Laura S. Cubit

ORCID: 0000-0002-3558-5614
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About
Contact & Profiles
Research Areas
  • Folate and B Vitamins Research
  • Memory and Neural Mechanisms
  • Parkinson's Disease Mechanisms and Treatments
  • Face recognition and analysis
  • Cardiomyopathy and Myosin Studies
  • Autism Spectrum Disorder Research
  • Speech and Audio Processing
  • Child and Animal Learning Development
  • Neural and Behavioral Psychology Studies
  • Bioinformatics and Genomic Networks
  • Face and Expression Recognition
  • Obsessive-Compulsive Spectrum Disorders
  • Amino Acid Enzymes and Metabolism
  • Genetic Associations and Epidemiology
  • Muscle metabolism and nutrition
  • Behavioral and Psychological Studies

Children's Hospital of Philadelphia
2021-2023

University of Pennsylvania
2023

Center for Autism and Related Disorders
2022

University of Rochester
2019-2021

Abstract Background Autistic individuals frequently experience social communication challenges. Girls are diagnosed with autism less often than boys even when their symptoms equally severe, which may be due to insufficient understanding of the way manifests in girls. Differences behavioral presentation autism, including how people talk about topics, could contribute these persistent problems identification. Despite a growing body research suggesting that autistic girls and present distinct...

10.1186/s13229-021-00483-1 article EN cc-by Molecular Autism 2022-01-10

How do children allocate their attention? There is too much information in the world to encode it all, so must pick and choose. they organize sampling make most of learning opportunities that surround them? Previous work shows infants actively seek intermediately predictable information. Here we employ eye-tracking computational modeling examine impact stimulus predictability across early childhood (ages 3-6 years, n = 72, predominantly Non-Hispanic White, middle- upper-middle-income), by...

10.1111/cdev.13536 article EN Child Development 2021-01-08

Creatine transporter deficiency (CTD) is a rare X-linked disorder of creatine transport caused by pathogenic variants in SLC6A8 (Xq28). The marked developmental delay, especially speech delay. biomarkers Aβ40, Aβ42 and total tau are abnormal Alzheimer disease (AD), common neurodegenerative pathologically characterized Aβ peptide containing amyloid plaques neurofibrillary tangles. Although CTD results neuronal energy deficiency, the pathological processes underlying phenotype not fully...

10.1016/j.ymgmr.2023.101001 article EN cc-by-nc-nd Molecular Genetics and Metabolism Reports 2023-08-21

3D morphable models (3DMMs) simultaneously reconstruct facial morphology, expression and pose from 2D images, thus could be an invaluable tool for capturing characterizing the face behavior in early childhood. However, 3DMM fitting on infants is a largely unexplored problem. All publicly available 3DMMs are developed adults, it unclear if to what extent they can used videos of infants. In this paper, we compare five state-of-the-art methods data naturalistic infant-caregiver interactions....

10.2312/3dor.20221178 article EN PubMed 2022-09-01
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