Results 141 to 150 of about 541 (199)
Human Capital Disclosure and Labor Market Outcomes: Evidence from Regulation S‐K
Journal of Accounting Research, Volume 64, Issue 4, Page 1685-1731, September 2026.ABSTRACT We examine the labor market consequences of the 2020 Regulation S‐K requiring human capital disclosure in 10K filings. Using large‐sample job‐level data and a Generative Large Language Model (GLLM), we observe that public firms subject to the regulation increase their disclosure of diversity, equity, and inclusion (DEI) information in job ...
Jung Ho Choi, Dan Li, Daniele Macciocchi
wiley +1 more source
Developmental Science, Volume 29, Issue 5, September 2026.ABSTRACT Poor reading has been associated with impaired simultaneous visual processing of multiple graphic symbols composed of separable features, a behavioral marker of reduced visual attention based on parietal dysfunction. We designed a visual search screening test, consisting of finding the (unique) black circle among circles combined with a bar of
Audrey Vialatte +4 more
wiley +1 more source
Review for "Preparation of saccade sequences and eye programming affect endogenous covert attention" [PDF]
, 2019 +5 more sources
Saccades oculaires, adaptation sensori-motrice et attention visuo-spatiale [PDF]
, 2015 The interaction of human beings with their static or dynamic environment requires detailed and precise exploration of objects. For this, our oculomotor system produces fast and accurate eye movements called "saccades" to bring the image of objects of ...
Habchi, Ouazna
core +3 more sources
The cerebral correlates of set-shifting: an fMRI study of the trail making test
Arquivos de Neuro-Psiquiatria, 2002 The trail making test (TMT) pertains to a family of tests that tap the ability to alternate between cognitive categories. However, the value of the TMT as a localizing instrument remains elusive.
Moll Jorge +4 more
doaj
American Journal of Medical Genetics Part A, Volume 200, Issue 8, Page 1850-1855, August 2026.ABSTRACT Griscelli Syndrome Type 2 (GS2) is a rare autosomal recessive disorder caused by pathogenic mutations in the RAB27A gene. Typically, it is characterized by cutaneous hypopigmentation, immunodeficiency, with or without neurological abnormalities secondary to hemophagocytic lymphohistiocytosis (HLH). Without treatment, GS2 often results in fatal
Dzhoy Papingi +6 more
wiley +1 more source
Multimodel Diffusion MRI Signatures in Atypical Parkinsonian Disorders
Human Brain Mapping, Volume 47, Issue 11, 01 August 2026.We implemented a diffusion MRI framework to analyze clinically compatible multishell data across 123 participants, including controls, Parkinson's disease (PD), corticobasal syndrome (CBS), and progressive supranuclear palsy Richardson's syndrome (PSP‐RS). Diffusion models included DTI, free‐water elimination (FWE), NODDI, and fixel‐based analysis (FBA)
Yuqi Tian +5 more
wiley +1 more source
Pre-saccadic Attention (and not Arousal) modulates the Size-Eccentricity Effect
Scientific ReportsPeripherally located objects are often perceived to be smaller than centrally located objects. This perceptual phenomenon, known as the Size-Eccentricity Effect (SEE), is mainly due to the structural properties of the visual system and is further ...
Jad Laaboudi +2 more
doaj +1 more source
Journal of Personality, Volume 94, Issue 4, Page 640-652, August 2026.ABSTRACT Introduction Alexithymia refers to difficulties in experiencing and expressing emotions, differentiating them from bodily sensations, restricted imagination, and externally oriented thinking. Mood and affective symptoms are often confounded with alexithymia due to the typical assessment through self‐report.
Jiyeon Seo +4 more
wiley +1 more source