专题:Genetic Associations and Epidemiology

This cluster of papers encompasses a wide range of topics in genomic studies, including genome-wide association analyses, genetic variation, haplotype mapping, population genetics, Mendelian randomization, polygenic risk scores, gene expression, and the study of complex diseases. It explores methods for analyzing genetic data and understanding the genetic basis of various traits and diseases.
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FinnGen provides genetic insights from a well-phenotyped isolated population

article Full Text OpenAlex 4126 FWCI1149.113

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

article Full Text OpenAlex 2786 FWCI452.7946

New insights into the genetic etiology of Alzheimer’s disease and related dementias

article Full Text OpenAlex 2487 FWCI405.737

Mendelian randomization

article Full Text OpenAlex 2177 FWCI350.597

Accurate proteome-wide missense variant effect prediction with AlphaMissense

article Full Text OpenAlex 2047 FWCI547.5108

The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource

article Full Text OpenAlex 1741 FWCI287.7299

Plasma proteomic associations with genetics and health in the UK Biobank

article Full Text OpenAlex 1519 FWCI407.4955

High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios

article Full Text OpenAlex 1051 FWCI77.577

Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases

article Full Text OpenAlex 981 FWCI272.7187

A saturated map of common genetic variants associated with human height

article Full Text OpenAlex 901 FWCI145.1242