Synthesis of genetic association studies for pertinent gene–disease associations requires appropriate methodological and statistical approaches
E Zintzaras, J Lau - Journal of clinical epidemiology, 2008 - Elsevier
OBJECTIVE: The aim of the study was to consider statistical and methodological issues
affecting the results of meta-analysis of genetic association studies for pertinent gene …
affecting the results of meta-analysis of genetic association studies for pertinent gene …
[HTML][HTML] Endothelial nitric oxide synthase–deficient mice: A model of spontaneous cerebral small-vessel disease
FF Liao, G Lin, X Chen, L Chen, W Zheng… - The American Journal of …, 2021 - Elsevier
Age-related cerebral small-vessel disease (CSVD) is a major cause of stroke and dementia.
Despite a widespread acceptance of small-vessel arteriopathy, lacunar infarction, diffuse …
Despite a widespread acceptance of small-vessel arteriopathy, lacunar infarction, diffuse …
White matter damage as a consequence of vascular dysfunction in a spontaneous mouse model of chronic mild chronic hypoperfusion with eNOS deficiency
X Chen, L Chen, G Lin, Z Wang, MC Kodali, M Li… - Molecular …, 2022 - nature.com
Vascular cognitive impairment and dementia (VCID) is the second most common form of
dementia after Alzheimer's disease (AD). Currently, the mechanistic insights into the …
dementia after Alzheimer's disease (AD). Currently, the mechanistic insights into the …
An updated meta-analysis of endothelial nitric oxide synthase gene: three well-characterized polymorphisms with hypertension
W Niu, Y Qi - PloS one, 2011 - journals.plos.org
Background Numerous individually underpowered association studies have been
conducted on endothelial nitric oxide synthase (eNOS) genetic variants across different …
conducted on endothelial nitric oxide synthase (eNOS) genetic variants across different …
Meta‐analysis methods
Meta‐analysis is the quantitative synthesis of information from several studies. It is
applicable to a variety of study designs in genetics, from family‐based linkage studies and …
applicable to a variety of study designs in genetics, from family‐based linkage studies and …
[HTML][HTML] Nitric oxide and hydrogen sulfide regulation of ischemic vascular growth and remodeling
Ischemic vascular remodeling occurs in response to stenosis or arterial occlusion leading to
a change in blood flow and tissue perfusion. Altered blood flow elicits a cascade of …
a change in blood flow and tissue perfusion. Altered blood flow elicits a cascade of …
Angiotensin-converting enzyme insertion/deletion gene polymorphic variant as a marker of coronary artery disease: a meta-analysis
Background Many studies have investigated the association between the angiotensin-
converting enzyme (ACE) gene insertion (I)/deletion (D) polymorphic variant and coronary …
converting enzyme (ACE) gene insertion (I)/deletion (D) polymorphic variant and coronary …
A review of the genetics of essential hypertension
A Binder - Current opinion in cardiology, 2007 - journals.lww.com
To date, linkage and association studies have not been convincing. Genome-wide
association studies may prove to be an effective approach to the problems posed by …
association studies may prove to be an effective approach to the problems posed by …
Genetic basis of polygenic hypertension
AY Deng - Human molecular genetics, 2007 - academic.oup.com
Essential hypertension is a common disorder that leads to significant morbidity and mortality;
however, the underlying mechanisms have remained elusive. Recent animal model studies …
however, the underlying mechanisms have remained elusive. Recent animal model studies …
[HTML][HTML] Angiotensin II type 1 receptor polymorphisms and susceptibility to hypertension: a HuGE review
The angiotensin II type 1 receptor (AGTR1) plays an integral role in blood pressure control,
and is implicated in the pathogenesis of hypertension. Polymorphisms within this gene have …
and is implicated in the pathogenesis of hypertension. Polymorphisms within this gene have …