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Biological Psychiatry|September 3, 2023
Beyond the Global Brain Differences: Intraindividual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion CarriersRune Boen, Tobias Kaufmann, Dennis van der Meer, et al.Medrxiv : the Preprint Server for Health Sciences|January 31, 2024
Unveiling the crucial neuronal role of the proteasomal ATPase subunit gene <i>PSMC5</i> in neurodevelopmental proteasomopathiesSébastien Küry, Janelle E Stanton, Geeske van Woerden, et al.JAMA Neurology|October 31, 2022
Genetic Testing to Inform Epilepsy Treatment Management From an International Study of Clinical PracticeDianalee McKnight, Ana Morales, Kathryn E Hatchell, et al.Nature Communications|November 26, 2025
Investigating the neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathiesSébastien Küry, Janelle E Stanton, Geeske M van Woerden, et al.Neuroimage|July 27, 2021
Frequency drift in MR spectroscopy at 3TSteve C N Hui, Mark Mikkelsen, Helge J Zöllner, et al.Translational Psychiatry|March 23, 2021
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humansIda E Sønderby, Dennis van der Meer, Clara Moreau, et al.Molecular Psychiatry|October 5, 2018
Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal gangliaIda E Sønderby, Ómar Gústafsson, Nhat Trung Doan, et al.Molecular Psychiatry|February 2, 2019
Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal gangliaIda E Sønderby, Ómar Gústafsson, Nhat Trung Doan, et al.Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.Science (New York, N.Y.)|June 23, 2018
Analysis of shared heritability in common disorders of the brain, Verneri Anttila, Brendan Bulik-Sullivan, et al.Pageof 139