NOS1AP c.178-38446C>T

Variant ID: 1-162218688-C-T

NM_014697.2(NOS1AP):c.178-38446C>T

This variant was identified in 8 publications

View GRCh38 version.




Publications:


Neurological Disorders and Risk of Arrhythmia.

International Journal Of Molecular Sciences
Bernardi, Joyce J; Aromolaran, Kelly A KA; Aromolaran, Ademuyiwa S AS
Publication Date: 2020-12-27

Variant appearance in text: rs4145621
PubMed Link: 33375447
Variant Present in the following documents:
  • Main text
  • ijms-22-00188.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: rs4145621
PubMed Link: 32111088
Variant Present in the following documents:
  • Main text
  • ijms-21-01604.pdf
View BVdb publication page



Role of nitric oxide and related molecules in schizophrenia pathogenesis: biochemical, genetic and clinical aspects.

Frontiers In Physiology
Nasyrova, Regina F RF; Ivashchenko, Dmitriy V DV; Ivanov, Mikhail V MV; Neznanov, Nikolay G NG
Publication Date: 2015

Variant appearance in text: rs4145621
PubMed Link: 26029110
Variant Present in the following documents:
  • Main text
  • fphys-06-00139.pdf
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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: rs4145621
PubMed Link: 23347024
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of a schizophrenia-associated functional noncoding variant in NOS1AP.

The American Journal Of Psychiatry
Wratten, Naomi S NS; Memoli, Holly H; Huang, Yungui Y; Dulencin, Anna M AM; Matteson, Paul G PG; Cornacchia, Michelle A MA; Azaro, Marco A MA; Messenger, Jaime J; Hayter, Jared E JE; Bassett, Anne S AS; Buyske, Steven S; Millonig, James H JH; Vieland, Veronica J VJ; Brzustowicz, Linda M LM
Publication Date: 2009-04

Variant appearance in text: rs4145621
PubMed Link: 19255043
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs4145621
PubMed Link: 19077434
Variant Present in the following documents:
  • Main text
View BVdb publication page



Increased expression in dorsolateral prefrontal cortex of CAPON in schizophrenia and bipolar disorder.

Plos Medicine
Xu, Bin B; Wratten, Naomi N; Charych, Erik I EI; Buyske, Steven S; Firestein, Bonnie L BL; Brzustowicz, Linda M LM
Publication Date: 2005-10

Variant appearance in text: rs4145621
PubMed Link: 16146415
Variant Present in the following documents:
  • Main text
  • pmed.0020263.pdf
View BVdb publication page



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: rs4145621
PubMed Link: 15065015
Variant Present in the following documents:
  • Main text
View BVdb publication page