Publications:

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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: rs1572495

PubMed Link: 35629257

Variant Present in the following documents:

• jpm-12-00835.pdf

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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: rs1572495

PubMed Link: 32111088

Variant Present in the following documents:

• Main text
• ijms-21-01604.pdf

View BVdb publication page

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Associations between NOS1AP single nucleotide polymorphisms (SNPs) and QT interval duration in four racial/ethnic groups in the Multi-Ethnic Study of Atherosclerosis (MESA).

Annals Of Noninvasive Electrocardiology : The Official Journal Of The International Society For Holter And Noninvasive Electrocardiology, Inc

Shah, Sidharth A SA; Herrington, David M DM; Howard, Timothy D TD; Divers, Jasmin J; Arnett, Donna K DK; Burke, Greg L GL; Kao, Weng Hong WH; Guo, Xiuqing X; Siscovick, David S DS; Chakravarti, Aravinda A; Lima, Joao A JA; Psaty, Bruce M BM; Tomaselli, Gordon F GF; Rich, Stephen S SS; Bowden, Donald W DW; Post, Wendy W

Publication Date: 2013-01

Variant appearance in text: rs1572495

PubMed Link: 23347024

Variant Present in the following documents:

• Main text

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NOS1AP variant associated with incidence of type 2 diabetes in calcium channel blocker users in the Atherosclerosis Risk in Communities (ARIC) study.

Diabetologia

Chu, A Y AY; Coresh, J J; Arking, D E DE; Pankow, J S JS; Tomaselli, G F GF; Chakravarti, A A; Post, W S WS; Spooner, P H PH; Boerwinkle, E E; Kao, W H L WH

Publication Date: 2010-03

Variant appearance in text: rs1572495

PubMed Link: 19943157

Variant Present in the following documents:

• Main text

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Evidence for a role of the NOS1AP (CAPON) gene in schizophrenia and its clinical dimensions: an association study in a South American population isolate.

Human Heredity

Kremeyer, Barbara B; García, Jenny J; Kymäläinen, Hanna H; Wratten, Naomi N; Restrepo, Gabriel G; Palacio, Carlos C; Miranda, Ana Lucía AL; López, Carlos C; Restrepo, Margarita M; Bedoya, Gabriel G; Brzustowicz, Linda M LM; Ospina-Duque, Jorge J; Arbeláez, María Patricia MP; Ruiz-Linares, Andrés A

Publication Date: 2009

Variant appearance in text: rs1572495

PubMed Link: 19077434

Variant Present in the following documents:

• Main text

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Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22.

American Journal Of Human Genetics

Brzustowicz, Linda M LM; Simone, Jaime J; Mohseni, Paria P; Hayter, Jared E JE; Hodgkinson, Kathleen A KA; Chow, Eva W C EW; Bassett, Anne S AS

Publication Date: 2004-05

Variant appearance in text: rs1572495

PubMed Link: 15065015

Variant Present in the following documents:

• Main text

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