User profiles for S. E. Legge
Sophie E LeggeCardiff University Verified email at cardiff.ac.uk Cited by 16661 |
Genetic architecture of schizophrenia: a review of major advancements
SE Legge, ML Santoro, S Periyasamy… - Psychological …, 2021 - cambridge.org
Schizophrenia is a severe psychiatric disorder with high heritability. Consortia efforts and
technological advancements have led to a substantial increase in knowledge of the genetic …
technological advancements have led to a substantial increase in knowledge of the genetic …
[HTML][HTML] Genomic findings in schizophrenia and their implications
There has been substantial progress in understanding the genetics of schizophrenia over
the past 15 years. This has revealed a highly polygenic condition with the majority of the …
the past 15 years. This has revealed a highly polygenic condition with the majority of the …
Schizophrenia polygenic risk and experiences of childhood adversity: a systematic review and meta-analysis
… Sophie E Legge Sophie E Legge … Grace E Woolway, Sophie E Smart, Amy J Lynham,
Jennifer L Lloyd, Michael J Owen, Ian R Jones, James TR Walters, Sophie E Legge, Schizophrenia …
Jennifer L Lloyd, Michael J Owen, Ian R Jones, James TR Walters, Sophie E Legge, Schizophrenia …
[PDF][PDF] Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases
…, AK Kähler, C Laurent, JLC Keong, SE Legge… - The American Journal of …, 2014 - cell.com
… g while accounting for error correlations (referred to here as the analytical SE27). All … We
evaluated the accuracy of the analytical SE for both quantitative and ascertained traits and …
evaluated the accuracy of the analytical SE for both quantitative and ascertained traits and …
[PDF][PDF] Modeling linkage disequilibrium increases accuracy of polygenic risk scores
…, C Laurent, JLC Keong, SH Lee, SE Legge… - The american journal of …, 2015 - cell.com
Polygenic risk scores have shown great promise in predicting complex disease risk and will
become more accurate as training sample sizes increase. The standard approach for …
become more accurate as training sample sizes increase. The standard approach for …
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Copy number variants (CNVs) have been strongly implicated in the genetic etiology of
schizophrenia (SCZ). However, genome-wide investigation of the contribution of CNV to risk has …
schizophrenia (SCZ). However, genome-wide investigation of the contribution of CNV to risk has …
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
Schizophrenia is a debilitating psychiatric condition often associated with poor quality of life
and decreased life expectancy. Lack of progress in improving treatment outcomes has been …
and decreased life expectancy. Lack of progress in improving treatment outcomes has been …
Analysis of copy number variations at 15 schizophrenia-associated loci
…, G Mahoney-Davies, SE Legge… - The British Journal of …, 2014 - cambridge.org
BackgroundA number of copy number variants (CNVs) have been suggested as susceptibility
factors for schizophrenia. For some of these the data remain equivocal, and the frequency …
factors for schizophrenia. For some of these the data remain equivocal, and the frequency …
[HTML][HTML] The penetrance of copy number variations for schizophrenia and developmental delay
…, AL Richards, KD Chambert, G Davies, SE Legge… - Biological …, 2014 - Elsevier
Background Several recurrent copy number variants (CNVs) have been shown to increase
the risk of developing schizophrenia (SCZ), developmental delay (DD), autism spectrum …
the risk of developing schizophrenia (SCZ), developmental delay (DD), autism spectrum …
A comparison of ten polygenic score methods for psychiatric disorders applied across multiple cohorts
…, AK Kähler, C Laurent, J Lee, SH Lee, SE Legge… - Biological …, 2021 - Elsevier
Background Polygenic scores (PGSs), which assess the genetic risk of individuals for a disease,
are calculated as a weighted count of risk alleles identified in genome-wide association …
are calculated as a weighted count of risk alleles identified in genome-wide association …