No Association Between Rare <scp> <i>TWNK</i> </scp> Variants and Parkinson's Disease in European Cohorts-Reference-Cited by-同舟云学术

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No Association Between Rare TWNK Variants and Parkinson's Disease in European Cohorts

Published:2022-09-04 Issue:11 Volume:37 Page:2318-2319
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Movement Disorders

Author:

Senkevich Konstantin¹²^ORCID,Gan‐Or Ziv¹²³^ORCID

Affiliation:

1. The Neuro (Montreal Neurological Institute‐Hospital) McGill University Montreal Quebec Canada

2. Department of Neurology and Neurosurgery McGill University Montréal Quebec Canada

3. Department of Human Genetics McGill University Montréal Quebec Canada

Funder

Canada First Research Excellence Fund

Consortium canadien en neurodégénérescence associée au vieillissement

Michael J. Fox Foundation for Parkinson's Research

Parkinson Canada

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.29216

Reference5 articles.

1. TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective Study

2. Precision medicine for disease modification in Parkinson disease

3. Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource

4. Effective filtering strategies to improve data quality from population-based whole exome sequencing studies

5. UK Biobank Whole-Exome Sequence Binary Phenome Analysis with Robust Region-Based Rare-Variant Test

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mitochondrial Parkinsonism: A Practical Guide to Genes and Clinical Diagnosis;Movement Disorders Clinical Practice;2024-06-28

2. Reply to: “Lack of Association between TWNK Rare Variants and Parkinson's Disease in a Chinese Cohort”;Movement Disorders;2023-04

3. Lack of Association between TWNK Rare Variants and Parkinson's Disease in a Chinese Cohort;Movement Disorders;2023-04

4. Reply to: No Association between Rare TWNK Variants and Parkinson's Disease in European Cohorts;Movement Disorders;2022-11

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