Marta Ribasés
A5020539457- Attention Deficit Hyperactivity Disorder
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Autism Spectrum Disorder Research
- Bipolar Disorder and Treatment
- Neurotransmitter Receptor Influence on Behavior
- Eating Disorders and Behaviors
- Functional Brain Connectivity Studies
- Nerve injury and regeneration
- Child and Adolescent Psychosocial and Emotional Development
- Epigenetics and DNA Methylation
- Health, Environment, Cognitive Aging
- Diet and metabolism studies
- Obsessive-Compulsive Spectrum Disorders
- Cancer-related molecular mechanisms research
- Genetic Syndromes and Imprinting
- Cannabis and Cannabinoid Research
- Tryptophan and brain disorders
- Alcohol Consumption and Health Effects
- Suicide and Self-Harm Studies
- Substance Abuse Treatment and Outcomes
- Cognitive Abilities and Testing
- Migraine and Headache Studies
- Neural and Behavioral Psychology Studies
- Genomic variations and chromosomal abnormalities
Vall d'Hebron Institut de Recerca
2016-2025
Universitat Autònoma de Barcelona
2016-2025
Universitat de Barcelona
2006-2025
Instituto de Salud Carlos III
2014-2025
Centro de Investigación Biomédica en Red de Salud Mental
2016-2025
Centre for Biomedical Network Research on Rare Diseases
2014-2025
Vall d'Hebron Hospital Universitari
2016-2025
Medical Research Network
2012-2024
Women and Children’s Health Research Institute
2024
University of Alberta
2024
Several genes with an essential role in the regulation of eating behavior and body weight are considered candidates involved etiology disorders (ED), but no relevant susceptibility a major effect on anorexia nervosa (AN) or bulimia (BN) have been identified. Brain-derived neurotrophic factor (BDNF) has implicated food intake rodents. We previously reported strong association Met66 allele Val66Met BDNF variant restricting AN (ANR) low minimum mass index Spanish patients. Another single...
Long QT syndrome (LQTS) is a rare genetic disorder and major preventable cause of sudden cardiac death in the young. A causal variant with large effect size identified up to 80% probands (genotype positive) cascade family screening shows incomplete penetrance variants. Furthermore, proportion cases meeting diagnostic criteria for LQTS remain genetically elusive despite testing established genes negative). These observations raise possibility that common variants small contribute clinical...
This study investigated the psychological impact of coronavirus disease 2019 (COVID-19) among youth by analyzing their emotional/behavioral problems before and during long-lasting lockdown in Spain. For that purpose, 699 parents with children aged 6-17 552 adolescents 12-17, who completed parent adolescent version Strengths Difficulties Questionnaire at beginning 2019, responded to a survey from 26 May 15 June 2020 assessed well-being life conditions quarantine (i.e., sociodemographic...
Cluster headache (CH) is a highly disabling primary disorder with complex underlying mechanism. However, there are currently no effective targeted therapeutic drugs available. Existing medications often have limited efficacy and numerous side effects, which frequently fail to meet clinical needs. This study aims identify potential new targets for CH through proteome-wide mendelian randomization (PWMR). We used PWMR estimate the causal effects of plasma proteins on CH. analysis integrated...
Air pollution and greenness are emerging as modifiable risk protective factors, respectively, in child psychopathology. However, research shows inconsistencies. Here, we examined associations between air surrounding with internalizing externalizing behaviors. In addition, the potential modifying role of genetic susceptibility for these traits socioeconomic status (SES) was explored. This population-based study included 4485 schoolchildren aged 5-18 years from Spain. Internalizing behaviors...
Attention-deficit/hyperactivity disorder (ADHD) is a common and highly heritable developmental characterized by persistent impairing pattern of inattention and/or hyperactivity-impulsivity. Using families from genetic isolate, the Paisa population Colombia, five independent datasets four different populations (United States, Germany, Norway Spain), consistent association was recently reported between ADHD latrophilin 3 (LPHN3) gene, brain-specific member LPHN subfamily G-protein-coupled...