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European Journal of Human Genetics : EJHG|April 23, 2015
Rare missense variants within a single gene form yin yang haplotypesDavid CurtisPlos One|December 12, 2024
Analysis of rare coding variants in 470,000 exome-sequenced subjects characterises contributions to risk of type 2 diabetesDavid CurtisAdvances and Applications in Bioinformatics and Chemistry : AABC|June 29, 2013
Approaches to the detection of recessive effects using next generation sequencing data from outbred populationsDavid CurtisHuman Heredity|January 7, 2021
Multiple Linear Regression Allows Weighted Burden Analysis of Rare Coding Variants in an Ethnically Heterogeneous PopulationDavid CurtisBMC Genetics|June 15, 2007
Allelic association studies of genome wide association data can reveal errors in marker position assignmentsDavid CurtisBMC Genetics|October 5, 2007
Extended homozygosity is not usually due to cytogenetic abnormalityDavid CurtisPsychiatric Genetics|March 17, 2016
Pathway analysis of whole exome sequence data provides further support for the involvement of histone modification in the aetiology of schizophreniaDavid CurtisAnnals of Human Genetics|March 31, 2015
Investigation of Recessive Effects in Schizophrenia Using Next-Generation Exome Sequence DataDavid CurtisHuman Heredity|December 9, 2025
Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMIDavid CurtisWork (Reading, Mass.)|January 18, 2013
The influence of environment on the fieldwork experience: exploring interprofessional student perspectivesSusan Mulholland, Mark HallPageof 35