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The impact of 22q11.2 copy-number variants on human traits in the general population
Authors:Malú   Zamariolli,Chiara Auwerx,Marie C. Sadler,Adriaan van der Graaf,Kaido Lepik,Tabea Schoeler,Mariana Moys  s-Oliveira,Anelisa G. Dantas,Maria Isabel Melaragno,Zolt  n Kutalik
Affiliation:1. Genetics Division, Universidade Federal de São Paulo, São Paulo, Brazil;2. Department of Computational Biology, University of Lausanne, Lausanne, Switzerland;3. Swiss Institute of Bioinformatics, Lausanne, Switzerland;4. University Center for Primary Care and Public Health, University of Lausanne, Lausanne, Switzerland;5. Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland;6. Sleep Institute, São Paulo, Brazil;7. Department of Clinical, Educational and Health Psychology, University College London, London, UK
Abstract:
Keywords:22q11.2  structural variant  CNV  UK Biobank  population cohort  deletion  duplication  HPO  Mendelian randomization  pleiotropy
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