CORDIS Project
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The project investigates the genetic factors contributing to autism and related disorders by analyzing copy number variations in the genome. It aims to identify rare genetic mutations that may increase the risk of these conditions, enhancing understanding of their genetic basis.
The recent technical improvements for the study of the cytogenetic basis of disease have led to the identification of many microdeletion and microduplication syndromes.
De novo copy number variants (CNVs) are seen more often than expected in autistic patients, and rare chromosomal aberrations are known to account for a small fraction of schizophrenia and bipolar disorder.
Recurrent spontaneous mutations at multiple sites across the genome may be a prime cause of these disorders, and the reduced…
ISLENSK ERFDAGREINING EHF
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LANDSPITALI UNIVERSITY HOSPITAL
Iceland, Reykjavik
Type: University / higher education
Activity type: Higher or Secondary Education Establishments
SME: No
United Kingdom, London
Type: University / higher education
Activity type: Higher or Secondary Education Establishments
SME: No
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