Anne S. Bassett, M.D.

University of Toronto, Toronto, ON, Canada 
"Anne Bassett"
Mean distance: 17.87 (cluster 11)
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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
Homans JF, de Reuver S, Heung T, et al. (2020) The Role of 22q11.2 Deletion Syndrome in the Relationship between Congenital Heart Disease and Scoliosis. The Spine Journal : Official Journal of the North American Spine Society
Vervoort L, Demaerel W, Rengifo LY, et al. (2019) Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins. Human Molecular Genetics. 28: 3724-3733
Zhao Y, Diacou A, Johnston HR, et al. (2019) Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects. American Journal of Human Genetics
Zarrei M, Burton CL, Engchuan W, et al. (2019) A large data resource of genomic copy number variation across neurodevelopmental disorders. Npj Genomic Medicine. 4: 26
Zinkstok JR, Boot E, Bassett AS, et al. (2019) Neurobiological perspective of 22q11.2 deletion syndrome. The Lancet. Psychiatry
Malecki SL, Van Mil S, Graffi J, et al. (2019) A genetic model for multimorbidity in young adults. Genetics in Medicine : Official Journal of the American College of Medical Genetics
Van L, Heung T, Graffi J, et al. (2019) All-cause mortality and survival in adults with 22q11.2 deletion syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics
Vlaskamp DRM, Bassett AS, Sullivan JE, et al. (2019) Schizophrenia is a later-onset feature of PCDH19 Girls Clustering Epilepsy. Epilepsia. 60: 429-440
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