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David Curtis

32PUBLICATIONS

88CO-AUTHORS

Epidemiological modellingGene expression (incl. microarray and other genome-wide approaches)Deep learningEpigenetics (incl. genome methylation and epigenomics)Human rights and justice issues (excl. law)

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Publications (32)

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|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 <i>ABCA7</i>, <i>PSEN1</i>, <i>SORL1</i> and <i>TREM2</i>.

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 <i>ABCA7, PSEN1, SORL1</i> and <i>TREM2</i>.

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

|Jun 27, 2025

Analysis of 470,000 exome-sequenced UK biobank participants identifies genes containing rare variants which confer dementia risk.

Lily Gibbons, 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

1 joint publications

Anders D Børglum

1 joint publications

Thomas D Als

1 joint publications

Jakob Grove

1 joint publications

David M Hougaard

1 joint publications

Jonas Byberg-Grauholm

1 joint publications

Tiffany A Greenwood

Frequent Collaborators

2 joint publications

Andrew McQuillin

1 joint publications

Nicholas J Bass

1 joint publications

Kamaldeep S Bhui

1 joint publications

Manuel Mattheisen

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