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March 29, 2026Nature Genetics3 citationsOpen Access

Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity

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HKHye In KimPfizer (United States)CDChristopher DeBoeverMaze (United States)KWKlaudia Walter

Key Points

  • This research aims to analyze exome sequencing data from a large cohort of British South Asians to identify gene variants and their associations with health traits.
  • Conducted whole-exome sequencing on 44,028 participants enriched for autozygosity.
  • Performed exome-wide association analyses for 645 health-related traits using additive and recessive models.
  • Conducted meta-analyses of 33 cardiometabolic traits in conjunction with UK Biobank data.
  • Identified over 100 novel gene–phenotype associations.
  • Detected 2,991 genes with rare biallelic knockout genotypes, including 546 previously unreported.
  • Found that drugs targeting knockout genes have a 2.2-fold higher chance of success in clinical trials.

Abstract

Abstract Genes & Health (G&H) is a biomedical study of adult British Pakistani and Bangladeshi research volunteers enriched for autozygosity. Here we performed whole-exome sequencing in 44,028 G&H participants, establishing a large publicly available South Asian exome resource linked to longitudinal electronic health records. We performed exome-wide association analyses for 645 electronic health record-derived traits under additive and recessive models, and meta-analyses of 33 cardiometabolic traits with UK Biobank, finding more than 100 novel gene–phenotype associations. We identified 2,991 genes with rare biallelic predicted loss-of-function (‘knockout’) genotypes, 546 of which had not been previously reported. We show that drugs targeting genes with knockouts in adults are associated with a 2.2-fold higher likelihood of progressing beyond phase 1 clinical trials. We further illustrate how phenotypic profiles associated with knockout genotypes can enhance efficacy and safety assessment of drug targets and aid in the interpretation of variants with ambiguous clinical significance in autosomal recessive disease genes.

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Cite This Study

Kim et al. (2026) studied this question.

synapsesocial.com/papers/69c8c384de0f0f753b39e550https://doi.org/10.1038/s41588-026-02553-7
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