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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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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.
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