Publications:

Association of a Common NOS1AP Variant with Attenuation of QTc Prolongation in Men with Heroin Dependence Undergoing Methadone Treatment.

Journal Of Personalized Medicine

Chang, Kuan-Cheng KC; Chen, Ke-Wei KW; Huang, Chieh-Liang CL; Liao, Wen-Ling WL; Wu, Mei-Yao MY; Lin, Yu-Kai YK; Shiao, Yi-Tzone YT; Chung, Wei-Hsin WH; Lin, Yen-Nien YN; Lane, Hsien-Yuan HY

Publication Date: 2022-05-20

Variant appearance in text: rs6683968

PubMed Link: 35629257

Variant Present in the following documents:

• jpm-12-00835.pdf

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Association of nitric oxide synthase 1 adaptor protein gene polymorphisms with schizophrenia in a Chinese Han population.

Indian Journal Of Psychiatry

Yang, Xueping X; Zhou, Jing J; Yuan, Zhen Z; Lin, Ailu A; Li, Xin X; Cong, Zhengtu Z; He, Ru R; Zhu, Gang G

Publication Date: 2022

Variant appearance in text: rs6683968

PubMed Link: 35494330

Variant Present in the following documents:

• Main text

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Genetic Factors of Nitric Oxide's System in Psychoneurologic Disorders.

International Journal Of Molecular Sciences

Nasyrova, Regina F RF; Moskaleva, Polina V PV; Vaiman, Elena E EE; Shnayder, Natalya A NA; Blatt, Nataliya L NL; Rizvanov, Albert A AA

Publication Date: 2020-02-26

Variant appearance in text: rs6683968

PubMed Link: 32111088

Variant Present in the following documents:

• Main text
• ijms-21-01604.pdf

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NOS1AP is a genetic modifier of the long-QT syndrome.

Circulation

Crotti, Lia L; Monti, Maria Cristina MC; Insolia, Roberto R; Peljto, Anna A; Goosen, Althea A; Brink, Paul A PA; Greenberg, David A DA; Schwartz, Peter J PJ; George, Alfred L AL

Publication Date: 2009-10-27

Variant appearance in text: rs6683968

PubMed Link: 19822806

Variant Present in the following documents:

• Main text

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Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study.

Bmc Medical Genetics

Newton-Cheh, Christopher C; Guo, Chao-Yu CY; Wang, Thomas J TJ; O'donnell, Christopher J CJ; Levy, Daniel D; Larson, Martin G MG

Publication Date: 2007-09-19

Variant appearance in text: rs6683968

PubMed Link: 17903306

Variant Present in the following documents:

• Main text
• 1471-2350-8-S1-S7.pdf

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