A. Bassett

发表

A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium

M. Owen, R. Gur, T. Lehner, 2017, Molecular Psychiatry.

Clinical use of clozapine in a major urban setting: one year experience.

E. Chow, A. Bassett, E. Collins, 1995, Journal of psychiatry & neuroscience : JPN.

Neuropathologic features in adults with 22q11.2 deletion syndrome.

D J Mikulis, T. Kiehl, D. Mikulis, 2009, Cerebral cortex.

Perceived burden and neuropsychiatric morbidities in adults with 22q11.2 deletion syndrome.

A. Bassett, G. Costain, E. Chow, 2014, Journal of intellectual disability research : JIDR.

Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia.

N. Freimer, T. Gilliam, C. Kaufmann, 1989, Genomics.

Clinical experience with single‐nucleotide polymorphism‐based non‐invasive prenatal screening for 22q11.2 deletion syndrome

A. Bassett, Z. Demko, J. Babiarz, 2016, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

A Genotype-Phenotype Research Strategy for Schizophrenia*

J. Kennedy, L. Kopala, A. Bassett, 1990, Canadian journal of psychiatry. Revue canadienne de psychiatrie.

Report of a workshop on genetic linkage studies in schizophrenia.

D. Weeks, T. Gilliam, T. Lehner, 1990, Schizophrenia bulletin.

Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndrome.

A. Bassett, G. Costain, P. Ray, 2012, Journal of intellectual disability research : JIDR.

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

R. Siebert, J. Coselli, K. Devriendt, 2020, bioRxiv.

Patterns of dysmorphic features in schizophrenia.

R. Weksberg, W. Honer, A. Bassett, 2001, American journal of medical genetics.

Mutation screening of the KCNN3 gene reveals a rare frameshift mutation

L. Jones, N. Norton, A. Cardno, 2001, Molecular Psychiatry.

A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats.

Paul W Goldberg, M. Hayden, P. Goldberg, 1994, The New England journal of medicine.

Low platelet count in a 22q11 deletion syndrome subtype of schizophrenia

E. Chow, K. Lazier, A. Bassett, 2001, Schizophrenia Research.

The natural history of a genetic subtype of arrhythmogenic right ventricular cardiomyopathy caused by a p.S358L mutation in TMEM43

A. Bassett, P. Parfrey, K. Hodgkinson, 2013, Clinical genetics.