The association between smoking cessation and lifestyle/genetic variant rs6265 among the adult population in Taiwan

YL Lai, CCR Gan, ON Nfor, WY Lu, SS Lee… - Scientific Reports, 2023 - nature.com
Recent studies showed significant associations between socio-demographic, lifestyle
factors, polymorphic variant rs6265, and smoking cessation behaviours. We examined …

Association of BDNF gene missense polymorphism rs6265 (Val66Met) with three quantitative traits, namely, intelligence quotient, body mass index, and blood …

R Fatma, W Chauhan, MH Shahi, M Afzal - Frontiers in Neurology, 2023 - frontiersin.org
Background Brain-derived neurotrophic factor (BDNF), a neurotransmitter modulator, plays a
significant role in neuronal survival and growth and participates in neuronal plasticity, thus …

Genetic association analysis of rs662799 ( − 1131A > G) polymorphism of APOA5 gene with morphometric and physio-metric traits using multiplex PCR

R Fatma, W Chauhan, S Riyaz, K Rasheed… - Egyptian Journal of …, 2023 - Springer
Abstract Background The apolipoprotein A5 (APOA5) gene, significantly expressed in liver,
has been involved in regulation of triglyceride metabolism, plasma lipid levels, serum …

Hypertension as a novel link for shared heritability in age at menarche and cardiometabolic traits

HY Fan, KL Chien, YT Huang, JBK Hsu… - The Journal of …, 2023 - academic.oup.com
Context Extremely early age at menarche, also called precocious puberty, has been
associated with various cardiometabolic traits, but their shared heritability remains unclear …

Association between ESR1 rs2234693 single nucleotide polymorphism and uterine fibroids in Taiwanese premenopausal and postmenopausal women

YS Tyan, CY Shen, DM Tantoh, SY Hsu… - Journal of Health …, 2023 - Springer
Abstract Background Uterine fibroids (UFs) are uterine smooth muscle neoplasms that affect
women, especially during the reproductive stage. Both genetic and lifestyle factors affect the …

[HTML][HTML] Advancing human genotyping: The Infinium HTS iSelect Custom microarray panel (Rita) development study

SP Matute, K Turvey, S Iyavoo - Forensic Science International: Genetics, 2024 - Elsevier
Abstract Single Nucleotide Polymorphisms (SNPs), as the most prevalent type of variation in
the human genome, play a pivotal role in influencing human traits. They are extensively …

[HTML][HTML] Nomogram developed with APOA5 genetic variant rs662799 and clinical characteristics predicting risk of essential hypertension in a Chinese population

D Abulaiti, S Abudureyimu, H Li, Y Cao… - … diagnosis and therapy, 2024 - ncbi.nlm.nih.gov
Background The apolipoprotein A5 (APOA5) gene has been identified as a key regulatory
factor in triglyceride (TG) metabolism and plasma lipid levels. Genetic polymorphisms of …

Significance of the rs754635 variant of the cholecystokinin gene in the development of obesity in children

A Nikulina - Сучасна педіатрія. Україна= Modern Pediatrics …, 2023 - repo.dma.dp.ua
Materials and methods. 252 obese children aged 6–18 years were examined. The main
group (n= 152) was represented by children with metabolically unhealthy obesity (MUO) …

Investigation of rs1746661 Polymorphism in FNDC5 Gene in Obese Patients

E Hadi, H Nayeri, AM Ahadi, ZR Sichani - Disease and Diagnosis, 2024 - ddj.hums.ac.ir
Background: Obesity is a multifactorial disorder that has considerably increased in
developing countries in recent years. This disease results from an imbalance between …

[PDF][PDF] Μελέτη γενετικών πολυμορφισμών σε ασθενείς με νόσο του κινητικού νευρώνα

ΙΝ Λιάμπας - 2023 - ir.lib.uth.gr
Περίληψη Εισαγωγή: Παρόλο που στην πλειοψηφία τους οι περιπτώσεις ασθενών με νόσο
κινητικού νευρώνα (ΝΚΝ) είναι σποραδικές, ένα 10% του συνόλου των περιπτώσεων πάσχει …