Skip to content
DraconiticResearch
Search Sources API
203,948 studies31 sourcesUpdated 40 min ago
Peer-reviewedCC BYFrontiers in human neuroscience

Vision In SyndrOmic Neurodevelopmental disorders-15q (VISiON-15q) study: eye tracking to supplement clinical examination for detection of cerebral/cortical visual impairment in children with Angelman and Duplication of 15q Syndromes

  1. 1Division of Ophthalmology, Department of Surgery, Children’s Hospital Los Angeles , , ,
  2. 2Department of Pediatrics, Children’s Hospital Los Angeles , , ,
  3. 3Department of Pediatrics, University of California, Los Angeles , , ,

Related

  1. KATNAL2 dysfunction impairs microtubule dynamics and contributes to syndromic neurodevelopmental disease.
    Ece Sönmezler, Semra Hız Kurul, Ozlem Erez +9
    Human molecular geneticsPeer-reviewedCC BY-NCFull textGenetics & genomicsEurope PMC
  2. Growth Impairment and Neurodevelopmental Features in Kabuki Syndrome Type 2: A Case Report With a Novel KDM6A Frameshift Mutation
    Sayan Najafzade, Haneieh Honarmand, Mortaza Bonyadi +1
    Case Reports in PediatricsPeer-reviewedCC BY 4.0Full textGenetics & genomicsPMC
  3. Unravelling the role of IRX4 variants in non-syndromic and Down syndrome associated congenital heart disease
    J. Maddhesiya, K. Jain, D. Jain +3
    bioRxivPreprintAll rights reservedFull textGenetics & genomicsbioRxiv
  4. Altered keratinization and vitamin D metabolism may be key pathogenetic pathways in syndromic hidradenitis suppurativa: a novel whole exome sequencing approach
    Lucas Brandao, Ronald Moura, Paola Maura Tricarico +7
    Journal of Dermatological SciencePeer-reviewedLicence not statedFull text43 citedGeneral biologyHAL
  5. Microduplication of the ARID1A gene causes intellectual disability with recognizable syndromic features
    Marie Bidart, Michèle El Atifi, Sarra Miladi +18
    Genetics in MedicinePeer-reviewedLicence not statedFull text17 citedGenetics & genomicsHAL
BibTeX
@article{chang2026vision,
  title = {{Vision In SyndrOmic Neurodevelopmental disorders-15q (VISiON-15q) study: eye tracking to supplement clinical examination for detection of cerebral/cortical visual impairment in children with Angelman and Duplication of 15q Syndromes}},
  author = {Melinda Y. Chang and Sydney Jacobs and Katherine Granger and Anna Achenbach and Charlotte DiStefano and Shafali S. Jeste},
  journal = {Frontiers in human neuroscience},
  year = {2026},
  month = oct,
  url = {https://europepmc.org/article/PMC/PMC13658069},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Vision In SyndrOmic Neurodevelopmental disorders-15q (VISiON-15q) study: eye tracking to supplement clinical examination for detection of cerebral/cortical visual impairment in children with Angelman and Duplication of 15q Syndromes
AU  - Melinda Y. Chang
AU  - Sydney Jacobs
AU  - Katherine Granger
AU  - Anna Achenbach
AU  - Charlotte DiStefano
AU  - Shafali S. Jeste
PY  - 2026
DA  - 2026/10/16
JO  - Frontiers in human neuroscience
UR  - https://europepmc.org/article/PMC/PMC13658069
SN  - 1662-5161
ER  -