Dineke S. Verbeek

University of Groningen

H指数:26

被引数:2,096

个人简介

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Becoming a physician–scientist: Early research participation as an identity sandbox for preclinical medical students

成为医师-科学家：早期研究参与作为临床前医学生的身份沙盒

Medical Education

IF5.2

2026-09-290

OAAI

Genetic Insights in Hindbrain Abnormalities Through Network Analysis Expose Key Biological Pathways in Hindbrain Development

通过网络分析揭示小脑发育中遗传学见解和小脑异常的关键生物学通路

The Cerebellum

IF0

2025-12-220

OAAI

Corrigendum to “Genetics of upper limb tremor in clinical practice: a systematic literature review” [Parkinsonism and Related disorders volume “in press” (2025) PRD 107981]

勘误：“临床实践中上肢震颤的遗传学：一项系统文献综述” [Parkinsonism and Related disorders volume “in press” (2025) PRD 107981]

Parkinsonism & Related Disorders

IF3.4

2025-09-260

OAAI

Genetics of upper limb tremor in clinical practice: a systematic literature review

上肢震颤的遗传学：临床实践中的系统文献综述

Parkinsonism & Related Disorders

IF3.4

2025-08-140

OAAI

Neurological diagnoses in children potentially fulfilling the criteria for developmental coordination disorder

儿童中可能符合发育性协调障碍诊断标准的神经系统诊断

developmental medicine and child neurology

IF0

2025-07-250

OAAI

High Prevalence of the Intronic GAA-FGF14 Repeat Expansion in Dutch Patients With Late-Onset Ataxia

NEUROLOGY-GENETICS

IF3.7

2025-04-010

PRE

Cross-species analysis uncovers the mitochondrial stress response in the hippocampus as a shared mechanism in mouse early life stress and human depression

NEUROBIOLOGY OF STRESS

IF3.6

2024-07-010

OAAI

Comprehensive analysis of genetic risk loci uncovers novel candidate genes and pathways in the comorbidity between depression and Alzheimer's disease

TRANSLATIONAL PSYCHIATRY

IF6.2

2024-06-110

OAAI

Copy Number Variant Analysis of Spinocerebellar Ataxia Genes in a Cohort of Dutch Patients With Cerebellar Ataxia

NEUROLOGY-GENETICS

IF3.7

2023-02-015

OAAI

ULK overexpression mitigates motor deficits and neuropathology in mouse models of Machado-Joseph disease

MOLECULAR THERAPY

IF12

2022-01-016

Systematic analysis of PINK1 variants of unknown significance shows intact mitophagy function for most variants

NPJ PARKINSONS DISEASE

IF8.2

2021-12-107

OAAI

Reply to: Childhood Onset Chorea Caused by a Recurrent De Novo DRD2 Variant

MOVEMENT DISORDERS

IF7.6

2021-06-182

OAAI

Parkinson's disease-associated VPS35 mutant reduces mitochondrial membrane potential and impairs PINK1/Parkin-mediated mitophagy

帕金森病相关的VPS35突变体降低线粒体膜电位并损害PINK1/Parkin介导的线粒体自噬

TRANSLATIONAL NEURODEGENERATION

IF15.2

2021-06-1532

OAAI

Does SCA45 Cause Very Late-Onset Pure Cerebellar Ataxia?

NEUROLOGY-GENETICS

IF3.7

2021-06-017

OAAI

A novel variant of the human dopamine D2 receptor, associated with a hyperkinetic movement disorder, mediates enhanced activation of G proteins

FASEB JOURNAL

IF4.2

2021-05-140

PRE

Signaling-Biased and Constitutively Active Dopamine D2 Receptor Variant

ACS CHEMICAL NEUROSCIENCE

IF3.9

2021-05-1111

OAAI

WDR45, one gene associated with multiple neurodevelopmental disorders

AUTOPHAGY

IF14.3

2021-04-1231

OAAI

Rare functional missense variants in CACNA1H: What can we learn from Writer's cramp?

CACNA1H中罕见的功能错义变体: 我们可以从作家的抽筋中学到什么？

MOLECULAR BRAIN

IF2.9

2021-01-213

OAAI

Early Onset Ataxia with Comorbid Dystonia: Clinical, Anatomical and Biological Pathway Analysis Expose Shared Pathophysiology

DIAGNOSTICS

IF3.3

2020-11-246

OAAI

A Gain-of-Function Variant in Dopamine D2 Receptor and Progressive Chorea and Dystonia Phenotype

MOVEMENT DISORDERS

IF7.6

2020-11-1621

OAAI

Dineke S. Verbeek

个人简介

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