Brain

Papers
(The H4-Index of Brain is 70. 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 2021-06-01 to 2025-06-01.)
ArticleCitations
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 o343
The axon initial segment as a source of neuropathic pain332
De novo variants in ATXN7L3 lead to developmental delay, hypotonia and distinctive facial features292
Clinical dimensions along the non-fluent variant primary progressive aphasia spectrum281
Impaired ribosome-associated quality control of C9orf72 arginine-rich dipeptide-repeat proteins170
Correction to: Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders164
Proust and his neurologists: the challenge of functional disorders164
Thalamostriatal disconnection underpins long-term seizure freedom in frontal lobe epilepsy surgery164
Methodological drawbacks in the alleged association between foetal sonographic anomalies and autism164
Dysregulated cortical excitability and tau phosphorylation in a β3 integrin mouse model of autism155
Lesion correlates of impaired acoustic-phonetic perception after unilateral left hemisphere stroke154
Clinical and genetic characterization of a progressive RBL2-associated neurodevelopmental disorder149
Peripherin is a biomarker of axonal damage in Guillain-Barré syndrome: a pathophysiological annotation147
Dysfunction of the magnocellular subdivision of the visual thalamus in developmental dyslexia145
Clinical and genetic spectrum of 355 Chinese children with epilepsy: a trio-sequencing-based study136
Associations between accelerated forgetting, amyloid deposition and brain atrophy in older adults136
Deep brain stimulation: a tale of two targets … and closing the loop136
Trigeminal nerve microstructure is linked with neuroinflammation and brainstem activity in migraine133
Choroid plexus mis-splicing and altered cerebrospinal fluid composition in myotonic dystrophy type 1127
Somatic variants of MAP3K3 are sufficient to cause cerebral and spinal cord cavernous malformations126
Source-sink connectivity: a novel interictal EEG marker for seizure localization124
Imaging protein aggregates in the serum and cerebrospinal fluid in Parkinson’s disease124
18F-MK-6240 tau-PET in genetic frontotemporal dementia123
The inferior fronto-occipital fasciculus: bridging phylogeny, ontogeny and functional anatomy121
3T MRI of rapid brain activity changes driven by subcallosal cingulate deep brain stimulation121
We’re all in this together: a rejoinder to Masud Husain’s (rant) editorial121
The efficacy and deficiency of contemporary treatment for spinal cord arteriovenous shunts120
Biallelic ADAM22 pathogenic variants cause progressive encephalopathy and infantile-onset refractory epilepsy117
The use of optical coherence tomography in neurology: a review113
Biallelic FRA10AC1 variants cause a neurodevelopmental disorder with growth retardation109
Cerebral amyloid angiopathy interacts with neuritic amyloid plaques to promote tau and cognitive decline106
‘Seeding’ the idea of early diagnostics in synucleinopathies105
Mapping the peripheral immune landscape of Parkinson’s disease patients with single-cell sequencing103
Distinct subcellular autophagy impairments in induced neurons from patients with Huntington's disease102
Brain cholesterol and Alzheimer's disease: challenges and opportunities in probe and drug development102
Brain repair mechanisms after cell therapy for stroke101
Diffusion MRI tracks cortical microstructural changes during the early stages of Alzheimer’s disease100
From bugs to brain: unravelling the GABA signalling networks in the brain–gut–microbiome axis100
A data-driven study of Alzheimer's disease related amyloid and tau pathology progression92
The vascular contribution of apolipoprotein E to Alzheimer’s disease91
‘Hippocampal innate inflammatory gliosis only’ in pharmacoresistant temporal lobe epilepsy88
Genetically identical twin-pair difference models support the amyloid cascade hypothesis87
Optogenetic stimulation of the superior colliculus suppresses genetic absence seizures87
Speech and language markers of neurodegeneration: a call for global equity85
ActivatingRAC1variants in the switch II region cause a developmental syndrome and alter neuronal morphology84
Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes83
Genetic evaluation of dementia with Lewy bodies implicates distinct disease subgroups83
Correction to: New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy81
Midbrain cytotoxic T cells as a distinct neuropathological feature of progressive supranuclear palsy79
Genome-wide association study of neuropathological features in Lewy body disease79
Hitching a ride on exosomes: a new approach for the delivery of siRNA-mediated therapies78
Multiple sclerosis in Denmark (1950–2023): mean age, sex distribution, incidence and prevalence78
Synaptic dysregulation in a mouse model of GRIN2D developmental and epileptic encephalopathy77
Reply: Unblinding in the lecanemab trial in Alzheimer’s disease76
The interictal suppression hypothesis is the dominant differentiator of seizure onset zones in focal epilepsy75
Defective lipid signalling caused by mutations inPIK3C2Bunderlies focal epilepsy75
Periventricular remyelination failure in multiple sclerosis: a substrate for neurodegeneration74
Multimodal mapping of regional brain vulnerability to focal cortical dysplasia74
Long-term neuropsychological trajectories in children with epilepsy: does surgery halt decline?74
Demystifying interictal discharges and seizure initiation in focal epilepsy74
Multiple lines of evidence for disruption of nuclear lamina and nucleoporins in FUS amyotrophic lateral sclerosis74
The three deceits of bureaucracy73
Evolutionary perspectives on mRNA signatures of neurodegeneration-related brain remodelling73
Reply: From early limbic inflammation to long COVID sequelae73
Extra-cranial cholinergic lesions in dementia with Lewy bodies73
GGC repeat expansions in NOTCH2NLC cause uN2CpolyG cerebral amyloid angiopathy72
Biallelic null variants in PNPLA8 cause microcephaly by reducing the number of basal radial glia72
New mechanistic insights into hereditary spastic paraplegias72
Cytotoxic T cells and plasma cells dominate early in temporal lobe epilepsy with GAD antibodies72
Functional network reorganization precedes apathy in Parkinson’s disease: a neural marker of risk?70
Preclinical type 2 diabetes mellitus subtypes: new insights into diabetes, depression and dementia70
The low dimensionality of post-stroke cognitive deficits: it’s the lesion anatomy!70
Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 4070
BMP receptor blockade overcomes extrinsic inhibition of remyelination and restores neurovascular homeostasis70
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