ORCA
Online Research @ CardiffÂ
Browse by Current Cardiff authors
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Up a levelNumber of items: 4.
Huang, Lam Opal, Montalbano, Simone, Lundberg, Mischa, Katzourou, Ioanna, Owen, David, Ali, Nabila, van den Bree, Marianne  ORCID: https://orcid.org/0000-0002-4426-3254, Vaez, Morteza, Pedersen, Ole B., Ostrowski, Sisse R., Erikstrup, Christian, Werge, Thomas, Mikkelsen, Dorte Helenius and Ingason, Andres
2026.
W23. Neurodevelopmental disorder copy number variants and risk of internalising-cardiometabolic multimorbidity in four large-scale population-based biobanks [Abstract].
European Neuropsychopharmacology
111
(S1)
, 113141.
10.1016/j.euroneuro.2026.113141
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Rammos, Alexandros, Blakey, Rachel, Dennison, Charlotte A. ORCID: https://orcid.org/0000-0002-7493-2041, Lewis, Sarah J., Ali, Nabila, Davies, Amy, Wren, Yvonne, Humphries, Kerry, Sandy, Jonathan, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Kendall, Kimberley Marie ORCID: https://orcid.org/0000-0002-6755-6121, Sharp, Gemma C., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, van den Bree, Marianne B. M. 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
34
(18)
, pp. 1563-1574.
10.1093/hmg/ddaf115
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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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