Anne S Bassett

41PUBLICATIONS
212CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Neurology and neuromuscular diseasesPsychology of ageingGene expression (incl. microarray and other genome-wide approaches)
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Publications (41)

|Apr 15, 2026
Genome-wide tandem repeat expansions modify schizophrenia risk in the presence of a 22q11.2 deletion.

|Mar 27, 2026
Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Jhih-Rong Lin, Daniella Miller, Dana Luong

|Nov 01, 2025
Single cell RNA-seq analysis of hematopoietic cell types in 22q11.2 deletion syndrome reveals significant changes to non-T cells.

Katherine Beigel, Nouf Alsaati, Kelly Maurer

|Jun 18, 2025
Dissecting the Phenotypic Spectrum and Complexity of Movement Disorders in 22q11.2 Deletion Syndrome.

Nikolai Gil D Reyes, Talyta Grippe, Marcus Callister

|Dec 06, 2024
Real-World Treatment of Schizophrenia in Adults With a 22q11.2 Microdeletion: Traitement dans le monde réel de la schizophrénie chez des adultes atteints du syndrome de microdélétion 22q11.2.

Lily Van, Tracy Heung, Nikolai Gil D Reyes

|Nov 27, 2024
Adult Phenotype of CHD2-Associated Disorders.

Marlene Rong, Quratulain Zulfiqar Ali, Angel Aledo-Serrano

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Frequent Collaborators

11 joint publications

Erik Boot

11 joint publications

Donna McDonald-McGinn

8 joint publications

Ann Swillen

7 joint publications

Carrie E Bearden