ORCA
Online Research @ Cardiff
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Ali, Nabila M.H, Chawner, Samuel, Kushan-Wells, Leila, Bearden, Carrie, Mulle, Jennifer Gladys, Pollak, Rebecca, Gur, Raquel, Ghung, Wendy, Owen, Michael  ORCID: https://orcid.org/0000-0003-4798-0862 and Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254
2025.
Comparison of autism domains across thirty rare variant genotypes.
EBioMedicine
112
, 105521.
10.1016/j.ebiom.2024.105521
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Rammos, Alexandros, Blakey, Rachel, Dennison, Charlotte ORCID: https://orcid.org/0000-0002-7493-2041, Lewis, Sarah, Ali, Nabila, Davies, Amy, Wren, Yvonne, Humphries, Kerry, Sandy, Jonathan, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Kendall, Kimberley ORCID: https://orcid.org/0000-0002-6755-6121, Sharp, Gemma, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 and Stergiakouli, Evie
2025.
Copy number variants and their implications for developmental and behavioural problems in cleft lip and/or palate.
Human Molecular Genetics
Item availability restricted. |
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Ali, Nabila
2023.
Neurodevelopmental and neuropsychiatric disorders in individuals with rare pathogenic genetic variants analysis in clinical and population-based cohorts.
PhD Thesis,
Cardiff University.
Item availability restricted. |
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