Janna Kenny
Royal College of Surgeons in Ireland(IE)Children's Health Ireland at Crumlin(IE)
Publications by Year
Research Areas
Prion Diseases and Protein Misfolding, Genomics and Rare Diseases, Neurological diseases and metabolism, Genetic Syndromes and Imprinting, Connective tissue disorders research
Most-Cited Works
- → Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy(2015)500 cited
- → Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome(2011)257 cited
- → Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer’s disease: a case series(2016)242 cited
- → Managing Bardet–Biedl Syndrome—Now and in the Future(2018)210 cited
- → R47H TREM2 variant increases risk of typical early‐onset Alzheimer's disease but not of prion or frontotemporal dementia(2014)116 cited
- → Age at onset in genetic prion disease and the design of preventive clinical trials(2019)110 cited
- → Validation of next-generation sequencing technologies in genetic diagnosis of dementia(2013)63 cited
- → Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series(2018)60 cited
- → Genetic testing in dementia — utility and clinical strategies(2020)52 cited
- → Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob Disease(2016)47 cited