Ling Weng

PROFILE

Homepage
No homepage is listed.
ORCID
No ORCID is listed.
Affiliations
No affiliations are listed.
Aliases
No aliases are listed.
Publication record
47 papers · 969 citations · H-index 17

PAPERS

Plasma p-tau species are elevated in presymptomatic and symptomatic neuronal intranuclear inclusion disease
20260 citationsauthor #11
Short tandem repeat expansions in patients with neurodegenerative dementia.
20260 citationsauthor #15
Genetic risk and plasma biomarkers of dementia with Lewy bodies in a Chinese population
20250 citationsauthor #3
Six‐month follow‐up of ARIA‐H and iron deposition in real‐world lecanemab therapy for Alzheimer's disease: Evidence from a Chinese 7T MRI cohort
20250 citationsauthor #7
Genetic risk and plasma biomarkers of dementia with Lewy bodies in a Chinese population
20250 citationsauthor #3
Retinal alterations induced by amyotrophic lateral sclerosis: An analysis using optical coherence tomography.
20250 citationsauthor #9
Genetic spectrum features and diagnostic accuracy of four plasma biomarkers in 248 Chinese patients with frontotemporal dementia
202412 citationsauthor #2
Genetic Spectrum Features and Diagnostic Performance of Four Plasma Biomarkers in 245 Patients with Frontotemporal Dementia
20240 citationsauthor #7
Diagnostic value of nerve conduction study in NOTCH2NLC‐related neuronal intranuclear inclusion disease
20238 citationsauthor #10
Corrigendum: Construction of an immune-related signature for predicting the ischemic events in patients undergoing carotid endarterectomy
20230 citationsauthor #3
GSN gene frameshift mutations in Alzheimer’s disease
20236 citationsauthor #11
Clinical features of progressive supranuclear palsy
202310 citationsauthor #9
Macular Microvascular Density as a Diagnostic Biomarker for Alzheimer’s Disease
202223 citationsauthor #10
Novel insight into m6A regulator-mediated methylation modification patterns and immune characteristics in intracranial aneurysm
202217 citationsauthor #3
Identification and Validation of Aging-Related Genes in Alzheimer’s Disease
202227 citationsauthor #3
Construction of an immune-related signature for predicting the ischemic events in patients undergoing carotid endarterectomy
20222 citationsauthor #3
Variants in the Niemann-pick type C genes are not associated with Alzheimer's disease: a large case-control study in the Chinese population.
20222 citationsauthor #4
A bibliometric analysis of COVID-19 publications in neurology by using the visual mapping method
202219 citationsauthor #3
The evolution of intracranial aneurysm research from 2012 to 2021: Global productivity and publication trends
20225 citationsauthor #2
Clinical features of NOTCH2NLC-related neuronal intranuclear inclusion disease
202285 citationsauthor #34
Comprehensive molecular analyses of an autoimmune-related gene predictive model and immune infiltrations using machine learning methods in moyamoya disease
202214 citationsauthor #6
The Protective Effects of Osteocyte‐Derived Extracellular Vesicles Against Alzheimer's Disease Diminished with Aging
202266 citationsauthor #12
Consistency analysis and conversion model establishment of mini-mental state examination and montreal cognitive assessment in Chinese patients with Alzheimer’s disease
20224 citationsauthor #8
Genetics of progressive supranuclear palsy in a Chinese population.
20227 citationsauthor #7
Comprehensive analysis of autoimmune-related genes in amyotrophic lateral sclerosis from the perspective of 3P medicine
20223 citationsauthor #4
Clinical characteristics and genotype-phenotype correlation analysis of familial Alzheimer’s disease patients with pathogenic/likely pathogenic amyloid protein precursor mutations
20225 citationsauthor #6
Mutation spectrum of amyotrophic lateral sclerosis in Central South China.
202125 citationsauthor #12
Performance of Plasma Amyloid β, Total Tau, and Neurofilament Light Chain in the Identification of Probable Alzheimer's Disease in South China
202120 citationsauthor #6
The role of genetics in neurodegenerative dementia: a large cohort study in South China
20210 citationsauthor #7
Primary familial brain calcification in a patient with a novel compound heterozygous mutation in MYORG presenting with an acute ischemic stroke: a case report
20216 citationsauthor #4
The role of genetics in neurodegenerative dementia: a large cohort study in South China
202126 citationsauthor #7
MicroRNA-200b inhibits the growth and metastasis of glioma cells via targeting ZEB2
20210 citationsauthor #6
Lack of association between LGMN and Alzheimer’s disease in the Southern Han Chinese population
20206 citationsauthor #3
Identification of expanded repeats in NOTCH2NLC in neurodegenerative dementias.
202074 citationsauthor #4
Performance of Plasma Amyloid β, Total Tau and Neurofilament Light Chain Levels for Alzheimer’s Disease Identification
20200 citationsauthor #6
Author response for "Lack of association between LGMN and Alzheimer’s disease in the Southern Han Chinese population"
20200 citationsauthor #3
[Analysis of spinocerebellar ataxia type 31 related mutations among patients from mainland China].
20183 citationsauthor #7
Piperine ameliorates SCA17 neuropathology by reducing ER stress
201837 citationsauthor #6
Alteration of methylation status in the ATXN3 gene promoter region is linked to the SCA3/MJD.
201724 citationsauthor #14
Association of folate metabolism gene polymorphisms and haplotype combination with pulmonary embolism risk in Chinese Han population
20175 citationsauthor #2
MicroRNA-200b inhibits the growth and metastasis of glioma cells via targeting ZEB2.
201634 citationsauthor #6
Analyses MAPT, GRN, and C9orf72 mutations in Chinese patients with frontotemporal dementia.
201630 citationsauthor #7
Regulatory landscape and clinical implication of MBD3 in human malignant glioma
20167 citationsauthor #3
Genetic Identification Is Critical for the Diagnosis of Parkinsonism: A Chinese Pedigree with Early Onset of Parkinsonism
201513 citationsauthor #3
Loss of Ahi1 Affects Early Development by Impairing BM88/Cend1-Mediated Neuronal Differentiation
201326 citationsauthor #1
Genetic variations of Omi/HTRA2 in Chinese patients with Parkinson's disease.
201120 citationsauthor #3
TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.
2010300 citationsauthor #5

TIMELINE

2010 300 citations

2011 20 citations

2013 26 citations

2015 13 citations

2016 71 citations

2017 29 citations

2018 40 citations

2020 80 citations

2021 77 citations

2022 279 citations

2023 24 citations

2024 12 citations

2025 0 citations

2026 0 citations

Ling Weng

PROFILE

PAPERS

TIMELINE

COAUTHOR MAP

CONCEPT FOOTPRINT