Psychiatric Comorbidities of Neurogenetic and Neurodegenerative Diseases

858
Total downloads
8,448
Total views and downloads

Articles

ORIGINAL RESEARCH

Published on 19 Nov 2025

Correlation study between serum uric acid level and cognitive impairment in middle-aged and elderly patients with hypertension: based on an explainable predictive model

Jiarui Wang
Hetong Liao
Ping Zheng
Qinfen Chen
Dongxu Lu
Yihong Huang
Di Wu
Jiajia Hu
Juan Du
Xiaoyun Zhang

doi 10.3389/fneur.2025.1708305

300 views

REVIEW

Accepted on 13 Nov 2025

IDEDNIK syndrome: a newly recognized rare genetic disorder caused by AP1S1 and AP1B1 mutations

Wu Rong
Xingguang Luo
Xiao-Ping Wang

120 views

ORIGINAL RESEARCH

Published on 15 Oct 2025

Stage-specific efficacy of pharmacological interventions on gait impairments in Parkinson’s disease

Jun Zhang
Le Chen
Jun Li

doi 10.3389/fneur.2025.1657884

1,257 views

REVIEW

Published on 12 Sep 2025

CADASIL or NOTCH3 mutaion spectrum diseases? Interpretation of NOTCH3 mutations and clinical heterogeneity in CADASIL

Yuehui Wang
Yiran Liu
Hongbin Mo
Yue Han
Yuanyuan Jing
Fang Deng

doi 10.3389/fneur.2025.1662012

2,415 views

BRIEF RESEARCH REPORT

Published on 22 Aug 2025

Novel loss-of-function mutations in VPS13A cause chorea-acanthocytosis in two families

Xiao-Hong Lin
Bin Xiao
Ru-Kai Chen
Jia-Ying Chen
Nai-Qing Cai
Chun-Yan Cao
Li-Qiong Zhan

doi 10.3389/fneur.2025.1643889

1,162 views

ORIGINAL RESEARCH

Published on 18 Aug 2025

Impaired glymphatic system function and its association with speech and language delay in children with ADHD: a prospective study

Yangchen Li
Jianhong Wang
Xinyu Yuan
Lili Zhang
Yuchun Yan
Yang Yang
Lin Wang

doi 10.3389/fnhum.2025.1612997

1,354 views

Share on

Frontiers in Neurology

Cognitive and Behavioral Neurology
Neurogenetics

Other participating journals

Frontiers in Genetics
- Genetics of Common and Rare Diseases
- 2.8 impact factor
- 6.2 citescore
Frontiers in Pediatrics
- Genetics of Common and Rare Diseases
- 2.0 impact factor
- 4.3 citescore

Manuscripts can be submitted to this Research Topic via the main journal or any other participating journal.

Impact

8,448Topic views
6,432Article views
858Article downloads

View impact

Articles

Correlation study between serum uric acid level and cognitive impairment in middle-aged and elderly patients with hypertension: based on an explainable predictive model

IDEDNIK syndrome: a newly recognized rare genetic disorder caused by AP1S1 and AP1B1 mutations

Stage-specific efficacy of pharmacological interventions on gait impairments in Parkinson’s disease

CADASIL or NOTCH3 mutaion spectrum diseases? Interpretation of NOTCH3 mutations and clinical heterogeneity in CADASIL

Novel loss-of-function mutations in VPS13A cause chorea-acanthocytosis in two families

Impaired glymphatic system function and its association with speech and language delay in children with ADHD: a prospective study

Frontiers in Neurology

Cognitive and Behavioral Neurology

Neurogenetics

Other participating journals

Frontiers in Genetics

Genetics of Common and Rare Diseases

Frontiers in Pediatrics

Genetics of Common and Rare Diseases