Cargando…
Rare variant associations with plasma protein levels in the UK Biobank
Integrating human genomics and proteomics can help elucidate disease mechanisms, identify clinical biomarkers and discover drug targets(1–4). Because previous proteogenomic studies have focused on common variation via genome-wide association studies, the contribution of rare variants to the plasma p...
Autores principales: | Dhindsa, Ryan S., Burren, Oliver S., Sun, Benjamin B., Prins, Bram P., Matelska, Dorota, Wheeler, Eleanor, Mitchell, Jonathan, Oerton, Erin, Hristova, Ventzislava A., Smith, Katherine R., Carss, Keren, Wasilewski, Sebastian, Harper, Andrew R., Paul, Dirk S., Fabre, Margarete A., Runz, Heiko, Viollet, Coralie, Challis, Benjamin, Platt, Adam, Vitsios, Dimitrios, Ashley, Euan A., Whelan, Christopher D., Pangalos, Menelas N., Wang, Quanli, Petrovski, Slavé |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10567546/ https://www.ncbi.nlm.nih.gov/pubmed/37794183 http://dx.doi.org/10.1038/s41586-023-06547-x |
Ejemplares similares
-
Cancer-driving mutations are enriched in genic regions intolerant to germline variation
por: Vitsios, Dimitrios, et al.
Publicado: (2022) -
Effects of protein-coding variants on blood metabolite measurements and clinical biomarkers in the UK Biobank
por: Nag, Abhishek, et al.
Publicado: (2023) -
Rare variant contribution to human disease in 281,104 UK Biobank exomes
por: Wang, Quanli, et al.
Publicado: (2021) -
Prioritizing non-coding regions based on human genomic constraint and sequence context with deep learning
por: Vitsios, Dimitrios, et al.
Publicado: (2021) -
Mantis-ml: Disease-Agnostic Gene Prioritization from High-Throughput Genomic Screens by Stochastic Semi-supervised Learning
por: Vitsios, Dimitrios, et al.
Publicado: (2020)