Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence
Jakub Kopál, Kuldeep Kumar, Karin Saltoun, Claudia Modenato, Clara Moreau, Sandra Martin‐Brevet, Guillaume Huguet, Martineau Jean‐Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Petra Tamer, Élise Douard, Anne Maillard, Borja Rodríguez‐Herreros, Aurélie Pain, Sonia Richetin, Leila Kushan, Ana Isabel Silva, Marianne van den Bree, David E.J. Linden, Michael J. Owen, Jérémy Hall, Sarah Lippé, Bogdan Draganski, Ida E. Sønderby, Ole A. Andreassen, David C. Glahn, Paul M. Thompson, Carrie E. Bearden, Sébastien Jacquemont, Danilo Bzdok
Topics & Concepts
PhenomeCopy-number variationBiologyPhenotypePleiotropyBiobankGeneticsNeuroscienceEvolutionary biologyGenomeGeneGenomic variations and chromosomal abnormalitiesGenomics and Rare DiseasesCongenital heart defects research