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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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Journal ArticleDOI
22q11.2 deletion syndrome
Donna M. McDonald-McGinn,Kathleen E. Sullivan,Bruno Marino,Nicole Philip,Ann Swillen,Jacob A. S. Vorstman,Elaine H. Zackai,Beverly S. Emanuel,Joris Vermeesch,Bernice E. Morrow,Peter J. Scambler,Anne S. Bassett +11 more
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.
Journal ArticleDOI
Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia
Cathryn M. Lewis,Douglas F. Levinson,Lesley H. Wise,Lynn E. DeLisi,Richard E. Straub,Iiris Hovatta,Nigel Williams,Sibylle G. Schwab,Ann E. Pulver,Stephen V. Faraone,Linda M. Brzustowicz,Linda M. Brzustowicz,Charles A. Kaufmann,David L. Garver,Hugh Gurling,Eva Lindholm,Hilary Coon,Hans W. Moises,William Byerley,Sarah H. Shaw,Andrea Mesén,Robin Sherrington,F. Anthony O'Neill,Dermot Walsh,Kenneth S. Kendler,Jesper Ekelund,Tiina Paunio,Jouko Lönnqvist,Leena Peltonen,Leena Peltonen,Michael Conlon O'Donovan,Michael John Owen,Dieter B. Wildenauer,Wolfgang Maier,Gerald Nestadt,Jean-Louis Blouin,Stylianos E. Antonarakis,Bryan J. Mowry,Jeremy M. Silverman,Raymond R. Crowe,C. Robert Cloninger,Ming T. Tsuang,Dolores Malaspina,Jill M. Harkavy-Friedman,Dragan M. Svrakic,Anne S. Bassett,Jennifer A. Holcomb,Gursharan Kalsi,Andrew McQuillin,Jon Brynjolfson,Thordur Sigmundsson,Hannes Petursson,Elena Jazin,Tómas Zoega,Tómas Helgason +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
Linda M. Brzustowicz,Kathleen A. Hodgkinson,Eva W.C. Chow,Eva W.C. Chow,William G. Honer,Anne S. Bassett,Anne S. Bassett +6 more
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
Nancy D. Merner,Kathy Hodgkinson,Annika F.M. Haywood,Sean Connors,Vanessa M. French,Jörg-Detlef Drenckhahn,Christine Kupprion,Kalina Ramadanova,Ludwig Thierfelder,William J. McKenna,Barry Gallagher,Lynn Morris-Larkin,Anne S. Bassett,Patrick S. Parfrey,Terry-Lynn Young +14 more
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.
Journal ArticleDOI
Clinical Features of 78 Adults With 22q11 Deletion Syndrome
Anne S. Bassett,Eva W.C. Chow,Eva W.C. Chow,Janice A. Husted,Janice A. Husted,Rosanna Weksberg,Oana Caluseriu,Gary Webb,Michael A. Gatzoulis +8 more
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.