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Translational Psychiatry|February 3, 2018
Whole-exome sequencing and gene-based rare variant association tests suggest that PLA2G4E might be a risk gene for panic disorderYoshiro Morimoto, Mihoko Shimada-Sugimoto, Takeshi Otowa, et al.Journal of Medical Virology|January 7, 2026
Molecular Variations in Glycoprotein B of Asian Human Cytomegalovirus: Potential Impact on Virus Entry and Immune Evasion in Ocular DiseasesTantri Lestari, Nobuyo Yawata, Gabriel Gonzalez, et al.Sleep and Biological Rhythms|March 12, 2024
Genome-wide association study of idiopathic hypersomnia in a Japanese populationKotomi Tanida, Mihoko Shimada, Seik-Soon Khor, et al.NPJ Genomic Medicine|April 13, 2022
A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomniaTaku Miyagawa, Susumu Tanaka, Mihoko Shimada, et al.Molecular Psychiatry|March 28, 2026
A key gene modulating oxytocin efficacy in autism: genome-wide discovery and verification in randomized controlled trials datasetsHitoshi Kuwabara, Masaki Kojima, Seico Benner, et al.Journal of Human Genetics|September 30, 2018
A variant at 9q34.11 is associated with HLA-DQB1*06:02 negative essential hypersomniaTaku Miyagawa, Seik-Soon Khor, Hiromi Toyoda, et al.Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Genome-wide association study identifies a new susceptibility locus in PLA2G4C for Multiple System AtrophyYasuo Nakahara, Jun Mitsui, Hidetoshi Date, et al.Nature Communications|May 15, 2023
Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsyHanna M Ollila, Eilon Sharon, Ling Lin, et al.Pageof 4