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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.Medrxiv : the Preprint Server for Health Sciences|May 20, 2024
Characterising the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 casesJonathan Mitchell, Niedzica Camacho, Patrick Shea, et al.Nature Communications|February 19, 2025
Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 casesJonathan Mitchell, Niedzica Camacho, Patrick Shea, et al.Nature Genetics|June 12, 2023
Rare coding variants in CHRNB2 reduce the likelihood of smokingVeera M Rajagopal, Kyoko Watanabe, Joelle Mbatchou, 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 Genetics|April 4, 2024
Protein-truncating variants in BSN are associated with severe adult-onset obesity, type 2 diabetes and fatty liver diseaseYajie Zhao, Maria Chukanova, Katherine A Kentistou, et al.Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Type 2 diabetes genetics in 125,000 admixed adults from Mexico CityJason M Torres, Jaime Berumen, Diego Aguilar-Ramirez, 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|October 11, 2023
Genotyping, sequencing and analysis of 140,000 adults from Mexico CityAndrey Ziyatdinov, Jason Torres, Jesús Alegre-Díaz, 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 9