Her primary areas of study are Genetics, Schizophrenia, Psychosis, 22q11 Deletion Syndrome and DiGeorge syndrome. Her Genetics research incorporates elements of Pediatrics and Bioinformatics. Her study in Schizophrenia is interdisciplinary in nature, drawing from both Neurocognitive and Genetic linkage.
Her studies in Psychosis integrate themes in fields like Severity of illness and Clinical psychology. The concepts of her 22q11 Deletion Syndrome study are interwoven with issues in Phenotype, White matter, Magnetic resonance imaging and Genetic determinism. Anne S. Bassett combines subjects such as Cognition, Hypoparathyroidism, Microdeletion syndrome, Etiology and Genetic testing with her study of DiGeorge syndrome.
Genetics, Schizophrenia, Psychosis, Psychiatry and Copy-number variation are her primary areas of study. Her Genetics study frequently draws parallels with other fields, such as Schizophrenia. Her Schizophrenia research is multidisciplinary, incorporating elements of Intellectual disability, Clinical psychology, Autism spectrum disorder, DiGeorge syndrome and Pediatrics.
Her biological study deals with issues like 22q11 Deletion Syndrome, which deal with fields such as Endocrinology. In her study, which falls under the umbrella issue of Psychiatry, Microdeletion syndrome is strongly linked to Genetic counseling. Anne S. Bassett usually deals with Copy-number variation and limits it to topics linked to Bioinformatics and Human genetics.
Her primary areas of investigation include Genetics, Schizophrenia, Copy-number variation, Deletion syndrome and Intellectual disability. Her Schizophrenia research is multidisciplinary, incorporating perspectives in Psychological intervention, Psychosis, Clinical psychology and Anxiety. Her research combines Bioinformatics and Psychosis.
Her Copy-number variation course of study focuses on Autism spectrum disorder and Etiology and Attention deficit hyperactivity disorder. Her work carried out in the field of Intellectual disability brings together such families of science as Genetic model, Microdeletion syndrome, Pediatrics and Cohort. Her studies deal with areas such as DiGeorge syndrome, Scoliosis and Epilepsy as well as Pediatrics.
Her scientific interests lie mostly in Schizophrenia, Copy-number variation, Genetics, Cohort and Psychosis. Her work deals with themes such as Chromosome and Disease, which intersect with Schizophrenia. Her work is dedicated to discovering how Copy-number variation, Autism spectrum disorder are connected with Etiology and Attention deficit hyperactivity disorder and other disciplines.
Her study on Haploinsufficiency, Allele and DiGeorge syndrome is often connected to Vascular endothelial growth factor A as part of broader study in Genetics. Her Cohort research incorporates themes from Gene, Intellectual disability and Increased risk. Her research integrates issues of Bioinformatics and Deletion syndrome in her study of Psychosis.
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22q11.2 deletion syndrome
Donna M. McDonald-McGinn;Kathleen E. Sullivan;Bruno Marino;Nicole Philip.
Nature Reviews Disease Primers (2015)
Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia
Cathryn M. Lewis;Douglas F. Levinson;Lesley H. Wise;Lynn E. DeLisi.
American Journal of Human Genetics (2003)
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.
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.
American Journal of Psychiatry (2014)
Practical Guidelines for Managing Patients with 22q11.2 Deletion Syndrome
Anne S Bassett;Donna M McDonald-McGinn;Koenraad Devriendt;Maria Cristina Digilio.
The Journal of Pediatrics (2011)
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.
American Journal of Medical Genetics Part A (2005)
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.
American Journal of Human Genetics (2008)
The schizophrenia phenotype in 22q11 deletion syndrome
Anne S. Bassett;Eva W.C. Chow;Philip AbdelMalik;Mirona Gheorghiu.
American Journal of Psychiatry (2003)
22q11 deletion syndrome: a genetic subtype of schizophrenia.
Anne S Bassett;Eva W.C Chow;Eva W.C Chow.
Biological Psychiatry (1999)
Meta-analysis of 32 genome-wide linkage studies of schizophrenia
M Y M Ng;D F Levinson;S Faraone;B K Suarez.
Molecular Psychiatry (2009)
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