Ryan S. Dhindsa

Rare variant contribution to human disease in 281,104 UK Biobank exomes

Quanli Wang, Ryan S. Dhindsa, Keren Carss et al. · Nature · 2021 · 604 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios

Xiaolin Zhu, Slavé Petrovski, Pingxing Xie et al. · Genetics in Medicine · 2015 · 342 citations · Full text

Life Sciences, Bioinformatics, Genetics +17

Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

Yen‐Chen Anne Feng, Daniel P. Howrigan, Liam Abbott et al. · The American Journal of Human Genetics · 2019 · 303 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Rare variant associations with plasma protein levels in the UK Biobank

Ryan S. Dhindsa, Oliver S. Burren, Benjamin B. Sun et al. · Nature · 2023 · 179 citations · Full text

Life Sciences, Biochemistry, Genetics +16

Orion: Detecting regions of the human non-coding genome that are intolerant to variation using population genetics

Ayal B. Gussow, Brett Copeland, Ryan S. Dhindsa et al. · PLoS ONE · 2017 · 171 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17