compulsivity and reshapes frontostriatal pathways45
Multimodal multicentre investigation of diagnostic and prognostic markers in disorders of consciousness45
Morc2a variants cause hydroxyl radical-mediated neuropathy and are rescued by restoring GHKL ATPase44
Interpretable surface-based detection of focal cortical dysplasias: a Multi-centre Epilepsy Lesion Detection study44
The functional role of the precuneus44
Motor network gamma oscillations in chronic home recordings predict dyskinesia in Parkinson’s disease44
Right temporal degeneration and socioemotional semantics: semantic behavioural variant frontotemporal dementia44
Elucidating the nociceptive role of CGRP in migraine headache44
Reply: Methodological drawbacks in the alleged association between foetal sonographic anomalies and autism43
Medial temporal lobe structural changes when Down syndrome and Alzheimer’s disease collide43
Chasing MOG antibodies down … assays and lumbar punctures43
ZSCAN10 deficiency causes a neurodevelopmental disorder with characteristic oto-facial malformations43
Reply: Putative benefits of vitamin D supplements in multiple sclerosis out of reach due to sample size43
Plasma biomarkers in chronic single moderate/severe traumatic brain injury43
Pure autonomic failure as an essential window into progression of synucleinopathies42
Interaction of motor behaviour, cortical oscillations and deep brain stimulation in Parkinson’s disease42
TGFβ4 alleviates the phenotype of Charcot–Marie–Tooth disease type 1A42
One transgene, two myopathies: an MTM1 ‘cross gene therapy’ for BIN1 deficiency?42
Reply: Neural substrates of the link between dual-task gait and dementia: an intermediary step in which direction?42
The complexity of interpreting TSPO PET neuroimaging in first-episode psychosis42
Ligand-free mitochondria-localized mutant AR-induced cytotoxicity in spinal bulbar muscular atrophy42
Reply: An epigenetic basis for genetic anticipation in facioscapulohumeral muscular dystrophy type 141
Mitochondrial damage is associated with an early immune response in inclusion body myositis41
Mitochondrial dynamics and bioenergetics in Alzheimer’s induced pluripotent stem cell-derived neurons41
Great science does not communicate itself: but who should and how?41
Brainstem cavernous malformations: observation, microsurgical resection or stereotactic radiosurgery41
Increase of HCN current in SOD1-associated amyotrophic lateral sclerosis41
Genome-wide epistasis analysis reveals significant epistatic signals associated with Parkinson’s disease risk40
The Wernicke conundrum revisited: evidence from connectome-based lesion-symptom mapping40
Clinical features and prognostic factors in adults with viral meningitis40
Neurophysiological consequences of synapse loss in progressive supranuclear palsy40
Uncovering the distinct macro-scale anatomy of dysexecutive and behavioural degenerative diseases40
Nifuroxazide rescues the deleterious effects due to CHCHD10-associated MICOS defects in disease models40
Oxytocin receptor neurons in the paraventricular thalamus as a nexus for social behaviour and fear39
Intra-putaminal muscarinic receptor agonist infusion induces a dystonic phenotype in non-human primates39
Genome-wide contribution of common short-tandem repeats to Parkinson’s disease genetic risk39
Cation leak through the ATP1A3 pump causes spasticity and intellectual disability39
Myelination potential and injury susceptibility of grey versus white matter human oligodendrocytes39
Reply: The challenge of assessing invasive biomarkers for epilepsy surgery and To plan efficacious epilepsy surgery39
Brain essay competition winner on artificial general intelligence39
Role of pattern recognition receptors in chemotherapy-induced neuropathic pain39
Noradrenergic alterations in Parkinson’s disease: a combined 11C-yohimbine PET/neuromelanin MRI study38
Memory deficits of MDMA users are linked to cortical thinning related to 5-HT receptor densities38
Expedited epilepsy surgery prior to drug resistance in children: a frontier worth crossing?38
Motivational and cognitive predictors of apathy after subthalamic nucleus stimulation in Parkinson’s disease38
Phenotypic individual clusters and metabolic tuber subtypes refine surgical strategy in tuberous sclerosis complex38
Data-driven modelling of tau pathology reveals distinct progressive supranuclear palsy subtypes37
Cerebellar pathology contributes to neurodevelopmental deficits in spinal muscular atrophy37
Neurovascular injury with complement activation and inflammation in COVID-1937
Connectivity as a universal predictor of tau progression in atypical Alzheimer’s disease37
Seronegative autoimmune encephalitis: clinical characteristics and factors associated with outcomes37
Efficacy of MEDI0618, a pH-dependent monoclonal antibody targeting PAR2, in preclinical models of migraine37
Heterozygous PRKN mutations are common but do not increase the risk of Parkinson’s disease37
Limitation of life sustaining therapy in disorders of consciousness: ethics and practice37
Clinicopathological correlates in the frontotemporal lobar degeneration–motor neuron disease spectrum37
Phenoconversion in pure autonomic failure: a multicentre prospective longitudinal cohort study37
CSF amyloid-β40 levels are not associated with efficacy outcomes in Alzheimer’s disease trials36
Astrocyte regeneration via FGF8-DBX1 signalling facilitates recovery in neuromyelitis optica rats36
Mutations inTAF8cause a neurodegenerative disorder36
Reply: Lack of statistical significance is not evidence against modularity in visual feature processing36
Methodological considerations in neuronal extracellular vesicle isolation for α-synuclein biomarkers36
Can immunological imprinting drive neurological dysfunction in long COVID?36
Missense variants in TUBA4A cause myo-tubulinopathies36
ILAE position on early surgery for drug sensitive lesional focal epilepsy36
Snatches of time. Fragments36
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