Anne S Bassett

发表

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

Brian Chung, Therese van Amelsvoort, Gregory Costain, 2015, Genetics in Medicine.

Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome.

Stephan Eliez, Tingwei Guo, Xiaowu Gai, 2015, American journal of human genetics.

Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome

David J Mikulis, D. Mikulis, A. Bassett, 2002, Biological Psychiatry.

Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia

David J Mikulis, Rosanna Weksberg, R. Weksberg, 1999, Biological Psychiatry.

Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications.

Ekaterina Rogaeva, Tim-Rasmus Kiehl, T. Kiehl, 2013, JAMA neurology.

Response to clozapine in a clinically identifiable subtype of schizophrenia.

A. Lang, A. Bassett, N. Butcher, 2015, The British journal of psychiatry : the journal of mental science.

Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome

A. Bassett, C. Silversides, E. Chow, 2014, Clinical endocrinology.

Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays.

Daniele Merico, Christian R Marshall, Tracy Yuen, 2013, Human molecular genetics.

The schizophrenia phenotype in 22q11 deletion syndrome.

Rosanna Weksberg, Mirona Gheorghiu, R. Weksberg, 2003, The American journal of psychiatry.

Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome

Daniele Merico, Christian R Marshall, Babak Alipanahi, 2015, G3: Genes, Genomes, Genetics.

Identification of a schizophrenia-associated functional noncoding variant in NOS1AP.

Steven Buyske, Veronica J Vieland, Yungui Huang, 2009, The American journal of psychiatry.

Association of schizophrenia in 22q11.2 deletion syndrome and gray matter volumetric deficits in the superior temporal gyrus.

Corie Wei, A. Crawley, A. Bassett, 2011, The American journal of psychiatry.

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.

Stephan Eliez, Abraham Weizman, Wanda Fremont, 2014, The American journal of psychiatry.

Complex congenital heart disease in unaffected relatives of adults with 22q11.2 deletion syndrome.

A. Bassett, C. Silversides, E. Chow, 2011, The American journal of cardiology.

Schizophrenia and 22q11.2 deletion syndrome

A. Bassett, E. Chow, Anne S Bassett, 2008, Current psychiatry reports.

22q11 deletion syndrome: a genetic subtype of schizophrenia

A. Bassett, E. Chow, Anne S Bassett, 1999, Biological Psychiatry.

Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness.

Dmitry Isaev, Kosha Ruparel, Eileen Daly, 2020, The American journal of psychiatry.

Hippocampal Malrotation is Associated with Chromosome 22q11.2 Microdeletion

Timo Krings, Tim-Rasmus Kiehl, T. Kiehl, 2013, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease.

Stephen W Scherer, S. Scherer, A. Bassett, 2010, The American journal of psychiatry.

Clinical applications of schizophrenia genetics: genetic diagnosis, risk, and counseling in the molecular era

Gregory Costain, A. Bassett, G. Costain, 2012, The application of clinical genetics.

Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene.

Sean Connors, Patrick S Parfrey, Barry Gallagher, 2008, American journal of human genetics.

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia.

Leena Peltonen, Andrew McQuillin, Jouko Lönnqvist, 2003, American journal of human genetics.