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Marta Ribases Haro

Institutions of which they are part

Main researcher
Psychiatry, Mental Health and Addictions
Vall Hebron Institut de Recerca

Marta Ribases Haro

Institutions of which they are part

Main researcher
Psychiatry, Mental Health and Addictions
Vall Hebron Institut de Recerca

Projects

Identificació de factors de risc en el Trastorn per Dèficit d'Atenció amb Hiperactivitat (TDAH) a través de l'estudi del perfil de metilació d'ADN a escala genòmica

IP: Marta Ribases Haro
Collaborators: -
Funding agency: Agència Gestió Ajuts Universitaris i de Recerca
Funding: 45600
Reference: 2016 FI_B 00899
Duration: 01/03/2016 - 28/02/2019

Bases biológicas subyacentes al Trastorno por Déficit de Atención con Hiperactividad (TDAH)

IP: Miquel Casas Brugué
Collaborators: Marta Ribases Haro
Funding agency: Instituto de Salud Carlos III
Funding: 101250
Reference: CPII15/00023
Duration: 14/01/2016 - 13/01/2019

Factors genètics de susceptibilitat al Transtorn per Dèficit d'Atenció amb Hiperactivitat

IP: Marta Ribases Haro
Collaborators: -
Funding agency: Instituto de Salud Carlos III
Funding: 80598
Reference: CD15/00199
Duration: 01/01/2016 - 31/12/2018

CoCA: Comorbid Conditions of Attention deficit / hyperactivity disorder

IP: José Antonio Ramos Quiroga
Collaborators: Marta Ribases Haro, Pol Ibañez Jimenez
Funding agency: EUROPEAN COMMISSION
Funding: 326996.25
Reference: COCA_H2020-PHC2015
Duration: 01/01/2016 - 30/06/2022

Related news

Over the course of one week, it will host in-person assessments for 35 families to better understand the progression of the disease and contribute to the development of new therapies.

A project led by the Vall d’Hebron Research Institute (VHIR) in collaboration with FIDMAG Germanes Hospitalàries Research Foundation describes structural and functional brain changes in adolescents with borderline personality disorder (BPD).

A large-scale study involving Vall d’Hebron confirms the genetic relatedness among 14 different psychiatric disorders and groups them into five new families, paving the way for new treatments targeting their shared underlying genetic causes

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