User profiles for Cathryn M Lewis
Cathryn LewisProfessor of Genetic Epidemiology & Statistics, King's College London Verified email at kcl.ac.uk Cited by 136708 |
Localization of a Breast Cancer Susceptibility Gene, BRCA2, to Chromosome 13q12-13
A small proportion of breast cancer, in particular those cases arising at a young age, is due
to the inheritance of dominant susceptibility genes conferring a high risk of the disease. A …
to the inheritance of dominant susceptibility genes conferring a high risk of the disease. A …
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
Major depression is a debilitating psychiatric illness that is typically associated with low
mood and anhedonia. Depression has a heritable component that has remained difficult to …
mood and anhedonia. Depression has a heritable component that has remained difficult to …
[PDF][PDF] Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia
CM Lewis, DF Levinson, LH Wise, LE DeLisi… - The American Journal of …, 2003 - cell.com
Schizophrenia is a common disorder with high heritability and a 10-fold increase in risk to
siblings of probands. Replication has been inconsistent for reports of significant genetic …
siblings of probands. Replication has been inconsistent for reports of significant genetic …
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility
…, D Strachan, G Bethel, C Bryan, CM Lewis… - Nature …, 2007 - nature.com
A genome-wide association scan in individuals with Crohn's disease by the Wellcome Trust
Case Control Consortium detected strong association at four novel loci. We tested 37 SNPs …
Case Control Consortium detected strong association at four novel loci. We tested 37 SNPs …
PRSice: polygenic risk score software
A polygenic risk score (PRS) is a sum of trait-associated alleles across many genetic loci,
typically weighted by effect sizes estimated from a genome-wide association study. The …
typically weighted by effect sizes estimated from a genome-wide association study. The …
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
Stroke has multiple etiologies, but the underlying genes and pathways are largely unknown.
We conducted a multiancestry genome-wide-association meta-analysis in 521,612 …
We conducted a multiancestry genome-wide-association meta-analysis in 521,612 …
Suberoylanilide hydroxamic acid, a histone deacetylase inhibitor, ameliorates motor deficits in a mouse model of Huntington's disease
Huntington's disease (HD) is an inherited, progressive neurological disorder that is caused
by a CAG/polyglutamine repeat expansion and for which there is no effective therapy. Recent …
by a CAG/polyglutamine repeat expansion and for which there is no effective therapy. Recent …
The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease
BACKGROUND &AIMS:: Mutations in the NOD2 gene are strongly associated with
susceptibility to Crohn's disease (CD). We analyzed a large cohort of European patients with …
susceptibility to Crohn's disease (CD). We analyzed a large cohort of European patients with …
Meta-analysis of the association between the level of cannabis use and risk of psychosis
A Marconi, M Di Forti, CM Lewis… - Schizophrenia …, 2016 - academic.oup.com
Cannabis use has been reported to induce long-lasting psychotic disorders and a dose-response
relationship has been observed. We performed a systematic review of studies that …
relationship has been observed. We performed a systematic review of studies that …
[HTML][HTML] Polygenic risk scores: from research tools to clinical instruments
Genome-wide association studies have shown unequivocally that common complex disorders
have a polygenic genetic architecture and have enabled researchers to identify genetic …
have a polygenic genetic architecture and have enabled researchers to identify genetic …