Anne S. Bassett, M.D.
Affiliations: | University of Toronto, Toronto, ON, Canada |
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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 |
Gur R, Bearden C, Jacquemont S, et al. (2023) Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research Square |
Freud LR, Galloway S, Crowley TB, et al. (2023) Prenatal versus Postnatal Diagnosis of 22q11.2 Deletion Syndrome: Cardiac and Non-Cardiac Outcomes through 1 Year of Age. American Journal of Obstetrics and Gynecology |
Zhao Y, Wang Y, Shi L, et al. (2023) Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS. Npj Genomic Medicine. 8: 17 |
Bassett AS, McDonald-McGinn DM, Boot E, et al. (2023) Approaches to studying the impact of 22q11.2 copy number variants. American Journal of Human Genetics. 110: 1216-1218 |
Lin JR, Zhao Y, Jabalameli MR, et al. (2023) Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia. Molecular Psychiatry |
Óskarsdóttir S, Boot E, Crowley TB, et al. (2023) Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100338 |
Boot E, Óskarsdóttir S, Loo JCY, et al. (2023) Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100344 |
Blagowidow N, Nowakowska B, Schindewolf E, et al. (2023) Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes. 14 |
Bassett AS. (2022) Clinical genetics of schizophrenia and related neuropsychiatric disorders. Psychiatry Research. 319: 114992 |