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Number of items: 4.

Smart, Sophie E. ORCID: https://orcid.org/0000-0002-6709-5425, Legge, Sophie E., Fenner, Eilidh, Pardiñas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Woolway, Grace, Lynham, Amy J. ORCID: https://orcid.org/0000-0002-3189-6888, Escott‐Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Wilkinson, Lawrence ORCID: https://orcid.org/0000-0002-9337-6124, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Walters, James T.R. ORCID: https://orcid.org/0000-0002-6980-4053 2025. The role of SLC39A8.p.( Ala391Thr ) in schizophrenia symptom severity and cognitive ability: cross‐sectional studies of schizophrenia and the general UK population. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics , e33037. 10.1002/ajmg.b.33037
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Kappel, Djenifer, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Fenner, Eilidh, King, Adrian, Jansen, John, Helthius, Marinka, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 and Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590 2024. Rare variants in pharmacogenes influence clozapine metabolism in individuals with schizophrenia. European Neuropsychopharmacology 80 , pp. 47-54. 10.1016/j.euroneuro.2023.12.007
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Fenner, Eilidh 2023. Discovery and impact of schizophrenia rare genetic variation using next generation sequencing. PhD Thesis, Cardiff University.
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Wadon, Megan, Fenner, Eilidh, Kendall, Kimberley ORCID: https://orcid.org/0000-0002-6755-6121, Bailey, Grace, Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222 and Peall, Kathryn J. ORCID: https://orcid.org/0000-0003-4749-4944 2022. Clinical and genotypic analysis in determining dystonia non-motor phenotypic heterogeneity: a UK Biobank study. Journal of Neurology 269 , pp. 6436-6451. 10.1007/s00415-022-11307-4
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