Maria Capovilla

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 6

Top Topics

Autism Spectrum Disorder

Network Analysis

Drosophila Melanogaster

Top Venues

International journal of molecular sciences

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Sara Milojevic, Arijit Ghosh, Vedrana Makevic, Maja Stojkovic, Maria Capovilla, Tomislav B Tosti, Dejan B Budimirovic, Dragana D Protic
Circadian Rhythm and Sleep Analyses in a Fruit Fly Model of Fragile X Syndrome Using a Video-Based Automated Behavioral Research System. International journal of molecular sciences 25 (14) (2024)
Maja Stojkovic, Milan Petrovic, Maria Capovilla, Sara Milojevic, Vedrana Makevic, Dejan B Budimirovic, Louise Corscadden, Shuhan He, Dragana D Protic
Using a Combination of Novel Research Tools to Understand Social Interaction in the Drosophila melanogaster Model for Fragile X Syndrome. Biology 13 (6) (2024)
Sara Milojevic, Arijit Ghosh, Vedrana Makevic, Maja Stojkovic, Maria Capovilla, Tomislav B Tosti, Dejan B Budimirovic, Dragana D Protic
Circadian Rhythm and Sleep Analyses in a Fruit Fly Model of Fragile X Syndrome Using a Video-Based Automated Behavioral Research System. International journal of molecular sciences 25 (14) (2024)
Maja Stojkovic, Milan Petrovic, Maria Capovilla, Sara Milojevic, Vedrana Makevic, Dejan B Budimirovic, Louise Corscadden, Shuhan He, Dragana D Protic
Using a Combination of Novel Research Tools to Understand Social Interaction in the Drosophila melanogaster Model for Fragile X Syndrome. Biology 13 (6) (2024)
Sara Milojevic, Arijit Ghosh, Vedrana Makevic, Maja Stojkovic, Maria Capovilla, Tomislav B Tosti, Dejan B Budimirovic, Dragana D Protic
Circadian Rhythm and Sleep Analyses in a Fruit Fly Model of Fragile X Syndrome Using a Video-Based Automated Behavioral Research System. International journal of molecular sciences 25 (14) (2024)
Arnaud Fernandez, Małgorzata Drozd, Susanne Thümmler, Barbara Bardoni, Florence Askenazy, Maria Capovilla
A novel microduplication in INPP5A segregates with schizophrenia spectrum disorder in the family of a patient with both childhood onset schizophrenia and autism spectrum disorder. American journal of medical genetics. Part A 185 (6) (2021)