OOIR: Observatory of International Research

Papers

(The TQCC of Neuropathology is 3. 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 2020-05-01 to 2024-05-01.)

Article	Citations
Where and how alpha‐synuclein pathology spreads in Parkinson’s disease:	38
A novel SNCA E83Q mutation in a case of dementia with Lewy bodies and atypical frontotemporal lobar degeneration	27
Sodium/glucose cotransporter 2 is expressed in choroid plexus epithelial cells and ependymal cells in human and mouse brains	26
Praja1 RING‐finger E3 ubiquitin ligase suppresses neuronal cytoplasmic TDP‐43 aggregate formation	25
Glioblastoma multiforme: Metabolic differences to peritumoral tissue and IDH‐mutated gliomas revealed by mass spectrometry imaging	25
Human brain pathology in myotonic dystrophy type 1: A systematic review	23
Intracellular amyloid hypothesis for ultra‐early phase pathology of Alzheimer's disease	22
Astrocytes release glutamate via cystine/glutamate antiporter upregulated in response to increased oxidative stress related to sporadic amyotrophic lateral sclerosis	16
Neuropathology of α‐synuclein in Parkinson's disease	15
Red nucleus IL‐6 mediates the maintenance of neuropathic pain by inducing the productions of TNF‐α and IL‐1β through the JAK2/STAT3 and ERK signaling pathways	14
Investigation of adult‐onset multiple acyl‐CoA dehydrogenase deficiency associated with peripheral neuropathy	12
Many roles for oligodendrocyte precursor cells in physiology and pathology	11
Multiple system aging‐related tau astrogliopathy with complex proteinopathy in an oligosymptomatic octogenarian	11
Abnormal prion protein deposits with high seeding activities in the skeletal muscle, femoral nerve, and scalp of an autopsied case of sporadic Creutzfeldt–Jakob disease	11
A case of CIC‐rearranged sarcoma with CIC‐LEUTX gene fusion in spinal cord	10
An autopsy case of adult‐onset neuronal intranuclear inclusion disease with perivascular preservation in cerebral white matter	10
An autopsy report of a familial amyotrophic lateral sclerosis case carrying VCP Arg487His mutation with a unique TDP‐43 proteinopathy	10
Neurofibrillary changes undergoing morphological and biochemical changes – How does tau with the profile shift of from four repeat to three repeat spread in Alzheimer brain?	10
Early ultrastructural lesions of anti‐neutrophil cytoplasmic antibody‐ versus complement‐associated vasculitis	9
Globular glial tauopathy Type I presenting with behavioral variant frontotemporal dementia	9
Diffuse midline glioma with H3 K27M mutation of the spinal cord: A series of 33 cases	9
Usefulness of intraoperative rapid immunohistochemistry in the surgical treatment of brain tumors	8
NLRP3 inflammasome inhibitor ameliorates ischemic stroke by reprogramming the phenotype of microglia/macrophage in a murine model of distal middle cerebral artery occlusion	8
Clinicopathological features of titinopathy from a Chinese neuromuscular center	8
Transactivation response DNA‐binding protein of 43 kDa proteinopathy and lysosomal abnormalities in spastic paraplegia type 11	8

