Maria Gudbrandsen
8PUBLICATIONS
30CO-AUTHORS
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Publications (8)
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|Jan 28, 2026
Navigating Services in the UK: The Lived Experiences of Families Affected by 22q11.2 Deletion Syndrome.Maria Gudbrandsen, Sophie Edmonds, Michelle Jayman
|Jan 24, 2025
Driving Innovation to Support Pupils with SEND Through Co-Production in Education and Research: Participatory Action Research with 22q11.2 Deletion Syndrome Families in England.Michelle Jayman, Sophie Edmonds, Maria Gudbrandsen
|Jun 23, 2021
Correction: Striatal dopaminergic alterations in individuals with copy number variants at the 22q11.2 genetic locus and their implications for psychosis risk: a [18F]-DOPA PET study.Maria Rogdaki, Céline Devroye, Mariasole Ciampoli
|May 13, 2021
Striatal dopaminergic alterations in individuals with copy number variants at the 22q11.2 genetic locus and their implications for psychosis risk: a [18F]-DOPA PET study.Maria Rogdaki, Céline Devroye, Mariasole Ciampoli
|Jun 10, 2020
Neuroanatomical underpinnings of autism symptomatology in carriers and non-carriers of the 22q11.2 microdeletion.Maria Gudbrandsen, Anke Bletsch, Caroline Mann
|Feb 05, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.Isabelle Cleynen, Worrawat Engchuan, Matthew S Hestand
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Frequent Collaborators
4 joint publications
Michael Owen
3 joint publications
Declan Murphy
3 joint publications
Maria Rogdaki
3 joint publications
Robert A McCutcheon
2 joint publications
Ania M Fiksinski
2 joint publications
Sameer Jauhar
2 joint publications
Michelle Jayman
2 joint publications
Carrie E Bearden
2 joint publications
Eileen Daly
2 joint publications
Abhishekh H Ashok
