Cargando…

Generalized Structured Component Analysis in candidate gene association studies: applications and limitations

Background: Generalized Structured Component Analysis (GSCA) is a component-based alternative to traditional covariance-based structural equation modelling. This method has previously been applied to test for association between candidate genes and clinical phenotypes, contrasting with traditional g...

Descripción completa

Detalles Bibliográficos
Autores principales:	Thompson, Paul A., Bishop, Dorothy V. M., Eising, Else, Fisher, Simon E., Newbury, Dianne F.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	F1000 Research Limited 2020
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818107/ https://www.ncbi.nlm.nih.gov/pubmed/33521327 http://dx.doi.org/10.12688/wellcomeopenres.15396.2

Ejemplares similares

Stage 1 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: protocol for a test of the double hit hypothesis
por: Newbury, Dianne F., et al.
Publicado: (2018)

Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis
por: Newbury, Dianne F., et al.
Publicado: (2021)

Using neuroimaging genomics to investigate the evolution of human brain structure
por: Alagöz, Gökberk, et al.
Publicado: (2022)

The Dyslexia Candidate Locus on 2p12 Is Associated with General Cognitive Ability and White Matter Structure
por: Scerri, Thomas S., et al.
Publicado: (2012)

Recent advances in the genetics of language impairment
por: Newbury, Dianne F, et al.
Publicado: (2010)

Generalized models for quantifying laterality using functional transcranial Doppler ultrasound
por: Thompson, Paul A., et al.
Publicado: (2022)

DCDC2, KIAA0319 and CMIP Are Associated with Reading-Related Traits
por: Scerri, Tom S., et al.
Publicado: (2011)

Generalized structured component analysis: a component-based approach to structural equation modeling
por: Hwang, Heungsun, et al.
Publicado: (2014)

Problems in using p-curve analysis and text-mining to detect rate of p-hacking and evidential value
por: Bishop, Dorothy V.M., et al.
Publicado: (2016)

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment
por: Chen, Xiaowei Sylvia, et al.
Publicado: (2017)

Candidate genes for limiting cholestatic intestinal injury identified by gene expression profiling
por: Alaish, Samuel M, et al.
Publicado: (2013)

Diffusion-Limited Processes in Hydrogels with Chosen Applications from Drug Delivery to Electronic Components
por: Lavrentev, Filipp V., et al.
Publicado: (2023)

Registered report: investigating a preference for certainty in conversation among autistic adults compared to dyslexic adults and the general population
por: Wilson, Alexander C., et al.
Publicado: (2020)

FOXP2
por: Nudel, Ron, et al.
Publicado: (2013)

Effect of apolipoprotein E polymorphism on cognition and brain in the Cambridge Centre for Ageing and Neuroscience cohort
por: Henson, Richard N., et al.
Publicado: (2020)

Fundamental limits in structured principal component analysis and how to reach them
por: Barbier, Jean, et al.
Publicado: (2023)

A randomized controlled trial of different methods of alcohol screening and brief intervention in routine probation settings: 12-month outcomes
por: Newbury-Birch, Dorothy, et al.
Publicado: (2012)

The shared genetic architecture and evolution of human language and musical rhythm
por: Alagöz, Gökberk, et al.
Publicado: (2023)

An experimental limit on the intrinsic charm component of the nucleon
por: Aubert, Jean-Jacques, et al.
Publicado: (1982)

Online incidental statistical learning of audiovisual word sequences in adults: a registered report
por: Kuppuraj, Sengottuvel, et al.
Publicado: (2018)

The understanding of complex syntax in children with Down syndrome
por: Frizelle, Pauline, et al.
Publicado: (2019)

Analysis of exome data in a UK cohort of 603 patients with syndromic orofacial clefting identifies causal molecular pathways
por: Wilson, Kate, et al.
Publicado: (2023)

Screening and brief alcohol intervention in routine primary care in the UK: 12-month outcomes
por: Kaner, Eileen, et al.
Publicado: (2012)

Epigenetic mechanisms in migraine: a promising avenue?
por: Eising, Else, et al.
Publicado: (2013)

Generalized Structured Component Analysis with Uniqueness Terms for Accommodating Measurement Error
por: Hwang, Heungsun, et al.
Publicado: (2017)

Candidates for Synergies: Linear Discriminants versus Principal Components
por: Vinjamuri, Ramana, et al.
Publicado: (2014)

Scorpion venom components as potential candidates for drug development
por: Ortiz, Ernesto, et al.
Publicado: (2015)

Are there any potentially dangerous pharmacological effects of combining ADHD medication with alcohol and drugs of abuse? A systematic review of the literature
por: Barkla, Xanthe M., et al.
Publicado: (2015)

Complex traits and candidate genes: estimation of genetic variance components across multiple genetic architectures
por: Feldmann, Mitchell J, et al.
Publicado: (2023)

Transcriptome Profiling of Wild Arachis from Water-Limited Environments Uncovers Drought Tolerance Candidate Genes
por: Brasileiro, Ana C. M., et al.
Publicado: (2015)

Schizophrenia Gene Networks and Pathways and Their Applications for Novel Candidate Gene Selection
por: Sun, Jingchun, et al.
Publicado: (2010)

Genetic structure and evolution of the Vps25 family, a yeast ESCRT-II component
por: Slater, Ruth, et al.
Publicado: (2006)

Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population
por: Paracchini, S, et al.
Publicado: (2011)

Reading and Language Disorders: The Importance of Both Quantity and Quality
por: Newbury, Dianne F., et al.
Publicado: (2014)

A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development
por: Eising, Else, et al.
Publicado: (2018)

A systematic strategy for the discovery of candidate genes responsible for phenotypic variation
por: Fisher, Paul, et al.
Publicado: (2007)

Generally Applicable Transformation Protocols for Fluorescent Nanodiamond Internalization into Cells
por: Hemelaar, Simon R., et al.
Publicado: (2017)

Generalized functions, convergence structures, and their applications
por: Stanković, Bogoljub, et al.
Publicado: (1988)

Generalized principal component analysis
por: Vidal, René, et al.
Publicado: (2016)

Investigation into inconsistent lateralisation of language functions as a potential risk factor for language impairment
por: Bradshaw, Abigail R., et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_i1bgpiohppkjsn5jjtmp42d3cv