This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a University of Toronto directory, so their courses and email address may be missing. Find their university profile.
Research
Latest papers
Autoantibodies in patients with 22q11.2 deletion syndrome and psychosis.
The Journal of allergy and clinical immunology · 2025
Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression.
Clinical genetics · 2023
Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome.
European journal of medical genetics · 2018
Latest funding
- $10,000
Family-friendly plain language renditions of clinical practice recommendations for children and adults with 22q11.2 deletion syndrome
CIHR · 2025 · Nominated PI
- $1,147,500
Identifying genetic and epigenetic modifiers for schizophrenia in a high-risk population
CIHR · 2024 · Principal investigator
- $15,000
Expanding access to clinical practice recommendations for 22q11.2 deletion syndrome across the lifespan
CIHR · 2024 · Nominated PI
5 publications.
Autoantibodies in patients with 22q11.2 deletion syndrome and psychosis.
Starkey SY, Maurer K, Bassett A, McDonald McGinn DM, Sullivan KE
Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression.
Campbell IM, Crowley TB, Jobaliya C, Bailey A, McGinn DE, Gaiser K, Bassett A, Gur RE, Morrow B, Emanuel BS, Franco AT, French D, Zackai EH, McDonald-McGinn DM, Lambert MP
Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome.
Unolt M, Barry J, Digilio MC, Marino B, Bassett A, Oechslin E, Low DW, Belasco JB, Kallish S, Sullivan K, Zackai EH, McDonald-McGinn DM
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.
Isles AR, Ingason A, Lowther C, Walters J, Gawlick M, Stöber G, Rees E, Martin J, Little RB, Potter H, Georgieva L, Pizzo L, Ozaki N, Aleksic B, Kushima I, Ikeda M, Iwata N, Levinson DF, Gejman PV, Shi J, Sanders AR, Duan J, Willis J, Sisodiya S, Costain G, Werge TM, Degenhardt F, Giegling I, Rujescu D, Hreidarsson SJ, Saemundsen E, Ahn JW, Ogilvie C, Girirajan SD, Stefansson H, Stefansson K, O'Donovan MC, Owen MJ, Bassett A, Kirov G
Deletion of 15q11.2(BP1-BP2) region: further evidence for lack of phenotypic specificity in a pediatric population.
Hashemi B, Bassett A, Chitayat D, Chong K, Feldman M, Flanagan J, Goobie S, Kawamura A, Lowther C, Prasad C, Siu V, So J, Tung S, Speevak M, Stavropoulos DJ, Carter MT
Family-friendly plain language renditions of clinical practice recommendations for children and adults with 22q11.2 deletion syndrome
Principal investigators: Bassett, Anne S
Keywords: Dissemination
Identifying genetic and epigenetic modifiers for schizophrenia in a high-risk population
Principal investigators: Yuen, Ryan; Bassett, Anne S
Keywords: 22q11.2 Deletion; Epigenetics; Polygenic Risk; Schizophrenia; Tandem Repeats
Expanding access to clinical practice recommendations for 22q11.2 deletion syndrome across the lifespan
Principal investigators: Bassett, Anne S
Keywords: Dissemination
Outcomes and disease burden in a model of young adult multimorbidity
Principal investigators: Bassett, Anne S
Keywords: 22q11.2 Deletion Syndrome; Copy Number Variation; Disease Burden; Genetic Syndrome; Genetics; Genomic Disorders; Natural History; Outcome; Variable Expression; Whole Genome Sequencing
Outcomes and disease burden in a model of young adult multimorbidity
Principal investigators: Bassett, Anne S
Keywords: 22q11.2 Deletion Syndrome; Copy Number Variation,; Disease Burden; Genetic Syndrome; Genetics; Genomic Disorders; Natural History; Outcome; Variable Expression; Whole Genome Sequencing
Impact of tandem repeat expansions in schizophrenia
Principal investigators: Bassett, Anne S; Yuen, Ryan
Keywords: Bioinformatics; Genetics; Genomic; Pathogenic Variants; Schizophrenia; Variable Expression; Whole Genome Sequencing
Determining genetic and non-genetic risk for schizophrenia in a high risk group
Principal investigators: Bassett, Anne S
Keywords: 22q11.2 Deletion Syndrome; Bioinformatics; Copy Number Variation; Genetics; Genomic; Microdeletion; Pathogenic Variants; Penetrance; Variable Expression; Whole Genome Sequencing
11th Biennial International 22q11.2 Conference
Principal investigators: Bassett, Anne S
Keywords: 22q11.2 Deletion Syndrome; Genetic Syndrome; Genetics; Genomic Disorders
Understanding and treating neurological phenotypes in the 15q13.3 microdeletion syndrome
Principal investigators: Singh, Karun
Keywords: Autism; Copy Number Variation; Disease Modelling; Genetic Sequencing; Human Neurones; Mouse Model; Neurodevelopmental Disorder; Psychiatric Disorder; Schizophrenia; Synapse Development
Predicting occurrence and lifetime expression of a major recurrent copy number variation
Principal investigators: Bassett, Anne S
Keywords: 22q11.2 Deletion Syndrome; Copy Number Variation; Genetic Syndrome; Genetics; Genomic Disorders; Microdeletion; Outcome; Penetrance; Variable Expression; Whole Genome Sequencing
From CIHR, NSERC and SSHRC funding decisions: CIHR since 2008, NSERC since 1991 and SSHRC since 1998, including their latest published competition results.
Frequent collaborators
- Psychiatry/Genetics
- Computer Science
- Other
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