Genomic Analysis of Trichotillomania
ABSTRACT Trichotillomania (TTM) is a psychiatric condition in which people feel an overwhelming urge to pull out their hair, resulting in noticeable hair loss and significant distress. Twin and family studies suggest that TTM is at least partly genetic, but no genome‐wide analyses have been completed.
Matthew W. Halvorsen+4 more
wiley +1 more source
Effects of sumac aqueous extract along with eating and drinking modification on functional dyspepsia symptoms in comparison with omeprazole: An open-label, randomized, controlled clinical trial. [PDF]
Saravani M+4 more
europepmc +1 more source
The Effect of Missing Values for Covariates
Gary Whitlock, Taane G. Clark
openalex +1 more source
ABSTRACT The missense SNP NC_000004.12:g.102267552C>T (also known as SLC39A8.p.(Ala391Thr), rs13107325) in SLC39A8 encodes a zinc transporter. This SNP has been linked to schizophrenia and is the likely causal variant for one of the genome‐wide association loci associated with the disorder. Using regression analyses, we tested whether the schizophrenia‐
Sophie E. Smart+12 more
wiley +1 more source
Imaging features and prognostic significance of immune checkpoint inhibitor-related pneumonitis in NSCLC. [PDF]
Wang X+7 more
europepmc +1 more source
Adjusting power for a baseline covariate in linear models
Deborah H. Glueck, Keith E. Muller
openalex +2 more sources
Genetics of Response to ECT, TMS, Ketamine and Esketamine
ABSTRACT Treatment‐resistant mood disorders are often managed with intensive interventions that include electroconvulsive therapy (ECT), transcranial magnetic stimulation (TMS), ketamine, and esketamine, but the role of genetics in clinical response to those interventions is yet to be clearly determined.
Clio E. Franklin+18 more
wiley +1 more source
Considering landscape heterogeneity improves the inference of inter-individual interactions from movement data. [PDF]
Fronville T+4 more
europepmc +1 more source
Genome‐Wide Insights and Polygenic Risk Scores in Common Epilepsies: A Narrative Review
ABSTRACT The research of single gene‐related disorders or pathogenic copy‐number variations (CNVs) has given a significant impetus to the shift from a diagnostic work‐up focused on epileptic syndromes to genomic approaches in individuals with severe pediatric‐onset epilepsies and in developmental and epileptic encephalopathies.
Mario Mastrangelo+5 more
wiley +1 more source
A new method for dealing with collider bias in the PWP model for recurrent events in randomized controlled trials. [PDF]
Shi C+5 more
europepmc +1 more source