Results 191 to 200 of about 484,885 (328)
Etiology of longitudinal associations between subjective effects and substance use disorders in a clinical sample. [PDF]
Gresko SA +5 more
europepmc +1 more source
M. Feinberg, A. Solmeyer, S. McHale
semanticscholar +1 more source
ABSTRACT Migrant healthcare workers in Australia find themselves at the centre of three intersecting concerns, often presented as ‘crises’ in contemporary discourse: the ‘care crisis’, the ‘housing crisis’ and the ‘migration crisis.’ Yet their own perspectives on these issues are rarely foregrounded. This paper explores the role of homeownership in the
Leah Williams Veazey
wiley +1 more source
Transdiagnostic Neurocognitive Endophenotypes for Schizophrenia, Bipolar I Disorder and a Broad Psychosis/Bipolar I Disorder Phenotype: A Mega-Analysis of Twin and Sibling Data. [PDF]
Kravariti E +19 more
europepmc +1 more source
Theoretical Perspectives on Sibling Relationships.
S. Whiteman, S. McHale, A. Soli
semanticscholar +1 more source
Objective Mutations in TARDBP (encoding TDP‐43) are associated with the neurodegenerative disease amyotrophic lateral sclerosis (ALS) and include familial missense mutations where there are a lack of models and mechanisms examining how they are pathogenic.
Ziyaan A. Harji +10 more
wiley +1 more source
The National Longitudinal Study of Adolescent Health (Add Health) Sibling Pairs Data
K. Harris +3 more
semanticscholar +1 more source
Diverse Genetic Etiologies of Unilateral Polymicrogyria
Objective Polymicrogyria (PMG) is one of the most common human malformations of cortical development and is often classified by its radiographic pattern of distribution. Unilateral polymicrogyria (uPMG) is a subtype of PMG affecting a portion or all of one cerebral hemisphere.
Abbe Lai +21 more
wiley +1 more source
Attachment network, interparental conflict, and older siblings' behavior predicting toddler behavior problems. [PDF]
Al Bcherraoui M +3 more
europepmc +1 more source
Fibroblast Transcriptomics in Molecular Diagnostics of a Comprehensive Dystonia Cohort
Objective Genomic sequencing leaves >50% of dystonia‐affected individuals without a diagnosis. Where DNA‐oriented approaches remain insufficient, integrating multiomics is essential to advance genome interpretation. Herein, we incorporated RNA sequencing (RNA‐seq) data from 167 patients with dystonia across a range of ages and presentations. Methods We
Alice Saparov +42 more
wiley +1 more source

