NOTCH2NLC Intermediate‐Length Repeat Expansions Are Associated with Parkinson Disease-Reference-Cited by-同舟云学术

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NOTCH2NLC Intermediate‐Length Repeat Expansions Are Associated with Parkinson Disease

Published:2020-10-19 Issue:1 Volume:89 Page:182-187
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol

Author:

Shi Chang‐he¹²³,Fan Yu¹⁴,Yang Jing¹²³^ORCID,Yuan Yan‐peng¹²,Shen Si¹,Liu Fen¹,Mao Cheng‐yuan¹²,Liu Han¹²,Zhang Shuo¹,Hu Zheng‐wei¹,Fan Li‐yuan¹,Li Meng‐jie¹,Fan Shi‐heng¹²,Liu Xiao‐jing¹²,Xu Yu‐ming¹²³^ORCID

Affiliation:

1. Department of Neurology, First Affiliated Hospital of Zhengzhou University Zhengzhou University Zhengzhou China

2. Henan Key Laboratory of Cerebrovascular Diseases First Affiliated Hospital of Zhengzhou University, Zhengzhou University Zhengzhou China

3. Institute of Neuroscience Zhengzhou University Zhengzhou China

4. Academy of Medical Sciences of Zhengzhou University Zhengzhou China

Funder

National Basic Research Program of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ana.25925

Reference16 articles.

1. Parkinson's disease

2. The genetic architecture of Parkinson's disease

3. Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion disease

4. Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease

5. Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders

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1. Microglia contribute to polyG-dependent neurodegeneration in neuronal intranuclear inclusion disease;Acta Neuropathologica;2024-08-16

2. High-depth whole-genome sequencing identifies structure variants, copy number variants and short tandem repeats associated with Parkinson’s disease;npj Parkinson's Disease;2024-07-23

3. Toward understanding the role of genomic repeat elements in neurodegenerative diseases;Neural Regeneration Research;2024-04-16

4. Review of Phenotypic Heterogeneity of Neuronal Intranuclear Inclusion Disease and NOTCH2NLC -Related GGC Repeat Expansion Disorders;Neurology Genetics;2024-04

5. Sequence composition changes in short tandem repeats: heterogeneity, detection, mechanisms and clinical implications;Nature Reviews Genetics;2024-03-11

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