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Bjpsych Bulletin|November 10, 2024
The Royal College of Psychiatrists should become British, not RoyalDavid Curtis
Journal of Genetics|October 6, 2023
Mendel did not study common, naturally occurring phenotypesDavid Curtis
The Behavioral and Brain Sciences|September 11, 2023
Social scientists would do well to steer clear of polygenic scoresDavid Curtis
Journal of Affective Disorders|December 17, 2020
Analysis of 50,000 exome-sequenced UK Biobank subjects fails to identify genes influencing probability of developing a mood disorder resulting in psychiatric referralDavid Curtis
The British Journal of Psychiatry : the Journal of Mental Science|August 3, 2016
Schizophrenia genetics moves into the lightDavid Curtis
Journal of Neurogenetics|May 10, 2021
Analysis of whole genome sequenced cases and controls shows that the association of variants in TOMM40, BCAM, NECTIN2 and APOC1 with late onset Alzheimer's disease is driven by linkage disequilibrium with APOE ε2/ε3/ε4 allelesDavid Curtis,
Journal of Medical Genetics|April 29, 2021
Analysis of 200 000 exome-sequenced UK Biobank subjects illustrates the contribution of rare genetic variants to hyperlipidaemiaDavid Curtis
European Journal of Human Genetics : EJHG|September 28, 2018
A weighted burden test using logistic regression for integrated analysis of sequence variants, copy number variants and polygenic risk scoreDavid Curtis
Annals of Human Genetics|June 17, 2011
Assessing the contribution family data can make to case-control studies of rare variantsDavid Curtis
Patient Preference and Adherence|July 28, 2011
Patient experience - the ingredient missing from cost-effectiveness calculationsDavid Curtis
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