Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicity
Year: 2022
Type: article
Source: Nature Genetics
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: green
Awards: G1021745955, From common to rare variant functional architectures of human diseases, G223491490, G3177290858, Leveraging functional data to predict disease risk in multi-ethnic populations, Network-based prediction and validation of causal schizophrenia genes and variants, G5850737185, G6254203004, New approaches for leveraging single-cell data to identify disease-critical genes and gene sets, Functionally specialized components of disease heritability in ENCODE data, G7523544532, G8088770145, G9000286330, Statistical methods to localize disease heritability and identify biological mechanisms, Training in Bioinformatics and Integrative Genomics, Functional and population genetic architectures of complex disease, Integrating case-control transcriptomic and genetic data in admixed individuals to identify disease genes for schizophrenia and bipolar disorder, Predicting the impact of genetic variants, genes and pathways on human Disease
OpenAlex ID: W4282915079