The Braak hypothesis in prion disease with a focus on Creutzfeldt–Jakob disease	8
Clinicopathological heterogeneity of Alzheimer's disease with pure Alzheimer's disease pathology: Cases associated with dementia with Lewy bodies, very early‐onset dementia, and primary progressive ap	8
Intracranial myxoid angiomatoid fibrous histiocytoma with “classic” histology and EWSR1:CREM fusion providing insight for reconciliation with intracranial myxoid mesenchymal tumors	8
Expression of programmed cell death ligand‐1 by immune cells in the microenvironment is a favorable prognostic factor for primary diffuse large B‐cell lymphoma of the central nervous system	7
A case of intracranial myxoid mesenchymal tumor with EWSR1:CREM fusion in an adult female: Extensive immunohistochemical evaluation	7
High‐grade gliomas with isocitrate dehydrogenase wild‐type and 1p/19q codeleted: Atypical molecular phenotype and current challenges in molecular diagnosis	7
Minocycline prevents depression‐like behavior in streptozotocin‐induced diabetic mice	7
Accumulation of phosphorylated TDP‐43 in the cytoplasm of Schwann cells in a case of sporadic amyotrophic lateral sclerosis	7
Lewy pathology of the submandibular gland in Lewy body disease: A report of autopsy cases	7
Experimental models of prion‐like protein propagation	6
Symmetrical glial hyperplasia in the brainstem of fibrodysplasia ossificans progressiva	6
A case of desmoplastic myxoid tumor, SMARCB1 mutant, in the pineal region	6
Neuropathology of the spinal nerve roots, spinal cord, and brain in the first autopsied case of Charcot–Marie–Tooth disease 4F with a D651N mutation in the periaxin gene	6
Amyotrophic lateral sclerosis with speech apraxia, predominant upper motor neuron signs, and prominent iron accumulation in the frontal operculum and precentral gyrus	6
FOXM1‐mediated NUF2 expression confers temozolomide resistance to human glioma cells by regulating autophagy via the PI3K/AKT/mTOR signaling path	6
Praja1 RING‐finger E3 ubiquitin ligase is a common suppressor of neurodegenerative disease‐associated protein aggregation	6
LINC01123 potentially correlates with radioresistance in glioma through the miR‐151a/CENPB axis	5
Cerebral embolization associated with parenchymal seeding of the left atrial myxoma: Potential role of interleukin‐6 and matrix metalloproteinases	5
Progressive supranuclear palsy: Neuropathology of patients with a short disease duration due to unexpected death	5
The clinical and neuropathological picture of adult neuronal intranuclear inclusion disease with no radiological abnormality	5
Four‐repeat tauopathies and late‐onset psychiatric disorders: Etiological relevance or incidental findings?	5
Distribution of amyloid‐β precursor protein‐immunoreactive axons differs according to the severity of cerebral ischemia in autopsy brains	5
Immunohistochemical expression of osteopontin and collagens in choroid plexus of human brains	5
The hot cross bun sign in corticobasal degeneration	5
Clinicopathological diversity of semantic dementia: Comparisons of patients with early‐onset versus late‐onset, left‐sided versus right‐sided temporal atrophy, and TDP‐type A versus type C pathology	5
Brain cutting and trimming	5
Identification and characterization of sex‐dependent gene expression profile in glioblastoma	5
Supratentorial ependymoma with YAP1:FAM118B fusion: A case report	5
Recurrent oligodendroglioma with changed 1p/19q status	4
A case of ganglioglioma grade 3 withH3 K27Mmutation arising in the medial temporal lobe in an elderly patient	4
Pembrolizumab‐caused polyradiculoneuropathy as an immune‐related adverse event	4
Intravascular large B‐cell lymphoma affecting multiple cranial nerves: A histopathological study	4
Diffuse Lewy body disease presenting as Parkinson's disease with progressive aphasia	4
Primary central nervous system other iatrogenic immunodeficiency‐associated lymphoproliferative disorders presenting as extraosseous plasmacytoma with a progressive clinical course: A case report and	4
A comparison of cerebral amyloid angiopathy in the cerebellum and CAA‐positive occipital lobe of 60 brains from routine autopsies	4
Unique Lewy pathology in myotonic dystrophy type 1	4
The autophagic marker p62 highlights Alzheimer type II astrocytes in metabolic/hepatic encephalopathy	4
Glioblastoma and malignant melanoma: Serendipitous or anticipated association?	4
High HMGA2 expression without gene rearrangement in meningiomas	3
Possible association of limbic tau pathology with psychosis or behavioral disturbances: Studies of two autopsied psychiatric patients	3
Brain parenchymal angiomatoid fibrous histiocytoma and spinal myxoid mesenchymal tumor with FET: CREB fusion, a spectrum of the same tumor type	3
Unexpected postmortem diagnoses in cases of clinically diagnosed amyotrophic lateral sclerosis	3
Amyloid‐β plaques may be reduced in advanced stages of cerebral amyloid angiopathy in the elderly	3
An autopsy case of progressive supranuclear palsy treated with monoclonal antibody against tau	3
Simple and clear differentiation of spinocerebellar degenerations: Overview of macroscopic and low‐power view findings	3
Cerebellar liponeurocytoma: clinical, histopathological and molecular features of a series of three cases, including one recurrent tumor	3
Genetic Creutzfeldt–Jakob disease‐M232R with the cooccurrence of multiple prion strains, M1 + M2C + M2T: Report of an autopsy case	3
Coexisting lipomatous meningioma and glioblastoma in Cowden syndrome: A unique tumor association	3
A juvenile case of epilepsy‐associated, isocitrate dehydrogenase wild‐type/histone 3 wild‐type diffuse glioma with a rare BRAF^A598T mutation	3
Evaluation of the prognostic potential of EGFL7 in pilocytic astrocytomas	3

Immunotherapy‐refractory vacuolar myopathy with mucin deposition in scleromyxedema: A possible role of fibroblast growth factor 2	3
Spinal cord‐predominant neuropathology in an adult‐onset case of POLR3A‐related spastic ataxia	3
An adult case of diffuse midline glioma with H3 K27M mutation	3
Macroscopic diagnostic clue for parkinsonism	3
Coexistence of dentatorubral‐pallidoluysian atrophy and Parkinson's disease: An autopsy case report	3
Macroscopic findings of brain with dementia	3
Clinicopathological findings of a mitochondrial encephalopathy, lactic acidosis, and stroke‐like episodes/Leigh syndrome overlap patient with a novel m.3482A>G mutation in MT‐ND1	3
Senile plaque calcification of the lamina circumvoluta medullaris in Alzheimer's disease	3
Neuropathology of a case of fragile X‐associated tremor ataxia syndrome without tremor	3
Calcifying pseudoneoplasms of the neuraxis (CAPNON). A case report	3
Tufted astrocyte‐like glia in two autopsy cases of multiple system atrophy: Is it a concomitant neurodegenerative disorder with multiple system atrophy and progressive supranuclear palsy?	3
Let's cluster cases in Neuropathology Case Cluster series!: Unveil clinical masqueraders (Neuropathology Cluster Case 1–13)	3