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BMC Psychiatry|October 21, 2006
Case report: rapidly fatal bowel ischaemia on clozapine treatmentGiles Townsend, David CurtisJournal of Neurogenetics|September 24, 2025
Analysis of whole genome sequence data shows association of Alzheimer's disease with rare coding variants in ABCA7, PSEN1, SORL1 and TREM2David Curtis, Shujaani Joseph, Schizophrenia Research|November 22, 2017
Association study of schizophrenia with variants in miR-137 binding sitesDavid Curtis, Warren EmmettHuman Heredity|July 10, 2026
Investigation of the effects of non-coding LDLR variants on hyperlipidaemia riskDaniela Rojano, David CurtisPsychiatric Genetics|January 22, 2019
In-silico investigation of coding variants potentially affecting the functioning of the glutamatergic N-methyl-D-aspartate receptor in schizophreniaAntonia Tsavou, David CurtisSchizophrenia Bulletin|May 22, 2019
Assessment of Potential Clinical Role for Exome Sequencing in SchizophreniaThivia Balakrishna, David CurtisMedrxiv : the Preprint Server for Health Sciences|August 8, 2025
Analysis of whole genome sequence data shows association of Alzheimer's disease with rare coding variants in ABCA7, PSEN1, SORL1 and TREM2David Curtis, Shujaani Joseph, Journal of Neurogenetics|June 27, 2025
Analysis of 470,000 exome-sequenced UK biobank participants identifies genes containing rare variants which confer dementia riskLily Gibbons, David CurtisInternational Journal of Immunogenetics|May 9, 2025
Analysis of Rare Coding Variants in 470,000 UK Biobank Participants Reveals Genetic Associations With Childhood Asthma PredispositionZhenzhen Liu, David CurtisBMC Genetics|June 29, 2007
Minor differences in haplotype frequency estimates can produce very large differences in heterogeneity test statisticsDavid Curtis, Ke XuPageof 35