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Anne S. Bassett

Researcher at University of Toronto

Publications -  172
Citations -  11708

Anne S. Bassett is an academic researcher from University of Toronto. The author has contributed to research in topics: Schizophrenia (object-oriented programming) & Psychosis. The author has an hindex of 49, co-authored 149 publications receiving 10771 citations. Previous affiliations of Anne S. Bassett include St. John's University & University of British Columbia.

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22q11.2 deletion syndrome

TL;DR: The first description in the English language of the constellation of findings now known to be due to this chromosomal difference was made in the 1960s in children with DiGeorge syndrome, who presented with the clinical triad of immunodeficiency, hypoparathyroidism and congenital heart disease as mentioned in this paper.
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Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia

Cathryn M. Lewis, +54 more
TL;DR: The GSMA produced significant genomewide evidence for linkage on chromosome 2q and suggests that some or all of these regions contain loci that increase susceptibility to schizophrenia in diverse populations.
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Location of a Major Susceptibility Locus for Familial Schizophrenia on Chromosome 1q21-q22

TL;DR: A genome-wide scan for schizophrenia susceptibility loci in 22 extended families with high rates of schizophrenia provided highly significant evidence of linkage to chromosome 1 (1q21-q22), with a maximum heterogeneity logarithm of the likelihood of linkage (lod) score of 6.50.
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Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene

TL;DR: It is concluded that ARVC at locus ARVD5 is a lethal, fully penetrant, sex-influenced morbid disorder and contains a response element for PPAR gamma, which may explain the fibrofatty replacement of the myocardium, a characteristic pathological finding in ARVC.
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Clinical Features of 78 Adults With 22q11 Deletion Syndrome

TL;DR: The results have implications for clinical assessment and management, genetic counseling and research into pathophysiological mechanisms, including several of later onset in 22q11DS.