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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

Genetic susceptibility factors in attention- deficit/hyperactivity disorder (ADHD): a two stage genome-wide association study

IP: Marta Ribases Haro
Collaborators: -
Funding agency: Fundació La Marató de TV3
Funding: 149712.5
Reference: MARATV3/2009/01
Duration: 01/01/2010 - 31/12/2013

Genetic susceptibility factors in Attention-Deficit/Hiperactivity Disorder (ADHD)

IP: Marta Ribases Haro
Collaborators: -
Funding agency: Instituto de Salud Carlos III
Funding: 44700
Reference: CP09/00119
Duration: 01/01/2010 - 31/12/2012

Genetic susceptibility factors in attention-deficit/hiperactivity disorder (ADHD)

IP: Miquel Casas Brugué
Collaborators: Marta Ribases Haro
Funding agency: Instituto de Salud Carlos III
Funding: 243000
Reference: MS09/00119
Duration: 14/01/2010 - 13/01/2016

El test de apomorfina como marcador biológico de recaídas en pacientes dependientes de cocaína.

IP: Miquel Casas Brugué
Collaborators: Marta Ribases Haro
Funding agency: Ministerio de Ciencia e Innovación-MICINN
Funding: 96000
Reference: JDCI0300888
Duration: 01/01/2007 - 13/01/2010

Ministerio de Ciencia

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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