Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome
Year: 2020
Type: article
Study design: Observational Study
Abstract: Chromosome 22q11.2 deletion syndrome is a neurogenetic disorder associated with high rates of schizophrenia and other psychiatric conditions. The authors report what is to their knowledge the first large-scale collaborative study of rates and sex distributions of psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome. The associations among psychopathology, intellect, and functioning were examined in a subgroup of participants.
DOI: 10.17615/ftev-qq33
Authors: Owen, Michael, Swillen, Ann, Boot, Erik, Murphy, Kieran C., Green, Tamar, Klaassen, Petra W.J., Bassett, Anne S., Chow, Eva W.C., Antshel, Kevin M., Gur, Raquel E., Gothelf, Doron, Evers, Laurens, Duijff, Sasja N., van den Bree, Marianne B.M., Armando, Marco, Murphy, Declan G., Shashi, Vandana, Fremont, Wanda, Schneider, Maude, Vorstman, Jacob, Bearden, Carrie E., Fung, Wai Lun Alan, Vicari, Stefano, Hooper, Stephen R., Jalbrzikowski, Maria, Van Amelsvoort, Therese, Debbané, Martin, Zackai, Elaine H., McDonald-McGinn, Donna M., Kates, Wendy R., Niarchou, Maria, Weizman, Abraham
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: green
Funders: National Science Foundation, March of Dimes Foundation, National Alliance for Research on Schizophrenia and Depression, Wellcome Trust, Hunter Medical Research Institute, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, Canadian Institutes of Health Research, Medical Research Council, National Health and Medical Research Council, National Institute of Mental Health, National Institute of Child Health and Human Development
OpenAlex ID: W4300530427