Interactions betweenMAOAandSYPpolymorphisms were associated with symptoms of attention-deficit/hyperactivity disorder in Chinese Han subjects-Reference-Cited by-全球学者库

Interactions betweenMAOAandSYPpolymorphisms were associated with symptoms of attention-deficit/hyperactivity disorder in Chinese Han subjects

Published:2014-12-08 Issue:1 Volume:168 Page:45-53
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Gao Qian¹²,Liu Lu¹²,Li Hai-Mei¹²,Tang Yi-Lang³,Wu Zhao-Min¹²,Chen Yun¹²,Wang Yu-Feng¹²,Qian Qiu-Jin¹²

Affiliation:

1. Peking University Sixth Hospital/Institute of Mental Health; Beijing China

2. Key Laboratory of Mental Health; Ministry of Health; Peking University; Beijing China

3. Department of Psychiatry and Behavioral Sciences; Emory University School of Medicine; Atlanta Georgia

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)

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4. Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: A preliminary study;Biederman;Am J Med Genet B Neuropsychiatr Genet,2008

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3. Predicting the Adult Clinical and Academic Outcomes in Boys With ADHD: A 7- to 10-Year Follow-Up Study in China;Frontiers in Pediatrics;2021-08-02

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