scholarly journals Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study population

2010 ◽  
Vol 155 (1) ◽  
pp. 14-21 ◽  
Author(s):  
Tonia C. Carter ◽  
Faith Pangilinan ◽  
James F. Troendle ◽  
Anne M. Molloy ◽  
Julia VanderMeer ◽  
...  
Keyword(s):  
Risk Factors ◽  
Single Nucleotide Polymorphisms ◽  
Neural Tube ◽  
Neural Tube Defects ◽  
Nucleotide Polymorphisms ◽  
Single Nucleotide ◽  
Study Population ◽  
Irish Study

scholarly journals Single nucleotide polymorphisms in the transcobalamin gene: relationship with transcobalamin concentrations and risk for neural tube defects

2002 ◽  
Vol 10 (7) ◽  
pp. 433-438 ◽  
Author(s):  
Lydia A Afman ◽  
Karin J A Lievers ◽  
Nathalie M J van der Put ◽  
Frans J M Trijbels ◽  
Henk J Blom
Keyword(s):  
Single Nucleotide Polymorphisms ◽  
Neural Tube ◽  
Neural Tube Defects ◽  
Nucleotide Polymorphisms ◽  
Single Nucleotide

Statin-induced adverse effects – facts and genes

2013 ◽  
Vol 154 (3) ◽  
pp. 83-92
Author(s):  
Mariann Harangi ◽  
Noémi Zsíros ◽  
Lilla Juhász ◽  
György Paragh
Keyword(s):  
Risk Factors ◽  
Single Nucleotide Polymorphisms ◽  
Adverse Effects ◽  
Adverse Events ◽  
Statin Therapy ◽  
Significant Proportion ◽  
Gene Mutations ◽  
Nucleotide Polymorphisms ◽  
Serious Adverse Events ◽  
Single Nucleotide

Statin therapy is considered to be safe and rarely associated with serious adverse events. However, a significant proportion of patients on statin therapy show some degree of intolerance which can lead to decreased adherence to statin therapy. The authors summarize the symptoms, signs and frequencies of the most common statin-induced adverse effects and their most important risk factors including some single nucleotide polymorphisms and gene mutations. Also, they review the available approaches to detect and manage the statin-intolerant patients. Orv. Hetil., 2013, 154, 83–92.

scholarly journals Role of six single nucleotide polymorphisms, risk factors in coronary disease, inOLR1alternative splicing

RNA ◽  
2015 ◽  
Vol 21 (6) ◽  
pp. 1187-1202 ◽  
Author(s):  
J. Ramón Tejedor ◽  
Hagen Tilgner ◽  
Camilla Iannone ◽  
Roderic Guigó ◽  
Juan Valcárcel
Keyword(s):  
Risk Factors ◽  
Single Nucleotide Polymorphisms ◽  
Coronary Disease ◽  
Nucleotide Polymorphisms ◽  
Single Nucleotide
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