Nancy J Butcher
Affiliations: | University of Toronto, Toronto, ON, Canada |
Area:
NeuroscienceGoogle:
"Nancy Butcher"Mean distance: 15.87 (cluster 11) | S | N | B | C | P |
Parents
Sign in to add mentor| Anne S. Bassett | grad student | University of Toronto (CAMH) | ||
| Ian A. Meinertzhagen | grad student | 2008-2010 | Dalhousie University | |
| (MSc) | ||||
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Publications
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| Ge R, Ching CRK, Bassett AS, et al. (2024) Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome. Human Brain Mapping. 45: e26553 |
| Pasternak M, Shirzadi Z, Mutsaerts HJ, et al. (2022) Elevated regional cerebral blood flow in adults with 22q11.2 deletion syndrome. The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry. 1-15 |
| Sønderby IE, Ching CRK, Thomopoulos SI, et al. (2021) Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs. Human Brain Mapping |
| Ching CRK, Gutman BA, Sun D, et al. (2020) Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness. The American Journal of Psychiatry. appiajp201919060583 |
| Cleynen I, Engchuan W, Hestand MS, et al. (2020) Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular Psychiatry |
| Zinkstok JR, Boot E, Bassett AS, et al. (2019) Neurobiological perspective of 22q11.2 deletion syndrome. The Lancet. Psychiatry |
| Sumitomo A, Horike K, Hirai K, et al. (2018) A mouse model of 22q11.2 deletions: Molecular and behavioral signatures of Parkinson's disease and schizophrenia. Science Advances. 4: eaar6637 |
| Fiksinski AM, Breetvelt EJ, Lee YJ, et al. (2018) Neurocognition and adaptive functioning in a genetic high risk model of schizophrenia. Psychological Medicine. 1-8 |
| Sun D, Ching CRK, Lin A, et al. (2018) Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size. Molecular Psychiatry |
| Butcher NJ, Boot E, Lang AE, et al. (2018) Neuropsychiatric expression and catatonia in 22q11.2 deletion syndrome: An overview and case series. American Journal of Medical Genetics. Part A |