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Psychiatric disorders in children with 16p11.2 deletion and duplication.
Maria Niarchou, Samuel JRA Chawner, Joanne L Doherty, Anne M Maillard, Sébastien Jacquemont, Wendy K Chung, LeeAnne Green-Snyder, Raphael A Bernier, Robin P Goin-Kochel, Ellen Hanson, David EJ Linden, Stefanie C Linden, F Lucy Raymond, David Skuse, Jeremy Hall, Michael J Owen, Marianne BM van den Bree
Feb 18, 2019
Deletion and duplication of 16p11.2 (BP4-BP5) have been associated with an increased risk of intellectual disability and psychiatric disorder. This is the first study to compare the frequency of a broad spectrum of psychiatric...
Genetic variation at 16q24.2 is associated with small vessel stroke.
Matthew Traylor, Rainer Malik, Mike A Nalls, Ioana Cotlarciuc, Farid Radmanesh, Gudmar Thorleifsson, Ken B Hanscombe, Carl Langefeld, Danish Saleheen, Natalia S Rost, Idil Yet, Tim D Spector, Jordana T Bell, Eilis Hannon, Jonathan Mill, Ganesh Chauhan, Stephanie Debette, Joshua C Bis, WT Longstreth, M Arfan Ikram, Lenore J Launer, Sudha Seshadri, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium METASTROKE, Monica Anne Hamilton-Bruce, Jordi Jimenez-Conde, John W Cole, Reinhold Schmidt, Agnieszka Słowik, Robin Lemmens, Arne Lindgren, Olle Melander, Raji P Grewal, Ralph L Sacco, Tatjana Rundek, Kathryn Rexrode, Donna K Arnett, Julie A Johnson, Oscar R Benavente, Sylvia Wasssertheil-Smoller, Jin-Moo Lee, Sara L Pulit, Quenna Wong, Stephen S Rich, Paul IW de Bakker, Patrick F McArdle, Daniel Woo, Christopher D Anderson, Huichun Xu, Laura Heitsch, Myriam Fornage, Christina Jern, Kari Stefansson, Unnur Thorsteinsdottir, Solveig Gretarsdottir, Cathryn M Lewis, Pankaj Sharma, Cathie LM Sudlow, Peter M Rothwell, Giorgio B Boncoraglio, Vincent Thijs, Chris Levi, James F Meschia, Jonathan Rosand, Steven J Kittner, Braxton D Mitchell, Martin Dichgans, Bradford B Worrall, Hugh S Markus, International Stroke Genetics Consortium
Feb 24, 2017
Developmental potential of aneuploid human embryos cultured beyond implantation.
Marta N Shahbazi, Tianren Wang, Xin Tao, Bailey AT Weatherbee, Li Sun, Yiping Zhan, Laura Keller, Gary D Smith, Antonio Pellicer, Richard T Scott, Emre Seli, Magdalena Zernicka-Goetz
Jul 20, 2020
Aneuploidy, the presence of an abnormal number of chromosomes, is a major cause of early pregnancy loss in humans. Yet, the developmental consequences of specific aneuploidies remain unexplored. Here, we determine the extent of...
Aneuploidy Antigens CD Cadherins Cell Adhesion Cell Cycle Checkpoints Cell Lineage Chromosome Segregation Chromosomes Human Pair 16 Chromosomes Human Pair 21 Embryo Implantation Embryo Mammalian Embryonic Development Female Genes erbB-1 Genetic Testing Humans Monosomy Mosaicism Pregnancy Stem Cells Trisomy