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A.S. Bassett

Brief research communication: No evidence for linkage of the CHRNA7 gene region in Canadian schizophrenia families
1998 · M. Neves-Pereira, A.S. Bassett, et al. · American Journal of Medical Genetics · 63
New Polymorphism for the Human Serotonin 1D Receptor Variant (5-HT1Dβ) not Linked to Schizophrenia in Five Canadian Pedigrees
1993 · D.G. Sidenberg, A.S. Bassett, et al. · Human Heredity · 41
NCAM and schizophrenia: genetic studies
1997 · A M Vicente, F Macciardi, et al. · Molecular Psychiatry · 39
Search for unstable DNA in schizophrenia families with evidence for genetic anticipation.
1996 · A Petronis, A S Bassett, et al. · PubMed Central · 34
Reproductive fitness in familial schizophrenia
1995 · A.S. Bassett, J. McAlduff, et al. · Schizophrenia Research · 16
The schizophrenia phenotype in 22Q deletion syndrome
2003 · A.S. Bassett, E. Chow, et al. · Schizophrenia Research · 10
Genetic linkage evaluation of twenty-four loci in an eastern Canadian family segregating Darier's disease (keratosis follicularis)
1994 · Deborah Gayle Sidenberg, Daniel Berg, et al. · Journal of the American Academy of Dermatology · 7
Clozapine-associated seizures in a 22Q deletion syndrome subtype of schizophrenia
2003 · O. Caluseriu, T. Tayyeb, et al. · Schizophrenia Research · 4
Dopamine D4 receptor gene variants and schizophrenia
1993 · J.L. Kennedy, H.H.M. Van Tol, et al. · Schizophrenia Research · 4
The temporal lobes, reversed asymmetry, and schizophrenia genetics
1996 · W.G. Honer, A.S. Bassett, et al. · Schizophrenia Research · 3
Clinical use of clozapine in a major urban setting: one year experience.
1995 · E W Chow, E J Collins, et al. · PubMed Central · 3
Investigation of genetic risk factors for schizophrenia on 11q
1993 · A. Petronis, A.S. Bassett, et al. · Schizophrenia Research · 3
Axis II personality features and disorder in subjects in the New York high-risk project
1991 · E. Squires-Wheeler, L. Erlenmeyer-Kimling, et al. · Schizophrenia Research · 2
417 Sudden death risk in patients with tetralogy of Fallot and 22q11.2 deletion syndrome
2011 · S. Liu, H. Balint, et al. · Canadian Journal of Cardiology · 1
Olfactory deficits in familial schizophrenia
1996 · L.C. Kopala, A.S. Bassett, et al. · Schizophrenia Research · 1
Genome-wide association study of modifiers for tetralogy of Fallot in 22q11DS identifies variants in the GPR98 locus on 5q14.3
2016 · Tianfu Guo, Gabriela M. Repetto, et al.
Micrornas and Genetic Risk for Tetralogy of Fallot
2015 · A.S. Bassett, G.A. Costain, et al. · Canadian Journal of Cardiology
The 22q11.2 Deletion Syndrome: Second Hit Copy Number Variants and Conotruncal Heart Defects
2011 · MB Sheridan, Tingwei Guo, et al.
Childhood behaviour in a 22Q deletion syndrome subtype of schizophrenia
2003 · M. Gheorghiu, E. Chow, et al. · Schizophrenia Research
Impulsivity and aggression in 22Q11 deletion syndrome and schizophrenia
2003 · E.W. Chow, R. Weksberg, et al. · Schizophrenia Research
Childhood head injury and illness expression in familial schizophrenia
2003 · P. AbdelMalik, A. Bassett, et al. · Schizophrenia Research
Distinguishing features for schizophrenia on MRI brain scans of 22qDS adults
2001 · Eva W.C. Chow, David J. Mikulis, et al.
379. 22q11 deletion syndrome (velocardiofacial syndrome) and schizophrenia: a genetic subtype?
2000 · R. Nicolson, K. Murphy, et al. · Biological Psychiatry
A study to evaluate the antiaggressive properties of clozapine
2000 · E. Chow, H. Desai, et al. · Schizophrenia Research
Delineating a 22q11 deletion subtype of schizophrenia
1998 · L. Scutt, S. Correia, et al. · Schizophrenia Research
Works count: 35
Citation count: 231
H-index: 7
I10-index: 6
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