Anne S. Bassett

Overview

Best Publications

• 22q11.2 deletion syndrome

  Donna M. McDonald-McGinn;Kathleen E. Sullivan;Bruno Marino;Nicole Philip

  1968
  Citations

• Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia

  Cathryn M. Lewis;Douglas F. Levinson;Lesley H. Wise;Lynn E. DeLisi

  1478
  Citations

• Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.

  Maude Schneider;Martin Debbané;Anne S. Bassett;Eva W.C. Chow

  814
  Citations

• QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

  Stefano Colella;Christopher Yau;Jennifer M. Taylor;Ghazala Mirza

  751
  Citations

• 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

  732
  Citations

• Practical Guidelines for Managing Patients with 22q11.2 Deletion Syndrome

  Anne S Bassett;Donna M McDonald-McGinn;Koenraad Devriendt;Maria Cristina Digilio

  652
  Citations

• Clinical Features of 78 Adults With 22q11 Deletion Syndrome

  Anne S. Bassett;Eva W.C. Chow;Eva W.C. Chow;Janice Husted;Janice Husted;Rosanna Weksberg

  597
  Citations

• 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 A. Hodgkinson;Annika F.M. Haywood;Sean Connors

  558
  Citations

• The schizophrenia phenotype in 22q11 deletion syndrome

  Anne S. Bassett;Eva W.C. Chow;Philip AbdelMalik;Mirona Gheorghiu

  447
  Citations

• 22q11 deletion syndrome: a genetic subtype of schizophrenia.

  Anne S Bassett;Eva W.C Chow;Eva W.C Chow

  436
  Citations

• Meta-analysis of 32 genome-wide linkage studies of schizophrenia

  M Y M Ng;D F Levinson;S Faraone;B K Suarez

  354
  Citations

• Clinical and genetic epidemiology of Bardet-Biedl syndrome in Newfoundland: A 22-year prospective, population-based, cohort study

  Susan J. Moore;Jane S. Green;Yanli Fan;Ashvinder K. Bhogal

  350
  Citations

• A Major Susceptibility Locus for Specific Language Impairment Is Located on 13q21

  Christopher W. Bartlett;Judy F. Flax;Mark W. Logue;Veronica J. Vieland

  322
  Citations

• 22q11 Deletion Syndrome in Adults With Schizophrenia

  Anne S. Bassett;Kathy Hodgkinson;Eva W.C. Chow;Susana Correia

  315
  Citations

• Linkage of familial schizophrenia to chromosome 13q32.

  Linda M. Brzustowicz;Linda M. Brzustowicz;William G. Honer;Eva W.C. Chow;Dawn Little

  307
  Citations

• Practical guidelines for managing adults with 22q11.2 deletion syndrome

  Wai Lun Alan Fung;Nancy J. Butcher;Gregory Costain;Danielle M. Andrade

  292
  Citations

• Copy Number Variations in Schizophrenia: Critical Review and New Perspectives on Concepts of Genetics and Disease

  Anne S. Bassett;Stephen W. Scherer;Linda M. Brzustowicz

  260
  Citations

• Cognitive Decline Preceding the Onset of Psychosis in Patients With 22q11.2 Deletion Syndrome

  Jacob A. S. Vorstman;Elemi J. Breetvelt;Sasja N. Duijff;Stephan Eliez

  258
  Citations

• Evidence for anticipation in schizophrenia

  A. S. Bassett;W. G. Honer

  243
  Citations

• Neurocognitive profile in 22q11 deletion syndrome and schizophrenia.

  Eva W.C. Chow;Eva W.C. Chow;Mark Watson;Donald A. Young;Donald A. Young;Anne S. Bassett;Anne S. Bassett

  240
  Citations