Showing results (1-10 of 168) with videos related to
Sort By:
Pageof 17
Psychiatric Genetics|June 24, 2022
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesisDavid CurtisAnnals of Human Genetics|September 13, 2017
Construction of an Exome-Wide Risk Score for Schizophrenia Based on a Weighted Burden TestDavid CurtisPsychiatric Genetics|December 19, 2012
Consideration of plausible genetic architectures for schizophrenia and implications for analytic approaches in the era of next generation sequencingDavid CurtisDiabetes/Metabolism Research and Reviews|July 3, 2021
Analysis of rare coding variants in 200,000 exome-sequenced subjects reveals novel genetic risk factors for type 2 diabetesDavid CurtisPsychiatric Genetics|June 2, 2021
Haploinsufficiency of the HIRA gene may not always produce severe neurodevelopmental consequencesDavid CurtisInternational Journal of Obesity (2005)|January 24, 2022
Weighted burden analysis in 200,000 exome-sequenced subjects characterises rare variant effects on BMIDavid CurtisAdvances and Applications in Bioinformatics and Chemistry : AABC|August 14, 2012
A rapid method for combined analysis of common and rare variants at the level of a region, gene, or pathwayDavid CurtisMolecular Genetics and Metabolism|August 5, 2020
Analysis of exome-sequenced UK Biobank subjects implicates genes affecting risk of hyperlipidaemiaDavid CurtisEuropean Journal of Human Genetics : EJHG|August 3, 2024
Assessment of ability of AlphaMissense to identify variants affecting susceptibility to common diseaseDavid CurtisJournal of Human Genetics|March 7, 2024
Weighted burden analysis of rare coding variants in 470,000 exome-sequenced UK Biobank participants characterises effects on hyperlipidaemia riskDavid CurtisPageof 17