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Nature Genetics|October 1, 2025
Limited overlap between genetic effects on disease susceptibility and disease survivalZhiyu Yang, Fanny-Dhelia Pajuste, Kristina Zguro, et al.American Journal of Human Genetics|February 2, 2010
The distribution and most recent common ancestor of the 17q21 inversion in humansMichael P Donnelly, Peristera Paschou, Elena Grigorenko, et al.Biological Psychiatry|March 14, 2021
Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity SpectrumZhiyu Yang, Hanrui Wu, Phil H Lee, et al.Research Square|September 2, 2025
Persistent Tic Disorders Are Associated With 17q12 DuplicationsMatthew Halvorsen, Sheng Wang, Tyne Miller-Fleming, et al.Journal of Medical Genetics|August 17, 2021
Myasthenia gravis genome-wide association study implicates AGRN as a risk locusApostolia Topaloudi, Zoi Zagoriti, Alyssa Camille Flint, et al.European Child & Adolescent Psychiatry|July 9, 2018
European Multicentre Tics in Children Studies (EMTICS): protocol for two cohort studies to assess risk factors for tic onset and exacerbation in children and adolescentsAnette Schrag, Davide Martino, Alan Apter, et al.Biological Psychiatry|October 8, 2015
Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European CohortBirgitte Bertelsen, Hreinn Stefánsson, Lars Riff Jensen, et al.Cell Reports|September 27, 2018
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in PathogenesisSheng Wang, Jeffrey D Mandell, Yogesh Kumar, et al.Annals of Neurology|July 22, 2014
Genetic association signal near NTN4 in Tourette syndromePeristera Paschou, Dongmei Yu, Gloria Gerber, et al.Nature Communications|November 13, 2024
Genome-wide meta-analysis of myasthenia gravis uncovers new loci and provides insights into polygenic predictionAlice Braun, Sudhanshu Shekhar, Daniel F Levey, et al.Pageof 8