[HTML][HTML] Human genetic background in susceptibility to tuberculosis

J Ghanavi, P Farnia, P Farnia… - The International Journal …, 2020 - journals.lww.com
Tuberculosis (TB), especially in developing countries, is a major threat to human health. The
pathogenesis of TB remains poorly understood, and< 5%–10% of individuals infected with …

Genome-wide association studies in asthma: what they really told us about pathogenesis

M Wjst, M Sargurupremraj, M Arnold - Current opinion in allergy …, 2013 - journals.lww.com
The next wave of asthma genetic studies will use full-genome sequencing and overcome
most GWAS-associated problems. It will be the last step of a century-long search for asthma …

The contribution of genetic variants of SLC2A1 gene in T2DM and T2DM-nephropathy: association study and meta-analysis

I Stefanidis, M Tziastoudi, EE Tsironi, E Dardiotis… - Renal failure, 2018 - Taylor & Francis
An association study was conducted to investigate the relation between 14 variants of
glucose transporter 1 gene (SLC2A1) and the risk of type 2 diabetes (T2DM) leading to …

Introduction to The Routledge Handbook of Social Work and Addictive Behaviors

AL Begun, MM Murray - The Routledge Handbook of Social Work …, 2020 - taylorfrancis.com
Addictive behaviors, such as substance misuse, gambling, and internet gaming, and their
attendant problems are associated with significant difficulties for individuals, families …

[HTML][HTML] Genetic signatures of asthma exacerbation

HW Park, KG Tantisira - Allergy, asthma & immunology research, 2017 - ncbi.nlm.nih.gov
Asthma exacerbation (AE) usually denotes worsening of asthma symptoms that requires
intense management to prevent further deterioration. AE has been reported to correlate with …

Association of TLR4‐T399I polymorphism with chronic obstructive pulmonary disease in smokers

M Speletas, V Merentiti, K Kostikas… - Journal of …, 2009 - Wiley Online Library
Tobacco smoking has been considered the most important risk factor for chronic obstructive
pulmonary disease (COPD) development. However, not all smokers develop COPD and …

[HTML][HTML] Genetic Factors for Coronary Heart Disease and Their Mechanisms: A Meta-Analysis and Comprehensive Review of Common Variants from Genome-Wide …

KA Zarkasi, N Abdullah, NA Abdul Murad, N Ahmad… - Diagnostics, 2022 - mdpi.com
Genome-wide association studies (GWAS) have discovered 163 loci related to coronary
heart disease (CHD). Most GWAS have emphasized pathways related to single-nucleotide …

The search for modifier genes in Huntington disease–Multifactorial aspects of a monogenic disorder

L Arning - Molecular and cellular probes, 2016 - Elsevier
It is becoming increasingly evident that the underlying mutation of a single locus is often
insufficient for the prediction of the comprehensive phenotype in human Mendelian …

Correlation between an intronic SNP genotype and ARL15 level in rheumatoid arthritis

AK Pandey, A Saxena, SK Dey, M Kanjilal, U Kumar… - Journal of genetics, 2021 - Springer
ADP ribosylation factor like protein 15 (ARL15) was identified as a novel susceptibility gene
for rheumatoid arthritis (RA) based on a genomewide association study in a north Indian …

Gamma-aminobutyric acid A receptor, α-2 (GABRA2) variants as individual markers for alcoholism: a meta-analysis

E Zintzaras - Psychiatric genetics, 2012 - journals.lww.com
Objectives The available evidence from the genetic association studies (GAS) published to
date on the association between variants in the GABRA2 gene and alcoholism has …