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Neuron|January 14, 2023
Machine learning dissection of human accelerated regions in primate neurodevelopmentSean Whalen, Fumitaka Inoue, Hane Ryu, et al.Human Mutation|May 21, 2019
Integration of multiple epigenomic marks improves prediction of variant impact in saturation mutagenesis reporter assayDustin Shigaki, Orit Adato, Aashish N Adhikari, et al.Biorxiv : the Preprint Server for Biology|March 22, 2023
TAD Evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and functionMariam Okhovat, Jake VanCampen, Ana C Lima, et al.Biorxiv : the Preprint Server for Biology|November 24, 2025
Large-scale discovery of neural enhancers for cis-regulation therapiesTroy A McDiarmid, Nicholas F Page, Florence M Chardon, et al.Biorxiv : the Preprint Server for Biology|June 9, 2023
Association of genetic variation inHao Yu, Anas M Khanshour, Aki Ushiki, et al.Elife|January 26, 2024
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosisHao Yu, Anas M Khanshour, Aki Ushiki, et al.Nature Medicine|June 1, 2023
Genetically adjusted PSA levels for prostate cancer screeningLinda Kachuri, Thomas J Hoffmann, Yu Jiang, et al.Human Molecular Genetics|November 6, 2018
Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility lociAnas M Khanshour, Ikuyo Kou, Yanhui Fan, et al.Nature Communications|December 7, 2023
TAD evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and functionMariam Okhovat, Jake VanCampen, Kimberly A Nevonen, et al.Nature|September 17, 2025
CRISPR activation for SCN2A-related neurodevelopmental disordersSerena Tamura, Andrew D Nelson, Perry W E Spratt, et al.Pageof 18