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A disanalogy with RCTs and its implications for second-generation causal knowledge.
Lynch, Kate E; Brown, Rachael L; Strasser, Jeremy; Yeo, Shang Long.
Afiliação
  • Lynch KE; Department of Philosophy, University of Sydney, Sydney, Australia kate.lynch@sydney.edu.au www.katelynch.net.
  • Brown RL; Charles Perkins Centre, University of Sydney, Sydney, Australia.
  • Strasser J; Centre for Philosophy of the Sciences, School of Philosophy, Australian National University, Canberra, Australia rachael.brown@anu.edu.auhttp://rachaelbrown.net.
  • Yeo SL; School of Philosophy, Australian National University, Canberra, Australia jeremy.strasser@anu.edu.au.
Behav Brain Sci ; 46: e194, 2023 09 11.
Article em En | MEDLINE | ID: mdl-37694935
ABSTRACT
We are less optimistic than Madole & Harden that family-based genome-wide association studies (GWASs) will lead to significant second-generation causal knowledge. Despite bearing some similarities, family-based GWASs and randomised controlled trials (RCTs) are not identical. Most RCTs assess a relatively homogenous causal stimulus as a treatment, whereas GWASs assess highly heterogeneous causal stimuli. Thus, GWAS results will not translate so easily into second-generation causal knowledge.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Conhecimento / Estudo de Associação Genômica Ampla Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Behav Brain Sci Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Conhecimento / Estudo de Associação Genômica Ampla Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Behav Brain Sci Ano de publicação: 2023 Tipo de documento: Article