Cargando…
Gene-based burden scores identify rare variant associations for 28 blood biomarkers
BACKGROUND: A relevant part of the genetic architecture of complex traits is still unknown; despite the discovery of many disease-associated common variants. Polygenic risk score (PRS) models are based on the evaluation of the additive effects attributable to common variants and have been successful...
Autores principales: | Aldisi, Rana, Hassanin, Emadeldin, Sivalingam, Sugirthan, Buness, Andreas, Klinkhammer, Hannah, Mayr, Andreas, Fröhlich, Holger, Krawitz, Peter, Maj, Carlo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10476296/ https://www.ncbi.nlm.nih.gov/pubmed/37667186 http://dx.doi.org/10.1186/s12863-023-01155-0 |
Ejemplares similares
-
GenRisk: a tool for comprehensive genetic risk modeling
por: Aldisi, Rana, et al.
Publicado: (2022) -
Assessing the performance of European-derived cardiometabolic polygenic risk scores in South-Asians and their interplay with family history
por: Hassanin, Emadeldin, et al.
Publicado: (2023) -
Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence
por: Hassanin, Emadeldin, et al.
Publicado: (2023) -
Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
por: Henne, Sabrina Katrin, et al.
Publicado: (2023) -
A statistical boosting framework for polygenic risk scores based on large-scale genotype data
por: Klinkhammer, Hannah, et al.
Publicado: (2023)