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Biorxiv : the Preprint Server for Biology|November 26, 2025
Mirror effect of genomic deletions and duplications on cognitive ability across the human cerebral cortexKuldeep Kumar, Sayeh Kazem, Guillaume Huguet, et al.
Nature Medicine|September 25, 2019
A framework for the investigation of rare genetic disorders in neuropsychiatryStephan J Sanders, Mustafa Sahin, Joseph Hostyk, et al.
Cell Genomics|December 12, 2024
Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processesGuillaume Huguet, Thomas Renne, Cécile Poulain, et al.
Trends in Neurosciences|April 26, 2018
Progress in Understanding and Treating SCN2A-Mediated DisordersStephan J Sanders, Arthur J Campbell, Jeffrey R Cottrell, et al.
Research Square|January 18, 2024
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and DuplicationsRuben Gur, Carrie Bearden, Sébastien Jacquemont, et al.
Nature Medicine|December 25, 2019
Autism risk in offspring can be assessed through quantification of male sperm mosaicismMartin W Breuss, Danny Antaki, Renee D George, et al.
The American Journal of Psychiatry|March 3, 2022
Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and PsychopathologySébastien Jacquemont, Guillaume Huguet, Marieke Klein, et al.
Nature Genetics|October 27, 2009
Microduplications of 16p11.2 are associated with schizophreniaShane E McCarthy, Vladimir Makarov, George Kirov, et al.
Nature Genetics|January 10, 2025
Cell state-dependent allelic effects and contextual Mendelian randomization analysis for human brain phenotypesAlexander Haglund, Verena Zuber, Maya Abouzeid, et al.
Molecular Psychiatry|July 24, 2024
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplicationsRuben C Gur, Carrie E Bearden, Sebastien Jacquemont, et al.
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