Medicina Legal, Psiquiatría y Patología
Departamento
Université de Genève
Ginebra, SuizaPublicaciones en colaboración con investigadores/as de Université de Genève (10)
2022
-
A normative chart for cognitive development in a genetically selected population
Neuropsychopharmacology, Vol. 47, Núm. 7, pp. 1379-1386
-
Burden of non-communicable diseases among adolescents aged 10–24 years in the EU, 1990–2019: a systematic analysis of the Global Burden of Diseases Study 2019
The Lancet Child and Adolescent Health, Vol. 6, Núm. 6, pp. 367-383
-
Clinical high risk for psychosis paradigm for CAP: do not throw the baby out with the bathwater
European Child and Adolescent Psychiatry
2021
-
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
Molecular Psychiatry, Vol. 26, Núm. 8, pp. 4496-4510
2020
-
Clinical high risk for psychosis model in children and adolescents: a joint position statement of ESCAP Clinical Division and Research Academy
European Child and Adolescent Psychiatry
-
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
Nature Medicine, Vol. 26, Núm. 12, pp. 1912-1918
-
What electrophysiology tells us about Alzheimer's disease: a window into the synchronization and connectivity of brain neurons
Neurobiology of Aging, Vol. 85, pp. 58-73
2019
-
EUREXIT? High time to consider the merits of European collaboration in child and adolescent psychiatry
European Child and Adolescent Psychiatry
2018
-
Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome
American Journal of Medical Genetics, Part A, Vol. 176, Núm. 10, pp. 2182-2191
-
Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects
American Journal of Medical Genetics, Part A, Vol. 176, Núm. 10, pp. 2172-2181