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Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Rare protein-coding variation and the genetic architecture of height in >1.4 million individualsJack A Kosmicki, Liron Ganel, Kyoko Watanabe, et al.Nature Genetics|August 9, 2023
Converging evidence from exome sequencing and common variants implicates target genes for osteoporosisSirui Zhou, Olukayode A Sosina, Jonas Bovijn, et al.Biorxiv : the Preprint Server for Biology|May 22, 2023
A deep catalog of protein-coding variation in 985,830 individualsKathie Y Sun, Xiaodong Bai, Siying Chen, et al.Nature|May 20, 2024
A deep catalogue of protein-coding variation in 983,578 individualsKathie Y Sun, Xiaodong Bai, Siying Chen, et al.Nature|November 30, 2022
Common and rare variant associations with clonal haematopoiesis phenotypesMichael D Kessler, Amy Damask, Sean O'Keeffe, et al.The New England Journal of Medicine|August 8, 2022
Germline Mutations in CIDEB and Protection against Liver DiseaseNiek Verweij, Mary E Haas, Jonas B Nielsen, et al.Nature Communications|August 23, 2022
Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetesParsa Akbari, Olukayode A Sosina, Jonas Bovijn, et al.Pageof 2