Mutation pattern and genotype-phenotype correlations of SETD2 in neurodevelopmental disorders-Reference-Cited by-同舟云学术

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Mutation pattern and genotype-phenotype correlations of SETD2 in neurodevelopmental disorders

Published:2021-05 Issue:5 Volume:64 Page:104200
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Chen Meilin,Quan Yingting,Duan Guiqin,Wu Huidan,Bai Ting,Wang Yazhe,Zhou Shimin,Ou Jianjun,Shen Yidong,Hu Zhengmao,Xia Kun,Guo Hui

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference38 articles.

1. A method and server for predicting damaging missense mutations;Adzhubei;Nat. Methods,2010

2. MIPgen: optimized modeling and design of molecular inversion probes for targeted resequencing;Boyle;Bioinformatics,2014

3. Comprehensive molecular characterization of clear cell renal cell carcinoma;Nature,2013

4. Histone methyltransferase SETD2 coordinates FACT recruitment with nucleosome dynamics during transcription;Carvalho;Nucleic Acids Res.,2013

5. SETD2 is required for DNA double-strand break repair and activation of the p53-mediated checkpoint;Carvalho;Elife,2014

Cited by 6 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. Epigenetic underpinnings of the autistic mind: Histone modifications and prefrontal excitation/inhibition imbalance;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2024-06-04

2. Cellular and molecular functions of SETD2 in the central nervous system;Journal of Cell Science;2023-11-01

3. Clinical Heterogeneity and Different Phenotypes in Patients with SETD2 Variants: 18 New Patients and Review of the Literature;Genes;2023-05-29

4. A novel SETD2 variant causing global development delay without overgrowth in a Chinese 3-year-old boy;Frontiers in Genetics;2023-03-21

5. The role of histone methyltransferases in neurocognitive disorders associated with brain size abnormalities;Frontiers in Neuroscience;2023-02-10

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