A Whole-Exome Sequencing Study of Tourette Disorder in a Chinese Population-Reference-Cited by-同舟云学术

A Whole-Exome Sequencing Study of Tourette Disorder in a Chinese Population

Published:2020-01-01 Issue:1 Volume:39 Page:63-68
ISSN:1044-5498
Container-title:DNA and Cell Biology
language:en
Short-container-title:DNA and Cell Biology

Author:

Zhao Xin¹,Wang Sheng²,Hao Juanjuan¹,Zhu Pengcheng¹,Zhang Xin¹,Wu Min¹

Affiliation:

1. Department of Traditional Chinese Medicine, Xinhua Hospital Affiliated to Shanghai Jiatong University School of Medicine, Shanghai, China.

2. Institute for Neurodegenerative Diseases, UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California.

Publisher

Mary Ann Liebert Inc

Subject

Cell Biology,Genetics,Molecular Biology,General Medicine

Link

https://www.liebertpub.com/doi/pdf/10.1089/dna.2019.4746

Reference26 articles.

1. Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability

2. Gusfield, D., and Nielsen, R. (2015). Association Mapping for Compound Heterozygous Traits Using Phenotypic Distance and Integer Programming. International Workshop on Algorithms in Bioinformatics. Springer, Berlin Heidelberg.

3. Integrated Model of De Novo and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes

4. Lifetime Prevalence, Age of Risk, and Genetic Relationships of Comorbid Psychiatric Disorders in Tourette Syndrome

5. Environmental factors in Tourette syndrome

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