User profiles for C. O'Dushlaine

Colm O'Dushlaine

Head of Statistical Genetics, insitro
Verified email at insitro.com
Cited by 37014

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

…, EF Thelander, P Sullivan, DW Morris, CT O'Dushlaine… - Nature, 2009 - nature.com
Schizophrenia is a severe mental disorder with a lifetime risk of about 1%, characterized by
hallucinations, delusions and cognitive deficits, with heritability estimated at up to 80% 1 , 2 . …

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

S Ripke, C O'dushlaine, K Chambert, JL Moran… - Nature …, 2013 - nature.com
Schizophrenia is an idiopathic mental disorder with a heritable component and a substantial
public health impact. We conducted a multi-stage genome-wide association study (GWAS) …

A polygenic burden of rare disruptive mutations in schizophrenia

…, D Ruderfer, N Solovieff, P Roussos, C O'dushlaine… - Nature, 2014 - nature.com
Schizophrenia is a common disease with a complex aetiology, probably involving multiple
and heterogeneous genetic factors. Here, by analysing the exome sequences of 2,536 …

[HTML][HTML] Computationally efficient whole-genome regression for quantitative and binary traits

…, JA Kosmicki, A Ziyatdinov, C Benner, C O'Dushlaine… - Nature …, 2021 - nature.com
Genome-wide association analysis of cohorts with thousands of phenotypes is computationally
expensive, particularly when accounting for sample relatedness or population structure. …

[HTML][HTML] Genetic and pharmacologic inactivation of ANGPTL3 and cardiovascular disease

…, C O'Dushlaine, C Schurmann… - … England Journal of …, 2017 - Mass Medical Soc
Background Loss-of-function variants in the angiopoietin-like 3 gene (ANGPTL3) have been
associated with decreased plasma levels of triglycerides, low-density lipoprotein (LDL) …

[HTML][HTML] A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease

…, MD Still, S McCarthy, C O'Dushlaine… - … England Journal of …, 2018 - Mass Medical Soc
Background Elucidation of the genetic factors underlying chronic liver disease may reveal
new therapeutic targets. Methods We used exome sequence data and electronic health …

Biobank-driven genomic discovery yields new insight into atrial fibrillation biology

…, U Thorsteinsdottir, A Baras, C O'Dushlaine… - Nature …, 2018 - nature.com
To identify genetic variation underlying atrial fibrillation, the most common cardiac arrhythmia,
we performed a genome-wide association study of >1,000,000 people, including 60,620 …

Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study

…, L Habegger, JB Leader, SN Fetterolf, C O'Dushlaine… - Science, 2016 - science.org
… with HDL-C levels in African Americans (41, 42). Our results provide further evidence of a
role for CD36 in the modulation of HDL-C levels in individuals of European ancestry. …

[HTML][HTML] Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease

FE Dewey, V Gusarova, C O'Dushlaine… - … England Journal of …, 2016 - Mass Medical Soc
Background Higher-than-normal levels of circulating triglycerides are a risk factor for ischemic
cardiovascular disease. Activation of lipoprotein lipase, an enzyme that is inhibited by …

[HTML][HTML] Exome sequencing and characterization of 49,960 individuals in the UK Biobank

…, C O'Dushlaine, A Marcketta, J Staples, C Schurmann… - Nature, 2020 - nature.com
The UK Biobank is a prospective study of 502,543 individuals, combining extensive phenotypic
and genotypic data with streamlined access for researchers around the world 1 . Here …