Categoría: Annual Review of Genomics and Human Genetics
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Population Diversity at the Single-Cell Level
Population-scale single-cell genomics is a transformative approach for unraveling the intricate links between genetic and cellular variation. This approach is facilitated by cutting-edge experimental methodologies, including the development of high-thr…
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Genome-Wide Screening Approaches for Biochemical Reactions Independent of Cell Growth
Genome-wide screening is a potent approach for comprehensively understanding the molecular mechanisms of biological phenomena. However, despite its widespread use in the past decades across various biological targets, its application to biochemical rea…
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Causes and Consequences of Varying Transposable Element Activity: An Evolutionary Perspective
Transposable elements (TEs) are genomic parasites found in nearly all eukaryotes, including humans. This evolutionary success of TEs is due to their replicative activity, involving insertion into new genomic locations. TE activity varies at multiple le…
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The prevalence and linkage disequilibrium of 21 genetic variations related to thrombophilia, folate cycle, and hypertension in reproductive age women of Rostov region (Russia)
Annals of Human Genetics, Volume 88, Issue 2, Page 171-181, March 2024.
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Issue Information
Annals of Human Genetics, Volume 88, Issue 2, March 2024.
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Clinical application of prospective whole‐exome sequencing in the diagnosis of genetic disease: Experience of a regional disease center in South Korea
Annals of Human Genetics, Volume 88, Issue 2, Page 101-112, March 2024.
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The effect of TRIM5 variants on the susceptibility to HIV‐1 infection and disease progression in the Polish population
Annals of Human Genetics, Volume 88, Issue 2, Page 154-170, March 2024.
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Low‐pass whole genome sequencing is a reliable and cost‐effective approach for copy number variant analysis in the clinical setting
Annals of Human Genetics, Volume 88, Issue 2, Page 113-125, March 2024.