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Cell Genomics|February 13, 2023
Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomesKonrad J Karczewski, Matthew Solomonson, Katherine R Chao, et al.American Journal of Human Genetics|June 11, 2021
Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individualsJack A Kosmicki, Julie E Horowitz, Nilanjana Banerjee, et al.Nature Genetics|March 31, 2026
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosisPaul J Hop, Maarten Kooyman, Brendan J Kenna, et al.Science Translational Medicine|February 23, 2022
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALSPaul J Hop, Ramona A J Zwamborn, Eilis Hannon, et al.Nature Genetics|May 22, 2019
Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestriesNick Shrine, Anna L Guyatt, A Mesut Erzurumluoglu, et al.Nature Genetics|February 27, 2019
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestriesNick Shrine, Anna L Guyatt, A Mesut Erzurumluoglu, et al.Nature|January 18, 2023
FinnGen provides genetic insights from a well-phenotyped isolated populationMitja I Kurki, Juha Karjalainen, Priit Palta, et al.Nature Communications|September 13, 2019
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuriaAlexander Teumer, Yong Li, Sahar Ghasemi, et al.Nature Genetics|December 7, 2021
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.Medrxiv : the Preprint Server for Health Sciences|September 11, 2023
Discovery of 95 PTSD loci provides insight into genetic architecture and neurobiology of trauma and stress-related disordersCaroline M Nievergelt, Adam X Maihofer, Elizabeth G Atkinson, et al.Pageof 10