DNA in extracellular vesicles: From evolution to its current application in health and disease

J Ghanam, VK Chetty, L Barthel, D Reinhardt… - Cell & Bioscience, 2022 - Springer
Extracellular vesicle (EV) secretion is a highly conserved evolutionary trait in all organisms
in the three domains of life. The packaging and release of EVs appears to be a bulk-flow …

Pathway analysis for genome-wide genetic variation data: Analytic principles, latest developments, and new opportunities

M Silberstein, N Nesbit, J Cai, PH Lee - Journal of genetics and genomics, 2021 - Elsevier
Pathway analysis, also known as gene-set enrichment analysis, is a multilocus analytic
strategy that integrates a priori, biological knowledge into the statistical analysis of high …

[HTML][HTML] Assessing the effect of interaction between gut microbiome and inflammatory bowel disease on the risks of depression

X Qin, C Pan, Q Cai, Y Zhao, D He, W Wei… - Brain, Behavior, & …, 2022 - Elsevier
Background Gut microbiome and inflammatory bowel disease (IBD) are implicated in the
development of depression, but the effect of their interactions on the risk of depression …

Gene-based testing of interactions using XGBoost in genome-wide association studies

Y Guo, C Wu, Z Yuan, Y Wang, Z Liang… - Frontiers in Cell and …, 2021 - frontiersin.org
Among the myriad of statistical methods that identify gene–gene interactions in the realm of
qualitative genome-wide association studies, gene-based interactions are not only powerful …

[HTML][HTML] Dielectrophoresis spectroscopy for nucleotide identification in DNA

MF Shahriar, J Kabir, D Piaopiao - Aspects of Molecular Medicine, 2023 - Elsevier
DNA sequence with a known physical position on a chromosome is called a genetic marker,
so the causal gene may identify with genetic markers in different kinds of hereditary …

Tailored graphical lasso for data integration in gene network reconstruction

C Lingjærde, TG Lien, Ø Borgan, H Bergholtz… - BMC …, 2021 - Springer
Background Identifying gene interactions is a topic of great importance in genomics, and
approaches based on network models provide a powerful tool for studying these. Assuming …

Genotypes of the UCP1 gene polymorphisms and cardiometabolic diseases: A multifactorial study of association with disease probability

AE Pravednikova, A Nikitich, A Witkowicz, L Karabon… - Biochimie, 2024 - Elsevier
Cardiometabolic diseases (CMDs) are complex disorders with a heterogenous phenotype,
which are caused by multiple factors including genetic factors. Single nucleotide …

[PDF][PDF] Aspects of Molecular Medicine

MF Shahriar, J Kabir, D Piaopiao - researchgate.net
ABSTRACT DNA sequence with a known physical position on a chromosome is called a
genetic marker, so the causal gene may identify with genetic markers in different kinds of …