Dawn L. Thiselton
Publications by Year
Research Areas
Retinal Development and Disorders, Genetic Associations and Epidemiology, RNA regulation and disease, Mitochondrial Function and Pathology, Lipoproteins and Cardiovascular Health
Most-Cited Works
- → OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28(2000)1,310 cited
- → Replication of association between schizophrenia and ZNF804A in the Irish Case–Control Study of Schizophrenia sample(2009)229 cited
- → Association of the NRG1 gene and schizophrenia: a meta-analysis(2006)220 cited
- → AKT1 Is Associated with Schizophrenia Across Multiple Symptom Dimensions in the Irish Study of High Density Schizophrenia Families(2007)157 cited
- → Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)(2012)152 cited
- → A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene(2001)139 cited
- → Genomewide linkage study in the Irish affected sib pair study of alcohol dependence: evidence for a susceptibility region for symptoms of alcohol dependence on chromosome 4(2006)110 cited
- A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophy.(2002)
- → No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF)(2004)103 cited
- → Association Study of 167 Candidate Genes for Schizophrenia Selected by a Multi-Domain Evidence-Based Prioritization Algorithm and Neurodevelopmental Hypothesis(2013)102 cited