Author

Imelda Barber

University of Nottingham

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Kevin MorganiD· 2 shared Afina Willemina LemstraiD· 1 shared Alberto LleóiD· 1 shared Andrew John LeesiD· 1 shared Andrew SingletoniD· 1 shared Anne BraaeiD· 1 shared Bradley F. BoeveiD· 1 shared Célia Kun‐RodriguesiD· 1 shared

Activity by Year

2018-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersNeuroscience

Kevin MorganORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Heritability and genetic variance of dementia with Lewy bodies

Rita João Guerreiro, Valentina Escott‐Price, Dena G. Hernandez, Célia Kun‐Rodrigues, Owen A. Ross, Tatiana Orme, João Luís Neto, Susana Carmona, Nadia Dehghani, John D. Eicher, Claire E. Shepherd, Laura Parkkinen, Lee Darwent, Michael G. Heckman, Sonja W. Scholz, , José Brás

This study estimates the heritability of dementia with Lewy bodies (DLB) and finds it to be higher than previous estimates, with low variance explained by polygenic risk scores from Parkinson's or Alzheimer's disease.

Neurobiology of Disease · Apr 3, 2019Peer-reviewedNeuroscience

Complement receptor 1 gene (CR1) intragenic duplication and risk of Alzheimer’s disease

Ezgi Kucukkilic, Keeley J. Brookes, Imelda Barber, Tamar Guetta‐Baranes, Kevin Morgan, Edward J. Hollox

This study develops assays to genotype CR1-B allele and confirms its association with late-onset Alzheimer’s disease risk.

Human Genetics · Apr 1, 2018Peer-reviewedGenetics