Author

Ruth E. March

AstraZeneca (United Kingdom)ORCID 0000-0001-5482-6324Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Research Focus:database / resource· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Adam PlattiD· 3 shared Slavé PetrovskiiD· 3 shared Abhishek NagiD· 2 shared AstraZeneca Genomics Initiative· 2 shared Carolina HaefligeriD· 2 shared Dimitrios VitsiosiD· 2 shared Henric OlssoniD· 2 shared Katherine R. SmithiD· 2 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Adam PlattORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 18, 2023

Genetic architecture of telomere length in 462,675 UK Biobank whole-genome sequences

Oliver S. Burren, Ryan S. Dhindsa, Sri V. V. Deevi…·Slavé Petrovski

The paper identifies 53 rare variants and 22 genes associated with telomere length using UK Biobank whole-genome sequences, highlighting their role in clonal haematopoiesis and disease.

7 citations

humanwhole-genome sequencing

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Genetic & Genomic MedicineNature GeneticsPeer-reviewedJun 28, 2021

Advancing Human Genetics Research and Drug Discovery through Exome Sequencing of the UK Biobank

Joseph D. Szustakowski, Suganthi Balasubramanian, Erika M. Kvikstad…·Adam Platt

The paper describes exome sequencing of 200,643 UK Biobank participants, providing a rich resource of coding variants for genetic and drug discovery research.

401 citationstop 1%

humanwhole-exome sequencing

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GenomicsbioRxivPreprintDec 13, 2020

Surveying the contribution of rare variants to the genetic architecture of human disease through exome sequencing of 177,882 UK Biobank participants

Quanli Wang, Ryan S. Dhindsa, Keren Carss…·AstraZeneca Genomics Initiative

This study uses exome sequencing of 177,882 UK Biobank participants to assess the role of rare variants in 10,533 phenotypes, identifying 911 significant gene-phenotype relationships.

10 citations

humanwhole-exome sequencing

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