David Curtis

33PUBLICATIONS
88CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epidemiological modellingDeep learningEpigenetics (incl. genome methylation and epigenomics)Human rights and justice issues (excl. law)
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Publications (33)

|Jul 29, 2026
Sequence effects on mutation rates investigated in whole-genome sequenced UK Biobank participants.

|Oct 22, 2025
Health effects of loss of function variants in gene targets for Alzheimer's disease prevention.

Yuan Ma, Allena Zhang, Sabrina Asri

|Sep 24, 2025
Analysis of whole genome sequence data shows association of Alzheimer's disease with rare coding variants in ABCA7, PSEN1, SORL1 and TREM2.

David Curtis, Shujaani Joseph

|Aug 14, 2025
Assessment of ability of a DNA language model to predict pathogenicity of rare coding variants.

David Curtis

|Aug 08, 2025
Analysis of whole genome sequence data shows association of Alzheimer's disease with rare coding variants in ABCA7, PSEN1, SORL1 and TREM2.

David Curtis, Shujaani Joseph

|Jun 30, 2025
Analysis of 470,000 exome-sequenced cases and controls fails to identify any genes impacting risk of developing affective disorder.

David Curtis

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Frequent Collaborators

2 joint publications

Andrew McQuillin

1 joint publications

Nicholas J Bass

1 joint publications

Kamaldeep S Bhui

1 joint publications

Manuel Mattheisen